(Q104393396)

English

Stypodiol

chemical compound

In more languages

Statements

type of chemical entity

0 references

(7S,8R,10aR)-1,1,4a,7,7',8a-hexamethylspiro[2,3,4,4b,5,6,7,9,10,10a-decahydrophenanthrene-8,2'-3H-1-benzofuran]-2,5'-diol

1 reference

based on heuristic

inferred from SMILES

(4aS,4bR,7S,8S,8aR,10aR)-1,1,4a,7,7',8a-hexamethylspiro[2,3,4,4b,5,6,7,9,10,10a-decahydrophenanthrene-8,2'-3H-1-benzofuran]-2,5'-diol

1 reference

based on heuristic

inferred from SMILES

1,1,4a,7,7',8a-hexamethylspiro[2,3,4,4b,5,6,7,9,10,10a-decahydrophenanthrene-8,2'-3H-1-benzofuran]-2,5'-diol

1 reference

based on heuristic

inferred from SMILES

412.29774514 dalton

1 reference

based on heuristic

inferred from SMILES

stereoisomer of

2 references

based on heuristic

inferred from InChIKey

based on heuristic

inferred from InChI

chemical formula

C₂₇H₄₀O₃

0 references

canonical SMILES

OC=1C=C(C=2OC3(CC2C1)C(C)CCC4C5(C)CCC(O)C(C)(C)C5CCC43C)C

0 references

isomeric SMILES

Cc1cc(O)cc2c1O[C@@]1(C2)[C@@H](C)CC[C@@H]2[C@@]3(C)CC[C@H](O)C(C)(C)[C@@H]3CC[C@]21C

0 references

Stypopodium zonale

2 references

Chemical variation in the tropical seaweed Stypopodium zonale (dictyotaceae)

Ichthyotoxic and cytotoxic metabolites of the tropical brown alga Stypopodium zonale (Lamouroux) Papenfuss

Stypopodium flabelliforme

2 references

Neurotoxic meroditerpenoids from the tropical marine brown alga Stypopodium flabelliforme.

Anti-proliferative activity of meroditerpenoids isolated from the brown alga Stypopodium flabelliforme against several cancer cell lines.

Identifiers

InChI=1S/C27H40O3/c1-16-13-19(28)14-18-15-27(30-23(16)18)17(2)7-8-21-25(5)11-10-22(29)24(3,4)20(25)9-12-26(21,27)6/h13-14,17,20-22,28-29H,7-12,15H2,1-6H3/t17-,20-,21+,22-,25-,26+,27-/m0/s1

0 references

JTFQPSRKDMDRKT-LYIAKFBWSA-N

0 references

1 reference

17 September 2022

based on heuristic

inferred from InChIKey

UniChem compound ID

1 reference

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