Poriferasterol (Q27108047)

Poriferasterol (English)

(3S,8S,9R,10R,13S,14S,17S)-17-[(E,2S,5S)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol

5 October 2016

stereoisomer of

2 references

(3S,8S,9S,10R,13R,14S,17R)-17-[(E,2S,5S)-5-Ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol

2 references

(3S,8R,9R,10R,13R,14R,17R)-17-[(E,2R,5R)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol

2 references

(3S,8S,9S,10R,13R,14S,17S)-17-[(Z,2S,5S)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol

2 references

2 references

(3S,8S,9S,10R,13R,14S,17R)-17-[(E,2S,5R)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol

2 references

(3S,8R,9R,10R,13R,14R,17R)-17-[(E,2S,5S)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol

2 references

(3R,8R,9R,10S,13R,14R,17R)-17-[(Z,2S,5S)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol

2 references

(3S,8R,9S,10R,13R,14S,17S)-17-[(E,2S,5S)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol

2 references

(3S,8S,9S,10R,13R,14S,17S)-17-[(E,2S,5S)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol

1 reference

(3S,8S,9S,10R,13R,14S,17S)-17-[(E,2R,5S)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol

1 reference

(3S,8R,9R,10R,13R,14R,17R)-17-[(Z,2S,5S)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol

1 reference

(3S,8R,9R,10R,13R,14R,17R)-17-[(E,2R,5S)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol

1 reference

(3S,8S,9S,10R,13R,14S,17R)-17-[(Z,2R,5R)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol

1 reference

(3S,8S,9S,10R,13R,14S,17R)-17-[(Z,2R,5S)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol

1 reference

chemical formula

C₂₉H₄₈O

1 reference

Poriferasterol (English)

5 October 2016

canonical SMILES

CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C

1 reference

Poriferasterol (English)

5 October 2016

isomeric SMILES

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

1 reference

Sterol composition of some gorgonians from the Senegalese coast

Poriferasterol (English)

5 October 2016

1 reference

Ellisella paraplexauroides

1 reference

Sterol composition of some gorgonians from the Senegalese coast

Eunicella labiata

1 reference

Sterol composition of some gorgonians from the Senegalese coast

Leptogorgia ruberrima

1 reference

Sterol composition of some gorgonians from the Senegalese coast

Leptogorgia viminalis

1 reference

Sterol composition of some gorgonians from the Senegalese coast

Leptogorgia violetta

1 reference

Sterol composition of some gorgonians from the Senegalese coast

Hydnora johannis

1 reference

Antibacterial activity, cytotoxicity and chemical constituents of Hydnora johannis roots

Salvia jaminiana

1 reference

Components and antibacterial activity of the roots of Salvia jaminiana

Teucrium leucocladum

1 reference

Chemical analysis and biological activities of the essential oil of Teucrium leucocladum Boiss. (Lamiaceae)

Achillea santolina

1 reference

Further constituents of Achillea ageratum

Aglaia lawii

1 reference

A pregnane steroid from Aglaia lawii and structure confirmation of cabraleadiol monoacetate by X-ray crystallography

Alysicarpus monilifer

1 reference

Alysinol--a new triterpene from Alysicarpus monolifer

Boodleopsis pusilla

1 reference

Sterol composition of twelve chlorophyceae from the senegalese coast and their chemotaxonomic significance

Caulerpa racemosa

1 reference

Sterol composition of twelve chlorophyceae from the senegalese coast and their chemotaxonomic significance

Chrysotila lamellosa

1 reference

Sterols of the unicellular algae Nematochrysopsis roscoffensis and Chrysotila lamellosa: isolation of (24E)-24-n-propylidenecholesterol and 24-n-propylcholesterol

Clerodendrum infortunatum

1 reference

The 24α- and 24β-epimers of 24-ethylcholesta-5,22-dien-3β-ol in two Clerodendrum species

Codium dichotomum

1 reference

Sterol composition of twelve chlorophyceae from the senegalese coast and their chemotaxonomic significance

Enteromorpha clathrata

1 reference

Sterol composition of twelve chlorophyceae from the senegalese coast and their chemotaxonomic significance

Ochromonas malhamensis

2 references

Biosynthesis of the C29-phytosterol side-chain: evidence that the same stereochemistry at C-25 can originate from different mechanisms

Biosynthesis of poriferasterol in Ochromonas malhamensis: 13C NMR assignment of the isopropyl methyl groups of 2-methylpentan-3-ol

