(Q27277014)

inferred from SMILES

mass

426.386±0 dalton

1 reference

(1R,3aR,5aR,5bR,7aS,9R,11aR,11bR,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]chrysen-9-ol

Epilupeol (English)

14 October 2016

2 references

(1R,3aR,5aR,5bR,7aR,9R,11aR,11bR,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]chrysen-9-ol

2 references

(1R,3aS,5aS,5bR,7aS,9S,11aR,11bS,13aS,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]chrysen-9-ol

2 references

(1R,3aR,5aR,5bR,7aR,9R,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]chrysen-9-ol

2 references

(1R,3aR,5aR,5bR,7aR,9R,11aS,11bR,13aS,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]chrysen-9-ol

2 references

(1S,3aR,5aR,5bR,7aR,9R,11aR,11bR,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]chrysen-9-ol

2 references

(1R,3aR,5aR,5bR,7aR,9S,11aR,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]chrysen-9-ol

2 references

(1R,3aR,5aR,5bR,7aS,9S,11aR,11bR,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]chrysen-9-ol

1 reference

1 reference

(1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aS,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]chrysen-9-ol

1 reference

(1R,3aR,5aS,5bR,7aR,9S,11aR,11bR,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]chrysen-9-ol

1 reference

(1R,3aR,5aR,5bR,7aR,9S,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]chrysen-9-ol

1 reference

(1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aS,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]chrysen-9-ol

1 reference

(1R,3aR,5aR,5bR,7aR,9R,11aR,11bS,13aS,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]chrysen-9-ol

1 reference

(1R,3aS,5aR,5bR,7aR,9R,11aR,11bR,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]chrysen-9-ol

1 reference

(1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,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]chrysen-9-ol

1 reference

(1R,3aR,5aR,5bR,7aR,9S,11aS,11bR,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]chrysen-9-ol

1 reference

chemical formula

C₃₀H₅₀O

1 reference

Epilupeol (English)

14 October 2016

CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C

1 reference

Epilupeol (English)

14 October 2016

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

1 reference

Notes: On the Chemical Nature of Epicuticular Waxes in Some Succulent Kalanchoe and Senecio Species

Epilupeol (English)

14 October 2016

1 reference

Bursera graveolens

2 references

A New and Known Cytotoxic Aryltetralin-Type Lignans from Stems of Bursera graveolens.

A new and known cytotoxic aryltetralin-type lignans from stems of Bursera graveolens

Bursera simaruba

1 reference

A New Triterpene from the Resin of Bursera simaruba

Commiphora dalzielii

2 references

Dammarane Triterpenes from the stem bark of Commiphora Dalzielii

Dammarane Triterpenes from the stem bark of Commiphora Dalzielii

Picramnia teapensis

1 reference

Triterpene benzoates from the bark of Picramnia teapensis (Simaroubaceae)

Pyrus communis

1 reference

Triterpenoids from the stembark ofPyrus Communis

Vicoa indica

1 reference

Antiviral Constituents from Vicoa indica

Euphorbia fischeriana

1 reference

Cycloartane-type triterpenes from Euphorbia fischeriana stimulate human CYP3A4 promoter activity

Sapium haematospermum

2 references

Mycobacterium tuberculosis growth inhibition by constituents of Sapium haematospermum

Mycobacterium tuberculosis growth inhibition by constituents of Sapium haematospermum

Alstonia boonei

1 reference

Triterpenes from Alstonia boonei

Arctotheca populifolia

1 reference

Sesquiterpene lactones and farnesol derivatives from Arctotis and Aarctotheca species

Hedlundia hybrida

1 reference

Isocedrene derivatives and other sesquiterpenes from moscharia pinnatifida

Blainvillea acmella

2 references

Acanthospermolides and other constituents from Blainvillea acmella

A further steiractinolide derivative from Spilanthes leiocarpa

Spilanthes acmella

2 references

Acanthospermolides and other constituents from Blainvillea acmella

A further steiractinolide derivative from Spilanthes leiocarpa

Boswellia sacra

2 references

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

Absolute stereostructures of olibanumols A, B, C, H, I, and J from olibanum, gum-resin of Boswellia carterii, and inhibitors of nitric oxide production in lipopolysaccharide-activated mouse peritoneal macrophages

Bruguiera cylindrica

1 reference

Triterpenoid Esters from Bruguiera cylindrica

Excoecaria agallocha

1 reference

Pentacyclic triterpenoids from leaves of Excoecaria agallocha

Glochidion eriocarpum

1 reference

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

Harungana madagascariensis

1 reference

Prenylated anthronoid antioxidants from the stem bark of Harungana madagascariensis.

Moscharia pinnatifida

1 reference

Isocedrene derivatives and other sesquiterpenes from moscharia pinnatifida

Neolitsea parvigemma

1 reference

Chemical Constituents ofNeolitsea parvigemmaandNeolitsea konishii

Onoseris lopezii

1 reference

Onognaphalin, a further 5-methyl coumarin from Onoseris gnaphalioides

Kleinia anteuphorbium

1 reference

Neue germacren-derivate aus Senecio-arten

Stilpnopappus glomeratus

1 reference

Germacranolides from Stilpnopappus species

Phyllanthus eriocarpus

1 reference

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

Sapium rigidifolium

1 reference

Rigidol, an unusual diterpene from Sapium rigidifolium

Euonymus carnosus

1 reference

Lupane triterpenoids from the stems of Euonymus carnosus

Boswellia carteri

1 reference

Absolute stereostructures of olibanumols A, B, C, H, I, and J from olibanum, gum-resin of Boswellia carterii, and inhibitors of nitric oxide production in lipopolysaccharide-activated mouse peritoneal macrophages

Identifiers

InChI

InChI=1S/C30H50O/c1-19(2)20-11-14-27(5)17-18-29(7)21(25(20)27)9-10-23-28(6)15-13-24(31)26(3,4)22(28)12-16-30(23,29)8/h20-25,31H,1,9-18H2,2-8H3/t20-,21+,22-,23+,24+,25+,27+,28-,29+,30+/m0/s1

1 reference

Epilupeol (English)

14 October 2016

1 reference

Global Substance Registration System

Epilupeol (English)

14 October 2016

2 references

UNII

E8SUT3IMRZ

epilupeol (English)

14 October 2016

https://commonchemistry.cas.org/detail?cas_rn=4439-99-0

10 April 2021

1 reference

(3alpha)-Lup-20(29)-en-3-ol (English)

14 October 2016

2 references

Epilupeol (English)

retrieved

14 October 2016

InChIKey

ChEBI ID

182364

mapping relation type

exact match

2 references

ChEBI release 2022-06-13

International Chemical Identifier

InChI

InChI=1S/C30H50O/c1-19(2)20-11-14-27(5)17-18-29(7)21(25(20)27)9-10-23-28(6)15-13-24(31)26(3,4)22(28)12-16-30(23,29)8/h20-25,31H,1,9-18H2,2-8H3/t20-,21+,22-,23+,24+,25+,27+,28-,29+,30+/m0/s1

1 reference

splash10-0a4i-2920100000-8689154e5ecb9cc0abf6

CHEMBL459702 (English)

14 October 2016

1 reference

0 references

DSSTox substance ID

DTXSID701318679

1 reference

InChIKey

UNII

E8SUT3IMRZ

2 references

Global Substance Registration System

UNII

E8SUT3IMRZ

epilupeol (English)

retrieved

14 October 2016

InChIKey