CSDB: Search results

Found 1 organism. Displayed organism 1
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1. (Organism ID: 220)

(bacteria)

on a lifemap

(NCBI TaxID 2, species name lookup)

Taxonomic group: bacteria

The following compound(s) are assigned to this organism:

Compound ID: 387

Leg5Ac7Ac Show graphically

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Structure type: monomer
Reference(s) to other database(s): GTC:G31304UF, GlycomeDB:25214

Carbohydrate Research 2001, "Synthesis and NMR spectroscopy of nine stereoisomeric 5,7-diacetamido-3,5,7,9-tetradeoxynon-2-ulosonic acids"
CSDB ID 5239 (all data & tools)
Compound ID: 486

Pse5Ac7Ac Show graphically

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Structure type: monomer
Reference(s) to other database(s): GTC:G78417LS

Carbohydrate Research 2001, "Synthesis and NMR spectroscopy of nine stereoisomeric 5,7-diacetamido-3,5,7,9-tetradeoxynon-2-ulosonic acids"
CSDB ID 5349 (all data & tools)
Compound ID: 384

8eLeg5Ac7Ac Show graphically

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Structure type: monomer
Reference(s) to other database(s): GTC:G49224VH, GlycomeDB:37732

Carbohydrate Research 2001, "Synthesis and NMR spectroscopy of nine stereoisomeric 5,7-diacetamido-3,5,7,9-tetradeoxynon-2-ulosonic acids"
CSDB ID 5350 (all data & tools)
Compound ID: 487

4eLeg5Ac7Ac Show graphically

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Structure type: monomer
Reference(s) to other database(s): GTC:G80495ES

Carbohydrate Research 2001, "Synthesis and NMR spectroscopy of nine stereoisomeric 5,7-diacetamido-3,5,7,9-tetradeoxynon-2-ulosonic acids"
CSDB ID 5351 (all data & tools)
Compound ID: 488

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Structure type: monomer
Reference(s) to other database(s): GTC:G14692IW

Carbohydrate Research 2001, "Synthesis and NMR spectroscopy of nine stereoisomeric 5,7-diacetamido-3,5,7,9-tetradeoxynon-2-ulosonic acids"
CSDB ID 5352 (all data & tools)
Compound ID: 489

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Structure type: monomer
Reference(s) to other database(s): GTC:G76203DH

Carbohydrate Research 2001, "Synthesis and NMR spectroscopy of nine stereoisomeric 5,7-diacetamido-3,5,7,9-tetradeoxynon-2-ulosonic acids"
CSDB ID 5353 (all data & tools)
Compound ID: 490

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Structure type: monomer
Reference(s) to other database(s): GTC:G75658TV

Carbohydrate Research 2001, "Synthesis and NMR spectroscopy of nine stereoisomeric 5,7-diacetamido-3,5,7,9-tetradeoxynon-2-ulosonic acids"
CSDB ID 5354 (all data & tools)
Compound ID: 491

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Structure type: monomer
Reference(s) to other database(s): GTC:G02144SU

Carbohydrate Research 2001, "Synthesis and NMR spectroscopy of nine stereoisomeric 5,7-diacetamido-3,5,7,9-tetradeoxynon-2-ulosonic acids"
CSDB ID 5355 (all data & tools)
Compound ID: 492

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Structure type: monomer
Reference(s) to other database(s): GTC:G52174ZG

Carbohydrate Research 2001, "Synthesis and NMR spectroscopy of nine stereoisomeric 5,7-diacetamido-3,5,7,9-tetradeoxynon-2-ulosonic acids"
CSDB ID 5356 (all data & tools)
Compound ID: 834

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Structure type: oligomer
Trivial name: Lewis X, Lewis x antigen
Compound class: LOS
Reference(s) to other database(s): GTC:G13314IB, GlycomeDB:1738

Glycoconjugate Journal 2000, "Progress in deciphering the information content of the 'glycome' - a crescendo in the closing years of the millennium"
CSDB ID 6940 (all data & tools)
Compound ID: 58

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Structure type: oligomer
Trivial name: Lewisa, Lewis a
Reference(s) to other database(s): GTC:G05450JY, GlycomeDB:1403

Glycoconjugate Journal 2000, "Progress in deciphering the information content of the 'glycome' - a crescendo in the closing years of the millennium"
CSDB ID 6941 (all data & tools)
Compound ID: 835

