(Q105348631)

English

YHVNCBGBSMUHPF-UHFFFAOYSA-N

group of stereoisomers with the chemical formula C₆₂H₁₀₄O₃₁

In more languages

Statements

group of stereoisomers

0 references

furostan steroid

1 reference

furostan steroid

1,344.656156548 dalton

1 reference

based on heuristic

inferred from SMILES

chemical formula

C₆₂H₁₀₄O₃₁

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canonical SMILES

OCC1OC(OCC(C)CCC2(OC)OC3CC4C5CCC6CC(OC7OC(CO)C(OC8OC(CO)C(O)C(OC9OCC(O)C(O)C9O)C8OC%10OCC(O)C(O)C%10O)C(O)C7OC%11OC(C)C(O)C(O)C%11O)CCC6(C)C5CCC4(C)C3C2C)C(O)C(O)C1O

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Tribulus terrestris

4 references

In vitro and in vivo antifungal activities of the eight steroid saponins from Tribulus terrestris L. with potent activity against fluconazole-resistant fungal pathogens.

Food supplements ofTribulus terrestris L.: An HPLC-ESI-MS method for an estimation of the saponin content

Antifungal activities and action mechanisms of compounds from Tribulus terrestris L

Terrestrinins A and B, two new steroid saponins from Tribulus terrestris

Identifiers

InChI=1S/C62H104O31/c1-23(20-81-54-47(77)44(74)41(71)34(17-63)86-54)9-14-62(80-6)24(2)37-33(93-62)16-30-28-8-7-26-15-27(10-12-60(26,4)29(28)11-13-61(30,37)5)85-58-52(91-57-48(78)43(73)38(68)25(3)84-57)49(79)50(36(19-65)88-58)89-59-53(92-56-46(76)40(70)32(67)22-83-56)51(42(72)35(18-64)87-59)90-55-45(75)39(69)31(66)21-82-55/h23-59,63-79H,7-22H2,1-6H3

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YHVNCBGBSMUHPF-UHFFFAOYSA-N

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2 references

15 September 2022

matched by identifier from

YHVNCBGBSMUHPF-UHFFFAOYSA-N

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