TN1691 |
Glabrol
|
59870-65-4
|
99.72%
|
|
Glabrol is a PTP1B inhibitor, it is also a CYP1B1 inhibitor, it shows inhibition of CYP1B1 in live cell assay with the IC50 value of 15uM.
|
T1650 |
Chlorzoxazone
|
95-25-0
|
99.72%
|
|
Chlorzoxazone (Chlorzoxazon) is a Muscle Relaxant. The physiologic effect of chlorzoxazone is by means of Centrally-mediated Muscle Relaxation.
|
T15641 |
K777
|
233277-99-1
|
99.71%
|
|
K777 is a potent, orally active and irreversible inhibitor of cysteine protease. K777 is a potent CYP3A4 inhibitor (IC50= 60 nM). K777 is also a selective CCR4 a...
|
T117521 |
7-BFC
|
220001-53-6
|
99.71%
|
|
7-BFC (7-Benzyloxy-4-(trifluoromethyl)coumarin) is a coumarin-like fluorescent substrate that serves as a biomarker for cytochrome P 450 and can be used to study...
|
T5715 |
(E)-Flavokawain A
|
37951-13-6
|
99.7%
|
|
(E)-Flavokawain A, a novel chalcone from kava extract, induces apoptosis in bladder cancer cells by involvement of Bax protein-dependent and mitochondria-depende...
|
T4567 |
Sulfaphenazole
|
526-08-9
|
99.67%
|
|
Sulfaphenazole (Plisulfan) is an inhibitor of CYP2C9 (Ki: 0.3 μM) that demonstrates at least 100-fold selectivity over other CYP450 isoforms (Ki: 63/29 μM for CY...
|
T0100 |
Atazanavir sulfate
|
229975-97-7
|
99.67%
|
|
Atazanavir sulfate (BMS-232632 sulfate) is an azapeptide and HIV-PROTEASE INHIBITOR that is used in the treatment of HIV INFECTIONS and AIDS in combination with ...
|
T70489 |
Enerisant HCl
|
1152749-07-9
|
99.66%
|
|
Enerisant HCl is a novel potent and selective histamine H3 receptor antagonist, a substrate for P-gp, mediated by cytochrome P450 (CYP) and transporter proteins....
|
T2175 |
Apigenin
|
520-36-5
|
99.66%
|
|
Apigenin (NSC 83244) is an aromatic oil extracted from the flowers or leaves of the daisy-like plants. Extracts, oils and teas made from chamomile are used for i...
|
T3811 |
Ginsenoside C-K
|
39262-14-1
|
99.65%
|
|
Ginsenoside C-K (Ginsenoside K) is a bacterial metabolite of G-Rb1 exhibiting anti-inflammatory effects by reducing iNOS and COX-2.
|
T21818 |
Pregnenolone Carbonitrile
|
1434-54-4
|
99.64%
|
|
Pregnenolone Carbonitrile (5-Pregnen-3β-ol-20-one-16α-carbonitrile) is an activator of rodent-PXR and induces the expression of CYP3A.
|
T9113 |
Myristicin
|
607-91-0
|
99.63%
|
|
Myristicin (Myristicine) is a natural product found in spices and umbelliferous plants. Myristicin has anti-cholinergic, Antibacterial, and hepatoprotective effe...
|
TQ0296L |
N-Nornuciferine hydrochloride(4846-19-9 free base)
|
TQ0296L
|
99.63%
|
|
N-Nornuciferine hydrochloride(4846-19-9 free base) (N-Nornuciferine hydrochloride) is an aporphine alkaloid in lotus leaf, significantly inhibits CYP2D6 (IC50: 3...
|
T6S0630 |
Hypaconitine
|
6900-87-4
|
99.63%
|
|
Hypaconitine, an active and highly toxic constituent derived from Aconitum species, has anti-inflammatory activity, is widely used to treat rheumatism.
|
T6246 |
Cobicistat
|
1004316-88-4
|
99.62%
|
|
Cobicistat (GS-9350) is a carbamate and thiazole derivative that functions as a CYTOCHROME P450 CYP3A INHIBITOR to enhance the concentration of ANTI-HIV AGENTS, ...
|
T0679 |
Ketoconazole
|
65277-42-1
|
99.62%
|
|
Ketoconazole (R-41400), a CYP3A4 inhibitor, is an imidazole anti-fungal agent.
|
T27918 |
LY 43578
|
26766-35-8
|
99.62%
|
|
LY 43578 is an orally active aromatase inhibitor. LY43578 could inhibit O-demethylation of P-450-dependent p-nitroanisole and N-demethylation of ethylmorphine (I...
|
T22254 |
Alflutinib
|
1869057-83-9
|
99.61%
|
|
Alflutinib (ASK120067) is an inhibitor of EGFR, and its targets including EGFR activating mutations and T790M, thus leading to tumor growth inhibition.
|
T3698 |
Alpha-Asarone
|
2883-98-9
|
99.59%
|
|
alpha-Asarone (trans-Asarone) is a psychoactive compound with antidepressant-like activity in mice.
|
T7056 |
Dronedarone
|
141626-36-0
|
99.58%
|
|
Dronedarone (SR 33589) is an amiodarone analogue which has an effective and promising treatment for Atrial fibrillation.
|