Pavlova gyrans

1 reference

Free and combined sterols ofPavlova gyrans

Ulva fasciata

1 reference

Sterol composition of twelve chlorophyceae from the senegalese coast and their chemotaxonomic significance

Sea lettuce

1 reference

Sterol composition of twelve chlorophyceae from the senegalese coast and their chemotaxonomic significance

Angelica sinensis

1 reference

Serotonergic activity-guided phytochemical investigation of the roots of Angelica sinensis

Armillaria mellea

1 reference

Steroids from Armillaria mellea rhizomorphs

Aureoumbra lagunensis

1 reference

Sterol composition of Aureoumbra lagunensis, the Texas brown tide alga

Glebionis coronaria

2 references

Novel plant growth inhibitors and an insect antifeedant from Chrysanthemum coronarium (Japanese name: shungiku).

Novel Plant Growth Inhibitors and an Insect Antifeedant fromChrysanthemum coronarium(Japanese Name: Shungiku)

Glebionis coronarium

2 references

Novel plant growth inhibitors and an insect antifeedant from Chrysanthemum coronarium (Japanese name: shungiku).

Novel Plant Growth Inhibitors and an Insect Antifeedant fromChrysanthemum coronarium(Japanese Name: Shungiku)

Cliona celata

1 reference

Sterols from the sponges Cliona celata grant and Hymeniacidon perleve montagu

Corbicula fluminea

1 reference

Sterols and Other Unsaponifiable Substances in the Lipids of Shell Fishes, Crustacea and Echinoderms. XIV. Unsaponifiable Components Other Than Corbisterol in the Lipid of Corbicula

Corbicula leana

1 reference

Sterols and Other Unsaponifiable Substances in the Lipids of Shell Fishes, Crustacea and Echinoderms. XIV. Unsaponifiable Components Other Than Corbisterol in the Lipid of Corbicula

Coriaria intermedia

1 reference

20-Epibryonolic acid, phytosterols and ellagic acid from Coriaria intermedia

Coriaria japonica

1 reference

20-Epibryonolic acid, phytosterols and ellagic acid from Coriaria intermedia

Dumortiera hirsuta

2 references

A 7-nordumortenone and other dumortane derivatives from the Argentine liverwort Dumortiera hirsuta

Sesquiterpene and other constituents of the liverwort Dumortiera hirsuta

Erythrina indica

1 reference

Cytotoxic isoflavones from Erythrina indica.

Erythrina variegata

1 reference

Cytotoxic isoflavones from Erythrina indica.

Eutreptia viridis

1 reference

Sterols of the cultured euglenid Eutreptia viridis: a novel delta 23-unsaturated sterol

Fatsia japonica

1 reference

The first naturally occurring phytyl esters and hexane soluble non-volatiles from leaves of Fatsia japonica

Diplopterygium glaucum

1 reference

Triterpene Alcohols and Sterols from the Fern Gleichenia japonica SPR.

Gleichenia japonica

1 reference

Triterpene Alcohols and Sterols from the Fern Gleichenia japonica SPR.

Exallage auricularia

1 reference

Chemical constituents of Actinodaphne augustifolia, Croton sparsiflorus, Duabanga sonneratiodes, Glycosmis mauritiana, Hedyotis auricularia, Lyonia ovalifolia, Micromelum pubescens, Pyrus pashia and Rhododendron niveum

Water net

1 reference

24-Methylene-25-methylcholesterol and both C-24 epimers of 24-ethyl-22-dehydrocholesterol in a freshwater green algaHydrodictyon reticulatum

Kalanchoe marmorata

1 reference

Co-occurrence of C-24 epimeric 24-ethylsterols possessing and lacking a Δ25-bond inKalanchoe petitiana

Kalanchoe petitiana

1 reference

Co-occurrence of C-24 epimeric 24-ethylsterols possessing and lacking a Δ25-bond inKalanchoe petitiana

Khaya senegalensis

1 reference

Rearranged limonoids from Khaya senegalensis

Ligularia veitchiana

1 reference

Eremophilanolides from the roots of Ligularia veitchiana

Ophioplocus japonicus

1 reference

On the Unsaponifiable Matters of the Echino derms. III. On the Sterol Components of " Ophioplocus japOnicus".

