TN1140 |
Onjisaponin B
|
35906-36-6
|
99.88%
|
|
Onjisaponin B induces autophagy via the AMPK-mTOR signaling pathway, increases the NGF level and accelerates both the removal of mutant huntingtin and A53T α±-sy...
|
T10990 |
Dehydrocorydaline chloride
|
10605-03-5
|
99.88%
|
|
Dehydrocorydaline chloride (13-Methylpalmatine chloride) is an alkaloid with anti-inflammatory and anti-cancer activity. Can improve the activation of p38 MAPK.
|
T0320 |
Colchicine
|
64-86-8
|
99.88%
|
|
Colchicine (Colcin) is a natural product that is an inhibitor of microtubule polymerization (IC50=3 nM) and blocks microtubule polymerization by binding to micro...
|
T1215 |
Nicardipine hydrochloride
|
54527-84-3
|
99.87%
|
|
Nicardipine hydrochloride (YC-93 Hydrochloride) is the hydrochloride salt form of nicardipine, a synthetic derivative of nitrophenyl-pyridine and potent calcium ...
|
T1178 |
Temozolomide
|
85622-93-1
|
99.87%
|
|
Temozolomide (TMZ) is a DNA alkylating agent with blood-brain barrier permeability and oral activity. Temozolomide has antitumor activity and antiangiogenic acti...
|
T1792 |
Regorafenib
|
755037-03-7
|
99.87%
|
|
Regorafenib (BAY 73-4506) is a multi-targeted receptor tyrosine kinase inhibitor that inhibits RET, C-RAF, VEGFR2, c-Kit, VEGFR1, and PDGFRβ and is orally active...
|
T3001 |
Honokiol
|
35354-74-6
|
99.87%
|
|
Honokiol (NSC-293100) is the active principle of magnolia extract. It inhibits the activation of Akt and enhances the phosphorylation of ERK1/ERK2.
|
T5842 |
Bromocriptine mesylate
|
22260-51-1
|
99.87%
|
|
Bromocriptine mesylate (CB-154) is a potent dopamine receptor agonist that binds the D2 receptor with highest affinity (Ki = 2.5 nM)
|
TL0004 |
FERULIC ACID METHYL ESTER
|
2309-07-1
|
99.87%
|
|
FERULIC ACID METHYL ESTER (Methyl ferulate) is a hydroxycinnamic acid that is abundant in plants and originally derived from giant fennel (F. communis). This nat...
|
T1764 |
Adezmapimod
|
152121-47-6
|
99.87%
|
|
Adezmapimod (SB 203580) is a p38 MAPK inhibitor (IC50=0.3-0.5 μM) that is selective and ATP-competitive. Adezmapimod possesses autophagy and mitochondrial autoph...
|
T2146 |
Fulvestrant
|
129453-61-8
|
99.87%
|
|
Fulvestrant (ZM 182780) is an estrogen receptor (ER) antagonist (IC50=9.4 nM) and an agonist of GPR30. Fulvestrant has antitumor activity, inhibiting cell prolif...
|
T2144 |
Tacrolimus
|
104987-11-3
|
99.87%
|
|
Tacrolimus (Fujimycin) can bind FKBP12 to form a high-affinity complex (Ki: 0.2 nM) which inhibits the activity of the calcium/calmodulin-dependent protein phosp...
|
T1050 |
Prazosin hydrochloride
|
19237-84-4
|
99.87%
|
|
Prazosin hydrochloride (Vasoflex) reduces peripheral resistance and relaxes vascular smooth muscles as a selective adrenergic alpha-1 antagonist by a mechanism n...
|
T3068 |
AT9283
|
896466-04-9
|
99.87%
|
|
AT9283 (J-504568) is an effective multi-targeted inhibitor of JAK2(IC50=1.2 nM) and JAK3(IC50=1.1 nM), Aurora A, Aurora B and Abl(T315I).
|
T0334 |
Rosiglitazone
|
122320-73-4
|
99.87%
|
|
Rosiglitazone (BRL49653) is a PPARγ agonist, TRPC5 activator, and TRPM3 inhibitor with oral activity. Rosiglitazone is also a hypoglycemic agent and a thiazolidi...
|
T0462 |
Cilostazol
|
73963-72-1
|
99.87%
|
|
Cilostazol (OPC 21) is a Phosphodiesterase 3 Inhibitor. The mechanism of action of cilostazol is as a Phosphodiesterase 3 Inhibitor.
|
T0951 |
Hydroxychloroquine sulfate
|
747-36-4
|
99.87%
|
|
Hydroxychloroquine sulfate (Acidum iopanoicum) inhibits plasmodial heme polymerase. It is a chemotherapeutic agent that acts against erythrocytic forms of malari...
|
T6641 |
Rilmenidine Phosphate
|
85409-38-7
|
99.87%
|
|
Rilmenidine Phosphate is a selective I(1) imidazoline receptor agonist, used to treat hypertension.
|
T0987 |
Gimeracil
|
103766-25-2
|
99.86%
|
|
Gimeracil (Gimestat) is a competitive, reversible inhibitor of dihydropyrimidine dehydrogenase.
|
TQ0064 |
Peretinoin
|
81485-25-8
|
99.86%
|
|
Peretinoin (NIK333) is an oral acyclic retinoid with a vitamin A-like structure that targets retinoid nuclear receptors such as RXR and RAR.
|