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Structure type: oligomer
Trivial name: 3'-sialyl-LeX
Reference(s) to other database(s): GTC:G82999RZ, GlycomeDB:1801

Glycoconjugate Journal 2000, "Progress in deciphering the information content of the 'glycome' - a crescendo in the closing years of the millennium"
CSDB ID 6942 (all data & tools)
Compound ID: 836

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Structure type: oligomer
Trivial name: 3'-sialyl-LeA
Reference(s) to other database(s): GTC:G68569PY, GlycomeDB:1804

Glycoconjugate Journal 2000, "Progress in deciphering the information content of the 'glycome' - a crescendo in the closing years of the millennium"
CSDB ID 6943 (all data & tools)
Compound ID: 837

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Structure type: oligomer
Trivial name: 3'-sulfo-LeX
Reference(s) to other database(s): GTC:G45489TR, GlycomeDB:1803

Glycoconjugate Journal 2000, "Progress in deciphering the information content of the 'glycome' - a crescendo in the closing years of the millennium"
CSDB ID 6944 (all data & tools)
Compound ID: 838

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Structure type: oligomer
Trivial name: 3'-sulfo-LeA
Reference(s) to other database(s): GTC:G58032OK, GlycomeDB:8865

Glycoconjugate Journal 2000, "Progress in deciphering the information content of the 'glycome' - a crescendo in the closing years of the millennium"
CSDB ID 6945 (all data & tools)
Compound ID: 839

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Structure type: oligomer
Trivial name: 6'-sulfo-sialyl-LeX
Reference(s) to other database(s): GTC:G77659VW, GlycomeDB:24829

Glycoconjugate Journal 2000, "Progress in deciphering the information content of the 'glycome' - a crescendo in the closing years of the millennium"
CSDB ID 6946 (all data & tools)
Compound ID: 840

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Structure type: oligomer
Trivial name: 6-sulfo-sialyl-LeX
Reference(s) to other database(s): GTC:G66194LI, GlycomeDB:1883

Glycoconjugate Journal 2000, "Progress in deciphering the information content of the 'glycome' - a crescendo in the closing years of the millennium"
CSDB ID 6947 (all data & tools)

Compound ID: 841

Compound 841

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Compound ID: 972

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Structure type: oligomer
Reference(s) to other database(s): GTC:G76375NR, GlycomeDB:27121

Chemical and Pharmaceutical Bulletin 1995, "Syntheses of three interglycosidic isomers of N-acetyl-b-D-mannosaminyl-L-rhamnoses associated with O-antigens of several gram-negative opportunistic pathogens"
CSDB ID 7224 (all data & tools)
Compound ID: 1604

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Structure type: monomer
Trivial name: componente of O-antigen, GDP-L-colitose
Compound class: nucleoside diphosphate sugar

Biochemistry 2004, "Biosynthesis of colitose: Expression, purification, and mechanistic characterization of GDP-4-keto-6-deoxy-D-mannose-3-dehydrase (ColD) and GDP-l-colitose synthase (ColC)"
CSDB ID 9218 (all data & tools)
Compound ID: 844

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Structure type: polymer chemical repeating unit
Trivial name: alginate, alginate oligosaccharide, alginic acid
Compound class: EPS
Reference(s) to other database(s): GTC:G94988EU, GlycomeDB:25989

Carbohydrate Research 2004, "Preparation and structure elucidation of alginate oligosaccharides degraded by alginate lyase from Vibro sp. 510"
CSDB ID 9241 (all data & tools)
Compound ID: 1638

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Structure type: oligomer
Reference(s) to other database(s): GTC:G35274JV

Carbohydrate Research 2004, "Preparation and structure elucidation of alginate oligosaccharides degraded by alginate lyase from Vibro sp. 510"
CSDB ID 9468 (all data & tools)
Compound ID: 1639

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Structure type: oligomer
Reference(s) to other database(s): GTC:G43351IL

Carbohydrate Research 2004, "Preparation and structure elucidation of alginate oligosaccharides degraded by alginate lyase from Vibro sp. 510"
CSDB ID 9469 (all data & tools)
Compound ID: 1640

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Structure type: oligomer
Reference(s) to other database(s): GTC:G10034GW

Carbohydrate Research 2004, "Preparation and structure elucidation of alginate oligosaccharides degraded by alginate lyase from Vibro sp. 510"
CSDB ID 9470 (all data & tools)
Compound ID: 1641

