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T9359PDL-1 cpd 10PDL 1 cpd 10,PDL1 cpd 10
PDL-1 cpd 10 is a novel small molecule PD-L1 inhititor.
价 格：￥电议型 号：T9359产 地：中国大陆
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T35349CU-CPD107CU-CPD-107,CUCPD107,CU CPD107
CU-CPD107是一种选择性的双活性小分子，对TLR8激动剂和ssRNA配体表现出不同的活性。在R848存在的情况下，CU-CPD107是TLR8信号抑制剂 (IC50=13.7 μM)。在ssRNA存在的情况下，CU-CPD107表现出协同激动剂活性，而CU-CPD107单独不能影响TLR8信号转导。
价 格：￥电议型 号：T35349产 地：中国大陆
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T8688(Rac)-X77SARS-CoV,(Rac)-X77,protease,SARS coronavirus,inhibit,Inhibitor,(Rac) X77,(Rac)-X-77,coronav
CPD77 is a potent SARS- CoV- 2 main protease inhibitor.
价 格：￥电议型 号：T8688产 地：中国大陆
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T3484trans-ACPD(±)-trans-ACPD；1-amino-1,3-dicarboxycyclopentane；Trans-(±)-ACP
(±)-trans-ACPD is an equimolecular mixture of (1S, 3R)- and (1R, 3S)-ACPD. (±)-trans-ACPD is a selective agonist of the mGluR (metabotropic glutamate receptor); active at the group I/II mGlu receptors (EC50: 2/15/23/800 μM, mGluR2/1/5/4).
价 格：￥电议型 号：T3484产 地：中国大陆
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T3199PTACHNCH-51；Cpd 51
PTACH (NCH-51) is a SAHA-based inhibitor of human HDAC. It can potently inhibit the growth of various human Y cells (EC50: 1 to 10 μM).
价 格：￥电议型 号：T3199产 地：中国大陆
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T134923,5-Diiodothyropropionic acid3,5-二碘甲腺丙酸；Ditpa cpd；C082182
3,5-Diiodothyropropionic acid is a thyroid hormone analog. It induces α-myosin heavy chain mRNA expression, binds to thyroid hormone receptor (Ka: 2.40/M and 4.06/M for TRα1 and TRβ1).
价 格：￥电议型 号：T13492产 地：中国大陆
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T10877CPDA
CPDA is a new potent inhibitor of SH2 domain-containing inositol phosphatase 2 (SHIP2).
价 格：￥电议型 号：T10877产 地：中国大陆
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T10877CPDACPDA
CPDA is a new potent inhibitor of SH2 domain-containing inositol phosphatase 2 (SHIP2).
价 格：￥电议型 号：T10877产 地：美洲
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T8688(Rac)-X77；化合物CPD77CPD77|||MUN91789；CPD77|||MUN91789
(Rac)-X77 (MUN91789) is a potent SARS- CoV- 2 main protease inhibitor.
价 格：￥电议型 号：T8688产 地：中国大陆
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T75140CPD-1224；化合物 CPD-1224CPD-1224
CPD-1224, an orally active derivative that binds cereblon ligands to ALK inhibitors, specifically targets and degrades EML4-ALK oncogenic fusions, including ALK and its mutants L1196M/G1202R.
价 格：￥电议型 号：T75140产 地：中国大陆
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T71989CPD7 HCl；化合物 CPD7 HClCPD7 HCl
CPD7 HCl is a novel non-RBD binding modulator to inhibit SARS-CoV-2 by prohibiting the conformational change of the spike (S) protein.
价 格：￥电议型 号：T71989产 地：中国大陆
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T69252CPD26；化合物 CPD26CPD26
CPD26 is a novel non-RBD binding modulator to inhibit SARS-CoV-2 by prohibiting the conformational change of the spike (S) protein.
价 格：￥电议型 号：T69252产 地：中国大陆
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T35349CU-CPD107；化合物CU-CPD107CU-CPD107；CU-CPD107
CU-CPD107 is a selective agonist of toll-like receptor 8 (TLR8) and also shows activation activity against ssRNA ligands. CU-CPD107 acts as an inhibitor of TLR8 signaling in the presence of R848 (IC50=13.7 μM). CU-CPD107 exhibited coagonist activity in the presence of ssRNA, while CU-CPD107 alone could not affect TLR8 signal transduction.
价 格：￥电议型 号：T35349产 地：中国大陆
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T3484trans-ACPD；化合物(±)-trans-ACPDTrans-(±)-ACP|||1-amino-1,3-dicarboxycyclopentane|||(±)-trans-ACPD；Trans
trans-ACPD ((±)-trans-ACPD) is an equimolecular mixture of (1S, 3R)- and (1R, 3S)-ACPD. trans-ACPD is a selective agonist of the mGluR (metabotropic glutamate receptor); active at the group I/II mGlu receptors (EC50: 2/15/23/800 μM, mGluR2/1/5/4).
价 格：￥电议型 号：T3484产 地：中国大陆
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T33610NC-174；化合物 T33610CPDpmGA|||CP Dpm GA|||CP-Dpm-GA|||CP-DpmGA|||CPDpm-GA；CPDpmGA|||CP Dpm GA|||CP-Dpm-
NC-174 is a trisubstituted guanidine high potency synthetic sweetener.
价 格：￥电议型 号：T33610产 地：中国大陆
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T33372MF 13；化合物 T33372MF13Cpd|||MF13 Cpd|||MF-13|||MF13|||MF13-Cpd；MF13Cpd|||MF13 Cpd|||MF-13|||MF13|||MF1
MF 13 exhibits tumor apoptosis activity.
价 格：￥电议型 号：T33372产 地：中国大陆
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T32311Jom 13；化合物 T32311DCFPE|||Htdcpdp-OH；DCFPE|||Htdcpdp-OH
Jom 13 is a selective tetrapeptide used as a cyclic delta receptor.
价 格：￥电议型 号：T32311产 地：中国大陆
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T3199PTACH；化合物PTACHNCH-51|||Cpd 51；NCH-51|||Cpd 51
PTACH (Cpd 51) (NCH-51) is a SAHA-based inhibitor of human HDAC. It can potently inhibit the growth of various human Y cells (EC50: 1 to 10 μM).
价 格：￥电议型 号：T3199产 地：中国大陆
