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Search Results for " bph "

20

Compounds

Cat No. Product Name Synonyms Targets
T14766 BPH-715 Others , Parasite
BPH-715 inhibits the liver-stage growth of P. falciparum with an IC50 of 10 μM for P. falciparum exoerythrocytic forms in HepG2 cells.
T10586L BPH-1358 NSC50460 Others , Antibacterial
BPH-1358 (NSC-50460) (NSC-50460) is a potent human farnesyl diphosphate synthase (FPPS) and undecaprenyl diphosphate synthase (UPPS) inhibitor. With IC50s of 1.8 μM and 110 nM, respectively. And it is active against S. a...
T30563 BPH-252 BPH 252
BPH-252 is a bioactive chemical.
T30567 BPH-675 BPH 675
BPH-675 is a bioactive chemical.
T30569 BPH-742 BPH 742,BPH742
BPH-742 is a bioactive chemical.
T30564 BPH-608
BPH-608 is a bioactive chemical.
T10587 BPH-652 Others
BPH-652 is an S. aureus dehydrosqualene synthase (CrtM) inhibitor (Ki: 1.5 nM; IC50: 100-300 nM for S. aureus pigment formation).
T30568 BPH-676
BPH-676 is a bioactive chemical.
T30566 BPH-629 BPH629
BPH-629 is a bioactive chemical.
T30565 BPH-628 BPH628
BPH-628 is a bioactive chemical.
T23814 BPH-1218 BPH1218
BPH-1218 is a SQS inhibitor.
T30570 BPH-830 BPH830
BPH-830 is a bioactive chemical.
T23815 BPH-651 BPH651,3ACW,3-ACW,3 ACW
BPH-651 is a CrtM inhibitor.
T72587 BPH-1358 mesylate NSC50460 mesylate
BPH-1358 mesylate (NSC50460 mesylate), a highly effective inhibitor of both human farnesyl diphosphate synthase (FPPS) and undecaprenyl diphosphate synthase (UPPS), exhibits IC50 values of 1.8 μM and 110 nM, respectively...
T10586 BPH-1358 free base NSC50460 free base Others
BPH-1358 (NSC50460) free base is a potent human undecaprenyl diphosphate synthase (UPPS) and farnesyl diphosphate synthase (FPPS) inhibitor (IC50s: 110 nM and 1.8 μM) and is active against S. aureus in vitro (MIC ~250 ng...
T60300 BPH-1086
BPH-1086 (compound 10) is an inhibitor of IspH. IspH domain fused with ribosomal protein S1 (RPS1) can bind to mRNA or form part of the bacterial ribosome [1] [2].
T0488 Finasteride MK-906 Reductase
Finasteride (MK-906) is an oral inhibitor of active testosterone 5-alpha-reductase and Ki value is 10 nM.
T0091 Alfuzosin hydrochloride SL 77499-10,Alfuzosin HCl Adrenergic Receptor
Alfuzosin hydrochloride (Alfuzosin HCl) is an α1 adrenergic receptor antagonist. It applies to treat benign prostatic hyperplasia (BPH).
T1284 Megestrol acetate SC10363,BDH1298 Glucocorticoid Receptor , Estrogen/progestogen Receptor , Progesterone Receptor , HIV Protease , Autophagy
Megestrol acetate (BDH1298) is a progestogen with actions and uses similar to those of the progestogens in general. Megestrol acetate also has anti-androgenic properties. It is given by mouth in the palliative treatment ...
T1504 Silodosin KAD 3213,KMD 3213 Adrenergic Receptor
Silodosin (KAD 3213) is an alpha-Adrenergic Blocker. The mechanism of action of silodosin is as an Adrenergic alpha-Antagonist.
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