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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. |