about
7alpha-Hydroxypregnenolone acts as a neuronal activator to stimulate locomotor activity of breeding newts by means of the dopaminergic systemCentral administration of a cytochrome P450-7B product 7 alpha-hydroxypregnenolone improves spatial memory retention in cognitively impaired aged ratsNeurosteroid biosynthesis in the quail brain: a review.Hormone-mediated reproductive behavior in the red-bellied newt.Identification of 7alpha-hydroxypregnenolone, a novel bioactive amphibian neurosteroid stimulating locomotor activity, and its physiological roles in the regulation of locomotion.Prolactin increases the synthesis of 7alpha-hydroxypregnenolone, a key factor for induction of locomotor activity, in breeding male Newts.In vitro metabolism of pregnenolone to 7alpha-hydroxypregnenolone by rainbow trout embryos.The role of CYP 1A1 in the in vitro metabolism of pregnenolone by the liver of rainbow trout embryos.Evidence for 15alpha- and 7alpha-hydroxylase activity in gonadal tissue of the early-life stages of sea lampreys, Petromyzon marinus.Diurnal changes in the synthesis of the neurosteroid 7alpha-hydroxypregnenolone stimulating locomotor activity in newts.Seasonal changes in the synthesis of the neurosteroid 7alpha-hydroxypregnenolone stimulating locomotor activity in newts.Identification, biosynthesis, and function of 7alpha-hydroxypregnenolone, a new key neurosteroid controlling locomotor activity, in nonmammalian vertebrates.Discovery of a novel avian neurosteroid, 7alpha-hydroxypregnenolone, and its role in the regulation of the diurnal rhythm of locomotor activity in Japanese quail.7Alpha-hydroxypregnenolone mediates melatonin action underlying diurnal locomotor rhythms.Seasonal changes in the production of two novel and abundant ovarian steroids in the channel catfish (Ictalurus punctatus).
P921
Q24558795-BC243EDB-85A2-44AC-9137-81762180945AQ28566776-4B96F88E-B7D3-4947-9609-5D547C8DB2B5Q36562948-FADCC1DA-A3F9-47F7-813B-89314B1F38B8Q37490054-38CB16B2-DD25-4B1B-8DB9-917D52EC2C9AQ37688475-D1745415-A0A6-4A61-B118-336DD700462AQ43134786-663660F3-4B95-47CC-A4BE-92FD5C66B8C6Q44416782-0BB8A6B2-1F97-49D2-BEF4-7EB7DFD3E7BEQ44555660-B3617047-BE27-46D2-8D24-4BF03D5EBD72Q44933154-2B1B6353-CEB5-4C70-9F72-9A8DF3CA3FFDQ46004038-C3811FF6-3816-4F1A-AE77-52A6A70DB902Q46004044-DE277660-A7FE-4A5C-818B-019AFFBDA314Q46004077-96EE5096-6D35-40DA-AB3D-C7DB3A5FBC48Q46053050-F97FAA57-1771-4C80-847B-E91756B25888Q46729670-9B6D2277-E730-46D8-8DFE-F7313BDFAEB6Q48935191-57F56644-C91F-48C5-AC91-AA240B186A40
P921
description
chemesch Verbindung
@lb
chemical compound
@en
chemical compound
@en-ca
chemical compound
@en-gb
chemická sloučenina
@cs
chemická zlúčenina
@sk
chemiese verbinding
@af
chemische Verbindung
@de
chemische Verbindung
@de-ch
chemische verbinding
@nl
name
7alpha-Hydroxypregnenolone
@en
type
label
7alpha-Hydroxypregnenolone
@en
altLabel
3beta,7alpha-Dihydroxy-5-pregnen-20-one
@en
prefLabel
7alpha-Hydroxypregnenolone
@en
P661
P662
P665
P683
P2017
CC(=O)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2[C@@H](C=C4[C@@]3(CC[C@@H](C4)O)C)O)C
P2067
P231
30626-96-1
P233
CC(=O)C1CCC2C1(CCC3C2C(C=C4C3(CCC(C4)O)C)O)C
P234
1S/C21H32O3/c1-12(22)15-4-5-16 ...... ,16-,17-,18+,19-,20-,21+/m0/s1
P235
UEWNVBNIVGLQPG-XXHSLLPRSA-N
P274
P3117
DTXSID10433466