About 30 results found for searched term "MP7" (0.02 seconds)
Cat.No. | Name | Target |
---|---|---|
M1865 | Bevirimat | HIV Protease |
BVM, MPC-4326, PA-457 | ||
Bevirimat (BVM), also known as PA-457 or MPC-4326, is a novel Human Immunodeficiency Virus type 1 (HIV-1) maturation inhibitor. | ||
M1918 | Amuvatinib | VEGFR/PDGFR |
MP470; HPK 56 | ||
Amuvatinib (MP470) is a novel receptor tyrosine kinase inhibitor that targets c-KIT and PDGFRα. | ||
M2475 | Bucladesine Sodium Salt | PKA |
Dibutyryl-cAMP sodium salt; DC2797; Sodium dibutyryl cAMP | ||
Bucladesine, a membrane permeable selective activator of PKA, has a critical role in up-regulation of ChAT and VAChT gene expression in PC12 cells by activation of extracellular signal regulated kinase (ERK) in Ca2+- and PKA-dependent manner. | ||
M2521 | Cinoxacin | Antibiotic |
Compound 64716 | ||
Cinoxacin is a synthetic antimicrobial related to the quinolone class of orally active antibacterial agent. Cinoxacin has antibacterial activity against many gram-negative aerobic bacteria and inhibits bacterial DNA synthesis. | ||
M2834 | Medetomidine hydrochloride | Adrenergic Receptor |
MPV785 | ||
Medetomidine is a selective α2-adrenoceptor agonist, with Ki of 1.08 nM, exhibts 1620-fold selectivity over α1-adrenoceptor. | ||
M2868 | MPI-0479605 | Kinesin |
MPI-0479605 is an ATP competitive and selective inhibitor of mitotic kinase Mps1 with IC50 of 1.8 nM, >40-fold selectivity over other kinases. | ||
M3768 | Ixabepilone | Microtubule |
Ixempra, BMS-247550, NSC 710428 | ||
Ixabepilone (BMS 247550) is an epothilone B analog and nontaxane microtubule-stabilizing compound with clinical activity in a range of solid tumors. | ||
M4238 | Kaempferol-7-O-β-D-glucopyranoside | Others |
Kaempferol-7-o -β-D-glucopyranoside is a kind of glucopyranoside extracted from Malus Pumila Mill. Flavonoids isolated from flowers with antioxidant, anti-inflammatory and procoagulant activities. | ||
M5174 | Icariin | PDE |
8-prenyl kaempferol 3,7-O-diglucoside | ||
Icariin is a flavonol glycoside. Icariin inhibited PDE5 and PDE4 activity with IC50 of 432 nM and 73.50 μM, respectively. Icariin is also a PPARα activator. Icariin can increase cardiovascular and cerebrovascular blood flow, promote hematopoiesis, immunity and bone metabolism. | ||
M9602 | Atamparib (RBN-2397) | PARP |
Atamparib | ||
Atamparib (RBN-2397) is a potent, orally active NAD+ competitive PARP7 inhibitor with an IC50 value of less than 3 nM. Atamparib (RBN-2397) can directly inhibit cell proliferation and restore type I interferon signaling by inhibiting PARP7 in tumor cells to stimulate innate or adaptive antitumor immune responses. | ||
M9720 | Aranidipine | Calcium Channel |
MPC1304; CCRIS-6724 | ||
Aranidipine (MPC1304) is a calcium channel blocker which may positively affect ambulatory blood pressure. *This compound is unstable in solutions, freshly prepared is recommended. | ||
M10035 | Semaglutide | GLP Receptor |
Rybelsus; Ozempic; NN9535; OG217SC; NNC 0113-0217 | ||
