Ergosterol

Ergosterol
Formula kimikoa	C28H44O
SMILES kanonikoa	2D eredua
SMILES isomerikoa	C[C@H](/C=C/[C@H](C)C(C)C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3C2=CC=C4[C@@]3(CC[C@@H](C4)O)C)C
MolView	3D eredua
Mota	ergostane steroid(en)
Estereoisomeroa	[[(3S,9S,10S,13R,14S,17R)-17-[(E,2S,5R)-5,6-dimethylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol|(3S,9S,10S,13R,14S,17R)-17-[(E,2S,5R)-5,6-dimethylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol]](en),[[(3S,9S,10R,13R,14R,17S)-17-[(E,2R,5S)-5,6-dimethylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol|(3S,9S,10R,13R,14R,17S)-17-[(E,2R,5S)-5,6-dimethylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol]](en),lumisterol(en),[[(3S,9S,10R,13R,14S,17R)-17-[(E,2S,5R)-5,6-dimethylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol|(3S,9S,10R,13R,14S,17R)-17-[(E,2S,5R)-5,6-dimethylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol]](en),[[(3S,9R,10R,13S,14S,17R)-17-[(Z,2S,5R)-5,6-dimethylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol|(3S,9R,10R,13S,14S,17R)-17-[(Z,2S,5R)-5,6-dimethylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol]](en),[[(3S,9S,10R,13R,14R,17R)-17-[(Z,2S,5R)-5,6-dimethylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol|(3S,9S,10R,13R,14R,17R)-17-[(Z,2S,5R)-5,6-dimethylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol]](en),[[(3S,9R,10R,13R,14S,17R)-17-[(E,2S,5R)-5,6-dimethylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol|(3S,9R,10R,13R,14S,17R)-17-[(E,2S,5R)-5,6-dimethylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol]](en),[[(3S,9R,10S,13R,14S,17R)-17-[(E,2S,5R)-5,6-dimethylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol|(3S,9R,10S,13R,14S,17R)-17-[(E,2S,5R)-5,6-dimethylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol]](en),ergosta-5,8,20(22)-trien-3-ol(en),[[(3S,9R,10R,13R,14S,17R)-17-[(Z,2S,5R)-5,6-dimethylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol|(3S,9R,10R,13R,14S,17R)-17-[(Z,2S,5R)-5,6-dimethylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol]](en),Epiergosterol(en),pyrocalciferol(en),isopyrocalciferol(en),(3beta,22E)-ergosta-5,7,22-trien-3-ol(en),[[(3S,9S,10R,13R,14R,17R)-17-[(Z,2R,5R)-5,6-dimethylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol|(3S,9S,10R,13R,14R,17R)-17-[(Z,2R,5R)-5,6-dimethylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol]](en)eta [[(3S,9R,10R,13R,14S,17R)-17-[(E,2R,5R)-5,6-dimethylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol|(3S,9R,10R,13R,14S,17R)-17-[(E,2R,5R)-5,6-dimethylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol]](en)
Masa molekularra	396,339 Da
Erabilera
Tratatzen du	hipoparatiroidismoetahipofosfatemia familiar
Rola	probitamina
Identifikatzaileak
InChlKey	DNVPQKQSNYMLRS-APGDWVJJSA-N
CAS zenbakia	57-87-4
ChemSpider	392539
PubChem	444679
Reaxys	2338604
Gmelin	16933
ChEMBL	CHEMBL1232562
EC zenbakia	200-352-7
ECHA	100.000.320
CosIng	33778
MeSH	D004875
Human Metabolome Database	HMDB0000878
KNApSAcK	C00023755etaC00003652
UNII	Z30RAY509F
KEGG	C01694
PDB Ligand	ERG

Ergosterolaesterolensailekoalkoholada(C₂₈H₄₄O).

Zekale-ainotik(Claviceps purpurea) lortzen da batez ere, bainagaragar-legamiatikere ateratzen da gaur egun. Animalia- eta landare-ehun batzuetan ere aurkitzen da. Mutur batean daukan hidroxilo taldeari eskermolekula anfipatikoada.

Erradiazio ultramoreajasotzen duenean,kaltziferoledoD₂bitaminabilakatzen da. Giza gorputzean,kaltzioahezurretanetahortzetankatalizatzea da haren eginkizun nagusia.

Erreferentziak

• Artikulu honen edukiaren zati batLur hiztegi entziklopedikotik edoLur entziklopedia tematikotik txertatu zen 2011/12/27 egunean. Egile-eskubideen jabeak,Eusko Jaurlaritzak,hiztegi horiekCC-BY 3.0 lizentziarekinargitaratu ditu,Open Data Euskadi webgunean.

Kanpo estekak

• Datuak:Q143263
• Multimedia:Ergosterol/Q143263