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ristocetin

group of stereoisomers
ChemicalSubstance group_of_stereoisomers Q904599
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ristocetin

Summary

ristocetin is a group of stereoisomers[1]. ristocetin draws 22 Wikipedia views per month (group_of_stereoisomers category, ranking #196 of 1,063).[2]

Key Facts

  • ristocetin's instance of is recorded as group of stereoisomers[3].
  • ristocetin's chemical structure is recorded as Ristocetin.png[4].
  • ristocetin's CAS Registry Number is recorded as 1404-55-3[5].
  • ristocetin's EC number is recorded as 215-770-5[6].
  • ristocetin's canonical SMILES is recorded as CC1C(C(CC(O1)OC2C3C(=O)NC(C4=CC(=CC(=C4C5=C(C=CC(=C5)C(C(=O)N3)NC(=O)C6C7=CC(=C(C(=C7)OC8=CC=C2C=C8)OC9C(C(C(C(O9)COC1C(C(C(C(O1)C)O)O)O)O)O)OC1C(C(C(C(O1)CO)O)O)OC1C(C(C(CO1)O)O)O)OC1=CC=C(C=C1)C(C1C(=O)NC(C2=CC(=C(C(=C2)O)C)OC2=C(C=CC(=C2)C(C(=O)N1)N)O)C(=O)N6)O)O)OC1C(C(C(C(O1)CO)O)O)O)O)C(=O)O)N)O[7].
  • ristocetin'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)/t31-,32-,44+,48+,54+,55-,56+,57+,59+,60+,61-,62+,63-,64+,65-,66-,67-,68+,69+,70+,71-,72+,73+,74-,75+,76-,77-,78+,79-,80+,82+,83+,91?,92-,93+,94-,95-/m0/s1[8].
  • ristocetin's InChIKey is recorded as VUOPFFVAZTUEGW-FBMDODLCSA-N[9].
  • ristocetin's chemical formula is recorded as C₉₄H₁₀₈N₈O₄₄[10].
  • ristocetin's subclass of is recorded as Ristocetin A[11].
  • ristocetin's MeSH descriptor ID is recorded as D012310[12].
  • ristocetin's ChEMBL ID is recorded as CHEMBL1095986[13].
  • ristocetin's Freebase ID is recorded as /m/0bx2xm[14].
  • ristocetin's ChemSpider ID is recorded as 21106475[15].
  • ristocetin's PubChem CID is recorded as 16204749[16].
  • ristocetin's PubChem CID is recorded as 170843004[17].
  • ristocetin's MeSH tree code is recorded as D09.400.420.800[18].
  • ristocetin's MeSH tree code is recorded as D12.644.233.697[19].
  • ristocetin's ChEBI ID is recorded as 85129[20].
  • ristocetin's found in taxon is recorded as Nocardia[21].
  • ristocetin's isomeric SMILES is recorded as COC(=O)[C@H]1NC(=O)[C@H]2NC(=O)C@Hc2ccc(O)c(c2)-c2c(O[C@@H]3OC@HC@@HC@H[C@@H]3O)cc(O)cc21C@HC@Hc4ccc(cc4)Oc4cc3cc(c4O[C@@H]3O[C@H](CO">[22].
  • ristocetin's mass is recorded as {'unit': 'Q483261', 'amount': '+2066.6615888'}[23].
  • ristocetin's ECHA Substance Infocard ID is recorded as 100.014.336[24].
  • ristocetin's subject has role is recorded as antibiotic[25].
  • ristocetin's DSSTox substance ID is recorded as DTXSID30894853[26].
  • ristocetin's Microsoft Academic ID is recorded as 2776057759[27].

Why It Matters

ristocetin draws 22 Wikipedia views per month (group_of_stereoisomers category, ranking #196 of 1,063).[2] ristocetin has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.[28]

References

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

Direct Wikidata claims

  1. [3] ↑ . wikidata.org.
  2. [4] ↑ . wikidata.org.
  3. [5] ↑ . wikidata.org.
  4. [6] ↑ . ECHA Substance Infocard database. Retrieved . wikidata.org.
  5. [7] ↑ . PubChem. wikidata.org.
  6. [8] ↑ . wikidata.org.
  7. [9] ↑ . ChEBI release 2020-09-01. wikidata.org.
  8. [10] ↑ . PubChem. wikidata.org.
  9. [11] ↑ . wikidata.org.
  10. [12] ↑ . wikidata.org.
  11. [13] ↑ . wikidata.org.
  12. [14] ↑ . Freebase Data Dumps. wikidata.org.
  13. [15] ↑ . wikidata.org.
  14. [16] ↑ . wikidata.org.
  15. [17] ↑ . wikidata.org.
  16. [18] ↑ . wikidata.org.
  17. [19] ↑ . wikidata.org.
  18. [20] ↑ . ChEBI release 2019-10-02. wikidata.org.
  19. [21] ↑ . Structure of the antibiotic ristocetin A. wikidata.org.
  20. [22] ↑ . wikidata.org.
  21. [23] ↑ . wikidata.org.
  22. [24] ↑ . ECHA Substance Infocard database. Retrieved . wikidata.org.
  23. [25] ↑ . Medical Subject Headings. Retrieved . wikidata.org.
  24. [26] ↑ . wikidata.org.
  25. [27] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikimedia Foundation. dumps.wikimedia.org.
  2. [28] ↑ . Wikidata sitelinks. wikidata.org.

📑 Cite this page

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. Retrieved May 3, 2026, from https://4ort.xyz/entity/ristocetin
MLA “ristocetin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/ristocetin.
BibTeX @misc{4ortxyz_ristocetin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{ristocetin}}, year = {2026}, url = {https://4ort.xyz/entity/ristocetin}, note = {Accessed: 2026-05-03}}
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