(Q104397720)

English

BJNQXJIQCPPOHN-LQSBXWATSA-N

group of stereoisomers with the chemical formula C₅₀H₈₂O₂₂

In more languages

Statements

group of stereoisomers

0 references

1 reference

1,034.529774264 dalton

1 reference

based on heuristic

inferred from SMILES

chemical formula

C₅₀H₈₂O₂₂

0 references

canonical SMILES

OCC1OC(OC2C(OC(CO)C(O)C2OC3OCC(O)C(O)C3O)OC4C(O)C(O)C(OC5CCC6(C)C(CCC7C6CCC8(C)C7CC9OC%10(OCC(C)CC%10)C(C)C98)C5)OC4CO)C(O)C(O)C1O

0 references

isomeric SMILES

CC1CC[C@@]2(OC1)O[C@H]1C[C@H]3[C@@H]4CC[C@H]5CC(OC6OC(CO)C(OC7OC(CO)C(O)C(OC8OCC(O)C(O)C8O)C7OC7OC(CO)C(O)C(O)C7O)C(O)C6O)CC[C@]5(C)[C@@H]4CC[C@]3(C)[C@@H]1C2C

0 references

Anemarrhena asphodeloides

1 reference

Saponins of anemarrhenae rhizoma

Solanum dulcamara

1 reference

Steroidal glycosides from Solanum torvum

1 reference

Further studies on steroidal glycosides from bulbs, roots and leaves of Allium sativum L.

Chlorophytum comosum

1 reference

Steroidal saponins from the underground parts of Chlorophytum comosum and their inhibitory activity on tumour promoter-induced phospholipids metabolism of HeLa cells

Solanum lyratum

1 reference

Steroidal glycoside and glycoalkaloid from Solanum lyratum

Identifiers

InChI=1S/C50H82O22/c1-20-7-12-50(64-18-20)21(2)32-28(72-50)14-26-24-6-5-22-13-23(8-10-48(22,3)25(24)9-11-49(26,32)4)65-45-40(62)37(59)41(31(17-53)68-45)69-47-43(71-46-39(61)36(58)34(56)29(15-51)66-46)42(35(57)30(16-52)67-47)70-44-38(60)33(55)27(54)19-63-44/h20-47,51-62H,5-19H2,1-4H3/t20?,21?,22-,23?,24+,25+,26-,27?,28-,29?,30?,31?,32+,33?,34?,35?,36?,37?,38?,39?,40?,41?,42?,43?,44?,45?,46?,47?,48-,49-,50+/m0/s1

0 references

BJNQXJIQCPPOHN-LQSBXWATSA-N

0 references

1 reference

15 September 2022

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q104397720&oldid=2129867428"