Petrosia weinbergi

1 reference

Sterols of the marine sponge Petrosia weinbergi: implications for the absolute configurations of the antiviral orthoesterols and weinbersterols

Axinella aruensis

1 reference

Minor and trace sterols in marine invertebrates. 61. Isolation and structure elucidation of new A-nor sterols from the marine sponge Phakellia aruensis

Ruprechtia tangarana

1 reference

Isolation and structure of ruprechstyril from Ruprechtia tangarana

Calyptocarpus vialis

1 reference

Sesquiterpene lactones and other constituents of Stevia maimarensis and Synedrellopsis grisebachii

Synedrellopsis grisebachii

1 reference

Sesquiterpene lactones and other constituents of Stevia maimarensis and Synedrellopsis grisebachii

Psorospermum laurentii

1 reference

Laurentixanthones A and B, antimicrobial xanthones from Vismia laurentii

Vismia laurentii

1 reference

Laurentixanthones A and B, antimicrobial xanthones from Vismia laurentii

Cipangopaludina japonica

1 reference

On the Sterols of “Viviparus Japonicus” (Fresh Water Rolled Shell Fish) .

Neoraputia magnifica

1 reference

A pyrano chalcone and a flavanone from Neoraputia magnifica

Leptogorgia rubroflavescens

1 reference

Sterol composition of some gorgonians from the Senegalese coast

Scandosorbus intermedia

1 reference

20-Epibryonolic acid, phytosterols and ellagic acid from Coriaria intermedia

Clerodendrum fragrans

1 reference

The 24α- and 24β-epimers of 24-ethylcholesta-5,22-dien-3β-ol in two Clerodendrum species

Hydnora abyssinica

1 reference

Antibacterial activity, cytotoxicity and chemical constituents of Hydnora johannis roots

Heterogen japonica

1 reference

On the Sterols of “Viviparus Japonicus” (Fresh Water Rolled Shell Fish) .

Ulva popenguinensis

1 reference

Sterol composition of twelve chlorophyceae from the senegalese coast and their chemotaxonomic significance

Salvia triloba

1 reference

Constituents from Salvia triloba

Ulva linza

1 reference

Sterol composition of twelve chlorophyceae from the senegalese coast and their chemotaxonomic significance

Clerodendrum chinense

1 reference

The 24α- and 24β-epimers of 24-ethylcholesta-5,22-dien-3β-ol in two Clerodendrum species

Salvia fruticosa

1 reference

Constituents from Salvia triloba

Achillea tenuifolia

1 reference

Further constituents of Achillea ageratum

Achillea cretica

1 reference

Further constituents of Achillea ageratum

Identifiers

InChI

InChI=1S/C29H48O/c1-7-21(19(2)3)9-8-20(4)25-12-13-26-24-11-10-22-18-23(30)14-16-28(22,5)27(24)15-17-29(25,26)6/h8-10,19-21,23-27,30H,7,11-18H2,1-6H3/b9-8 /t20-,21 ,23 ,24 ,25-,26 ,27 ,28 ,29-/m1/s1

1 reference

Poriferasterol (English)

5 October 2016

2 references

Poriferasterol (English)

5 October 2016

ChEBI release 2020-09-01

2 references

Poriferasterol (English)

5 October 2016

https://commonchemistry.cas.org/detail?cas_rn=481-16-3

8 April 2021

1 reference

Poriferasterol (English)

5 October 2016

2 references

Poriferasterol (English)

5 October 2016

ChEBI ID

8334

mapping relation type

2 references

Poriferasterol (English)

5 October 2016

International Chemical Identifier

InChI

InChI=1S/C29H48O/c1-7-21(19(2)3)9-8-20(4)25-12-13-26-24-11-10-22-18-23(30)14-16-28(22,5)27(24)15-17-29(25,26)6/h8-10,19-21,23-27,30H,7,11-18H2,1-6H3/b9-8 /t20-,21 ,23 ,24 ,25-,26 ,27 ,28 ,29-/m1/s1

SureChEMBL ID

SCHEMBL156814

2 references

1 reference

1 reference

EC number

207-561-2

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.006.875

27 December 2018

ECHA Substance Infocard ID

(3β,22E,24R)-stigmasta-5,22-dien-3-ol (English)

quotation

CAS no.: 481-16-3 (English)

100.006.875

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.006.875

27 December 2018

(3β,22E,24R)-stigmasta-5,22-dien-3-ol (English)

quotation

CAS no.: 481-16-3 (English)

1 reference

Poriferasterol (English)

5 October 2016

1 reference

Poriferasterol (English)

5 October 2016

1 reference

http://www.lipidmaps.org/rest/compound/lm_id/LM/all/download

Poriferasterol (English)

5 October 2016

1 reference