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Structure type: oligomer
Reference(s) to other database(s): GTC:G35635XI

Carbohydrate Research 2004, "Preparation and structure elucidation of alginate oligosaccharides degraded by alginate lyase from Vibro sp. 510"
CSDB ID 9471 (all data & tools)
Compound ID: 1642

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Structure type: oligomer
Reference(s) to other database(s): GTC:G90412UL

Carbohydrate Research 2004, "Preparation and structure elucidation of alginate oligosaccharides degraded by alginate lyase from Vibro sp. 510"
CSDB ID 9472 (all data & tools)
Compound ID: 1643

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Structure type: oligomer
Reference(s) to other database(s): GTC:G40854NE

Carbohydrate Research 2004, "Preparation and structure elucidation of alginate oligosaccharides degraded by alginate lyase from Vibro sp. 510"
CSDB ID 9473 (all data & tools)
Compound ID: 1644

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Structure type: oligomer
Reference(s) to other database(s): GTC:G75562DR

Carbohydrate Research 2004, "Preparation and structure elucidation of alginate oligosaccharides degraded by alginate lyase from Vibro sp. 510"
CSDB ID 9474 (all data & tools)
Compound ID: 2058

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Structure type: monomer
Reference(s) to other database(s): GTC:G46605HW, GlycomeDB:25193

Carbohydrate Research 1996, "The synthesis of five L-glycero-D-manno-heptose monophosphates"
CSDB ID 448 (all data & tools)
Compound ID: 2059

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Structure type: monomer
Reference(s) to other database(s): GlycomeDB:25194

Carbohydrate Research 1998, "Five monophosphates of methyl L-glycero-a-D-manno-heptopyranoside: synthesis, hydrolysis and migrations"
CSDB ID 449 (all data & tools)
Compound ID: 2067

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Structure type: oligomer
Aglycon: 4-methoxyphenyl
Reference(s) to other database(s): GTC:G35556TW, GlycomeDB:25201

Carbohydrate Research 1998, "Synthesis of hyaluronic-acid-related oligosaccharides and analogues, as their 4-methoxyphenyl glycosides, having N-acetyl-b-D-glucosamine at the reducing end"
CSDB ID 473 (all data & tools)
Compound ID: 2088

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Structure type: oligomer ; 597.6
Reference(s) to other database(s): GlycomeDB:5576

Biochemistry 1999, "NMR experiments reveal distinct antibody-bound conformations of a synthetic disaccharide representing a general structural element of bacterial lipopolysaccharide epitopes"
CSDB ID 496 (all data & tools)
Compound ID: 2102

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Structure type: monomer
Reference(s) to other database(s): GTC:G47272XX, GlycomeDB:25225

Carbohydrate Research 1996, "The synthesis of five L-glycero-D-manno-heptose monophosphates"
CSDB ID 513 (all data & tools)
Compound ID: 2103

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Structure type: monomer
Reference(s) to other database(s): GTC:G66328OX, GlycomeDB:25226

Carbohydrate Research 1996, "The synthesis of five L-glycero-D-manno-heptose monophosphates"
CSDB ID 514 (all data & tools)
Compound ID: 2104

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Structure type: monomer
Reference(s) to other database(s): GTC:G60290GH, GlycomeDB:25227

Carbohydrate Research 1996, "The synthesis of five L-glycero-D-manno-heptose monophosphates"
CSDB ID 515 (all data & tools)
Compound ID: 2105

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Structure type: monomer
Reference(s) to other database(s): GTC:G84872CU, GlycomeDB:25228

Carbohydrate Research 1996, "The synthesis of five L-glycero-D-manno-heptose monophosphates"
CSDB ID 516 (all data & tools)

Compound ID: 2106

Compound 2106

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Compound ID: 2138

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Structure type: oligomer ; 597.6
Reference(s) to other database(s): GlycomeDB:5769

Biochemistry 1999, "NMR experiments reveal distinct antibody-bound conformations of a synthetic disaccharide representing a general structural element of bacterial lipopolysaccharide epitopes"
CSDB ID 565 (all data & tools)
Compound ID: 2145

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Structure type: oligomer
Aglycon: 4-methoxyphenyl
Reference(s) to other database(s): GTC:G01866TT, GlycomeDB:25265

Carbohydrate Research 1998, "Synthesis of hyaluronic-acid-related oligosaccharides and analogues, as their 4-methoxyphenyl glycosides, having N-acetyl-b-D-glucosamine at the reducing end"
CSDB ID 572 (all data & tools)
Compound ID: 2146

