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T10792LCHK1-IN-4 hydrochloride；化合物CHK1-IN-4盐酸盐CHK1-IN-4 hydrochloride（2120398-41-4 Free base）；CHK1-IN-4 hyd
CHK1-IN-4 hydrochloride is a potent inhibitor of checkpoint kinase 1 (chk1). CHK1-IN-4 hydrochloride potently inhibits chk1 phosphorylation in the tumor cells. CHK1-IN-4 hydrochloride has anti-tumor activity.
价 格：￥电议型 号：T10792L产 地：中国大陆
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T10788LChitinase-IN-2 hydrochloride；化合物 T10788LChitinase-IN-2 hydrochloride (1579991-63-1 free base)；Chitin
Chitinase-IN-2 hydrochloride functions as an inhibitor of both insect chitinase and N-acetyl hexosaminidase, and also serves as a pesticide. At concentrations of 50 ?M and 20 ?M, it demonstrates inhibitory effectiveness of 98% and 92% against chitinase and N-acetyl-hexosaminidase, respectively.
价 格：￥电议型 号：T10788L产 地：中国大陆
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T10759CEP-28122 mesylate salt (1022958-60-6 free base)；化合物CEP-28122 mesylate saltCEP-28122 mesylate salt；C
CEP-28122 mesylate salt (1022958-60-6 free base) is a highly selective orally active ALK inhibitor (IC50: 1.9 nM in an enzyme-based TRF assay).
价 格：￥电议型 号：T10759产 地：中国大陆
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T10750Cecropin A TFA (80451-04-3 free base)；化合物 T10750Cecropin A TFA；Cecropin A TFA
Cecropin A TFA is an antimicrobial polypeptide isolated from Hyalaphora cecropia pupae with anti-inflammatory, anti-bacterial, and anti-cancer activity.
价 格：￥电议型 号：T10750产 地：中国大陆
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T10699L2CBB1007 trihydrochloride (1379573-92-8 free base)；化合物 T10699L2CBB1007 trihydrochloride；CBB1007 trihy
CBB1007 trihydrochloride is a selective, reversible, and substrate competitive LSD1 inhibitor (IC50: 5.27 μM for hLSD1).
价 格：￥电议型 号：T10699L2产 地：中国大陆
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T10699CBB1007 hydrochloride (1379573-92-8 free base)；化合物 T10699CBB1007 hydrochloride；CBB1007 hydrochloride
CBB1007 Hcl is a selective, reversible, and substrate competitive LSD1 inhibitor (IC50: 5.27 μM for hLSD1).
价 格：￥电议型 号：T10699产 地：中国大陆
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T10698LCBB1003 hydrochloride (1379573-88-2 free base)；化合物 T10698LCBB1003 hydrochloride；CBB1003 hydrochlorid
CBB1003 hydrochloride is a new inhibitor of histone demethylase LSD1 (IC50: 10.54 μM).
价 格：￥电议型 号：T10698L产 地：中国大陆
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T10692CB-1158 dihydrochloride (2095732-06-0 free base)；化合物 T10692INCB01158 dihydrochloride|||CB-1158 dihyd
CB-1158 dihydrochloride is an effective and orally active inhibitor of arginase (IC50s: 86 nM and 296 nM for recombinant human arginase 1 and 2).
价 格：￥电议型 号：T10692产 地：中国大陆
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T10631LBucindolol Formate；化合物Bucindolol FormateBucindolol Formate (71119-11-4 Free base)；Bucindolol Formate
Bucindolol Formatel is a blocker of β1-adrenergic receptor. Bucindolol exhibits intrinsic sympathomimetic activity. Bucindolol can be used in the research of heart failure.
价 格：￥电议型 号：T10631L产 地：中国大陆
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T10625L(Rac)-IBT6A hydrochloride (1412418-47-3 free base)；化合物 T10625L(Rac)-IBT6A hydrochloride；(Rac)-IBT6A
(Rac)-IBT6A hydrochloride is a racemate of IBT6A. IBT6A is an impurity of Ibrutinib. IBT6A can be used in the synthesis of IBT6A Ibrutinib dimer and IBT6A adduct. Ibrutinib is a Btk inhibitor (IC50: 0.5 nM).
