(Q27137663)

inferred from SMILES

mass

428.365431±0 dalton

1 reference

6beta-Hydroxystigmast-4-en-3-one (English)

(6R,8S,9S,10S,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-6-hydroxy-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one

7 October 2016

stereoisomer of

1 reference

6alpha-Hydroxystigmast-4-en-3-one

1 reference

(6S,8R,9R,10S,13R,14R,17S)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-6-hydroxy-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one

1 reference

(6S,8S,9S,10R,13R,14S,17R)-17-[(2R,5S)-5-ethyl-6-methylheptan-2-yl]-6-hydroxy-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one

1 reference

chemical formula

C₂₉H₄₈O₂

1 reference

6beta-Hydroxystigmast-4-en-3-one (English)

7 October 2016

canonical SMILES

CCC(CCC(C)C1CCC2C1(CCC3C2CC(C4=CC(=O)CCC34C)O)C)C(C)C

1 reference

6beta-Hydroxystigmast-4-en-3-one (English)

7 October 2016

isomeric SMILES

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

1 reference

6beta-Hydroxystigmast-4-en-3-one (English)

7 October 2016

found in taxon

Pilocarpus grandiflorus

3 references

A New Imidazole Alkaloid and Other Constituents from Pilocarpus grandiflorus and their Antifungal Activity

A New Imidazole Alkaloid and Other Constituents from Pilocarpus grandiflorus and their Antifungal Activity

A New Imidazole Alkaloid and Other Constituents from Pilocarpus grandiflorus and their Antifungal Activity

Azolla nilotica

2 references

Chemical constituents of aquatic fern Azolla nilotica

Chemical constituents of aquatic fern Azolla nilotica

Acorus calamus

1 reference

A New Steroid Glycoside Derivative fromAcorus CalamusL.

Aframomum cereum

1 reference

Labdane diterpenoids from Aframomum sceptrum: NMR study and antiparasitic activities

Aframomum sceptrum

1 reference

Labdane diterpenoids from Aframomum sceptrum: NMR study and antiparasitic activities

Ailanthus altissima

1 reference

Sterones and indole alkaloid from Ailanthus altissima callus cultures

Aristolochia zollingeriana

1 reference

Sodium Aristolochates from the Flowers and Fruits ofAristolochia zollingeriana

Bauhinia purpurea

1 reference

Studies on the Constituents from the Bark ofBauhinia Purpurea

Beilschmiedia erythrophloia

1 reference

Endiandric Acid Analogues from the Roots of Beilschmiedia erythrophloia

Beilschmiedia tsangii

2 references

New cytotoxic tetrahydrofuran- and dihydrofuran-type lignans from the stem of Beilschmiedia tsangii

Anti-inflammatory endiandric acid analogues from the roots of Beilschmiedia tsangii

Castanopsis lamontii

1 reference

Terpenoids and steroids from Castanopsis lamontii: A new triterpene ketol

Cremanthodium discoideum

1 reference

Epoxide Sesquiterpenes and Steroids from Cremanthodium discoideum

Cymodocea nodosa

1 reference

3-Keto steroids from the marine organisms Dendrophyllia cornigera and Cymodocea nodosa

Etlingera elatior

1 reference

Antioxidative constituents of Etlingera elatior

Garcinia linii

1 reference

Benzopyrans, biphenyls and xanthones from the root of Garcinia linii and their activity against Mycobacterium tuberculosis

Semialarium mexicanum

1 reference

Triterpenoids from Hippocratea excelsa. The Crystal Structure of 29-Hydroxytaraxerol

Illigera luzonensis

1 reference

Aporphine alkaloids and cytotoxic lignans from the roots of Illigera luzonensis

Isolona congolana

1 reference

Constituents of Isolona maitlandii

Isolona maitlandii

1 reference

Constituents of Isolona maitlandii

Ixora coccinea

1 reference

Ixorapeptide I and ixorapeptide II, bioactive peptides isolated from Ixora coccinea

Macaranga tanarius

1 reference

Terpenoids and steroids from Macaranga tanarius

Mangifera indica

1 reference

Triterpenoids from Mangifera indicafn1fn1Part iii in the series Triterpenoids from Mangifera indica. For part ii see Anjaneyulu et al., 1989.

Magnolia compressa

1 reference

Chemical constituents from the stems of Michelia compressa VAR. lanyuensis

Muntingia calabura

1 reference

Flavones and Cytotoxic Constituents from the Stem Bark of Muntingia Calabura

Osmanthus armatus

1 reference

Constituents from the heartwoods of Osmanthus armatus

Patrinia rupestris

1 reference

Chemical Constituents from the Roots ofPatrinia Rupestris

Rhinacanthus nasutus

1 reference

A quinol and steroids from the leaves and stems of Rhinacanthus nasutus

Saussurea hieracioides

1 reference

Chemical constituents of Saussurea superba

Saussurea superba

1 reference

Chemical constituents of Saussurea superba

Veronica anagallis

1 reference

Aquaticol, a bis-sesquiterpene and iridoid glucosides from Veronica anagallis-aquatica

blue water-speedwell

1 reference

Aquaticol, a bis-sesquiterpene and iridoid glucosides from Veronica anagallis-aquatica

Xanthium sibiricum

1 reference

Chemical constituents from the roots of Xanthium sibiricum

Xanthium strumarium

1 reference

Chemical constituents from the roots of Xanthium sibiricum

Xylocarpus moluccensis

1 reference

Chemistry of Fijian Plants. XIV An Unsaturated Aryl Keto Acid from Xylocarpus moluccensis

Zantedeschia aethiopica

1 reference

Antialgal compounds from zantedeschia aethiopica

Zingiber officinale

1 reference

Diarylheptanoids from the rhizomes of Zingiber officinale

Pontederia africana

1 reference

One Alkenylphenol and Steroids from the Aquatic PlantMonochoria Vaginalis

Veronica americana

1 reference

Aquaticol, a bis-sesquiterpene and iridoid glucosides from Veronica anagallis-aquatica

Bistorta officinalis

1 reference

Chemical constituents from the roots of Polygonum bistorta

Persicaria amphibia

1 reference

Chemical constituents from the roots of Polygonum bistorta

Identifiers

InChI

InChI=1S/C29H48O2/c1-7-20(18(2)3)9-8-19(4)23-10-11-24-22-17-27(31)26-16-21(30)12-14-29(26,6)25(22)13-15-28(23,24)5/h16,18-20,22-25,27,31H,7-15,17H2,1-6H3/t19-,20-,22+,23-,24+,25+,27-,28-,29-/m1/s1

1 reference

6beta-Hydroxystigmast-4-en-3-one (English)

IWNCBADONFSAAW-NFVQQQKOSA-N

7 October 2016

InChIKey

2 references

6beta-Hydroxystigmast-4-en-3-one (English)

7 October 2016

ChEBI release 2020-09-01

CAS Registry Number

36450-02-9

1 reference

CAS (formerly Chemical Abstracts Service)

25 January 2022

1 reference

(6beta)-6-Hydroxystigmast-4-en-3-one (English)

7 October 2016

1 reference

6beta-Hydroxystigmast-4-en-3-one (English)

7 October 2016

ChEBI ID

69321

mapping relation type

2 references

6beta-hydroxystigmast-4-en-3-one (English)