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Structure type: oligomer
Aglycon: 4-methoxyphenyl
Reference(s) to other database(s): GlycomeDB:36762

Carbohydrate Research 1998, "Synthesis of hyaluronic-acid-related oligosaccharides and analogues, as their 4-methoxyphenyl glycosides, having N-acetyl-b-D-glucosamine at the reducing end"
CSDB ID 573 (all data & tools)
Compound ID: 2147

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Structure type: oligomer
Reference(s) to other database(s): GlycomeDB:25265

Carbohydrate Research 1998, "Synthesis of hyaluronic-acid-related oligosaccharides and analogues, as their 4-methoxyphenyl glycosides, having N-acetyl-b-D-glucosamine at the reducing end"
CSDB ID 574 (all data & tools)
Compound ID: 2151

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Structure type: monomer
Trivial name: methyl glycosyde
Reference(s) to other database(s): GlycomeDB:25269

Carbohydrate Research 1998, "Five monophosphates of methyl L-glycero-a-D-manno-heptopyranoside: synthesis, hydrolysis and migrations"
CSDB ID 578 (all data & tools)
Compound ID: 2152

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Structure type: monomer
Trivial name: methyl glycosyde
Reference(s) to other database(s): GlycomeDB:25270

Carbohydrate Research 1998, "Five monophosphates of methyl L-glycero-a-D-manno-heptopyranoside: synthesis, hydrolysis and migrations"
CSDB ID 579 (all data & tools)

Carbohydrate Research 1998, "Studies of alkaline mediated phosphate migration in synthetic phosphoethanolamine L-glycero-D-manno-heptoside derivatives"
CSDB ID 5040 (all data & tools)
Compound ID: 2153

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Structure type: monomer
Trivial name: methyl glycosyde
Reference(s) to other database(s): GlycomeDB:25271

Carbohydrate Research 1998, "Five monophosphates of methyl L-glycero-a-D-manno-heptopyranoside: synthesis, hydrolysis and migrations"
CSDB ID 580 (all data & tools)

Carbohydrate Research 1998, "Studies of alkaline mediated phosphate migration in synthetic phosphoethanolamine L-glycero-D-manno-heptoside derivatives"
CSDB ID 5041 (all data & tools)
Compound ID: 2154

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Structure type: monomer
Trivial name: methyl glycosyde
Reference(s) to other database(s): GlycomeDB:25272

Carbohydrate Research 1998, "Five monophosphates of methyl L-glycero-a-D-manno-heptopyranoside: synthesis, hydrolysis and migrations"
CSDB ID 581 (all data & tools)

Carbohydrate Research 1998, "Studies of alkaline mediated phosphate migration in synthetic phosphoethanolamine L-glycero-D-manno-heptoside derivatives"
CSDB ID 5042 (all data & tools)
Compound ID: 66

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Structure type: oligomer
Trivial name: globotriose
Reference(s) to other database(s): GTC:G07992YV, GlycomeDB:1306

Glycoconjugate Journal 1999, "Synthesis of oligosaccharides by bacterial enzymes"
CSDB ID 813 (all data & tools)
Compound ID: 2181

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Structure type: oligomer
Trivial name: globotetraose
Reference(s) to other database(s): GTC:G82907DV, GlycomeDB:1308

Glycoconjugate Journal 1999, "Synthesis of oligosaccharides by bacterial enzymes"
CSDB ID 914 (all data & tools)
Compound ID: 2352

-1)-b-D-Fruf-(2- Show graphically

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Structure type: polymer chemical repeating unit
Trivial name: inulin
Reference(s) to other database(s): GTC:G25631OI, GlycomeDB:25637

Carbohydrate Research 1998, "Structure of the enzymatically synthesized fructan inulin"
CSDB ID 2417 (all data & tools)
Compound ID: 2705

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Structure type: monomer
Aglycon: 4-methylumbelliferyl
Reference(s) to other database(s): GTC:G34165VZ, GlycomeDB:13262

Journal of Biological Chemistry 1997, "a-KDOase activity in oyster and synthesis of a- and b-4-methylumbelliferyl ketosides of 3-deoxy-D-manno-octulosonic acid (KDO)"
CSDB ID 3148 (all data & tools)
Compound ID: 2706

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Structure type: monomer
Aglycon: 4-methylumbelliferyl
Reference(s) to other database(s): GTC:G38327SI, GlycomeDB:25943

