搜索结果

Search Results for " i 37 "

抑制剂 & 化合物

天然产物

如果没找到您满意的产品或者您对产品有其他要求，可以联系我们专业顾问为您提供针对性的合理建议。 QQ咨询网站留言咨询

Cat. No.	Product Name	Target	Signaling Pathways
T8721L	I-37 free base( 2359690-13-2(free base))	Raf	MAPK
	I-37 free base( 2359690-13-2(free base)) 是一种新型苄氨基取代的吡啶并嘧啶酮，可作为 SOS1 抑制剂。
T8721	I-37 Pyrido[4,3-d]pyrimidin-7(6H)-one, 2-methyl-6-(1-methylcyclopropyl)-4-[[(1R)-1-[2-methyl-3-(trifluoromethyl)phenyl]ethyl]amino]-	Raf	MAPK
	I-37 (Pyrido[4,3-d]pyrimidin-7(6H)-one, 2-methyl-6-(1-methylcyclopropyl)-4-[[(1R)-1-[2-methyl-3-(trifluoromethyl)phenyl]ethyl]amino]-) 是一种新型苄氨基取代的吡啶并嘧啶酮，可作为 SOS1 抑制剂。
T67748	ROCK-IN-5	ROCK; ERK	Cell Cycle/Checkpoint; Cytoskeletal Signaling; MAPK; Stem Cells
	ROCK-IN-5（化合物I-B-37）是一种有效的蛋白激酶抑制剂，包括ROCK、ERK、GSK 和AGC。ROCK-IN-5在心脏病、增殖性疾病和神经退行性疾病研究方面具有潜力。
TP1730L	β-catenin peptide acetate(265669-37-2 free base)	Others	Others
	β-catenin peptide acetate(265669-37-2 free base) 是一种由 Kb 呈递的天然存在的自身肽，可非常有效地介导 OT-I 胸腺细胞的阳性选择。
T81373	Proteasome β2c/i-IN-1	Proteasome	Proteases/Proteasome; Ubiquitination
	Proteasomeβ2c/i-IN-1（compound 37）为针对β2c和β2i亚基的选择性蛋白酶抑制剂。
T125185	Kudinoside I
	Kudinoside I 是一种有用的有机化合物，可用于生命科学领域的相关研究。其产品编号为 T125185，CAS号为 258343-37-2。
T79355	PRMT4-IN-3	Histone Methyltransferase	Chromatin/Epigenetic
	PRMT4-IN-3 (compound 56) 作为一种针对 I 类蛋白质精氨酸甲基转移酶 (PRMT) 的抑制剂，对 PRMT4 具有高效抑制作用，表现出对PRMT4(IC50: 37 nM) 和PRMT6(IC50: 253 nM) 的选择性。
TP1971	Pseudo RACK1
	Activator of protein kinase C; attached to cell permeabilization Antennapedia domain vector peptide. Consists of peptide derived from the C2 domain of PKC β linked by a disulfide bridge to the Antennapedia domain vector peptide. The Antennapedia peptide i
T38101	Bisucaberin
	Bisucaberin is a siderophore and bacterial metabolite that has been found inA. haloplanktisand has anticancer activity.1,2It inhibits the growth of L1210 and 1MC carcinoma cells (IC50s = 9.7 and 12.7 μM, respectively) and sensitizes fibrosarcoma 1023 cells to macrophage-mediated cytolysis. 1.Hou, Z., Raymond, K.N., O’Sullivan, B., et al.A preorganized siderophore: Thermodynamic and structural characterization of alcaligin and bisucaberin, microbial macrocyclic dihydroxamate chelating agentsInorg...
T35814	Urocortin III (human) (trifluoroacetate salt)
	Urocortin III is a neuropeptide hormone and member of the corticotropin-releasing factor (CRF) family which includes mammalian CRF , urocortin , urocortin II , frog sauvagine, and piscine urotensin I.1 Human urocortin III shares 90, 40, 37, and 21% identity to mouse urocortin III , mouse urocortin II , human urocortin , and mouse urocortin, respectively. Urocortin III selectively binds to type 2 CRF receptors (Kis = 21.7, 13.5, and >100 nM for rat CRF2α, rat CRF2β, and human CRF1, respectively)....

化合物

I-37 free base( 2359690-13-2(free base))

Synonym: Pyrido[4,3-d]pyrimidin-7(6H)-one, 2-methyl-6-(1-methylcyclopropyl)-4-[[(1R)-1-[2-methyl-3-(trifluoromethyl)phenyl]ethyl]amino]-

Target: ROCK, ERK

β-catenin peptide acetate(265669-37-2 free base)

Cat.No: TP1730L

Synonym:

Target: Others

Proteasome β2c/i-IN-1

Cat.No: T81373

Synonym:

Target: Proteasome

Target: Histone Methyltransferase

Urocortin III (human) (trifluoroacetate salt)

Cat.No: T35814

Synonym:

Target:

Cat. No.	Product Name	Target	Signaling Pathways
T36417	Nargenicin Antibiotic 47444
	Nargenicin is a macrolide antibiotic that selectively inhibits the growth of S. aureus, methicilin resistant S. aureus (MRSA), and M. luteus (MICs = 0.6, 0.3, and 2.5 μg/ml, respectively) over a panel of 11 Gram-positive and Gram-negative bacteria (MICs = >80 μg/ml). [1] It dose-dependently inhibits S. aureus DnaE in the presence of DNase I-activated DNA and E. coli DnaE when used at concentrations of 0.00001-0.1 and 0.01-100 μg/mL, respectively. [2] In murine BV-2 microglial cells, nargenicin (...

天然产物

Nargenicin

Cat.No: T36417

Synonym: Antibiotic 47444

Target:

* 搜索：		* 机关/企业：
* 邮箱：		* 电话：
备注：
验证码：

搜索结果

抑制剂 & 化合物

天然产物

提交您的定制咨询

化合物

天然产物