Ristocetin A

group of stereoisomers with the chemical formula C₉₅H₁₁₀N₈O₄₄
ChemicalSubstance group_of_stereoisomers Q105297347
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Ristocetin A

Summary

Ristocetin An is a group of stereoisomers[1].

Key Facts

  • Ristocetin A's instance of is recorded as group of stereoisomers[2].
  • Ristocetin A's CAS Registry Number is recorded as 11021-66-2[3].
  • Ristocetin A's canonical SMILES is recorded as COC(=O)C1NC(=O)C2NC(=O)C(NC(=O)C3NC(=O)C4NC(=O)C(NC(=O)C(N)c5ccc(O)c(c5)Oc5cc4cc(O)c5C)C(O)c4ccc(cc4)Oc4cc3cc(c4OC3OC(COC4OC(C)C(O)C(O)C4O)C(O)C(O)C3OC3OC(CO)C(O)C(O)C3OC3OCC(O)C(O)C3O)Oc3ccc(cc3)C2OC2CC(N)C(O)C(C)O2)c2ccc(O)c(c2)-c2c(OC3OC(CO)C(O)C(O)C3O)cc(O)cc21[4].
  • Ristocetin A's InChI is recorded as InChI=1S/C95H110N8O44/c1-30-47(109)18-37-20-49(30)139-50-19-35(9-16-46(50)108)59(97)84(125)102-64-68(113)33-5-11-40(12-6-33)137-52-21-38-22-53(81(52)145-95-83(76(121)72(117)56(143-95)29-134-91-78(123)73(118)67(112)32(3)136-91)147-94-82(75(120)71(116)55(27-105)142-94)146-92-77(122)69(114)48(110)28-133-92)138-41-13-7-34(8-14-41)80(144-57-25-44(96)66(111)31(2)135-57)65-89(130)101-63(90(131)132-4)43-23-39(106)24-51(140-93-79(124)74(119)70(115)54(26-104)141-93)58(43)42-17-36(10-15-45(42)107)60(85(126)103-65)98-87(128)62(38)99-86(127)61(37)100-88(64)129/h5-24,31-32,44,48,54-57,59-80,82-83,91-95,104-124H,25-29,96-97H2,1-4H3,(H,98,128)(H,99,127)(H,100,129)(H,101,130)(H,102,125)(H,103,126)[5].
  • Ristocetin A's InChIKey is recorded as VUOPFFVAZTUEGW-UHFFFAOYSA-N[6].
  • Ristocetin A's chemical formula is recorded as C₉₅H₁₁₀N₈O₄₄[7].
  • Ristocetin A's subclass of is recorded as chemical compound[8].
  • Ristocetin A's PubChem CID is recorded as 16131418[9].
  • Ristocetin A's PubChem CID is recorded as 163196150[10].
  • Ristocetin A's found in taxon is recorded as Amycolatopsis japonica[11].
  • Ristocetin A's found in taxon is recorded as Amycolatopsis lurida[12].
  • Ristocetin A's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+2066.6615888'}[13].
  • Ristocetin A's SureChEMBL ID is recorded as 31241173[14].
  • Ristocetin A's DSSTox substance ID is recorded as DTXSID801317931[15].
  • Ristocetin A's UniChem compound ID is recorded as 62672882[16].

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [2] . wikidata.org.
  2. [3] . Chemical Abstracts Service. Retrieved . wikidata.org.
  3. [4] . wikidata.org.
  4. [5] . wikidata.org.
  5. [6] . wikidata.org.
  6. [7] . wikidata.org.
  7. [8] . wikidata.org.
  8. [9] . PubChem. Retrieved . wikidata.org.
  9. [10] . PubChem. Retrieved . wikidata.org.
  10. [11] . Overproduction of Ristomycin A by activation of a silent gene cluster in Amycolatopsis japonicum MG417-CF17.. wikidata.org.
  11. [12] . Antibiotic resistance mechanisms inform discovery: identification and characterization of a novel amycolatopsis strain producing ristocetin. wikidata.org.
  12. [13] . wikidata.org.
  13. [14] . wikidata.org.
  14. [15] . wikidata.org.
  15. [16] . UniChem. wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

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Use these citations when quoting this entity in research, articles, AI prompts, or wherever provenance matters. We aggregate Wikidata + Wikipedia + authoritative open-data sources; the stitched, scored, cross-referenced view is what 4ort.xyz contributes.

APA 4ort.xyz Knowledge Graph. (2026). Ristocetin A. Retrieved May 3, 2026, from https://4ort.xyz/entity/ristocetin-a
MLA “Ristocetin A.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/ristocetin-a.
BibTeX @misc{4ortxyz_ristocetin-a_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Ristocetin A}}, year = {2026}, url = {https://4ort.xyz/entity/ristocetin-a}, note = {Accessed: 2026-05-03}}
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