Journal of Biological Chemistry 1997, "a-KDOase activity in oyster and synthesis of a- and b-4-methylumbelliferyl ketosides of 3-deoxy-D-manno-octulosonic acid (KDO)"
CSDB ID 3225 (all data & tools)
Compound ID: 3100

Mur Show graphically

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Structure type: monomer
C9H17N1O7
Trivial name: muramic acid
Reference(s) to other database(s): GTC:G53503VR

Carbohydrate Research 1997, "A simple approach to the synthesis of muramic acid and isomuramic acid: 1H and 13C NMR characterisation"
CSDB ID 4301 (all data & tools)
Compound ID: 3241

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Structure type: oligomer
Aglycon: Allyl or 3-(2-aminoethylthio)propyl)
Reference(s) to other database(s): GTC:G00109NL, GlycomeDB:26350

Journal of the Chemical Society, Perkin Transactions 1 1997, "Synthesis of neoglycoprotreins containing L-glycero-a-D-manno-heptopyranosyl-(1->4)- and -(1->5)-linked 3-deoxy-a-D-manno-oct-2-ulopyranosylonic acid (Kdo) phosphate determinants"
CSDB ID 4629 (all data & tools)
Compound ID: 3242

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Structure type: oligomer
Aglycon: Allyl or 3-(2-aminoethylthio)propyl)
Reference(s) to other database(s): GTC:G99535BO, GlycomeDB:26481

Journal of the Chemical Society, Perkin Transactions 1 1997, "Synthesis of neoglycoprotreins containing L-glycero-a-D-manno-heptopyranosyl-(1->4)- and -(1->5)-linked 3-deoxy-a-D-manno-oct-2-ulopyranosylonic acid (Kdo) phosphate determinants"
CSDB ID 4828 (all data & tools)
Compound ID: 3243

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Structure type: oligomer
Aglycon: Allyl or 3-(2-aminoethylthio)propyl)
Reference(s) to other database(s): GTC:G32223HD, GlycomeDB:26482

Journal of the Chemical Society, Perkin Transactions 1 1997, "Synthesis of neoglycoprotreins containing L-glycero-a-D-manno-heptopyranosyl-(1->4)- and -(1->5)-linked 3-deoxy-a-D-manno-oct-2-ulopyranosylonic acid (Kdo) phosphate determinants"
CSDB ID 4829 (all data & tools)
Compound ID: 3244

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Structure type: oligomer
Aglycon: Allyl or 3-(2-aminoethylthio)propyl)
Reference(s) to other database(s): GTC:G40857AB, GlycomeDB:26483

Journal of the Chemical Society, Perkin Transactions 1 1997, "Synthesis of neoglycoprotreins containing L-glycero-a-D-manno-heptopyranosyl-(1->4)- and -(1->5)-linked 3-deoxy-a-D-manno-oct-2-ulopyranosylonic acid (Kdo) phosphate determinants"
CSDB ID 4830 (all data & tools)
Compound ID: 3370

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Structure type: oligomer
Reference(s) to other database(s): GlycomeDB:15387

Journal of the Chemical Society, Perkin Transactions 2 1998, "Synthesis, NMR spectroscopy and conformational studies of the four anomeric methyl glycosides of the tetrasaccharide D-Glcp-(1->3)-[D-Glcp-(1->4)]-a-D-Glcp"
CSDB ID 4925 (all data & tools)
Compound ID: 3371

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Structure type: oligomer
Reference(s) to other database(s): GlycomeDB:274

Carbohydrate Research 1998, "Synthesis of site-specific, deuterium-substituted a-L-Rhap-(1→2)-a-L-Rhap-OMe"
CSDB ID 4926 (all data & tools)

Journal of the American Chemical Society 2002, "Conformational distribution function of a disaccharide in a liquid crystalline phase determined using NMR spectroscopy"
CSDB ID 4954 (all data & tools)
Compound ID: 3382

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Structure type: monomer

Carbohydrate Research 1998, "Synthesis of site-specific deuterium substituted methyl 6-O-[(R)- and (S)-1-carboxyethyl]-a-D-galactopyranoside and conformational analysis thereof based on J couplings"
CSDB ID 4952 (all data & tools)

Carbohydrate Research 2003, "The absolute configuration of 1-carboxyethyl substituents on common hexoses by circular dichroism"
CSDB ID 6439 (all data & tools)
Compound ID: 3383

