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T8151MobocertinibAP-32788,Epidermal growth factor receptor,TAK-788,H1975,Inhibitor,Mobocertinib,HCC827,in
Mobocertinib is a potent inhibitor of epidermal growth factor receptor (EGFR) and an antineoplastic agent
价 格：￥电议型 号：T8151产 地：中国大陆
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T7499TAK-779TAK-779,TAK 779,CCR,HIV,Human immunodeficiency virus,Takeda779,Takeda-779,TAK779,CXCR,inhibit
TAK-779 is an antagonist of chemokine receptor 5 (CCR5), CCR2b, and CXC chemokine receptor 3 (CXCR3).
价 格：￥电议型 号：T7499产 地：中国大陆
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T6692TAK-733inhibit,Inhibitor,TAK-733,MAP2K,MAPKK,MEK,Mitogen-activated protein kinase kinase
MEK Inhibitor TAK-733 is an orally bioavailable small-molecule inhibitor of MEK1 and MEK2 (MEK1/2) with potential antineoplastic activity.
价 格：￥电议型 号：T6692产 地：中国大陆
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T6050TAK-700(S/R)-Orteronel；Orteronel
TAK-700 (Orteronel) is a potent and highly selective human 17, 20-lyase inhibitor with IC50 of 38 nM, exhibits >1000-fold selectivity over other CYPs (e.g. 11-hydroxylase and CYP3A4). Phase 3.
价 格：￥电议型 号：T6050产 地：中国大陆
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T5490AK-7
AK-7 is a brain-permeable SIRT2 inhibitor and to characterize its cholesterol-reducing properties in neuronal models with an IC50 of 15.5 μM.
价 格：￥电议型 号：T5490产 地：中国大陆
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T5490AK-7AK-7
AK-7 is a brain-permeable SIRT2 inhibitor and to characterize its cholesterol-reducing properties in neuronal models.with an IC50 of 15.5 μM
价 格：￥电议型 号：T5490产 地：美洲
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T80880Valziflocept；化合物 ValzifloceptBAX1810|||TAK-752；BAX1810|||TAK-752
Valziflocept (BAX1810; TAK-752) is a recombinant soluble human FcγRIIb receptor designed to act as a "decoy" or "scavenger" by targeting Fc and FcγR, binding and neutralizing pathogenic IgG. Its utility lies in mitigating the impact of autoimmune diseases, making it a focus in systemic lupus erythematosus (SLE) research [1].
价 格：￥电议型 号：T80880产 地：中国大陆
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T7499TAK-779；化合物TAK-779Takeda 779；Takeda 779
TAK-779 (Takeda 779) is an antagonist of chemokine receptor 5 (CCR5), CCR2b, and CXC chemokine receptor 3 (CXCR3).
价 格：￥电议型 号：T7499产 地：中国大陆
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T6692TAK-733；化合物TAK733TAK733|||TAK 733；TAK733|||TAK 733
TAK-733 is an orally bioavailable small-molecule inhibitor of MEK1 and MEK2 (MEK1/2) with potential antineoplastic activity.
价 格：￥电议型 号：T6692产 地：中国大陆
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T61802AK-778-XXMU；化合物 AK-778-XXMUAK-778-XXMU
AK-778-XXMU is an ID2 antagonist with a KD value of 129 nM.AK-778-XXMU has potential antitumor and anticancer activity and can be used for the study of gliomas.
价 格：￥电议型 号：T61802产 地：中国大陆
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T6051Orteronel化合物(S)-OrteronelTAK-700|||(S)-Orteronel
Orteronel ((S)-Orteronel)(TAK-700) was selected as a candidate for clinical evaluation. orteronel (TAK-700) is currently in phase III clinical trials for the treatment of castration-resistant prostate cancer.
价 格：￥电议型 号：T6051产 地：中国大陆
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T6050TAK-700；化合物(S/R)-Orteronel(S/R)-Orteronel|||Orteronel；(S/R)-Orteronel|||Orteronel
TAK-700 (Orteronel) (Orteronel) is a potent and highly selective human 17, 20-lyase inhibitor with IC50 of 38 nM, exhibits >1000-fold selectivity over other CYPs (e.g. 11-hydroxylase and CYP3A4). Phase 3.
价 格：￥电议型 号：T6050产 地：中国大陆
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T5490AK-7；化合物AK-7AK-7
AK-7 is a brain-permeable SIRT2 inhibitor and to characterize its cholesterol-reducing properties in neuronal models with an IC50 of 15.5 μM.
价 格：￥电议型 号：T5490产 地：中国大陆
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T37790TAK-700 salt；TAK-700 saltTAK700 (salt)|||TAK 700 (salt)|||TAK-700 salt；TAK700 (salt)|||TAK 700 (salt
TAK-700 salt is a potent and highly selective inhibitor of human 17,20-lyase with an IC50 of 38 nM and is over 1000-fold more selective than other CYPs such as 11-hydroxylase and CYP3A4.
价 格：￥电议型 号：T37790产 地：中国大陆
