(Q105279730)

English

(1S,4S,5R,8R,10S,13S,14R,17S,18R,19S,20R)-10-hydroxy-4,5,9,9,13,19,20-heptamethyl-24-oxahexacyclo[15.5.2.0¹,¹⁸.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracos-15-en-23-one

chemical compound

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Statements

instance of

type of chemical entity

0 references

1 reference

454.344695332 dalton

1 reference

based on heuristic

inferred from SMILES

stereoisomer of

(1S,4R,5R,8R,10S,13R,14S,17S,18S,19R,20S)-10-hydroxy-4,5,9,9,13,19,20-heptamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracos-15-en-23-one

1 reference

based on heuristic

inferred from InChI

(1S,4S,5R,8S,10S,13S,14R,17S,18R,19S,20S)-10-hydroxy-4,5,9,9,13,19,20-heptamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracos-15-en-23-one

1 reference

based on heuristic

inferred from InChI

chemical formula

C₃₀H₄₆O₃

0 references

canonical SMILES

O=C1OC23C=CC4C5(C)CCC(O)C(C)(C)C5CCC4(C)C3(C)CCC16CCC(C)C(C)C26

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isomeric SMILES

C[C@H]1[C@H](C)CC[C@@]23CC[C@]4(C)[C@@](C=C[C@@H]5[C@@]6(C)CC[C@H](O)C(C)(C)[C@@H]6CC[C@]54C)(OC2=O)[C@H]13

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found in taxon

Bursera penicillata

1 reference

stated in

Two triterpenoid lactones from the resin of Bursera delpechiana

Centella asiatica

1 reference

stated in

Antiproliferative constituents from Umbelliferae plants VII. Active triterpenes and rosmarinic acid from Centella asiatica

Dracocephalum forrestii

1 reference

stated in

Three New Triterpenoids fromDracocephalum forrestii

Eriobotrya japonica

1 reference

stated in

Anti-inflammatory and antitumor-promoting effects of the triterpene acids from the leaves of Eriobotrya japonica

Eucalyptus camaldulensis

2 references

stated in

Triterpenoidal constituents from Eucalyptus camaldulensis var. obtusa leaves

stated in

Ovarian antiproliferative activity directed isolation of triterpenoids from fruits of Eucalyptus camaldulensis Dehnh

Eucalyptus tereticornis

2 references

stated in

Determination of ursolic acid and ursolic acid lactone in the leaves of Eucalyptus tereticornis by HPLC

stated in

Triterpene esters from Eucalyptus tereticornis

Hymenodictyon excelsum

1 reference

stated in

Acetylenic fatty acids, triglyceride and triterpenes from the leaves of Hymenodictyon excelsum

Hymenodictyon orixense

1 reference

stated in

Acetylenic fatty acids, triglyceride and triterpenes from the leaves of Hymenodictyon excelsum

yerba mate

1 reference

stated in

Brazilian natural medicines. III. structures of triterpene oligoglycosides and lipase inhibitors from mate, leaves of ilex paraguariensis

Incarvillea arguta

1 reference

stated in

A New Cyclooxygenase Inhibitor from Incarvillea arguta

Incarvillea diffusa

1 reference

stated in

A New Cyclooxygenase Inhibitor from Incarvillea arguta

Lavandula angustifolia

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stated in

Triterpenoids from lavandula spica

Lavandula spica

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stated in

Triterpenoids from lavandula spica

Bursera linanoe

1 reference

stated in

Two triterpenoid lactones from the resin of Bursera delpechiana

Rhaphiolepis loquata

1 reference

stated in

Anti-inflammatory and antitumor-promoting effects of the triterpene acids from the leaves of Eriobotrya japonica

Lavandula latifolia

1 reference

stated in

Triterpenoids from lavandula spica

Identifiers

InChI

InChI=1S/C30H46O3/c1-18-8-14-29-17-16-28(7)27(6)13-9-20-25(3,4)22(31)11-12-26(20,5)21(27)10-15-30(28,33-24(29)32)23(29)19(18)2/h10,15,18-23,31H,8-9,11-14,16-17H2,1-7H3/t18-,19+,20+,21-,22+,23-,26+,27-,28+,29+,30+/m1/s1

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InChIKey

UVBLDLGZDSGCSN-RUOWOPRNSA-N

0 references

2 references

17 September 2022

inferred from InChIKey

matched by identifier from

InChIKey

UVBLDLGZDSGCSN-RUOWOPRNSA-N

1 reference

(Q105279730)

(1S,4S,5R,8R,10S,13S,14R,17S,18R,19S,20R)-10-hydroxy-4,5,9,9,13,19,20-heptamethyl-24-oxahexacyclo[15.5.2.0¹,¹⁸.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracos-15-en-23-one

Statements

Identifiers

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