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T10371ArotinololArotinolol
Arotinolol is a nonselective α/β-adrenergic receptor blocker and a vasodilating β-blocker. Arotinolol also shows potency for inhibiting the binding of the radioligand 125I-ICYP to 5HT1B-serotonergic receptor sites. It is an antihypertensive agent.
价 格:¥电议型 号:T10371产 地:美洲
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T10373(R)-Filanesib(R)-Filanesib,(R)-ARRY-520,
(R)-Filanesib is the R-enantiomer of ARRY-520. (R)-Filanesib is a synthetic kinesin spindle protein (KSP) inhibitor (IC50: 6 nM).
价 格:¥电议型 号:T10373产 地:美洲
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T10375ARS-1323ARS-1323
ARS-1323 (the racemate of ARS-1620) is a mutant K-ras G12C inhibitor extracted from patent WO 2015054572 A1.
价 格:¥电议型 号:T10375产 地:美洲
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T10376ARS-1630ARS-1630
ARS-1630 is a mutant K-ras G12C inhibitor extracted from patent WO 2015054572 A1. It is a less active enantiomer of ARS-1620.
价 格:¥电议型 号:T10376产 地:美洲
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T10377ArtefenomelArtefenomel,OZ439,
Artefenomel (OZ439) is a synthetic antimalarial agent with the artemisinin pharmacophore.
价 格:¥电议型 号:T10377产 地:美洲
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T10705CCG 203769CCG 203769
CCG 203769 is a selective inhibitor of G protein signaling (RGS4). It blocks the RGS4-Gαo protein-protein interaction in vitro (IC50: 17 nM).
价 格:¥电议型 号:T10705产 地:美洲
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T12037MifamurtideMifamurtide,MTP-PE,L-MTP-PE
Mifamurtide is a drug against osteosarcoma, is an immunomodulator with antitumor effects.
价 格:¥电议型 号:T12037产 地:美洲
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T140373α-Aminocholestane3α-Aminocholestane
3α-Aminocholestane , a selective SH2 domain-containing inositol-5′-phosphatase 1 (SHIP1) , inhibitor with an IC50 of ~2.5 μM.
价 格:¥电议型 号:T14037产 地:美洲
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T15506HTS01037HTS01037
HTS01037 is an inhibitor of fatty acid-binding. HTS01037 is a competitive antagonist of protein-protein interactions mediated by AFABP/aP2 (Ki: 0.67 μM).
价 格:¥电议型 号:T15506产 地:美洲
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T1601LomustineLomustine,NSC 79037,CCNU
Lomustine is an alkylating agent of value against both hematologic malignancies and solid tumors.
价 格:¥电议型 号:T1601产 地:美洲
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T1841UNC0379UNC0379
UNC0379 is a selective, substrate-competitive inhibitor of the lysine methyltransferase SETD8.
价 格:¥电议型 号:T1841产 地:美洲
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T2037TH588TH588
TH588 is nudix hydrolase family inhibitor that effectively and selectively engages and inhibits the MTH1(IC50: 5 nM) in cells.
价 格:¥电议型 号:T2037产 地:美洲
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T5037MidecamycinMidecamycin,Antibiotic SF-837,Espinomycin A
Midecamycin, an acetoxy-substituted macrolide antibiotic, has effective on gram-positive and gram-negative bacteria acts by inhibiting bacterial protein synthesis.
价 格:¥电议型 号:T5037产 地:美洲
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T5383D3-βArrD3-βArr,NCGC00379308,
D3-βArr is a positive allosteric modulator for thyrotropin receptor (TSHR), which initiates translocation of β-Arr 1 (EC50: 11.6 μM) by direct TSHR activation.
价 格:¥电议型 号:T5383产 地:美洲
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T5411SEP-0372814SEP-0372814
PDE10-IN-1 is PDE10-IN-1 inhibitor extracted from Patent WO 2013192273 A1, for treating CNS and metabolic disorders.
价 格:¥电议型 号:T5411产 地:美洲
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T5597ZT-12-037-01ZT-12-037-01
Zt-12-037-01 is a ATP competitive STK19 inhibitor(IC50 values of 23.96 nM and 27.94 nM for STK19 (WT) and STK19 (D89N),respectively).
价 格:¥电议型 号:T5597产 地:美洲
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T6254IdasanutlinIdasanutlin,RG7388,Ro 5503781
Idasanutlin (RG-7388) is an effective and specific p53-MDM2 inhibitor (IC50: 6 nM).
价 格:¥电议型 号:T6254产 地:美洲
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T6438Cefoselis SulfateCefoselis Sulfate,FK-037,FK 037 Sulfate
Cefoselis is a widely used beta-lactam antibiotic.
价 格:¥电议型 号:T6438产 地:美洲
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T8585TA-03;化合物TA-037-Methoxytacrine|||7-Meota;7-Methoxytacrine|||7-Meota
TA-03 (7-Meota) is a potent inhibitor of AChE in treatment of cognitive manifestation of AD.
价 格:¥电议型 号:T8585产 地:中国大陆
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T8454SEP-0372814;化合物SEP-0372814SEP-0372814
SEP-0372814 is a potent inhibitor of PDE10.
价 格:¥电议型 号:T8454产 地:中国大陆