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UM-164 is a highly potent, dual c-Src/p38inhibitor of c-Src with a binding constant Kd of 2.7 nM for c-Src and inhibits both p38α and p38β.
AZ628 is a new pan-Raf inhibitor for BRAF, BRAFV600E, and c-Raf-1 with IC50 of 105 nM, 34 nM and 29 nM in cell-free assays, also inhibits VEGFR2, DDR2, Lyn, Flt1, FMS, etc.
YN321657 Serotonin hydrochloride 153-98-0
Serotonin HCl is a monoamine neurotransmitter and Endogenous 5-HT receptor agonist.
YN320455 Syk Inhibitor II 726695-51-8
Syk Inhibitor II is a potent, high selective and ATP-competitiveSykinhibitor with an IC50 of 41nM. Syk Inhibitor II inhibits5-HTrelease from RBL-cells with an IC50 of 460nM. Syk Inhibitor II shows less potent ag...
YN321265 Xanthotoxol 2009-24-7
Xanthotoxol is a biologically active linear furocoumarin, shows strong pharmacological activities as anti-inflammatory, antioxidant, 5-HT antagonistic, and neuroprotective effects.
YQ128 is a potent and selective second-generationNLRP3 (NOD-like receptor P3) inflammasomeinhibitor with an IC50 of 0.30 µM. YQ128 significantly and selectively suppresses the production ofIL-1β, but not TNF-α, a...
YN330535 Cardamonin 18956-16-6
Cardamonin, isolated from the fruits of Alpinia species, is a chalconoid with anti-inflammatory and anti-tumor activity. It has been shown to be a novel antagonist of hTRPA1 cation channel with IC50 of 454 nM while does not intera...
YN350220 Ginsenoside Re 52286-59-6
Ginsenoside Re is a major ginsenoside in ginseng and belongs to 20(S)-protopanaxatriol group. It has diverse in vitro and in vivo effects, including vasorelaxant, antioxidant, antihyperlipidemic, and angiogenic actions.
YN321589 Thioridazine hydrochloride 130-61-0
Thioridazine is a potent antianxiety and antipsychotic agent.
YN350053 Guggulsterone 95975-55-6
Guggulsterone is one of the active constituent of Commiphora mukul. It occurs in two isomeric forms, namely Z-GS and E-GS. Guggulsterone act as antagonist ligands for the bile acid receptor, farnesoid X receptor, and as active in...
YN350194 Anisomycin 22862-76-6
Anisomycin is an antibiotic, which inhibits protein synthesis, and also act as a JNK activator.
UNBS5162 is a pan-antagonist ofCXCL chemokineexpression, with anti-tumor activity.
L 888607 is a potent, and selectiveCRTH2(also known as DP2) agonist with a Ki of 0.8nM.
Asenapine is an antagonist ofserotonin receptors(5-HT2A, 5-HT2B, 5-HT2C, 5-HT6, 5-HT7),adrenoceptors(α1, α2A, α2B, α2C),dopamine receptors(D2, D3, D4) and histamine receptors(H1, H2), withpKis of 8.4-10.5, 8.9-9....
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