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T10643c-Fms-IN-1；化合物c-Fms-IN-1c-Fms-IN-1
c-Fms-IN-1 is an inhibitor of c-FMS kinase (IC50 = 0.8 nM).
价 格：￥电议型 号：T10643产 地：中国大陆
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T10634Bunaftide；丁萘夫汀Bunaphtide|||Meregon|||Bunaftine；Bunaphtide|||Meregon|||Bunaftine
Bunaftide (Bunaphtid) has antiarrhythmic effects and inhibits aconitine-induced ventricular tachycardia.
价 格：￥电议型 号：T10634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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T10618Broflanilide；溴虫氟苯双酰胺Broflanilide
Broflanilide is metabolized to desmethyl-broflanilide, which is a potent antagonist at the insect resistant-to-dieldrin GABA receptor and inhibits S. litura RDL GABAR with IC50 of 1.3 nM.
价 格：￥电议型 号：T10618产 地：中国大陆
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T10617Brofaromine；化合物 T10617CGP 11305A；CGP 11305A
Brofaromine (CGP 11305A) is an MAO inhibitor (IC50: 0.2 μM for MAO-A).
价 格：￥电议型 号：T10617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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T1060Flumequine；氟甲喹Flumigal|||R-802；Flumigal|||氟甲喹|||R-802
Flumequine (R-802) is a broad-spectrum antibiotic that is active against both Gram-positive and Gram-negative bacteria. It functions by inhibiting DNA gyrase, a type II topoisomerase, and topoisomerase IV, enzymes necessary to separate bacterial DNA, thereby inhibiting cell division.
价 格：￥电议型 号：T1060产 地：中国大陆
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T10599BRAF inhibitor；化合物BRAF inhibitorBRAF inhibitor
BRAF inhibitor is an inhibitor of B-Raf.
价 格：￥电议型 号：T10599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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T10580BOC-D-FMK；3-[[叔丁氧羰基]氨基]-5-氟-4-氧代戊酸甲酯BOC-D-FMK
Boc-D-FMK is an irreversible, cell-permeable, and broad-spectrum caspase inhibitor and inhibits apoptosis stimulated by TNF-α (IC50: 39 μM).
价 格：￥电议型 号：T10580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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T10570Fostemsavir Tris；化合物Fostemsavir TrisBMS-663068 Tris；BMS-663068 Tris
Fostemsavir Tris (BMS-663068 Tris) is the prodrug of BMS-626529,is a oral, safe and effective inhibitor of HIV-1 attachment. It inhibits human immunodeficiency virus type 1 (HIV-1) infection by binding to gp120 and interfering with the attachment of virus to CD4+ T-cells.
价 格：￥电议型 号：T10570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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T10551Bithionol sulfoxide；硫双二氯酚亚砜Bithionol sulfoxide
Bithionol sulfoxide is a clinically approved antiparasitic drug with the inhibitory against solid tumor growth in several preclinical cancer models.
价 格：￥电议型 号：T10551产 地：中国大陆
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T1055Ifosfamide；异环磷酰胺NSC109724|||Isophosphamide；NSC109724|||Isophosphamide|||异环磷酰胺
Ifosfamide (NSC-109724) alkylates and forms DNA crosslinks, thereby preventing DNA strand separation and DNA replication. Ifosfamide is a synthetic analog of the nitrogen mustard cyclophosphamide with antineoplastic activity. This agent is a prodrug that must be activated through hydroxylation by hepatic microsomal enzymes.
价 格：￥电议型 号：T1055产 地：中国大陆
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T10548Biotin-VAD-FMK；化合物 T10548Biotin-VAD-FMK
Biotin-VAD-FMK is a cell-permeable, irreversible biotin-labeled inhibitor of caspase. It is used to identify active caspases in cell lysates.
价 格：￥电议型 号：T10548产 地：中国大陆
