(Q15410967)

inferred from SMILES

chemical structure

Fungisterol.svg
512 × 390; 5 KB

0 references

mass

400.370516 dalton

1 reference

Fungisterol (English)

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

7 October 2016

stereoisomer of

2 references

inferred from InChIKey

1 reference

Campest-7-en-3beta-ol

1 reference

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

inferred from InChI

1 reference

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

inferred from InChI

1 reference

inferred from InChI

chemical formula

C₂₈H₄₈O

1 reference

Fungisterol (English)

20 November 2016

canonical SMILES

CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C

1 reference

Fungisterol (English)

20 November 2016

isomeric SMILES

C[C@H](CC[C@H](C)C(C)C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3C2=CC[C@@H]4[C@@]3(CC[C@@H](C4)O)C)C

1 reference

Identification of 23-demethylacanthasterol in an asteroid, Acanthaster planci and its synthesis

Fungisterol (English)

20 November 2016

1 reference

Baccharoides anthelmintica

1 reference

4α-methylvernosterol and other sterols from Vernonia anthelmintica seeds

Ganoderma

1 reference

New lanostanoids from the fungus Ganoderma concinna.

Carthamus tinctorius

1 reference

Carthami flos extract and its component, stigmasterol, inhibit tumour promotion in mouse skin two-stage carcinogenesis

Pisolithus arhizus

1 reference

Triterpenoids of the fungus Pisolithus tinctorius*

Pisolithus tinctorius

1 reference

Triterpenoids of the fungus Pisolithus tinctorius*

Roseofomes

1 reference

Roseolide a, a novel dimeric drimane sesquiterpenoid from the basidiomycete Roseoformes subflexibilis

Saccharomyces cerevisiae

1 reference

Episterol and fungisterol from mutant strains of the yeast Saccharomyces cerevisiae

Fuligo septica

1 reference

Ueber Paracholesterin aus Aethalium septicum

Axinella cannabina

1 reference

Minor and trace sterols in marine invertebrates. Part 35. Isolation and structure elucidation of seventy-four sterols from the sponge Axinella cannabina

Candida lipolytica

1 reference

Sterols from Candida lipolytica yeast grown on n-alkanes

Yarrowia lipolytica

1 reference

Sterols from Candida lipolytica yeast grown on n-alkanes

Ophiocordyceps sinensis

1 reference

Anti-inflammatory principles from Cordyceps sinensis

Dunaliella tertiolecta

1 reference

Minor and trace sterols of Dunaliella tertiolecta

Hohenbuehelia serotina

1 reference

New sterols from two edible mushrooms, Pleurotus eryngii and Panellus serotinus

Panellus serotinus

1 reference

New sterols from two edible mushrooms, Pleurotus eryngii and Panellus serotinus

Venturia inaequalis

1 reference

Sterol analysis of DMI-resistant and -sensitive strains of Venturia inaequalis

Arabidopsis thaliana

2 references

Brassinosteroids, microtubules and cell elongation in Arabidopsis thaliana. I. Molecular, cellular and physiological characterization of the Arabidopsis bull mutant, defective in the delta 7-sterol-C5-desaturation step leading to brassinosteroid bio

Plant sterol metabolism. Δ(7)-Sterol-C5-desaturase (STE1/DWARF7), Δ(5,7)-sterol-Δ(7)-reductase (DWARF5) and Δ(24)-sterol-Δ(24)-reductase (DIMINUTO/DWARF1) show multiple subcellular localizations in Arabidopsis thaliana (Heynh) L

Vitis vinifera

1 reference

Chemical composition of seeds of four Bulgarian grape varieties

Polyporus annulatus

1 reference

Antifungal activity of sterols and triterpenes isolated from Ganoderma annulare

Ganoderma tornatum

1 reference

Antifungal activity of sterols and triterpenes isolated from Ganoderma annulare

Sarcomyxa serotina

1 reference

New sterols from two edible mushrooms, Pleurotus eryngii and Panellus serotinus

Identifiers

InChI

InChI=1S/C28H48O/c1-18(2)19(3)7-8-20(4)24-11-12-25-23-10-9-21-17-22(29)13-15-27(21,5)26(23)14-16-28(24,25)6/h10,18-22,24-26,29H,7-9,11-17H2,1-6H3/t19-,20+,21-,22-,24+,25-,26-,27-,28+/m0/s1

1 reference

Fungisterol (English)

PUGBZUWUTZUUCP-ZRKHGVCBSA-N

20 November 2016

InChIKey

2 references

Fungisterol (English)

20 November 2016

ChEBI release 2020-09-01

CAS Registry Number

516-78-9

2 references

Global Substance Registration System

γ-ergostenol (English)

PUGBZUWUTZUUCP-ZRKHGVCBSA-N

20 November 2016

InChIKey

9 April 2021

https://commonchemistry.cas.org/detail?cas_rn=516-78-9

1 reference

Fungisterol (English)

20 November 2016

1 reference

Fungisterol (English)

20 November 2016

Reaxys registry number

3216965

1 reference

fungisterol (English)

7 October 2016

ChEBI ID

69432

mapping relation type

1 reference

fungisterol (English)

7 October 2016

1 reference

208-225-8

1 reference

Global Substance Registration System

γ-ergostenol (English)

ECHA Substance Infocard ID

20 November 2016

100.007.479

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.007.479

27 December 2018

5-α-ergost-7-en-3-β-ol (English)

quotation

CAS no.: 516-78-9 (English)

1 reference

Global Substance Registration System

γ-ergostenol (English)