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Structure type: monomer
Reference(s) to other database(s): GlycomeDB:26497

Carbohydrate Research 1998, "Studies of alkaline mediated phosphate migration in synthetic phosphoethanolamine L-glycero-D-manno-heptoside derivatives"
CSDB ID 4955 (all data & tools)
Compound ID: 3402

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Structure type: oligomer
Reference(s) to other database(s): GlycomeDB:15389

Journal of the Chemical Society, Perkin Transactions 2 1998, "Synthesis, NMR spectroscopy and conformational studies of the four anomeric methyl glycosides of the tetrasaccharide D-Glcp-(1->3)-[D-Glcp-(1->4)]-a-D-Glcp"
CSDB ID 5006 (all data & tools)
Compound ID: 3403

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Structure type: oligomer
Reference(s) to other database(s): GlycomeDB:15392

Journal of the Chemical Society, Perkin Transactions 2 1998, "Synthesis, NMR spectroscopy and conformational studies of the four anomeric methyl glycosides of the tetrasaccharide D-Glcp-(1->3)-[D-Glcp-(1->4)]-a-D-Glcp"
CSDB ID 5007 (all data & tools)
Compound ID: 3404

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Structure type: oligomer
Reference(s) to other database(s): GlycomeDB:15398

Journal of the Chemical Society, Perkin Transactions 2 1998, "Synthesis, NMR spectroscopy and conformational studies of the four anomeric methyl glycosides of the tetrasaccharide D-Glcp-(1->3)-[D-Glcp-(1->4)]-a-D-Glcp"
CSDB ID 5008 (all data & tools)
Compound ID: 3411

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Structure type: monomer

Carbohydrate Research 1998, "Synthesis of site-specific deuterium substituted methyl 6-O-[(R)- and (S)-1-carboxyethyl]-a-D-galactopyranoside and conformational analysis thereof based on J couplings"
CSDB ID 5017 (all data & tools)

Carbohydrate Research 2003, "The absolute configuration of 1-carboxyethyl substituents on common hexoses by circular dichroism"
CSDB ID 6440 (all data & tools)
Compound ID: 3430

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Structure type: monomer
Reference(s) to other database(s): GlycomeDB:26538

Carbohydrate Research 1998, "Studies of alkaline mediated phosphate migration in synthetic phosphoethanolamine L-glycero-D-manno-heptoside derivatives"
CSDB ID 5037 (all data & tools)
Compound ID: 3431

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Structure type: monomer
Reference(s) to other database(s): GlycomeDB:26539

Carbohydrate Research 1998, "Studies of alkaline mediated phosphate migration in synthetic phosphoethanolamine L-glycero-D-manno-heptoside derivatives"
CSDB ID 5038 (all data & tools)
Compound ID: 3432

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Structure type: monomer
Reference(s) to other database(s): GlycomeDB:627

Carbohydrate Research 1998, "Studies of alkaline mediated phosphate migration in synthetic phosphoethanolamine L-glycero-D-manno-heptoside derivatives"
CSDB ID 5039 (all data & tools)
Compound ID: 3433

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Structure type: monomer
Reference(s) to other database(s): GlycomeDB:26540

Carbohydrate Research 1998, "Studies of alkaline mediated phosphate migration in synthetic phosphoethanolamine L-glycero-D-manno-heptoside derivatives"
CSDB ID 5043 (all data & tools)
Compound ID: 3434

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Structure type: monomer

Carbohydrate Research 1998, "Studies of alkaline mediated phosphate migration in synthetic phosphoethanolamine L-glycero-D-manno-heptoside derivatives"
CSDB ID 5044 (all data & tools)
Compound ID: 3435

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Structure type: monomer

Carbohydrate Research 1998, "Studies of alkaline mediated phosphate migration in synthetic phosphoethanolamine L-glycero-D-manno-heptoside derivatives"
CSDB ID 5045 (all data & tools)
Compound ID: 3436

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Structure type: monomer

Carbohydrate Research 1998, "Studies of alkaline mediated phosphate migration in synthetic phosphoethanolamine L-glycero-D-manno-heptoside derivatives"
CSDB ID 5046 (all data & tools)
Compound ID: 3606

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Structure type: monomer

Carbohydrate Research 2003, "The absolute configuration of 1-carboxyethyl substituents on common hexoses by circular dichroism"
CSDB ID 6214 (all data & tools)
Compound ID: 3607

