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T11603Ibrutinib-MPEA；化合物 T11603Ibrutinib-MPEA
Ibrutinib-MPEA is ibrutinib derivative. Ibrutinib is a covalent and irreversible BTK inhibitor that has been used to treat hematological malignancies.
价 格：￥电议型 号：T11603产 地：中国大陆
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T11602Ibrutinib dimer；依鲁替尼二聚体Ibrutinib dimer
Ibrutinib dimer is an impurity of Ibrutinib. IIbrutinib dimer is a Dimer of Ibrutinib. Ibrutinib is an irreversible Btk inhibitor (IC50: 0.5 nM).
价 格：￥电议型 号：T11602产 地：中国大陆
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T11601Ibrutinib-d5；化合物 T11601PCI-32765 D5|||Ibrutinib D5；PCI-32765 D5|||Ibrutinib D5
Ibrutinib D5 is a deuterium-labeled Ibrutinib. Ibrutinib is an irreversible Btk inhibitor.
价 格：￥电议型 号：T11601产 地：中国大陆
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T11600IBR2；化合物IBR2Isoquinoline；Isoquinoline
IBR2 (Isoquinoline) is a potent and specific RAD51 inhibitor known for its ability to suppress RAD51-mediated DNA double-strand break repair. By interfering with RAD51 multimerization, accelerating proteasome-mediated RAD51 protein degradation, inhibiting cancer cell growth, and inducing apoptosis, IBR2 has proved to be an effective compound in these aspects.
价 格：￥电议型 号：T11600产 地：中国大陆
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T1160Fusidic acid；夫西地酸Fusidine；Fusidine|||夫西地酸
Fusidic acid (Fusidine) is an antibiotic isolated from the fermentation broth of Fusidium coccineum.
价 格：￥电议型 号：T1160产 地：中国大陆
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T11525LGW311616 hydrochloride；化合物 T11525LGW311616A；GW311616A
GW-311616 hydrochloride is a long duration, orally bioavailable, and selective human neutrophil elastase (HNE) inhibitor (IC50: 22 nM; Ki: 0.31 nM).
价 格：￥电议型 号：T11525L产 地：中国大陆
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T11525GW311616；化合物 T11525GW311616
GW-311616 is a long duration, orally bioavailable, and selective human neutrophil elastase (HNE) inhibitor (IC50: 22 nM; Ki: 0.31 nM).
价 格：￥电议型 号：T11525产 地：中国大陆
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T11169Eicosatetraynoic acid；化合物 T11169ETYA；ETYA
Eicosatetraynoic acid (ETYA) activates PPARα and PPARγ chimeras at 10 μM. Eicosatetraynoic acid (ETYA) is a nonspecific inhibitor of cyclooxygenase and lipoxygenase (ID50=8 μM and 4 μM, respectively).
价 格：￥电议型 号：T11169产 地：中国大陆
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T11168EHNA hydrochloride；外消旋-9-(2-羟基-3-壬基)腺嘌呤盐酸盐EHNA hydrochloride
EHNA hydrochloride is a chemical compound recognized for its antiviral, antitumor, and antiarrhythmic properties. It functions as a potent and selective inhibitor of both cyclic nucleotide phosphodiesterase 2 (PDE2) with an IC50 of 4 μM and adenosine deaminase (ADA). Additionally, it effectively inhibits the activity of cGMP-stimulated PDE II (cGs-PDE) with IC50 values of 0.8 μM in humans and 2 μM in porcine myocardium, although its inhibitory effects on unstimulated PDE2 activity are less prono
价 格：￥电议型 号：T11168产 地：中国大陆
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T11167EHMT2-IN-2；化合物 T11167EHMT2-IN-2
EHMT2-IN-2 Used in the research of blood disease or cancer. EHMT2-IN-2 is a potent EHMT inhibitor, with IC50s of all <100 nM for EHMT1 peptide, EHMT2 peptide and cellular EHMT2.
