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Trisporic acid information


Trisporic acid

Trisporic acid A

Trisporic acid B

Trisporic acid C
Identifiers
CAS Number
  • A: 161023-29-6
  • B: 26057-02-3
  • C: 26055-09-4
3D model (JSmol)
  • A: Interactive image
  • B: Interactive image
  • C: Interactive image
ChEBI
  • CHEBI:91017
PubChem CID
  • A: 90471808
  • B: 90470632
  • C: 101306749
InChI
  • A: InChI=1S/C18H26O3/c1-5-6-7-8-13(2)9-10-15-14(3)16(19)11-12-18(15,4)17(20)21/h8-10H,5-7,11-12H2,1-4H3,(H,20,21)/b10-9+,13-8+/t18-/m0/s1
    Key: OSQWPUQNCKZCOA-WVPSHWIESA-N
  • B: InChI=1S/C18H24O4/c1-12(6-5-7-13(2)19)8-9-15-14(3)16(20)10-11-18(15,4)17(21)22/h6,8-9H,5,7,10-11H2,1-4H3,(H,21,22)/b9-8+,12-6+/t18-/m0/s1
    Key: AUOKEERYXZUYBN-YEOBPPCSSA-N
  • C: InChI=1S/C18H26O4/c1-12(6-5-7-13(2)19)8-9-15-14(3)16(20)10-11-18(15,4)17(21)22/h6,8-9,13,19H,5,7,10-11H2,1-4H3,(H,21,22)/b9-8+,12-6+/t13-,18+/m1/s1
    Key: JYCOWXFWTZCULN-KSUWSPNXSA-N
SMILES
  • A: CCCC/C=C(\C)/C=C/C1=C(C(=O)CC[C@]1(C)C(=O)O)C
  • B: CC1=C([C@@](CCC1=O)(C)C(=O)O)/C=C/C(=C/CCC(=O)C)/C
  • C: CC1=C([C@@](CCC1=O)(C)C(=O)O)/C=C/C(=C/CC[C@@H](C)O)/C
Properties
Chemical formula
A: C18H26O3
B: C18H24O4
C: C18H26O4
Molar mass A: 290.40 g/mol
B: 304.39 g/mol
C: 306.40 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Trisporic acids (TSAs) are C-18 terpenoid compounds synthesized via β-carotene and retinol pathways in the zygomycetes. They are pheromone compound responsible for sexual differentiation in those fungal species. TSAs and related compounds make up the trisporoid group of chemicals.[1]

  1. ^ Gooday GW, Carlile MJ (August 1997). "The discovery of fungal sex hormones: III. Trisporic acid and its precursors". Mycologist. 11 (3): 126–130. doi:10.1016/S0269-915X(97)80017-1.

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