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Home > Products
| Cat.No. | Product name | Product Description |
| R10696 | 2-Chloro-N-[[2'-[(cyanoamino)sulfonyl][1,1'-biphenyl]-4-yl]methyl]-N-[(4-methylphenyl)methyl]-benzamide | S0859, an N-cyanosulphonamide compound, reversibly inhibit NBC-mediated pH(i) re |
| R10697 | HDAC-IN-7 (Chidamide impurity) | Chidamide(CS055; HBI-8000) is a class I HDAC inhibitor with IC50s of 95/160/67/7 |
| R10698 | J147 | J-147 is a broad spectrum neuroprotective phenyl hydrazide compound(EC50=60-115 |
| R10699 | AG18 | AG-18 inhibits EGFR with IC50 of 35 μM. |
| R10700 | ELR510444 | ELR510444 is a novel microtubule disruptor; inhibits MDA-MB-231 cell proliferati |
| R10701 | CCG1423 | CCG-1423 is a specific RhoA pathway inhibitor, which inhibits SRF-mediated trans |
| R10702 | RG108;N-Phthalyl-L-tryptophan | RG108 is an inhibitor of DNA methyltransferase with IC50 of 115 nM in a cell-fre |
| R10703 | STATIL | |
| R10704 | SRPIN340 | SRPIN340 is a selective SRPK inhibitor with Ki of 0.89 μM for SRPK1, showing no |
| R10705 | KY02111 | KY02111 promotes differentiation of hPSCs to cardiomyocytes by inhibiting Wnt si |
| R10706 | MHY1485 | MHY1485 is a potent, and cell-permeable mTOR activator, and also potently inhibi |
| R10707 | PURVALANOLA | Purvalanol A is a potent, and cell-permeable CDK inhibitor with IC50 of 4 nM, 70 |
| R10708 | NG-52 | NG 52 (Compound 52 ) is a potent, cell-permeable, reversible, selective, and ATP |
| R10709 | JANEX-1 (Synonyms: WHI-P131; Jak3 inhibitor I) | Janex-1 is a cell-permeable, reversible, potent, ATP-competitive, and specific i |
| R10710 | WHI-P180 | WHI-P180 (Janex 3) is a multi-kinase inhibitor; inhibits RET, KDR and EGFR with |
| R10711 | AG-1517 | PD153035 HCl is a potent and specific inhibitor of EGFR with Ki and IC50 of 5.2 |
| R10713 | Bohemine | Bohemine is a CDK inhibitor with IC50s of 4.6, 83, and 2.7 μM for Cdk |
| R10714 | WHI-P258 | WHI-P258, a quinazoline compound, binds to the active site of JAK3 with an estim |
| R10715 | Methoxy-PMS | Methoxy-PMS (1-Methoxy PMS; 1-Methoxyphenazine methosulfate) is stable electron- |
| R10716 | CZC54252;CZC-54252 | CZC-54252 is a potent inhibitor of LRRK2 with IC50s of 1.28 nM and 1.85 nM for w |
| R10717 | NS11394 | NS11394 is a potent and subtype-selective GABA(A) receptor-positive modulator; p |
| R10718 | kbNB142-70 | kb NB 142-70 is a selective protein kinase D (PKD) inhibitor (IC50 values are 28 |
| R10719 | APY0201 | APY0201 is a potent, highly selective, ATP-competitive PIKfyve inhibitor (IC50=5 |
| R10721 | ACT058362; Palosuran | Palosuran is a new potent and specific antagonist of the human UT receptor with |
| R10722 | CASIN | CASIN is a selective GTPase Cdc42 inhibitor with IC50 of 2 uM. In vitro: Treatme |
