20(29)-lupene-1beta,3alpha-diol (Q27136068)

(1R,3aR,5aR,5bR,7aS,9R,11R,11aR,11bS,13aR,13bS)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-9,11-diol

glochidiol (English)

7 October 2016

2 references

2 references

1 reference

20(29)-lupene-1beta,3beta-diol

2 references

(1R,3aS,5aR,5bR,7aR,9R,11R,11aS,11bS,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-9,11-diol

1 reference

1 reference

(1R,3aS,5aR,5bR,7aR,9S,11R,11aS,11bS,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-9,11-diol

inferred from InChI

1 reference

(1R,3aR,5aR,5bR,7aS,9S,11R,11aR,11bS,13aR,13bS)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-9,11-diol

inferred from InChI

1 reference

inferred from InChI

chemical formula

C₃₀H₅₀O₂

1 reference

glochidiol (English)

7 October 2016

CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(C(CC(C5(C)C)O)O)C)C)C

1 reference

glochidiol (English)

7 October 2016

CC(=C)[C@@H]1CC[C@]2([C@H]1[C@H]3CC[C@H]4[C@]([C@@]3(CC2)C)(CC[C@@H]5[C@@]4([C@@H](C[C@H](C5(C)C)O)O)C)C)C

1 reference

glochidiol (English)

7 October 2016

Phyllanthus velutinus

1 reference

Triterpenoids from Glochidion heyneanum*

Phyllanthus sellowianus

1 reference

A Biflavonoid from Phyllanthus sellowianus

Boswellia sacra

1 reference

Four new ursane-type triterpenes, olibanumols K, L, M, and N, from traditional egyptian medicine olibanum, the gum-resin of Boswellia carterii

Glochidion eriocarpum

2 references

Lupene triterpenoids from Glochidion eriocarpum

Cytotoxic activity of lupane-type triterpenes from Glochidion sphaerogynum and Glochidion eriocarpum two of which induce apoptosis.

Phyllanthus hohenackeri

1 reference

Chemical constituents of glochidion hohenackeri

Glochidion puberum

1 reference

Triterpenoids from Glochidion macrophyllum and G. puberum

Phyllanthus puberus

1 reference

Triterpenoids from Glochidion macrophyllum and G. puberum

Glochidion sphaerogynum

1 reference

Cytotoxic activity of lupane-type triterpenes from Glochidion sphaerogynum and Glochidion eriocarpum two of which induce apoptosis.

Phyllanthus sphaerogynus

1 reference

Cytotoxic activity of lupane-type triterpenes from Glochidion sphaerogynum and Glochidion eriocarpum two of which induce apoptosis.

Glochidion zeylanicum

1 reference

Potential anti-tumor promoting activity of lupane-type triterpenoids from the stem bark of Glochidion zeylanicum and Phyllanthus flexuosus

Monteverdia cuzcoina

2 references

Lupane triterpenoids from Maytenus species

Activity of lupane triterpenoids from Maytenus species as inhibitors of nitric oxide and prostaglandin E2.

Phyllanthus eriocarpus

2 references

Lupene triterpenoids from Glochidion eriocarpum

Cytotoxic activity of lupane-type triterpenes from Glochidion sphaerogynum and Glochidion eriocarpum two of which induce apoptosis.

Breynia fruticosa

1 reference

Triterpene and Sterol Derivatives from the Roots of Breynia fruticosa

Identifiers

InChI

InChI=1S/C30H50O2/c1-18(2)19-11-13-27(5)15-16-28(6)20(25(19)27)9-10-22-29(28,7)14-12-21-26(3,4)23(31)17-24(32)30(21,22)8/h19-25,31-32H,1,9-17H2,2-8H3/t19-,20+,21-,22-,23+,24+,25+,27+,28+,29+,30-/m0/s1

1 reference

SWEUJTWPRYKNNX-DZEONHSJSA-N

glochidiol (English)

7 October 2016

2 references

glochidiol (English)

7 October 2016

ChEBI release 2020-09-01

CAS Registry Number

6610-56-6

1 reference

CAS (formerly Chemical Abstracts Service)

25 January 2022

1 reference

glochidiol (English)

7 October 2016

2 references

matched by identifier from

English

title

glochidiol (English)

retrieved

7 October 2016

InChIKey

SWEUJTWPRYKNNX-DZEONHSJSA-N

Reaxys registry number

6575511

1 reference

English

title

20(29)-lupene-1beta,3alpha-diol (English)

retrieved

7 October 2016

ChEBI ID

67598

mapping relation type

2 references