cycloart-23-ene-3beta,25-diol (Q27138958)

inferred from SMILES

mass

442.381081±0 dalton

1 reference

Cycloart-23-en-3beta,25-diol

Handianol (English)

7 October 2016

2 references

inferred from InChIKey

(1S,3R,6S,8S,11S,12R,15R,16R)-15-[(E,2S)-6-hydroxy-6-methylhept-4-en-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol

inferred from InChI

2 references

inferred from InChIKey

9beta,19-cyclo-lanost-23Z-en-3beta,25-diol

inferred from InChI

1 reference

inferred from InChI

chemical formula

C₃₀H₅₀O₂

1 reference

Handianol (English)

7 October 2016

CC(CC=CC(C)(C)O)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C

1 reference

Handianol (English)

7 October 2016

C[C@H](C/C=C/C(C)(C)O)[C@H]1CC[C@@]2([C@@]1(CC[C@]34[C@H]2CC[C@@H]5[C@]3(C4)CC[C@@H](C5(C)C)O)C)C

1 reference

Lupane triterpenes with a δ-lactone at ring E, from Lippia mexicana.

Handianol (English)

7 October 2016

2 references

Lupane triterpenes with a δ-lactone at ring E, from Lippia mexicana.

Aglaia andamanica

1 reference

Phytochemical investigation of Aglaia andamanica

Aglaia rubiginosa

1 reference

Phytochemical investigation of Aglaia rubiginosa

Amberboa ramosa

1 reference

Tyrosinase inhibitory cycloartane type triterpenoids from the methanol extract of the whole plant of Amberboa ramosa Jafri and their structure-activity relationship

Artemisia argyi

1 reference

Bioactive constituents of Chinese natural medicines. I. New sesquiterpene ketones with vasorelaxant effect from Chinese moxa, the processed leaves of Artemisia argyi Levl. et Vant.: moxartenone and moxartenolide

breadfruit

1 reference

Sterols and triterpenes from the fruit of Artocarpus altilis

Artocarpus heterophyllus

1 reference

Triterpenoids from Artocarpus heterophyllus

Euphorbia bungei

1 reference

Macrocyclic diterpenoids from the Iranian plant Euphorbia bungei Boiss

Euphorbia esula

2 references

Ingenane diterpenoids from Euphorbia esula

Sesquiterpenoids from Euphorbia wangii

Euphorbia myrsinites

1 reference

Four diterpene esters from Euphorbia myrsinites

Euphorbia petiolata

1 reference

Sesquiterpenoids from Euphorbia wangii

Euphorbia pulcherrima

1 reference

Cytotoxic triterpenoids from the leaves of Euphorbia pulcherrima.

Guarea macrophylla

1 reference

Cycloartane triterpenoids from Guarea macrophylla.

Houttuynia cordata

1 reference

The constituents and their bioactivities of Houttuynia cordata

Oligochaeta divaricata

1 reference

Tyrosinase inhibitory cycloartane type triterpenoids from the methanol extract of the whole plant of Amberboa ramosa Jafri and their structure-activity relationship

Aglaia lawii

1 reference

Phytochemical investigation of Aglaia andamanica

Identifiers

InChI

InChI=1S/C30H50O2/c1-20(9-8-14-25(2,3)32)21-12-15-28(7)23-11-10-22-26(4,5)24(31)13-16-29(22)19-30(23,29)18-17-27(21,28)6/h8,14,20-24,31-32H,9-13,15-19H2,1-7H3/b14-8+/t20-,21-,22+,23+,24+,27-,28+,29-,30+/m1/s1

1 reference

JSPGKOBNHWTKNT-CPGXJQKCSA-N

Handianol (English)

7 October 2016

2 references

Handianol (English)

7 October 2016

ChEBI release 2020-09-01

1 reference

(3beta,9beta,23E)-9,19-Cyclolanost-23-ene-3,25-diol (English)

7 October 2016

2 references

matched by identifier from

Handianol (English)

retrieved

7 October 2016

InChIKey

JSPGKOBNHWTKNT-CPGXJQKCSA-N

ChEBI ID

70625

mapping relation type

2 references

matched by identifier from

cycloart-23-ene-3beta,25-diol (English)

retrieved

7 October 2016

International Chemical Identifier

InChI

InChI=1S/C30H50O2/c1-20(9-8-14-25(2,3)32)21-12-15-28(7)23-11-10-22-26(4,5)24(31)13-16-29(22)19-30(23,29)18-17-27(21,28)6/h8,14,20-24,31-32H,9-13,15-19H2,1-7H3/b14-8+/t20-,21-,22+,23+,24+,27-,28+,29-,30+/m1/s1

1 reference