carzinophilin a

chemical compound
ChemicalSubstance group_of_stereoisomers Q27236057
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carzinophilin a

Summary

carzinophilin an is a group of stereoisomers[1].

Key Facts

  • carzinophilin a's instance of is recorded as group of stereoisomers[2].
  • carzinophilin a's CAS Registry Number is recorded as 106486-76-4[3].
  • carzinophilin a's canonical SMILES is recorded as CC1=CC=CC2=C(C=C(C=C12)OC)C(=O)OC(C(=O)NC(=C3C(C(C4N3C4)O)OC(=O)C)C(=O)NC(=CO)C(=O)C)C5(CO5)C[4].
  • carzinophilin a's InChI is recorded as InChI=1S/C31H33N3O11/c1-14-7-6-8-18-19(14)9-17(42-5)10-20(18)30(41)45-27(31(4)13-43-31)29(40)33-23(28(39)32-21(12-35)15(2)36)24-26(44-16(3)37)25(38)22-11-34(22)24/h6-10,12,22,25-27,35,38H,11,13H2,1-5H3,(H,32,39)(H,33,40)/b21-12-,24-23+/t22-,25+,26+,27+,31-,34?/m0/s1[5].
  • carzinophilin a's InChIKey is recorded as QIKVYJOCQXXRSJ-PKDLRSQSSA-N[6].
  • carzinophilin a's chemical formula is recorded as C₃₁H₃₃N₃O₁₁[7].
  • carzinophilin a's subclass of is recorded as chemical compound[8].
  • carzinophilin a's UNII is recorded as 051R55X44C[9].
  • carzinophilin a's ChemSpider ID is recorded as 10270414[10].
  • carzinophilin a's PubChem CID is recorded as 14476972[11].
  • carzinophilin a's found in taxon is recorded as Streptomyces sahachiroi[12].
  • carzinophilin a's found in taxon is recorded as Streptomyces griseofuscus[13].
  • carzinophilin a's isomeric SMILES is recorded as CC1=CC=CC2=C(C=C(C=C12)OC)C(=O)OC@H[C@@]5(CO5)CC@H[C@@]5(CO5)C">[14].
  • carzinophilin a's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+623.212'}[15].
  • carzinophilin a's SureChEMBL ID is recorded as 413073[16].
  • carzinophilin a's DSSTox substance ID is recorded as DTXSID9040421[17].
  • carzinophilin a's DSSTOX compound identifier is recorded as DTXCID7020421[18].
  • carzinophilin a's UniChem compound ID is recorded as 43329998[19].

References

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

Direct Wikidata claims

  1. [2] . wikidata.org.
  2. [3] . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  3. [4] . PubChem. Retrieved . wikidata.org.
  4. [5] . PubChem. Retrieved . wikidata.org.
  5. [6] . PubChem. Retrieved . wikidata.org.
  6. [7] . PubChem. Retrieved . wikidata.org.
  7. [8] . wikidata.org.
  8. [9] . Global Substance Registration System. Retrieved . wikidata.org.
  9. [10] . Q2311683. Retrieved . wikidata.org.
  10. [11] . PubChem. Retrieved . wikidata.org.
  11. [12] . Essential role of an unknown geneaziU3in the production of antitumor antibiotic azinomycin B verified by utilizing optimized genetic manipulation systems forStreptomyces sahachiroi. wikidata.org.
  12. [13] . Azinomycins A and B, new antitumor antibiotics. III. Antitumor activity.. wikidata.org.
  13. [14] . PubChem. Retrieved . wikidata.org.
  14. [15] . PubChem. Retrieved . wikidata.org.
  15. [16] . wikidata.org.
  16. [17] . wikidata.org.
  17. [18] . wikidata.org.
  18. [19] . 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). carzinophilin a. Retrieved May 3, 2026, from https://4ort.xyz/entity/carzinophilin-a
MLA “carzinophilin a.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/carzinophilin-a.
BibTeX @misc{4ortxyz_carzinophilin-a_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{carzinophilin a}}, year = {2026}, url = {https://4ort.xyz/entity/carzinophilin-a}, note = {Accessed: 2026-05-03}}
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