价 格：￥电议型 号：T10625L产 地：中国大陆
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T10602BRD 4354 ditrifluoroacetate；化合物 T10602BRD 4354 ditrifluoroacetate (315698-07-8 free base)；BRD 4354 d
BRD 4354 (ditrifluoroacetate) is a moderately potent inhibitor of HDAC5 and HDAC9 (IC50s: 0.85 and 1.88 μM).
价 格：￥电议型 号：T10602产 地：中国大陆
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T10589BPN-15606 besylate (1914989-49-3 free base)；化合物 T10589BPN-15606 besylate；BPN-15606 besylate
BPN-15606 besylate is a highly potent, orally active γ-secretase modulator, attenuates the production of Aβ40 and Aβ42 by SHSY5Y neuroblastoma cells (IC50s: 7 nM and 17nM).
价 格：￥电议型 号：T10589产 地：中国大陆
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T10586BPH-1358 free base；化合物 T10586NSC50460 free base；NSC50460 free base
BPH-1358 (NSC50460) free base is a potent human undecaprenyl diphosphate synthase (UPPS) and farnesyl diphosphate synthase (FPPS) inhibitor (IC50s: 110 nM and 1.8 μM) and is active against S. aureus in vitro (MIC ~250 ng/mL).
价 格：￥电议型 号：T10586产 地：中国大陆
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T10581Boc-MLF TFA (67247-12-5 free base)；化合物 T10581Boc-Met-Leu-Phe-OH (TFA)|||Boc-MLF TFA；Boc-Met-Leu-Phe-
Boc-MLF (TFA) is a specific antagonist of formyl peptide receptor (FPR) and also inhibits signaling through FPRL1 at higher concentrations.
价 格：￥电议型 号：T10581产 地：中国大陆
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T10572LBMT-124110 Formate；BMT-124110甲酸盐BMT-124110 Formate（1679371-59-5 Free base）；BMT-124110 Formate（167937
BMT-124110 Formate is a selective AAK1 inhibitor (IC50: 0.9 nM) with anti-injury sensory activity.BMT-124110 Formate inhibits the BMP-2-inducible protein kinase BIKE with an IC50: 17 nM.BMT-124110 Formate inhibits the cell-cycle protein G-related BMT-124110 Formate inhibits the cell cycle protein G-associated kinase GAK with an IC50:99 nM.
价 格：￥电议型 号：T10572L产 地：中国大陆
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T10563L2BM635 mesylate (1493762-74-5 free base)；化合物 T10563L2BM635 mesylate；BM635 mesylate
BM635 mesylate is an MmpL3 inhibitor with outstanding anti-mycobacterial activity (MIC50: 0.12 μM against M. tuberculosis H37Rv).
价 格：￥电议型 号：T10563L2产 地：中国大陆
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T10563LBM635 hydrochloride (1493762-74-5 free base)；化合物 T10563LBM635 hydrochloride；BM635 hydrochloride
BM635 hydrochloride is an MmpL3 inhibitor with outstanding anti-mycobacterial activity (MIC50: 0.12 μM against M. tuberculosis H37Rv).
价 格：￥电议型 号：T10563L产 地：中国大陆
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T10501YM158 free base；化合物 T10501YM-57158；YM-57158
YM158 free base is a potent and selective antagonist of TXA2 and LTD4 receptor (pA2s: about 8.81 and 8.87).
价 格：￥电议型 号：T10501产 地：中国大陆
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T10482LBB-Cl-Amidine hydrochloride化合物 T10482LBB-Cl-Amidine hydrochloride (1802637-39-3 free base)
BB-Cl-Amidine hydrochloride is an inhibitor of peptidylarginine deminase (PAD) [1].
价 格：￥电议型 号：T10482L产 地：中国大陆
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T10472LBay 65-1942 free base；化合物 T10472LBay 65-1942 free base
Bay 65-1942 free base is an inhibitor of ATP-competitive and selective IKKβ.
价 格：￥电议型 号：T10472L产 地：中国大陆
