Dutasteride, dual 5alpha reductase type 1 and type 2 inhibitor
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MW 528.5 Da, Purity >99%. Selective, competitive dual 5α reductase type 1 and type 2 inhibitor. Blocks the conversion of testosterone into dihydrotestosterone. Shows antitumor effects in vivo. Orally active.
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ABC member 16, MDR/TAP subfamily, ABC16, ABCB1, ABCBB_HUMAN, AIS, ANDR_HUMAN, AR, AR8, ATP binding cassette sub family B (MDR/TAP) member 11, ATP-binding cassette sub-family B member 11, Androgen nuclear receptor variant 2, Androgen receptor, Androgen receptor (dihydrotestosterone receptor, testicular feminization, spinal and bulbar muscular atrophy, Kennedy disease), BRIC2, Bile salt export pump, Bsep, DHTR, Dihydro testosterone receptor, Dihydrotestosterone receptor (DHTR), Eag-related protein 1, Ether a go go related potassium channel protein, Ether-a-go-go-related gene potassium channel 1, Ether-a-go-go-related protein 1, GCCR, GCRST, GCR_HUMAN, GLRA1_HUMAN, GR, Glucocorticoid receptor, Glycine receptor 48 kDa subunit, Glycine receptor alpha 1, Glycine receptor strychnine-binding subunit, Glycine receptor subunit alpha-1, Glycine receptor, alpha 1 subunit, Grl1, H-ERG, HKPX1, HUMARA, HYSP1, KCNH2_HUMAN, KD, Kennedy disease (KD), Kv11.1, LQT 2, NR3C4, Nuclear receptor subfamily 3 group C member 1, Nuclear receptor subfamily 3 group C member 4, Nuclear receptor subfamily 3 group C member 4 (NR3C4), PFIC 2, PGY4, Potassium channel HERG, Potassium voltage gated channel subfamily H (eag related) member 2, Potassium voltage-gated channel subfamily H member 2, SBMA, SMAX1, SQT1, STHE, Sister of P glycoprotein, Spgp, Spinal and bulbar muscular atrophy, Spinal and bulbar muscular atrophy (SBMA), TFM, Testicular Feminization (TFM), Voltage gated potassium channel, subfamily H, member 2, Voltage-gated potassium channel subunit Kv11.1, androgen receptor splice variant 4b, eag homolog, glucocorticoid nuclear receptor variant 1, hERG-1, nr3c1, nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor), progressive familial intrahepatic cholestasis 2
- Chemical Structure
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Chemical Structure - Dutasteride, dual 5alpha reductase type 1 and type 2 inhibitor (AB141278)
2D chemical structure image of ab141278, Dutasteride, dual 5alpha reductase type 1 and type 2 inhibitor
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Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.
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Toxic, refer to SDS for further information.
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