价 格：￥电议型 号：T11167产 地：中国大陆
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T11166EHMT2-IN-1；化合物 T11166EHMT2-IN-1
EHMT2-IN-1 is a potent EHMT inhibitor, . Used in the research of blood disorder or cancer.with IC50s of all <100 nM for EHMT1 peptide, EHMT2 peptide and cellular EHMT2.
价 格：￥电议型 号：T11166产 地：中国大陆
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T11165EGLU；化合物 T11165(2S)-α-EGLU|||(2S)-α-Ethylglutamic acid；(2S)-α-EGLU|||(2S)-α-Ethylglutamic acid
EGLU, also known as (2S)-α-Ethylglutamic acid or (2S)-α-EGLU, is a potent and competitive antagonist of the mGluR-2 receptor, demonstrating a Kd value of 66 μM when interacting with the (lS,3S)-ACPD-sensitive site. This chemical compound functions as an antidepressant agent.
价 格：￥电议型 号：T11165产 地：中国大陆
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T11164EGFR mutant-IN-1；化合物 T11164EGFR mutant-IN-1
EGFR mutant- in-1, A 5-methylpyrimidopyridone derivative are effective selective EGFRL858R/T790M/C797S mutant inhibitors with IC50 of 27.5 nM, which significantly weakened EGFRWT effect.
价 格：￥电议型 号：T11164产 地：中国大陆
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T11163EGFR-IN-9；化合物EGFR-IN-9EGFR-IN-9
EGFR-IN-9 is a potent EGFR kinase inhibitor with IC50s of 7 nM, 28 nM for the wild type EGFR kinase and double mutant EGFR kinase (L858R/T790M). EGFR-IN-9 has antitumor activity.
价 格：￥电议型 号：T11163产 地：中国大陆
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T11162EGFR-IN-8；化合物EGFR-IN-8EGFR-IN-8
EGFR-IN-8, a dual inhibitor targeting both EGFR and c-Met, shows potential as a promising candidate for further development in treating EGFR TKI-resistant NSCLC.
价 格：￥电议型 号：T11162产 地：中国大陆
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T11161EGFR-IN-7；化合物EGFR-IN-7TQB3804；TQB3804
EGFR-IN-7 (TQB3804) is a selective and potent EGFR kinase inhibitor.
价 格：￥电议型 号：T11161产 地：中国大陆
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T11160EGFR-IN-5；化合物EGFR-IN-5EGFR-IN-5|||inhibit|||Epidermal growth factor receptor|||HER1|||ErbB-1|||Inhib
EGFR-IN-5 is a selective inhibitor of EGFR. The IC50s for EGFR, EGFR(L858R), EGFR(L858R/T790M), and EGFR(L858R/T790M/C797S) are 10.4, 1.1, 34, 7.2 nM, respectively.
价 格：￥电议型 号：T11160产 地：中国大陆
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T1116Biotin；生物素Vitamin B7|||D-Biotin|||Vitamin H；Vitamin B7|||生物素|||D-Biotin|||Vitamin H|||D-生物素（维生素H）
Biotin (Vitamin H) is a naturally occurring, water-soluble B vitamin involved in fatty acid production, fat and amino acid metabolism, and cell growth. Biotin is often used for biotin labeling.
价 格：￥电议型 号：T1116产 地：中国大陆
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T11116Duocarmycin MA；倍癌霉素 MADuocarmycin MA
Duocarmycin MA can be used against multi-drug resistant cell lines.Duocarmycin MA is an antibody drug conjugates (ADCs) toxin. Duocarmycin is a DNA alkylating agent that binds in the minor groove.
价 格：￥电议型 号：T11116产 地：中国大陆
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T11073Dofetilide N-oxide；化合物 T11073UK-116856；UK-116856
Dofetilide N-oxide (UK-116856) is a metabolite of dofetilide. Dofetilide can block potassium channels and is a tertiary antiarrhythmic drug.
价 格：￥电议型 号：T11073产 地：中国大陆
