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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T7824 | Eberconazole Nitrate | Ebernet | Antifungal |
Eberconazole Nitrate (Ebernet) is an azole antifungal agent and broad-spectrum imidazole derivative. | |||
T22976 | MFZ 10-7 | Others , GluR | |
MFZ 10-7 is anegative allosteric modulator of the mGluR5. | |||
T8959 | OS-3-106 | Dopamine Receptor | |
OS-3-106 is a novel arylamide phenylpiperazines, as partial agonists at the D3R in the adenylyl cyclase inhibition assay. | |||
T15799 | LY2940094 | LY-2940094 | Opioid Receptor |
LY2940094 (LY-2940094) decreases ethanol self-administration in animal models. LY2940094 is an effective, selective, and orally available nociceptin receptor antagonist with high affinity (Ki=0.105 nM) and antagonist pot... | |||
T39161 | Ro60-0175 | Ro60-0175 | 5-HT Receptor |
Ro60-0175 a selective agonist for both the 5-hydroxytryptamine 2B (5-HT2B) and 5-hydroxytryptamine 2C (5-HT2C)serotonin receptor subtypes, commonly used as fumarate salt. It has a role as a 5-hydroxytryptamine 2B recept... | |||
T6322 | Copanlisib | BAY 80-6946 | Apoptosis , PI3K |
Copanlisib (BAY 80-6946) is a phosphoinositide 3-kinase (PI3K) inhibitor with potential antineoplastic activity. Copanlisib inhibits the activation of the PI3K signaling pathway, which may result in inhibition of tumor c... | |||
T14998 | Copanlisib dihydrochloride | BAY 80-6946 dihydrochloride | Apoptosis , PI3K , mTOR |
Copanlisib dihydrochloride (BAY 80-6946 dihydrochloride) is an ATP-competitive pan-class I PI3K inhibitor (IC50s: 0.5 nM, 0.7 nM, 3.7 nM and 6.4 nM for PI3Kα, PI3Kδ, PI3Kβ and PI3Kγ). Copanlisib dihydrochloride has super... | |||
T1459 | Cisatracurium besylate | 51W89 | Adrenergic Receptor , AChR , Autophagy |
Cisatracurium besylate (51W89) is a nondepolarizing skeletal muscle relaxant for intravenous administration. | |||
T21983L | PKI 14-22 amide, myristoylated Acetate | PKI 14-22 amide, myristoylated Acetate(201422-03-9 Free base) | PKA |
PKI 14-22 amide, myristoylated Acetate inhibit cAMP-dependent protein kinase (PKA) and blocks hyperalgesia produced by spinal administration of 8-bromo-cAMP. | |||
T28396 | PGP-4008 | PGP 4008,PGP4008 | P-gp |
PGP-4008 is a selective and potent P-glycoprotein (Pgp) inhibitor that inhibits tumor growth by co-administration with Doxorubicin. | |||
T5467 | SAR125844 | SAR125884 | Apoptosis , c-Met/HGFR |
SAR125844, a potent and highly selective inhibitor of the MET receptor tyrosine kinase (RTK), for intravenous administration. (IC50 value of 4.2 nmol/L) | |||
T10124 | Antiulcer Agent 1 | Others | |
Antiulcer Agent 1 is a 2-(3,4-dimethoxyphenyl)ethylamine derivative for oral administration. | |||
T5S2245 | Alisol C 23-acetate | Alisol C monoacetate | Others |
Alisol C 23-acetate (Alisol C monoacetate) is a natural product isolated from Alisma orientale, can significantly and strongly inhibit DTH response after oral administration,has antibacterial activity. | |||
TN2023 | 8-Oxoepiberberine | Oxyepiberberine | Others |
8-Oxoepiberberine (Oxyepiberberine) is an alkaloid metabolite in the plasma after oral administration of Zuojin formula. Zuojin formula is a traditional chinese medicine used to treat gastrointestinal disease. | |||
T2322 | Fimasartan | BR-A-657,Kanarb | Apoptosis , RAAS |
Fimasartan (BR-A-657) is a non-peptide angiotensin II receptor antagonist (ARB) used for the treatment of hypertension and heart failure. Concurrent administration of fimasartan with diuretic hydrochlorothiazide has show... | |||
T69467 | Azacosterol | IMD760,Diazasterol | Others |
Azacosterol (Diazasterol) is a DHCR24 inhibitor.Azacosterol undergoes a series of reactions in cortical neurons following oral or intraperitoneal administration. | |||
T79909 | AEF0117 | Cannabinoid Receptor | |
AEF0117, a signaling-specific inhibitor of cannabinoid receptor 1 (CB1-SSi), inhibits cannabinoid self-administration and behavioral disorders associated with THC, and can be used to study cannabis withdrawal. | |||
T71012 | Nemazoline Free Base | ||
Nemazoline Free Base is a nasal decongestant. It has alpha 1-agonist/alpha 2-antagonist activity and was more effective and long-acting than oxymetazoline on canine nasal mucosa, in-vitro and in-vivo. Upon intranasal adm... | |||
T9422 | Fosciclopirox | CPX-POM | Gamma-secretase |
Fosciclopirox (CPX-POM), the phosphoryloxymethyl ester of CPX (Ciclopirox Prodrug, CPX-POM), selectively delivers the active metabolite, CPX, to the entire urinary tract following parenteral administration. | |||
T1551 | Tegaserod maleate | HTF-919,SDZ-HTF-919 | 5-HT Receptor |
Tegaserod maleate (SDZ-HTF-919) is a 5-HT4 agonist manufactured by Novartis and used for the management of irritable bowel syndrome and constipation. Its use was the only drug approved by the United States Food and Drug ... |