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T12291Olanzapine D3；化合物 T12291LY170053 D3；LY170053 D3
Olanzapine D3 is the deuterium labeled Olanzapine.
价 格：￥电议型 号：T12291产 地：中国大陆
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T12290OICR-0547；化合物 T12290OICR-0547
OICR-0547 is a closely related derivative of OICR-9429. OICR-9429 is a novel small-molecule Wdr5-MLL interaction antagonist.
价 格：￥电议型 号：T12290产 地：中国大陆
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T1229Erdosteine；厄多司坦RV 144|||KW-9144；厄多司坦|||RV 144|||KW-9144
Erdosteine (RV 144) is a homocysteine-derived thiol derivative with mucolytic and free radical scavenging properties. Erdosteine and its metabolites modulate mucus production and viscosity, by which facilitating mucociliary transport and improving expectoration. This agent also suppresses the chemical-induced cough reflex as well as protects lung tissues from damages caused by cigarette smoking mediated through free radicals scavenging.
价 格：￥电议型 号：T1229产 地：中国大陆
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T12289ODM-204；化合物 T12289ODM-204
ODM-204 is novel nonsteroidal dual inhibitor of both androgen receptor and CYP17A1 enzyme(IC50s of 80 nM and 22 nM, respectively).
价 格：￥电议型 号：T12289产 地：中国大陆
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T12288Odapipam；化合物 T12288NNC 756；NNC 756
Odapipam is a selective and high affinity antagonist of benzazepine dopamine D1 receptor (Kd of 0.18 nM).
价 格：￥电议型 号：T12288产 地：中国大陆
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T12287Octadecanedioic acid；十八烷二酸Octadecanedioic acid
Octadecanedioic acid is an endogenous metabolite, is a long-chain dicarboxylic acid.
价 格：￥电议型 号：T12287产 地：中国大陆
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T12286Obtusifoliol；化合物 T12286Obtusifoliol
Obtusifoliol is a specific inhibitor of CYP51(Trypanosoma brucei (TB) and human CYP51 with Kd values of 1.2 μM and 1.4 μM, respectively).
价 格：￥电议型 号：T12286产 地：中国大陆
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T12285Ebopiprant；化合物EbopiprantOBE022|||OBE-022；OBE022|||OBE-022
Ebopiprant (OBE022) is an orally available, selective and potent prostaglandin F2α (PGF2α) receptor antagonist that interferes with the binding of PGF0126α to the FPR and can be used in the study of obesity.
价 格：￥电议型 号：T12285产 地：中国大陆
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T12284O-Propargyl-Puromycin；OP-嘌呤霉素OP-puro|||O-Propargylpuromycin；OP-puro|||O-Propargylpuromycin
O-Propargyl-Puromycin (OP-puro) is a potent protein synthesis inhibitor, a puromycin acetylene analog.
价 格：￥电议型 号：T12284产 地：中国大陆
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T12283O-Methyl Atorvastatin hemicalcium；化合物 T12283O-Methyl Atorvastatin hemicalcium
O-Methyl Atorvastatin is an impurity of Atorvastatin that is an orally active inhibitor of 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase, has the ability to effectively decrease blood lipids.
价 格：￥电议型 号：T12283产 地：中国大陆
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T12282Benzyl-α-GalNAc；化合物Benzyl-α-GalNAcO-glycosylation-IN-1；O-glycosylation-IN-1
Benzyl-α-GalNAc (O-glycosylation-IN-1) is a potent inhibitor of O-glycosylation and is used to reduce mucin on cell surfaces.
价 格：￥电议型 号：T12282产 地：中国大陆
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T12280O-Desmethyl Midostaurin；化合物 T12280CGP62221|||O-Desmethyl PKC412；CGP62221|||O-Desmethyl PKC412
O-Desmethyl Midostaurin is the active Midostaurin metabolite via cytochrome P450 liver enzyme metabolism.
价 格：￥电议型 号：T12280产 地：中国大陆
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T1228Cefonicid sodium头孢尼西钠Monocid sodium|||头孢尼西钠|||Cefonicid disodium salt
Cefonicid binds to and inactivates penicillin-binding proteins (PBPs) located on the inner membrane of the bacterial cell wall. Cefonicid sodium (Monocid sodium) is the sodium salt form of cefonicid, a semisynthetic second-generation cephalosporin with antibacterial activity. PBPs are enzymes involved in the terminal stages of assembling the bacterial cell wall and in reshaping the cell wall during growth and division. Inactivation of PBPs interferes with the cross-linkage of peptidoglycan chain
价 格：￥电议型 号：T1228产 地：中国大陆
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T12279O-Desmethyl apixaban；化合物 T12279O-Desmethyl apixaban
O-Desmethyl apixaban is a metabolite of Apixaban that is a highly selective, reversible inhibitor of Factor Xa with Ki of 0.08 nM and 0.17 nM in human and rabbit, respectively.
价 格：￥电议型 号：T12279产 地：中国大陆
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T12278NXT629；化合物 T12278NXT629
NXT629 is a selective and competitive antagonist of PPAR-α(human PPARα with an IC50 of 77 nM).
价 格：￥电议型 号：T12278产 地：中国大陆
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T12277NVS-ZP7-4；化合物NVS-ZP7-4NVS-ZP7-4
NVS-ZP7-4 is a inhibitor of Zinc transporter SLC39A7 (ZIP7).
价 格：￥电议型 号：T12277产 地：中国大陆
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T12276NVS-CRF38；化合物 T12276NVS-CRF38
NVS-CRF38 is an antagonist of corticotropin-releasing factor receptor 1 (CRF1).
价 格：￥电议型 号：T12276产 地：中国大陆
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T12275NVP-QAV-572；化合物 T12275NVP-QAV-572
NVP-QAV-572 is a inhibitor of PI3K(IC50 of 10 nM).
价 格：￥电议型 号：T12275产 地：中国大陆
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T12274Siremadlin (R Enantiomer)化合物 T12274Siremadlin R Enantiomer|||HDM201 R Enantiomer|||NVP-HDM201 R Enan
Siremadlin R Enantiomer is the R enantiomer of Siremadlin. Siremadlin is a potent and highly specific inhibitor of MDM-2/p53.
价 格：￥电议型 号：T12274产 地：中国大陆
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T12273NVP-CGM097 sulfate；化合物 T12273CGM097 sulfate；CGM097 sulfate
NVP-CGM097 sulfate is a potent and selective inhibitor of MDM2 (hMDM2, IC50 of 1.7±0.1 nM).
价 格：￥电议型 号：T12273产 地：中国大陆
