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Search for "Androstenedione" returned 11 results

Showing 1-11 out of 11
DrugBank ID Name Formula Weight
DB01536
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4-Androstenedione C19H26O2 286.4085
Depending on the tissue type, androstenedione can serve as a precursor to testosterone as well as estrone and estradiol. [PubChem] DB01536 AEMFNILZOJDQLW-QAGGRKNEBJ (8R,9S,10R,13S,14S)-10,13 ...
DB00655
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Estrone C18H22O2 270.3661
Estrone is naturally derived from the peripheral conversion of androstenedione by an aromatase enzyme found in adipose tissues and is converted to estradiol in peripheral tissues. Estropipate is ...
DB01443
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19-Nor-5-androstenedione
Humans and other mammals Experimental Illicit Small Molecule DB01443 19-Nor-5-androstenedione estr-5-en-3,17-dione ...
DB01448
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19-Nor-4-androstenedione
Experimental Illicit Small Molecule DB01448 19-Nor-4-androstenedione ...
DB01451
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1-Androstenedione
Experimental Illicit Small Molecule DB01451 1-Androstenedione ...
DB01456
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5-Androstenedione
Experimental Illicit Small Molecule DB01456 5-Androstenedione ...
DB01217
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Anastrozole C17H19N5 293.3663
... primarily estradiol) is conversion of adrenally-generated androstenedione to estrone by aromatase in peripheral tissues. Therefore, aromatase inhibition leads to a decrease in circulatin ...
DB01708
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3-Beta-Hydroxy-5-Androsten-17-One C19H28O2 288.4244
Dehydroepiandrosterone (DHEA) can be converted to testosterone; androstenedione; estradiol; and estrone. Most of DHEA is sulfated (dehydroepiandrosterone sulfate) before secretion. [PubChem ...
DB02854
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Aetiocholanolone C19H30O2 290.4403
Etiocholanolone is a major metabolite of testosterone and androstenedione in many mammalian species including humans. It is excreted in the urine. [PubChem] DB02854 AE2 QGXBDMJGAMFCBF-UHFFFAOYAM ...
DB00990
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Exemestane C20H24O2 296.4034
... inactivator, structurally related to the natural substrate androstenedione. It acts as a false substrate for the aromatase enzyme, and is processed to an intermediate that binds irreversibly ...
DB00894
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Testolactone C19H24O3 300.3921
... and consequent reduction in estrone synthesis from adrenal androstenedione, the major source of estrogen in postmenopausal women. Based on in vitro studies, the aromatase inhibition may be ...
Showing 1-11 out of 11

This project is supported by Genome Alberta & Genome Canada, a not-for-profit organization that is leading Canada's national genomics strategy with $600 million in funding from the federal government. This project is also supported in part by GenomeQuest, Inc., an enterprise genomic information company serving the life science community.