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T63928KRAS inhibitor-21；化合物 KRAS inhibitor-21KRAS inhibitor-21
KRAS inhibitor-21 (22b) is a KRAS G12C inhibitor (IC50<0.01 μM) that can be used in cancer research.
价 格：￥电议型 号：T63928产 地：中国大陆
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T63900VEGFR-2-IN-11；化合物 VEGFR-2-IN-11VEGFR-2-IN-11
VEGFR-2-IN-11 is a potent inhibitor of VEGFR-2 (IC50: 60.27 nM) with an IC50 value of 60.27 nM, which induces apoptosis and has anticancer activity.
价 格：￥电议型 号：T63900产 地：中国大陆
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T63890HIV-1 inhibitor-22；化合物 HIV-1 inhibitor-22HIV-1 inhibitor-22
HIV-1 inhibitor-22 is a potent inhibitor of HIV-1 non-nucleoside reverse transcriptase (RT) (HIV-1 RT: IC50=3.63 μM). M and also showed low cytotoxicity with a CC50 > 227 μM.
价 格：￥电议型 号：T63890产 地：中国大陆
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T63822VEGFR-2-IN-22；化合物 VEGFR-2-IN-22VEGFR-2-IN-22
VEGFR-2-IN-22 (Compound 25) is an inhibitor of VEGFR-2 and β-tubulin polymerization with an IC50=19.82 nM for VEGFR-2. VEGFR-2-IN-22 is capable of inducing apoptosis.
价 格：￥电议型 号：T63822产 地：中国大陆
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T63804VEGFR-2-IN-28；化合物 VEGFR-2-IN-28VEGFR-2-IN-28
VEGFR-2-IN-28 is a potent inhibitor of VEGFR-2 (IC50: 0.83 μM). VEGFR-2-IN-28 induces apoptosis and exhibits antitumor effects.
价 格：￥电议型 号：T63804产 地：中国大陆
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T63722VEGFR-2-IN-24；化合物 VEGFR-2-IN-24VEGFR-2-IN-24
VEGFR-2-IN-24 is a potent inhibitor of VEGFR-2 (IC50: 0.22 μM) and can be used to study tumors.
价 格：￥电议型 号：T63722产 地：中国大陆
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T63499HIV-1 inhibitor-28；化合物 HIV-1 inhibitor-28HIV-1 inhibitor-28
HIV-1 inhibitor-28 is a potent and selective HIV-1 inhibitor with EC50=58 nM for wild-type HIV-1, IC50=3.37 μM for wild-type HIV-1 reverse transcription, and relatively low toxicity to MT-4 cells with CC50= 38.6 μM. HIV-1 inhibitor-28 can be used in AIDS research.
价 格：￥电议型 号：T63499产 地：中国大陆
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T63391Calpain Inhibitor-2；化合物 Calpain Inhibitor-2Calpain Inhibitor-2
Calpain Inhibitor-2 is a lipophilic calpain inhibitor, and they showed moderate to good anti-proliferative effects in vitro compared to melanoma cell lines (A-375 and B-16F1) and PC-3 prostate cancer cells. was able to inhibit the invasion of 80% of DU-145 cells.
价 格：￥电议型 号：T63391产 地：中国大陆
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T63279ATM Inhibitor-2；化合物 ATM Inhibitor-2ATM Inhibitor-2
ATM Inhibitor -2 is a potent and selective inhibitor of ATM (IC50<1 nM).
价 格：￥电议型 号：T63279产 地：中国大陆
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T63168VEGFR-2-IN-26；化合物 VEGFR-2-IN-26VEGFR-2-IN-26
VEGFR-2-IN-26 (compound 5h) is a potent inhibitor of VEGFR-2 (IC50: 15.5 nM).VEGFR-2-IN-26 exhibits good anti-proliferative effects on leukaemia, CNS, non-small lung, ovarian, renal, prostate and breast cancer cells.
