(Q27133411)

Dehydroergosterol (English)

(3S,10S,13R,14S,17R)-17-[(E,2R,5S)-5,6-dimethylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,12,14,15,16,17-octahydro-1H-cyclopenta[a]phenanthren-3-ol

7 October 2016

stereoisomer of

2 references

inferred from InChIKey

(3S,10S,13R,14R,17R)-17-[(E,2R,5S)-5,6-dimethylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,12,14,15,16,17-octahydro-1H-cyclopenta[a]phenanthren-3-ol

inferred from InChI

1 reference

inferred from InChI

chemical formula

C₂₈H₄₂O

1 reference

Dehydroergosterol (English)

7 October 2016

canonical SMILES

CC(C)C(C)C=CC(C)C1CCC2C1(CC=C3C2=CC=C4C3(CCC(C4)O)C)C

1 reference

Dehydroergosterol (English)

7 October 2016

isomeric SMILES

C[C@H](/C=C/[C@H](C)C(C)C)[C@H]1CC[C@@H]2[C@@]1(CC=C3C2=CC=C4[C@@]3(CC[C@@H](C4)O)C)C

1 reference

Antimycobacterial ergosterol-5,8-endoperoxide from Ajuga remota

Dehydroergosterol (English)

7 October 2016

1 reference

Chlorella vulgaris

1 reference

Inhibitory effects of sterols isolated from Chlorella vulgaris on 12-0-tetradecanoylphorbol-13-acetate-induced inflammation and tumor promotion in mouse skin

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

Conium maculatum

1 reference

Steroids from Poison Hemlock (Conium maculatum L.): A GC-MS analysis

Eutypa lata

1 reference

Sterol composition of the woody plant pathogenic fungus Eutypa lata

Leptosphaeria maculans

1 reference

Sterol composition of mycelia of the plant pathogenic ascomycete Leptosphaeria maculans

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

Phycomyces blakesleeanus

1 reference

Phycomysterols and other sterols from the fungus Phycomyces blakesleeanus

Sphaeria macula

1 reference

Sterol composition of mycelia of the plant pathogenic ascomycete Leptosphaeria maculans

Biscogniauxia macula

1 reference

Sterol composition of mycelia of the plant pathogenic ascomycete Leptosphaeria maculans

Sarcomyxa serotina

1 reference

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

Identifiers

InChI

InChI=1S/C28H42O/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/h7-10,14,18-20,22,24-25,29H,11-13,15-17H2,1-6H3/b8-7+/t19-,20+,22-,24+,25-,27-,28+/m0/s1

1 reference

Dehydroergosterol (English)

7 October 2016

2 references

Dehydroergosterol (English)

7 October 2016

ChEBI release 2020-09-01

2 references

dehydroergosterol (English)

7 October 2016

https://commonchemistry.cas.org/detail?cas_rn=516-85-8

10 April 2021

1 reference

Ergosta-5,7,9(11),22-tetraen-3b-ol (English)

7 October 2016

2 references

Dehydroergosterol (English)

7 October 2016

Reaxys registry number

3218613

1 reference

dehydroergosterol (English)

7 October 2016

ChEBI ID

64762

mapping relation type

2 references

dehydroergosterol (English)

7 October 2016

International Chemical Identifier

InChI

InChI=1S/C28H42O/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/h7-10,14,18-20,22,24-25,29H,11-13,15-17H2,1-6H3/b8-7+/t19-,20+,22-,24+,25-,27-,28+/m0/s1

SureChEMBL ID

SCHEMBL887147

2 references

inferred from InChIKey

1 reference

1 reference

UNII

123R6KJQ51

2 references

Global Substance Registration System

UNII

123R6KJQ51

DEHYDROERGOSTEROL (English)

7 October 2016