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抑制剂 & 化合物

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Cat. No.	Product Name	Target	Signaling Pathways
T26674	AT-130 AT 130	HBV; DNA/RNA Synthesis	Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology
	AT-130 是一种苯基丙烯酰胺衍生物，是乙型肝炎病毒复制的非核苷抑制剂。它抑制病毒 DNA 的合成，EC50为 0.13 μM。
T77920	ZXH-4-130 TFA	PROTACs	PROTAC
	ZXH-4-130 TFA为高效、选择性CRBN降解剂，属于CRBN-VHL类(hetero-PROTAC)化合物。在MM1.S细胞中，10 nM ZXH-4-130 TFA可诱导约80%的CRBN降解。
T36208	15(R)-Pinane Thromboxane A2 15(R)-Pinane Thromboxane A2
	15(R)-Pinane thromboxane A2 is the (R)-epimer of pinane thromboxane A2 . 15(R)-PTA2 does not inhibit collagen-induced platelet aggregation (IC50s = 120-130 μM). It does not affect gastric tone in isolated rat gastric fundus when used at concentrations of 0.5 or 1.5 μg/ml and is less effective than PTA2 at inhibiting prostaglandin-induced contraction of isolated rat stomach muscle.
T39194	PLX647 dihydrochloride
	PLX647 dihydrochloride is a potent and selective dual inhibitor of FMS and KIT kinases, with IC50 values of 28 nM and 16 nM, respectively. At a concentration of 1 μM, PLX647 dihydrochloride demonstrates superior selectivity against a wide range of 400 kinases, except FLT3 and KDR, where IC50 values are 91 nM and 130 nM, respectively. This orally active compound holds great potential for targeted kinase inhibition.
T38276	Benzomalvin C
	Benzomalvin C is a weak antagonist of the neurokinin-1 (NK1) receptor inhibiting binding of substance P by 46% when used at 100 μg/ml in vitro. It is also a weak inhibitor of indolamine 2,3-dioxygenase (IDO) with an IC50 value of 130 μM for recombinant IDO. It was isolated from Penicillium and contains an epoxide group at C-19 and C-20, which is not present in benzomalvins A, B, or E.
T74668	Zicronapine fumarate
	Zicronapine (Lu 31-130) fumarate 是抗精神病药，主要通过拮抗多巴胺D1/D2受体和5-HT2A受体发挥作用，在动物模型中显示出显著的前认知效果，展现出治疗多种神经和精神疾病的可能性。
T35989	CAY10565
	S-Nitrosothiols (RSNOs) are a class of molecules that function as exogenous and endogenous nitric oxide (NO) donors. RSNOs found in vivo include proteins such as S-nitrosohemoglobin and S-nitrosoalbumin, as well as low molecular weight species such as S-nitrosoglutathione (GSNO) and S-nitrosocysteine (CysNO). CAY10565 is a member of a new class of S-nitrosothiol species that act as NO donors under acidic conditions. It decomposes with a half-life of 130 minutes in 0.1 M phosphate buffer, pH 5.0,...
T83811	2'(3')-O-Anthraniloyladenosine-5'-O-triphosphate sodium 2'(3')-ANT-ATP
	2'(3')-O-Anthraniloyladenosine-5'-O-triphosphate（2'-ANT-ATP）与3'-ANT-ATP是荧光ATP衍生物，可自发地进行异构化。在水中，2'(3')-ANT-ATP的激发波长为330 nm时，发射最大波长为428 nm。它对哺乳动物腺苷酸环化酶（AC1）、AC2及AC5显示出抑制作用，抑制常数(Kis)分别为130、640和120 nM。此外，它还能抑制百日咳杆菌腺苷酸环化酶毒素CyaA（在锰和镁存在下，Kis分别为1.3和20 µM）、炭疽杆菌腺苷酸环化酶毒素水肿因子（在锰和镁存在下，Kis分别为0.44和5.15 µM）以及大肠杆菌重组酶A（RecA；Ki = 6.3 µM）。
T38077	TLQP-21 TFA
	TLQP-21 TFA, a VGF-derived peptide endowed of endocrine and extraendocrine properties, is a potent G-protein-coupled receptor complement-3a receptor1 (C3aR1) agonist (EC50: mouse TLQP-21=10.3 μM; human TLQP-21=68.8μM). TLQP-21 TFA activates C3aR1 to induce an increase of intracellular Ca2+. TLQP-21 TFA is used for the research in regulation of nociception and other relevant physiologic functions[1][2]. TLQP-21 TFA is a peptide of 21 amino acids. At a dose of 3 μM TLQP-21 induces up to ~69% of th...

化合物

AT-130

Cat.No: T26674

Synonym: AT 130

Target: HBV, DNA/RNA Synthesis

15(R)-Pinane Thromboxane A2

Cat.No: T36208

Synonym: 15(R)-Pinane Thromboxane A2

Target:

PLX647 dihydrochloride

2'(3')-O-Anthraniloyladenosine-5'-O-triphosphate sodium

Cat.No: T83811

Synonym: 2'(3')-ANT-ATP

Cat. No.	Product Name	Target	Signaling Pathways
T37751	Streptazolin
	Streptazolin is a fungal metabolite originally isolated from S. viridochromogenes. It increases NF-κB activity when used at concentrations ranging from 60 to 130 μg/ml, at least in part, via PI3K signaling. Streptazolin enhances TNF-α secretion induced by LPS and enhances IL-8 secretion when used alone or in combination with LPS in THP-1 Blue cells.

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