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Structure type: monomer

Carbohydrate Research 2003, "The absolute configuration of 1-carboxyethyl substituents on common hexoses by circular dichroism"
CSDB ID 6434 (all data & tools)
Compound ID: 3608

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Structure type: monomer

Carbohydrate Research 2003, "The absolute configuration of 1-carboxyethyl substituents on common hexoses by circular dichroism"
CSDB ID 6435 (all data & tools)
Compound ID: 3609

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Structure type: monomer

Carbohydrate Research 2003, "The absolute configuration of 1-carboxyethyl substituents on common hexoses by circular dichroism"
CSDB ID 6436 (all data & tools)
Compound ID: 3610

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Structure type: monomer

Carbohydrate Research 2003, "The absolute configuration of 1-carboxyethyl substituents on common hexoses by circular dichroism"
CSDB ID 6437 (all data & tools)
Compound ID: 3611

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Structure type: monomer

Carbohydrate Research 2003, "The absolute configuration of 1-carboxyethyl substituents on common hexoses by circular dichroism"
CSDB ID 6438 (all data & tools)
Compound ID: 3612

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Structure type: monomer

Carbohydrate Research 2003, "The absolute configuration of 1-carboxyethyl substituents on common hexoses by circular dichroism"
CSDB ID 6441 (all data & tools)
Compound ID: 3613

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Structure type: monomer

Carbohydrate Research 2003, "The absolute configuration of 1-carboxyethyl substituents on common hexoses by circular dichroism"
CSDB ID 6442 (all data & tools)

Compound ID: 10274

Compound 10274

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Compound ID: 13429

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Structure type: monomer ; 860
Compound class: glycolipid

Applied Microbiology and Biotechnology 1992, "Marine biosurfactants. IV. Production, characterization and biosynthesis of an anionic glucose lipid from the marine bacterial strain MM1"
CSDB ID 45709 (all data & tools)
Compound ID: 13661

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Structure type: polymer chemical repeating unit ; 260000
Trivial name: gellan
Compound class: EPS
Reference(s) to other database(s): GTC:G41181BF

International Journal of Biological Macromolecules 1990, "Evidence for microbial polysaccharide preparations containing polyester substituents"
CSDB ID 1015 (all data & tools)
Compound ID: 13906

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Structure type: oligomer
Trivial name: inulin
Compound class: EPS
Reference(s) to other database(s): GTC:G98273ZJ

Frontiers in Microbiology 2015, "Bacterial exopolysaccharides: biosynthesis pathways and engineering strategies"
CSDB ID 2270 (all data & tools)
Compound ID: 2454

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Structure type: structural motif or average structure
Trivial name: alginate
Compound class: polysaccharide
Reference(s) to other database(s): GTC:G94988EU, GlycomeDB:25731

Journal of Biological Chemistry 2019, "Structural and functional aspects of mannuronic acid-specific PL6 alginate lyase from the human gut microbe Bacteroides cellulosilyticus"
CSDB ID 1122 (all data & tools)
Compound ID: 13956

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Structure type: oligomer
Trivial name: alginate
Reference(s) to other database(s): GTC:G44502XX

Journal of Biological Chemistry 2019, "Structural and functional aspects of mannuronic acid-specific PL6 alginate lyase from the human gut microbe Bacteroides cellulosilyticus"
CSDB ID 2325 (all data & tools)

Compound ID: 6006

Compound 6006

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Compound ID: 14185

Compound 14185

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Compound ID: 15011

Compound 15011

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Compound ID: 15026

Compound 15026

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Compound ID: 15962

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Structure type: oligomer
Trivial name: kojibiose
Compound class: disaccharide, oligosaccharide
Reference(s) to other database(s): GTC:G46435VD

Current Medicinal Chemistry 2000, "Medicinal chemistry based on the sugar code: fundamentals of lectinology and experimental strategies with lectins as targets"
CSDB ID 67517 (all data & tools)
Compound ID: 5881

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Structure type: oligomer
C12H22O11
Trivial name: trehalose, trehalose dihydrate
Compound class: glucan, disaccharide, oligosaccharide, trehalose
Reference(s) to other database(s): GTC:G92130SN, GlycomeDB:245

Current Medicinal Chemistry 2000, "Medicinal chemistry based on the sugar code: fundamentals of lectinology and experimental strategies with lectins as targets"
CSDB ID 67525 (all data & tools)

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