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T3586Compound 4012-morpholino-4H-pyrimido[2,1-a]isoquinolin-4-one
Compound 401 is a synthetic DNA-PK inhibitor (IC50 = 0.28 μM) that also targets mTOR but not PI3K.
价 格：￥电议型 号：T3586产 地：中国大陆
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T35856BMS-986176
AAK1-IN-1 is a highly selective and potent inhibitor of adaptor associated kinase 1 (AAK1, IC50 = 2 nM).
价 格：￥电议型 号：T35856产 地：中国大陆
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T358415-Benzyloxygramine
5-Benzyloxygramine blocks the Dopamin receptors and antagonizes the effects of 5-HT on the rat uterus and the rabbit ear.
价 格：￥电议型 号：T35841产 地：中国大陆
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T35834L(Sar?)-Angiotensin II acetate
(Sar?)-Angiotensin II acetate, an analogue of Angiotensin II, is a specific agonist of angiotensin AT1 receptor. It binds to brain membrane-rich particles, with a Kd of 2.7 nM. It can stimulate protein synthesis and cell growth in embryonic chick myocytes
价 格：￥电议型 号：T35834L产 地：中国大陆
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T3583MacozinonePBTZ169
PBTZ169 inhibits decaprenylphosphoryl-β-d-ribose 2′-oxidase (DprE1), more efficiently than BTZ043.
价 格：￥电议型 号：T3583产 地：中国大陆
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T35827LPKCε Inhibitor Peptide acetatePKCε Inhibitor Peptide acetate(182683-50-7 Free base)
PKCε Inhibitor Peptide acetate is a selective PKCε inhibitor containing the site for its specific receptor for activated C kinase (RACK). PKCε Inhibitor Peptide acetate inhibits the translocation of PKCε, but not α-, β-, and δPKC.
价 格：￥电议型 号：T35827L产 地：中国大陆
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T3582BTZ043
BTZ043 is a DprE1 inhibitor with nanomolar bactericidal activity against Mycobacterium tuberculosis in vitro.
价 格：￥电议型 号：T3582产 地：中国大陆
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T3581KS176
KS176 is a potent and selective inhibitor of the breast cancer resistance protein (BCRP) multidrug transporter, showing no inhibitory activity against P-gp or MRP1.
价 格：￥电议型 号：T3581产 地：中国大陆
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T3580FIPI5-Fluoro-2-indolyl deschlorohalopemide
FIPI is a derivative of halopemide which potently inhibits both PLD1 (IC50 = 25 nM) and PLD2 (IC50 = 20 nM); prevents PLD regulation of F-actin cytoskeleton reorganization, cell spreading, and chemotaxis.
价 格：￥电议型 号：T3580产 地：中国大陆
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T3558EBE-A22PD153035 Analog 63
EBE-A22 is a derivative of PD 153035 which can inhibit ErbB-1-phosphorylation, whereas EBE-A22 is inactive.
价 格：￥电议型 号：T3558产 地：中国大陆
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T3537GSK583
GSK583 is a highly effective and specific RIP2 kinase inhibitor (IC50: 5 nM).
价 格：￥电议型 号：T3537产 地：中国大陆
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T3462BMS-582949 hydrochlorideBMS-582949 HCl
The BMS-582949 hydrochloride is a highly specific p38α MAPK inhibitor (IC50: 13 nM).
价 格：￥电议型 号：T3462产 地：中国大陆
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T3458EED226
EED226 is a potent, selective, and orally bioavailable embryonic ectoderm development (EED) inhibitor with an IC50 of 22 nM.
价 格：￥电议型 号：T3458产 地：中国大陆
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T3358ITSA-1ITSA1
ITSA-1 is membrane permeable and specifically suppresses TSA inhibition of HDAC (histone deacetylase), but shows no activity towards other HDAC inhibitors.
价 格：￥电议型 号：T3358产 地：中国大陆
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T3334Velpatasvir维帕他韦；GS-5816
Velpatasvir, also known as GS-5816, is a potent and selective Hepatitis C virus NS5A inhibitor. GS-5816 has demonstrated pan-genotypic activity and a high barrier to resistance in HCV replicon assays. GS-5816 demonstrated pangenotypic antiviral activity i
价 格：￥电议型 号：T3334产 地：中国大陆
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T32658LLeteprinimAIT082 acid；AIT-082 acid；AIT 082 acid
Leteprinim is an hypoxanthine derivative that stimulates in vitro neurite outgrowth and the production of adenosine and neurotrophins from astrocytes.
价 格：￥电议型 号：T32658L产 地：中国大陆
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T3258PonesimodACT-128800
Ponesimod is an orally available sphingosine-1-phosphate receptor 1 (S1PR1, S1P1) agonist with potential immunomodulating activity.
价 格：￥电议型 号：T3258产 地：中国大陆
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T3188NSC5844RE-640
NSC5844 (RE640) is a bisquinoline compound with C-C chemokine receptor type 1 (CCR1)-agonistic activities.
价 格：￥电议型 号：T3188产 地：中国大陆
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T3186NU2058O(6)-Cyclohexylmethylguanine；O6-(Cyclohexylmethyl)guanine
NU2058 is a guanine-based CDK inhibitor, also inhibits DNA topoisomerase II ATPase activity.
价 格：￥电议型 号：T3186产 地：中国大陆
