Xi'an ruixi Biological Technology Co

Home > Keywords >

Catalog	name	Description	price
R-R-2321	GSK2646264 CAS No.1398695-47-0	GSK2646264 (Compound 44)/CAS No.1398695-47-0 is a potent and selective spleen tyrosine kinase (SYK) inhibitor with a pIC50 of 7.1. GSK2646264 also inhibits other kinases with pIC50 values of 5.4, 5.4, 5.3, 5, 4.5, <4.6 and <4.3 against LCK, LRRK2, GSK3β, JAK2, VEGFR2, Aurora B and Aurora A, respectively. GSK2646264 is penetrable into the epidermis and dermis of the skin.	price>
R-C-622	AT9283 cas:896466-04-9	AT9283 inhibits aurora kinase A and B and targets other tyrosine and serine/threonine kinases associated with myeloid cell proliferation.	price>
R-R-2322	JAK3-IN-1 CAS No.1805787-93-2	JAK3-IN-1/CAS No.1805787-93-2 is a potent, selective and orally active JAK3 inhibitor with an IC50 of 4.8 nM. JAK3-IN-1 shows over 180-fold more selective for JAK3 than JAK1 (IC50 of 896 nM) and JAK2 (IC50 of 1050 nM).	price>
R-C-623	GSK2838232A cas:1443461-21-9	GSK2838232, a betulin derivative,is an inhibitor of human immune virus (HIV) maturation which is potential for the treatment of chronic HIV infection.	price>
R-R-2323	(E/Z)-Zotiraciclib citrate CAS No.1204918-73-9	(E/Z)-Zotiraciclib citrate/CAS No.1204918-73-9 is a potent CDK2, JAK2, and FLT3 inhibitor.	price>
R-C-624	TAK875 CAS:1000413-72-8	Fasiglifam(TAK-875) is a selective GPR40 agonist with EC50 of 14 nM in human GPR40 expressing CHO cell line,400-fold more potent than oleic acid.	price>
R-R-2324	JAK2 JH2 binder-1 CAS No.2923309-41-3	JAK2 JH2 binder-1 (compound 11)/CAS No.2923309-41-3 is a potent and selective JAK2 JH2 binder, with a Kd of 37.1 nM. JAK2 JH2 binder-1 has the potential for various myeloproliferative neoplasms research.	price>
R-C-625	CP690550 cas:540737-29-9	Tofacitinib citrate(CP-690550 citrate)is a novel inhibitor of JAK with IC50 of 1 nM,20 nM and 112 nM against JAK3,JAK2,and JAK1,respectively.Tofacitinib citrate has anti-infection activity.	price>
R-R-2325	G5-7 CAS No.939681-36-4	G5-7/CAS No.939681-36-4, an orally active and allosteric JAK2 inhibitor, selectively inhibits JAK2 mediated phosphorylation and activation of EGFR (Tyr1068) and STAT3 by binding to JAK2. G5-7 induces cell cycle arrest, apoptosis and possesses antiangiogenic effect. G5-7 has the potential for glioma study.	price>
R-C-626	Rivaroxaban cas:366789-02-8	Rivaroxaban(BAY 59-7939)is a direct inhibitor of Factor Xa with Ki and IC50 of 0.4 nM and 0.7 nM in cell-free assays,respectively. It is selective for human factor Xa,for which it has>10 000-fold greater selectivity than for other biologically relevant serine proteases (IC50 >20μM).	price>
R-R-2326	a7 nAchR-JAK2-STAT3 agonist 1 CAS No.2108714-20-9	α7 nAchR-JAK2-STAT3 agonist 1/CAS No.2108714-20-9 is a potent α7 nAchR-JAK2-STAT3 agonist, with an IC50 value of 0.32 μM for nitric oxide (NO). α7 nAchR-JAK2-STAT3 agonist 1 effectively suppresses the expression of iNOS, IL-1β, and IL-6 in murine RAW264.7 macrophages. α7 nAchR-JAK2-STAT3 agonist 1 can inhibit LPS-induced NO release, NF-κB activation and cytokine production. α7 nAchR-JAK2-STAT3 can be used for researching sepsis.	price>
R-C-627	RI-1 (RAD51 inhibitor) cas:415713-60-9	RI-1 is a small molecule that inhibits the central recombination protein RAD51. RI-1 specifically reduces gene conversion in human cells while stimulating single strand annealing.RI-1 binds covalently to the surface of RAD51 protein at cysteine 319 that likely destabilizes an interface used by RAD51 monomers to oligomerize into filaments on DNA.	price>
R-R-2327	(2R,5S)-Ritlecitinib CAS No.1792180-79-0	(2R,5S)-Ritlecitinib ((2R,5S)-PF-06651600)/CAS No.1792180-79-0 is a potent and selective JAK3 inhibitor (IC50=144.8 nM) extracted from patent US20150158864A1, example 68.	price>
R-C-628	SRPIN340 cas:218156-96-8	SRPIN340 is a cell-permeable isonicotinamide that acts as an ATP-competitive SRPK1-selective inhibitor (IC50=0.14 and 1.8 μM,respectively,against mSRPK1 and mSRPK2)with much reduced activity against 143 other kinases.	price>
R-R-2328	JAK-IN-14 CAS No.1973485-06-1	JAK-IN-14/CAS No.1973485-06-1 is a potent and selective JAK1 inhibitor, with an IC50 of <5 μM. JAK-IN-14 is >8-fold more selective for JAK1 than JAK2 and JAK3 (Patent WO2016119700A1, compound 16).	price>
R-C-629	Tarafenacin cas:385367-47-5	Tarafenacin is a highly selective M3 muscarinic receptor antagonist.It was the most potent in inhibiting carbachol-induced bladder contractions of the anti-cholinergic agents tested,without affecting atrial contractions over the same range of concentrations.	price>
R-R-2329	SD-1029 CAS No.118372-34-2	SD-1029/CAS No.118372-34-2 is a JAK2/STAT3 inhibitor. SD-1029 inhibits STAT3 nuclear translocation. SD-1029 is an inhibitor of STAT3 activation due to inhibition of JAK2 phosphorylation.	price>
R-C-630	Sancycline cas:808-26-4	Sancycline is a rare semi-synthetic tetracycline prepared by hydrogenolysis of the chloro and benzylic hydroxy moieties of Declomycin.	price>
R-R-2330	SJ988497 CAS No.2595365-41-4	SJ988497/CAS No.2595365-41-4 is a PROTAC JAK2 degrader. SJ988497 potently inhibits CRLF2-rearranged (CRLF2r) cell proliferation and degrades the CRBN neosubstrate GSPT1. SJ988497 consists of a Ruxolitinib (HY-50856) derivative, linker, and CRBN ligand Pomalidomide. SJ988497 can be used in the research of acute lymphoblastic leukemia (ALL).	price>
R-C-631	MK4305 cas1030377-33-3	Suvorexant(MK-4305)is a potent,selective,and orally bioavailable antagonist of OX1R and OX2R currently under clinical investigation as a novel therapy for insomnia.	price>

442443444445446447 448449450451452