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抑制剂 & 化合物

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Cat. No.	Product Name	Target	Signaling Pathways
T29137	VU0453595 VU 0453595,VU-0453595	AChR	Neuroscience
	VU0453595 是有效的、高选择性的、全身活性的M1正变构调节剂 (PAM, EC50=2140 nM)，在精神分裂症方面有研究价值。
T68060	Elgodipine
	Elgodipine 显著降低了运动诱导的心绞痛系统的发生率和严重程度，能够通过独立于转录因子c-fos 和c-jun 表达的机制抑制血管平滑肌增殖。 Elgodipine 诱导的抑制是电压依赖性的。Elgodipine 是治疗心绞痛的潜在化合物。
T27680	JNJ-40068782 JNJ 40068782
	JNJ-40068782 is a potent, selective and systemically active positive allosteric modulator of the mGlu2 receptor.
T27909	LY 274614
	LY 274614 is a structurally novel systemically active competitive NMDA receptor antagonist.
T71931	Clencyclohexerol
	Clencyclohexerol is an analog of clenbuterol. β-Adrenoceptor agonists, including clenbuterol, modulate protein synthesis and degradation and have therapeutic potential in muscle wasting disorders. β-adrenoceptor agonists have deleterious cardiovascular side effects when used systemically and at high concentrations.
T70619	LY2934747
	LY2934747 is a novel, potent, and systemically bioavailable mGlu2/3 receptor agonist, exhibiting both antipsychotic and analgesic properties in vivo.
T41184	Clocinnamox mesylate C-CAM,NIH 10443
	Clocinnamox mesylate is a systemically active, irreversibleμ-opioid receptor antagonist (apparent Kivalues are 0.7, 1.9 and 5.7 nM for mouseμ,δandκreceptors respectively).
T27897	LY 215490 LY215490,LY-215490
	LY 215490 is a selective, competitive and systemically active antagonist of AMPA receptor. LY 215490 has neuroprotective effect against focal ischaemia in a model of permanent MCA occlusion in the rat.
T68321	AS1940477
	AS1940477 is p38 MAPK inhibitor. AS1940477 inhibited the enzymatic activity of recombinant p38α and β isoforms but showed no effect against other 100 protein kinases including p38γ and δ isoforms. In human peripheral blood mononuclear cells, AS1940477 inhibited lipopolysaccharide (LPS)- or phytohemagglutinin A (PHA)-induced production of proinflammatory cytokines, including TNFα, IL-1β, and IL-6 at low concentrations (LPS/TNFα, IC(50)=0.45n M; PHA/TNFα, IC(50)=0.40 nM). In addition, equivalent c...
T36204	Methylatropine (nitrate)
	Methylatropine is an antagonist of muscarinic acetylcholine receptors (IC50= <0.1 nM in a radioligand binding assay using isolated porcine brain membranes) and a derivative of atropine .1,2It reduces acetylcholine-induced decreases in blood pressure in rats when administered intravenously with an ED50value of 5.5 μg/kg.2Methylatropine reduces salivation, induces mydriasis, and increases heart rate in dogs.3 1.Schmeller, T., Sporer, F., Sauerwein, M., et al.Binding of tropane alkaloids to nicotin...
T38844	MK-8245 Trifluoroacetate
	MK-8245 trifluoroacetate is a liver-targeting inhibitor of stearoyl-CoA desaturase (SCD) with IC50 of 1 nM for human SCD1 and 3 nM for both rat SCD1 and mouse SCD1, with anti-diabetic and anti-dyslipidemic efficacy. IC50 value: 1 nM (hSCD1) Target: SCD1 in vitro: MK-8245, a phenoxy piperidine isoxazole derivative, has been identified as a potent and liver-specific SCD inhibitor. It contains a tetrazole acetic acid moiety, which is the key molecule for OATPs recognition and liver-targeting. MK...

化合物

VU0453595

Cat.No: T29137

Synonym: VU 0453595,VU-0453595

Synonym: JNJ 40068782

Synonym: C-CAM,NIH 10443

Target:

LY 215490

Cat.No: T27897

Synonym: LY215490,LY-215490

Methylatropine (nitrate)

Cat.No: T36204

Synonym:

Target:

MK-8245 Trifluoroacetate

Cat.No: T38844

Synonym:

Target:

Cat. No.	Product Name	Target	Signaling Pathways
T0281	Meclocycline sulfosalicylate salt 磺基水杨酸甲氯环素,Meclutin,Mecloderm,甲环素磺基水杨酸盐,Meclan Cream	Antibacterial; Antibiotic	Microbiology/Virology
	Meclocycline sulfosalicylate salt (Mecloderm) 是一种具有广谱抗菌活性的四环素抗生素，可预防皮肤细菌感染。

天然产物

Meclocycline sulfosalicylate salt

Cat.No: T0281

Synonym: 磺基水杨酸甲氯环素,Meclutin,Mecloderm,甲环素磺基水杨酸盐,Meclan Cream

Target: Antibacterial, Antibiotic

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