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alvespimycin

chemical compound
ChemicalSubstance type_of_chemical_entity Q4552287
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alvespimycin

Summary

alvespimycin is a type of chemical entity[1]. alvespimycin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (2 views/month).[2]

Key Facts

  • alvespimycin's instance of is recorded as type of chemical entity[3].
  • alvespimycin's chemical structure is recorded as 17-(dimethylaminoethylamino)-17-demethoxygeldanamycin.png[4].
  • alvespimycin's CAS Registry Number is recorded as 467214-20-6[5].
  • alvespimycin's canonical SMILES is recorded as CC1CC(C(C(C=C(C(C(C=CC=C(C(=O)NC2=CC(=O)C(=C(C1)C2=O)NCCN(C)C)C)OC)OC(=O)N)C)C)O)OC[6].
  • alvespimycin's InChI is recorded as InChI=1S/C32H48N4O8/c1-18-14-22-27(34-12-13-36(5)6)24(37)17-23(29(22)39)35-31(40)19(2)10-9-11-25(42-7)30(44-32(33)41)21(4)16-20(3)28(38)26(15-18)43-8/h9-11,16-18,20,25-26,28,30,34,38H,12-15H2,1-8H3,(H2,33,41)(H,35,40)/b11-9-,19-10+,21-16+/t18-,20+,25+,26+,28-,30+/m1/s1[7].
  • alvespimycin's InChIKey is recorded as KUFRQPKVAWMTJO-LMZWQJSESA-N[8].
  • alvespimycin's chemical formula is recorded as C₃₂H₄₈N₄O₈[9].
  • alvespimycin's subclass of is recorded as carbamic acid [21-[2-(dimethylamino)ethylamino]-6-hydroxy-5,11-dimethoxy-3,7,9,15-tetramethyl-16,20,22-trioxo-17-azabicyclo[16.3.1]docosa-1(21),8,12,14,18-pentaen-10-yl] ester[10].
  • alvespimycin's ChEMBL ID is recorded as CHEMBL383824[11].
  • alvespimycin's Guide to Pharmacology Ligand ID is recorded as 9828[12].
  • alvespimycin's PDB structure ID is recorded as 1OSF[13].
  • alvespimycin's Freebase ID is recorded as /m/047fcfj[14].
  • alvespimycin's UNII is recorded as 001L2FE0M3[15].
  • alvespimycin's ChemSpider ID is recorded as 16744073[16].
  • alvespimycin's PubChem CID is recorded as 5288674[17].
  • alvespimycin's ChEBI ID is recorded as 65324[18].
  • alvespimycin's found in taxon is recorded as Cullen corylifolia[19].
  • alvespimycin's found in taxon is recorded as Cullen corylifolium[20].
  • alvespimycin's found in taxon is recorded as Trichosanthes kirilowii[21].
  • alvespimycin's found in taxon is recorded as Morus[22].
  • alvespimycin's DrugBank ID is recorded as DB12442[23].
  • alvespimycin's Reaxys registry number is recorded as 9890433[24].
  • alvespimycin's isomeric SMILES is recorded as C[C@H]1CC@@HOCC@@HOC">[25].
  • alvespimycin's mass is recorded as {'unit': 'Q483261', 'amount': '+616.347'}[26].
  • alvespimycin's SureChEMBL ID is recorded as 5449716[27].

Why It Matters

alvespimycin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (2 views/month).[2] alvespimycin is known by 4 alternative names across languages and contexts.[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] ↑ . ChEBI. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  4. [6] ↑ . PubChem. Retrieved . wikidata.org.
  5. [7] ↑ . PubChem. Retrieved . wikidata.org.
  6. [8] ↑ . PubChem. Retrieved . wikidata.org.
  7. [9] ↑ . PubChem. Retrieved . wikidata.org.
  8. [10] ↑ . wikidata.org.
  9. [11] ↑ . ChEMBL. Retrieved . wikidata.org.
  10. [12] ↑ . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  11. [13] ↑ . Protein Data Bank. Retrieved . wikidata.org.
  12. [14] ↑ . Freebase Data Dumps. wikidata.org.
  13. [15] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  14. [16] ↑ . Q2311683. Retrieved . wikidata.org.
  15. [17] ↑ . PubChem. Retrieved . wikidata.org.
  16. [18] ↑ . ChEBI. Retrieved . wikidata.org.
  17. [19] ↑ . Hypoxia-inducible factor-1 and nuclear factor-kappaB inhibitory meroterpene analogues of bakuchiol, a constituent of the seeds of Psoralea corylifolia.. wikidata.org.
  18. [20] ↑ . Hypoxia-inducible factor-1 and nuclear factor-kappaB inhibitory meroterpene analogues of bakuchiol, a constituent of the seeds of Psoralea corylifolia.. wikidata.org.
  19. [21] ↑ . An isoaurone and other constituents from Trichosanthes kirilowii seeds inhibit hypoxia-inducible factor-1 and nuclear factor-kappaB.. wikidata.org.
  20. [22] ↑ . Hypoxia-inducible factor-1 inhibitory benzofurans and chalcone-derived diels-alder adducts from Morus species.. wikidata.org.
  21. [23] ↑ . wikidata.org.
  22. [24] ↑ . ChEBI. Retrieved . wikidata.org.
  23. [25] ↑ . PubChem. Retrieved . wikidata.org.
  24. [26] ↑ . PubChem. Retrieved . 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 aliases. 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). alvespimycin. Retrieved May 3, 2026, from https://4ort.xyz/entity/alvespimycin
MLA “alvespimycin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/alvespimycin.
BibTeX @misc{4ortxyz_alvespimycin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{alvespimycin}}, year = {2026}, url = {https://4ort.xyz/entity/alvespimycin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): alvespimycin — https://4ort.xyz/entity/alvespimycin (retrieved 2026-05-03)

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