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T23439TC-N 1752TCN 1752,TC N 1752
TC-N 1752 is an orally active inhibitor of Nav1.7 channel with IC50 of 0.17 μM. TC-N 1752 shows analgesic activities.
价 格：￥电议型 号：T23439产 地：中国大陆
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T3574Sematilide hydrochloride司美利特；CK-1752；Sematilide HCl；CK-1752A
Sematilide (CK-1752) is a class III antiarrhythmic. It is a selectively delayed rectifier K+ current (IKr) channel blocker. It inhibits rapidly activating Ik in guinea pig atrial myocytes, resulting in the prolongation of refractoriness and action potenti
价 格：￥电议型 号：T3574产 地：中国大陆
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T2375BX471ZK-811752；BX 471；BX-471
BX471 is a potent, selective non-peptide CCR1 antagonist.
价 格：￥电议型 号：T2375产 地：中国大陆
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T17522Azido-PEG9-azide
Azido-PEG9-azide is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.
价 格：￥电议型 号：T17522产 地：中国大陆
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T17521Azido-PEG9-alcohol叠氮-九聚乙二醇
Azido-PEG9-alcohol is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.
价 格：￥电议型 号：T17521产 地：中国大陆
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T1752NS6180
NS6180 is a potent and selective KCa3.1 channel inhibitor(IC50= 9 nM). It prevents T-cell activation and inflammation.
价 格：￥电议型 号：T1752产 地：中国大陆
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T14845BX471 hydrochlorideBX471 hydrochloride,ZK-811752 hydrochloride,
BX471 hydrochloride (ZK-811752 hydrochloride) is a potent, selective non-peptide CCR1 antagonist with Ki of 1 nM for human CCR1. And it exhibits 250-fold selectivity for CCR1 over CCR2, CCR5 and CXCR4.
价 格：￥电议型 号：T14845产 地：美洲
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T1752NS6180NS6180
NS6180 is a potent and selective KCa3.1 channel inhibitor(IC50= 9 nM). It prevents T-cell activation and inflammation.
价 格：￥电议型 号：T1752产 地：美洲
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T81752MP-PEG8-Val-Lys-Gly-7-MAD-MDCPT；化合物 MP-PEG8-Val-Lys-Gly-7-MAD-MDCPTMP-PEG8-Val-Lys-Gly-7-MAD-MDCPT
MP-PEG8-Val-Lys-Gly-7-MAD-MDCPT is an agent-linker conjugate designed for antibody-drug conjugate (ADC) applications, with potential use in cancer and autoimmune disease research.
价 格：￥电议型 号：T81752产 地：中国大陆
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T71752Metoprolol fumarate；化合物 Metoprolol FumarateLopressor OROS|||CGP 2175C|||CGP 2175C ; Lopressor OROS；
Metoprolol fumarate (CGP 2175C) is a selectively active β1-adrenoceptor antagonist administered orally. It exhibits anti-inflammatory, antitumor, and anti-angiogenic properties.
价 格：￥电议型 号：T71752产 地：中国大陆
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T68870SU-11752；化合物 SU-11752SU-11752
SU-11752 is a potent and selective DNA-PK inhibitor. Inhibition kinetics and a direct assay for ATP binding showed that SU11752 inhibited DNA-PK by competing with ATP. SU11752 inhibited DNA double-strand break repair in cells and gave rise to a five-fold sensitization to ionizing radiation. At concentrations of SU11752 that inhibited DNA repair, cell cycle progression was still normal and ATM kinase activity was not inhibited.
价 格：￥电议型 号：T68870产 地：中国大陆
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T3574Sematilide hydrochloride；司美利特CK-1752A|||CK-1752|||Sematilide HCl；司美利特|||CK-1752A|||CK-1752|||Sematil
Sematilide hydrochloride (CK-1752) is a class III antiarrhythmic. It is a selectively delayed rectifier K+ current (IKr) channel blocker. It inhibits rapidly activating Ik in guinea pig atrial myocytes, resulting in the prolongation of refractoriness and action potential duration.
价 格：￥电议型 号：T3574产 地：中国大陆
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T34091p-Methoxybenzylideneacetone；化合物 T34091NSC-31752|||NSC31752|||NSC 31752；NSC-31752|||NSC31752|||NSC 31
p-Methoxybenzylideneacetone is a biochemical.
价 格：￥电议型 号：T34091产 地：中国大陆
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T31752FD&C Yellow No. 4；化合物 T31752NSC-11234|||NSC11234|||Yellow OB|||NSC 11234；NSC-11234|||NSC11234|||
FD&C Yellow No. 4 is a dye.
价 格：￥电议型 号：T31752产 地：中国大陆
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T30815Cgp 17520；化合物 T30815Cgp-17520|||Cgp17520；Cgp-17520|||Cgp17520
Cgp 17520 is a bio-active chemical.
价 格：￥电议型 号：T30815产 地：中国大陆
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T2375BX471；化合物BX-471BX 471|||BX-471|||ZK-811752；BX 471|||BX-471|||ZK-811752
BX471 (BX 471) is a potent, selective non-peptide CCR1 antagonist.
价 格：￥电议型 号：T2375产 地：中国大陆
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T23439TC-N 1752；化合物TC-N 1752TC-N 1752
TC-N 1752 is an orally active inhibitor of Nav1.7 channel with IC50 of 0.17 μM. TC-N 1752 shows analgesic activities.
价 格：￥电议型 号：T23439产 地：中国大陆
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T21752AL 8810；化合物 T21752AL 8810
AL-8810 is an 11β-fluoro analog of PGF 2α with selective antagonist effects at the PGF 2α receptor (FP receptor) [1].
价 格：￥电议型 号：T21752产 地：中国大陆
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T17529BCN-PEG3-Biotin；化合物 T17529BCN-PEG3-Biotin
BCN-PEG3-Biotin is a non-cleavable three-unit PEG linker employed in the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T17529产 地：中国大陆
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T17528BCN-PEG1-Val-Cit-PABC-OH；化合物 T17528BCN-PEG1-Val-Cit-PABC-OH
BCN-PEG1-Val-Cit-PABC-OH is a cleavable 1-unit PEG linker specifically utilized in the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T17528产 地：中国大陆
