5α,8α-epidioxyergosta-6,22-dien-3β-ol

bioactive natural product
ChemicalSubstance group_of_stereoisomers Q77279237
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5α,8α-epidioxyergosta-6,22-dien-3β-ol

Summary

5α,8α-epidioxyergosta-6,22-dien-3β-ol is a group of stereoisomers[1].

Key Facts

  • 5α,8α-epidioxyergosta-6,22-dien-3β-ol's instance of is recorded as group of stereoisomers[2].
  • 5α,8α-epidioxyergosta-6,22-dien-3β-ol's canonical SMILES is recorded as OC1CCC2(C)C3CCC4(C)C(CCC4C53OOC2(C=C5)C1)C(C=CC(C)C(C)C)C[3].
  • 5α,8α-epidioxyergosta-6,22-dien-3β-ol's InChI is recorded as InChI=1S/C28H44O3/c1-18(2)19(3)7-8-20(4)22-9-10-23-25(22,5)13-12-24-26(6)14-11-21(29)17-27(26)15-16-28(23,24)31-30-27/h7-8,15-16,18-24,29H,9-14,17H2,1-6H3/b8-7+/t19-,20+,21-,22+,23?,24?,25+,26+,27+,28-/m0/s1[4].
  • 5α,8α-epidioxyergosta-6,22-dien-3β-ol's InChIKey is recorded as VXOZCESVZIRHCJ-PHICIKCOSA-N[5].
  • 5α,8α-epidioxyergosta-6,22-dien-3β-ol's chemical formula is recorded as C₂₈H₄₄O₃[6].
  • 5α,8α-epidioxyergosta-6,22-dien-3β-ol's subclass of is recorded as (5R,6R,10R,13S)-5-[(E,2R,5R)-5,6-dimethylhept-3-en-2-yl]-6,10-dimethyl-16,17-dioxapentacyclo[13.2.2.01,9.02,6.010,15]nonadec-18-en-13-ol[7].
  • 5α,8α-epidioxyergosta-6,22-dien-3β-ol's PubChem CID is recorded as 6475145[8].
  • 5α,8α-epidioxyergosta-6,22-dien-3β-ol's ChEBI ID is recorded as 200580[9].
  • 5α,8α-epidioxyergosta-6,22-dien-3β-ol's found in taxon is recorded as Ficus nervosa[10].
  • 5α,8α-epidioxyergosta-6,22-dien-3β-ol's found in taxon is recorded as Ruprechtia[11].
  • 5α,8α-epidioxyergosta-6,22-dien-3β-ol's found in taxon is recorded as Biemna ehrenbergi[12].
  • 5α,8α-epidioxyergosta-6,22-dien-3β-ol's isomeric SMILES is recorded as CC(C)C@@H/C=C/C@@H[C@H]1CCC2[C@@]34C=C[C@]5(CC@@HCC[C@]5(C)C3CC[C@@]21C)OO4C@@H/C=C/C@@H[C@H]1CCC2[C@@]34C=C[C@]5(CC@@HCC[C@]5(C)C3CC[C@@]21C)OO4">[13].
  • 5α,8α-epidioxyergosta-6,22-dien-3β-ol's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+428.329045268'}[14].
  • 5α,8α-epidioxyergosta-6,22-dien-3β-ol's Natural Product Atlas ID is recorded as NPA003521[15].
  • 5α,8α-epidioxyergosta-6,22-dien-3β-ol's UniChem compound ID is recorded as 32049810[16].

References

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

Direct Wikidata claims

  1. [2] . wikidata.org.
  2. [3] . wikidata.org.
  3. [4] . wikidata.org.
  4. [5] . PubChem. wikidata.org.
  5. [6] . wikidata.org.
  6. [7] . wikidata.org.
  7. [8] . PubChem. wikidata.org.
  8. [9] . wikidata.org.
  9. [10] . Secondary metabolites and antimycobacterial activities from the roots of Ficus nervosa. wikidata.org.
  10. [11] . Inhibitory effect of sterols from Ruprechtia triflora and diterpenes from Calceolaria pinnifolia on the growth of Mycobacterium tuberculosis. wikidata.org.
  11. [12] . Ehrenasterol and biemnic acid; new bioactive compounds from the Red Sea sponge Biemna ehrenbergi. 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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