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Home > Products > APIs
Cat.No. Product name Product Description
R21082315 L-778123HCL L-778123 hydrochloride is a dual inhibitor of FPTase and GGptase-I with IC50 val
R21082316 TP434 Eravacycline is an effective broad-spectrum antimicrobial.
R21082317 CYC-116 Cyc-116 is A potent inhibitor of aurora A and B with Ki values of 8 and 9 nM, re
R21082318 AV-412 Tosylate Av-412 (MP412) is an EGFR inhibitor with IC50 values of 0.75, 0.5, 0.79, 2.3, 19
R21082319 JNJ5207852 Jnj-5207852 is an effective and selective antagonist of histamine H3 receptor wi
R21082320 SQ109 SQ109 effectively inhibited the adult stage of the parasite, killing cells with
R21082321 WAY181187 hydrochloride
R21082322 MK7622 Mk-7622 is a positive allosteric regulator of muscarine M1 receptor.
R21082323 LU AE58054 Idalopirdine (Lu AE58054) is a potent, selective 5-HT6 receptor antagonist with
R21082324 Pardoprunox hydrochloride Pardoprunox hydrochloride is an agonist of dopamine receptors D2, D3, and 5-HT1A
R21082325 AL 082D06 AL 082D06 is a selective nonsteroidal glucocorticoid receptor (GR) antagonist wi
R21082326 eliprodil
R21082327 Sertindole Sertindole is a 5-HT2A, 5-HT2C, D2 and α L receptor antagonist.
R21082328 Carbazeran Carbazeran is a PDE-II and PDE-III inhibitor that produces concentration-depende
R21082329 Deracoxib Deracoxib is a non-narcotic, non-steroidal anti-inflammatory compound that is a
R21082330 SB21664 hydrochloride SB 216641 has been reported as a selective SR-1B antagonist with approximately 2
R21082331 Talnetant Talnetant (SB 223412) is a highly active NK3 receptor selective antagonist with
R21082332 Tepoxalin Tepoxalin is a 5-lipoxygenase inhibitor potentially for the treatment of asthma,
R21082333 Pagoclone Pagoclone is an active (+)-RP59037, A local activator of GABA(A) receptor, which
R21082334 Trovafloxacin Trovafloxacin is a broad-spectrum quinolone antibiotic with potent activity agai
R21082335 PRE 084 PRE-084 hydrochloride is a high affinity, selective σ1 agonist (Ki values are 2.
R21082336 GSK8573 GSK8573 is an inactive control compound of GSK2801. GSK8573 had binding activit
R21082337 NCH 51 PTACH (NCH-51) is a novel HDAC inhibitor. PTACH is effective in inhibiting the g
R21082338 MK0812 Mk-0812 is an effective and selective CCR2 antagonist that acts on human mononuc
R21082339 FUB359 Ciproxifan(FUB-359) maleate is a highly active H3 receptor antagonist with IC50
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