价 格：￥电议型 号：T63168产 地：中国大陆
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T63166L(S, R)-LSN 3318839；化合物(S,R)-LSN 3318839(S, R)-LSN 3318839(Isomer-2764704-18-7)；(S, R)-LSN 3318839(Is
产品可用于生物细胞实验
价 格：￥电议型 号：T63166L产 地：中国大陆
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T63113HIV-1 inhibitor-21；化合物 HIV-1 inhibitor-21HIV-1 inhibitor-21
HIV-1 inhibitor-21 (compound 9b) is a potent inhibitor of HIV-1 non-nucleoside reverse transcriptase (RT) and acts on HIV-1 RT (IC50: 0.55 μM). HIV-1 inhibitor-21 inhibits both wild-type HIV-1 (EC50: 12.7 nM) and mutant virus strain K103N (EC50: 10.4 nM) with relatively low cytotoxicity (CC50 for MT-4: 10.2 μM).
价 格：￥电议型 号：T63113产 地：中国大陆
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T6301Tosedostat；托舍多特CHR-2797；CHR-2797|||托舍多特
Tosedostat (CHR-2797) is an orally bioavailable inhibitor of the M1 family of aminopeptidases with potential antineoplastic activity. Tosedostat is converted intracellularly into a poorly membrane-permeable active metabolite (CHR-79888) which inhibits the M1 family of aminopeptidases, particularly puromycin-sensitive aminopeptidase (PuSA), and leukotriene A4 (LTA4) hydrolase; inhibition of these aminopeptidases in tumor cells may result in amino acid deprivation, inhibition of protein synthesis
价 格：￥电议型 号：T6301产 地：中国大陆
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T63002VEGFR-2-IN-15；化合物 VEGFR-2-IN-15VEGFR-2-IN-15
VEGFR-2-IN-15 (Compound 14b) is a potent inhibitor of VEGFR-2. VEGFR-2-IN-15 inhibits the growth of HepG2 cells in the Pre-G1 phase and induces apoptosis.
价 格：￥电议型 号：T63002产 地：中国大陆
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T62965TDP1 Inhibitor-2；化合物 TDP1 Inhibitor-2TDP1 Inhibitor-2
TDP1 Inhibitor-2 is a potent inhibitor of TDP1 (tyrosyl-DNA phosphodiesterase 1) (IC50: 99 nM) and inhibits SCAN1 (spinal cerebellar ataxia syndrome with axonal neuropathy) (IC50: 3.5 μM).
价 格：￥电议型 号：T62965产 地：中国大陆
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T6296RAF265；化合物RAF265CHIR-265；CHIR-265
RAF265 (CHIR-265) (CHIR-265) is a potent selective inhibitor of C-Raf/B-Raf/B-Raf V600E with IC50 of 3-60 nM, and exhibits potent inhibition on VEGFR2 phosphorylation with EC50 of 30 nM. Phase 2.
价 格：￥电议型 号：T6296产 地：中国大陆
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T62901VEGFR-2-IN-27；化合物 VEGFR-2-IN-27VEGFR-2-IN-27
VEGFR-2-IN-27 (compound 7a) is a potent inhibitor of VEGFR-2 (IC50: 14.8 nM) and can be used in anticancer studies.
价 格：￥电议型 号：T62901产 地：中国大陆
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T6289Dovitinib；多韦替尼TKI258|||CHIR-258；TKI258|||多韦替尼|||CHIR-258|||度维替尼
Dovitinib (CHIR-258) (TKI258, CHIR258) is a multitargeted RTK inhibitor, mostly for class III (FLT3/c-Kit, IC50: 1/2 nM), also effective to class IV (FGFR1/3) and class V (VEGFR1-4) RTKs (IC50: 8-13 nM), less potent to EGFR, InsR, EphA2, c-Met, IGF-1R, Tie2, and HER2.
价 格：￥电议型 号：T6289产 地：中国大陆
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T62885GABAA receptor modulator-2；化合物 GABAA?receptor?modulator-2GABAA receptor modulator-2
GABAA receptor modulator-2 (Compound 20) is a selective, orally active α5-GABAAR negative conformation modulator (Ki: 4.1 nM). gABAA receptor modulator-2 exhibits high metabolic stability and a good central nervous system safety profile.
价 格：￥电议型 号：T62885产 地：中国大陆
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T62883BRD4 Inhibitor-23；化合物 BRD4 Inhibitor-23BRD4 Inhibitor-23
BRD4 Inhibitor-23 is a potent, orally active BRD4 inhibitor that acts on BRD4 BD-1 (IC50: 6.21 nM) and BRD4 BD-2 (IC50: 1.44 nM).
价 格：￥电议型 号：T62883产 地：中国大陆
