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Cat. No. Product Name Target Signaling Pathways
T11925 M‑89

Epigenetic Reader Domain; Histone Methyltransferase Chromatin/Epigenetic
M-89 可抑制 Menin-MLL 蛋白之间的相互作用,有研究混合谱系白血病的潜力。它是一种强特异性 menin 抑制剂,结合到 menin 的Kd 值为 1.4 nM。
T69629 M‑89 MLL inhibitor

M‑89 is a Highly Potent Inhibitor of the Menin-Mixed Lineage Leukemia (Menin-MLL) Protein−Protein Interaction (Kd = 1.4 nM; IC50 = 25nM). M-89 binds to menin with a Kd value of 1.4 nM and effectively engages cellular menin protein at low nanomolar concentrations. M-89 inhibits cell growth in the MV4;11 and MOLM-13 leukemia cell lines carrying MLL fusion with IC50 values of 25 and 55 nM, respectively, and demonstrates >100-fold selectivity over the HL-60 leukemia cell line lacking MLL fusion.
T69628 Iptacopan hydrochloride hydrate

Iptacopan hydrochloride hydrate is a highly potent and highly selective factor B inhibitor.
T11930 M8891

Others Others
M8891 is an orally active, reversible and brain penetrant Methionine Aminopeptidase-2 (MetAP-2) inhibitor(IC50 :54nM;Ki:4.33 nM).M8891 inhibits growth of primary endothelial cells as well as tumor cells and demonstrates antiangiogenic and antitumoral acti
T16839 sAJM589

c-Myc Cell Cycle/Checkpoint
sAJM589 is a Myc inhibitor(IC50: 1.8 μM).
T37053 Z-(L-Arg)-AMC (hydrochloride)

Z-(L-Arg)-AMC is a fluorogenic substrate for trypsin, cathepsin B, and cathepsin H.1,2Upon enzymatic cleavage by trypsin, cathepsin B, or cathepsin H, 7-amino-4-methylcoumarin (AMC) is released and its fluorescence can be used to quantify trypsin, cathepsin B, and cathepsin H activity. AMC displays excitation/emission maxima of 340-360/440-460 nm, respectively. 1.Zimmerman, M., Ashe, B., Yurewicz, E.C., et al.Sensitive assays for trypsin, elastase, and chymotrypsin using new fluorogenic substrat...
T37963 Methylchloroisothiazolinone/Methylisothiazolinone Mixture

Methylchloroisothiazolinone/methylisothiazolinone mixture (MCIT/MIT) is a mixture of isothiazolinone-derived biocides.1,2It is effective against Gram-positive and Gram-negative bacteria with MIC values of 0.0002, 0.0002, 0.00005, and 0.00005% (w/w) forS. aureus,P. aeruginosa,A. niger, andC. albicans, respectively.2MCIT/MIT can elicit contact sensitization.3Formulations containing MCIT/MIT have been used for controlling microbial growth in industrial and household products. 1.Frenzel, E., Schmidt...
T36844 Inostamycin A

Inostamycin A is a bacterial metabolite that has been found inStreptomycesand has anticancer activity.1It is an inhibitor of CDP-diacylglycerol:inositol 3-phosphatidyltransferase (IC50= 0.02 μg/ml in A431 cell membranes) and is selective for CDP-diacylglycerol:inositol 3-phosphatidyltransferase over phospholipase C (PLC) and phosphatidylinositol kinase at 10 μg/ml.2Inostamycin A decreases viability of YCU-T892, KCC-TC873, KB, HSC-4, and YCU-T891 oral squamous cell carcinoma (OSCC) cells in a con...

化合物

M‑89
Cat.No: T11925
Synonym:
Target: Epigenetic Reader Domain, Histone Methyltransferase
M‑89 MLL inhibitor
Cat.No: T69629
Synonym:
Target:
Iptacopan hydrochloride hydrate
Cat.No: T69628
Synonym:
Target:
M8891
Cat.No: T11930
Synonym:
Target: Others
sAJM589
Cat.No: T16839
Synonym:
Target: c-Myc
Z-(L-Arg)-AMC (hydrochloride)
Cat.No: T37053
Synonym:
Target:
Methylchloroisothiazolinone/Methylisothiazolinone Mixture
Cat.No: T37963
Synonym:
Target:
Inostamycin A
Cat.No: T36844
Synonym:
Target:
TargetMol Loading
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