Semaglutide (Rybelsus, Ozempic, NN9535, OG217SC, NNC 0113-0217) is a long-acting human GLP-1 analog, it is also a GLP-1 receptor agonist with the potential for the treatment of type 2 diabetes mellitus (T2DM). | ||
M10690 | Sulanemadlin | p53 |
ALRN-6924; MP-4897 | ||
Sulanemadlin (ALRN-6924) is a stapled peptide that blocks interactions between p53 and both MDM2 and MDMX. | ||
M10749 | Verubulin | Microtubule |
MPC 6827 | ||
Verubulin (MPC-6827) is a highly effective, broad-spectrum microtubule blocker with in vivo and in vitro cytotoxic activity, promising as a potential drug candidate for a wide range of cancers. | ||
M10847 | LMP744 hydrochloride | Topoisomerase |
MJ-III65 hydrochloride | ||
LMP744 hydrochloride (MJ-III65 hydrochloride) is a DNA chimeric agent that is an inhibitor of topoisomerase 1 (Top1) with antitumor activity. | ||
M11480 | Recombinant Human BMP-7 protein (E. coli) | Cytokines and Growth Factors |
Bone morphogenetic protein 7 | ||
The BMP-7 protein, Human is a potent bone morphogenetic protein and part of the transforming growth factor (TGF-β) superfamily. | ||
M11546 | CD38 inhibitor 1 | Others |
compound 78c;CD38-IN-78c;CD38 inhibitor 78c | ||
CD38 inhibitor 1 (COMPOUND 78c, CD38-in-78C) was an effective INHIBITOR of CD38, with IC50 of 7.3 nM and 1.9 nM for human AND mouse CD38 respectively. | ||
M14074 | C3a (70-77) (TFA) | Complement System |
Complement 3a (70-77) (TFA) | ||
C3a (70-77) TFA (Complement 3a (70-77) TFA) is an octapeptide corresponding to the COOH terminus of C3a, exhibits the specificity and 1 to 2% biologic activities of C3a. | ||
M14333 | DMP 777 | Elastase |
L-694458 | ||
DMP 777 is a potent, selective, and orally active human leukocyte elastase (HLE) inhibitor. | ||
M14524 | Tarenflurbil | RAR/RXR |
(R)-Flurbiprofen; MPC7869 | ||
Tarenflurbil ((R)-Flurbiprofen) is the R-enantiomer of the racemate NSAID Flurbiprofen, Tarenflurbil ((R)-Flurbiprofen) inhibits the binding of [3H]9-cis-RA to RXRα LBD with IC50 of 75 μM. | ||
M16555 | Kaempferol 3-O-neohesperidoside 7-O-glucoside | Flavonoids |
Kaempferol 3-O-neohesperidoside 7-O-glucoside | ||
M16561 | Kaempferol 3-O-sophoroside-7-O-glucoside | Flavonoids |
Kaempferol 3-O-sophoroside-7-O-glucoside | ||
M16581 | Kaempferol 3,7,4'-trimethyl ether | Flavonoids |
Kaempferol 3,7,4'-trimethyl ether | ||
M16582 | Kaempferol 5,7,4'-trimethyl ether | Flavonoids |
Kaempferol 5,7,4'-trimethyl ether | ||
M16591 | Kaempferol 7,4'-dimethyl ether | Flavonoids |
Kaempferol 7,4'-dimethyl ether | ||
M16619 | Kaempferol 7-O-rhamnoside | Flavonoids |
Kaempferol 7-O-rhamnoside | ||
M18016 | Kaempferol 3-O-rutinoside 7-O-glucoside | Others |
Kaempferol 3-O-rutinoside 7-O-glucoside | ||
M18020 | Kaempferol 3-O-robinoside-7-O-glucoside | Others |
Kaempferol 3-O-robinoside-7-O-glucoside | ||
M18035 | Kaempferol 3-sophoroside-7-rhamnoside | Others |
Kaempferol 3-sophoroside-7-rhamnoside | ||
M18141 | Isokaempferide 7-O-glucuronide | Others |
Isokaempferide 7-O-glucuronide |
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