About 20 results found for searched term "TA 01" (0.055 seconds)
Cat.No. | Name | Target |
---|---|---|
M2154 | TAK-901 | Aurora Kinase |
TAK901 | ||
TAK-901 is a novel small-molecule inhibitor of Aurora A and Aurora B with IC50 of 21 nM and 15 nM. | ||
M3274 | Pentagastrin | Cholecystokinin Receptor |
Peptavlon; ICI-50123 | ||
Pentagastrin (ICI-50123) is a synthetic polypeptide that has effects like gastrin when given parenterally. | ||
M3729 | TAC-101 | CDK |
Amsilarotene | ||
TAC-101 is a retinobenzoic acid with potential antineoplastic activity. | ||
M3973 | Tazarotene | RAR/RXR |
Tazorac; Zorac; AGN 190168 | ||
Tazarotene (AGN 190168) is a new member of the acetylenic class of RARβ/γ selective retinoids which is approved to treat a variety of skin diseases, exhibits an anti-proliferative effect in human basal cell carcinoma (BCC) by triggering caspase-dependent apoptosis. | ||
M5291 | Sufugolix | LHRH/GnRH |
TAK-013 | ||
Sufugolix (TAK-013) is a highly potent and orally available luteinizing hormone-releasing hormone LHRH receptor antagonist with an IC50 of 0.1 nM. | ||
M5928 | Riboflavin | Vitamin |
Vitamin B2; E101 | ||
Riboflavin is an easily absorbed micronutrient with a key role in maintaining health in humans and other animals. | ||
M6070 | EDO-S101 | HDAC |
Tinostamustine; EDO-S-101; EDO-S 101 | ||
EDO-S101 is a pan HDAC inhibitor; inhibits HDAC1, HDAC2 and HDAC3 with IC50 values of 9, 9 and 25 nM, respectively. | ||
M6140 | TA 01 | Casein Kinase |
TA-01; TA01 | ||
TA-01 potently inhibits CK1ε, CK1δ,and p38α (IC50values are 6.4, 6.8, and 6.7 nM respectively). | ||
M7355 | TAS 301 | Others |
TAS 301 is a inhibitor of smooth muscle cell migration and proliferation. | ||
M9041 | PF-03084014 (Nirogacestat) | Gamma-secretase/Beta-secretase |
Nirogacestat; PF-3084014 | ||
PF-03084014 (Nirogacestat) is a potent and selective γ-secretase inhibitor with IC50 of 6.2 nM. | ||
M9197 | Relugolix | LHRH/GnRH |
Orgovyx; TAK-385; RVT-601 | ||
Relugolix, also known as TAK-385, is an orally active gonadotropin-releasing hormone (GnRH) antagonist with an IC50 of 0.12 nM. | ||
M11283 | Inolitazone dihydrochloride | PPAR |
Efatutazone dihydrochloride; CS-7017 dihydrochloride; RS5444 dihydrochloride | ||
Inolitazone dihydrochloride (Efatutazone dihydrochloride) is a PPARγ agonist with high affinity, activity dependent on PPARγ, inhibiting growth, IC50 is 0.8 nM. | ||
M11549 | Palifosfamide | DNA Alkylator/Crosslinker |
Isophosphoramide mustard; IPM; ZIO-201 | ||
Palifosfamide(Isophosphoramide mustard; IPM; Zio-201) is a new DNA alkylation agent and active metabolite of isocyclophosphamide, which has anticancer activity. | ||
M21064 | Bradanicline | Others |
ATA-101; TC-5619 | ||
Bradanicline (ATA-101; TC-5619) is a highly selective α7 nicotinic acetylcholine receptor (nAChR) agonist (EC50=17 nM for human α7 nAChR; Ki=1.4 nM). Bradanicline can be used to study cognitive impairment. | ||
M24910 | Olinvacimab | VEGFR/PDGFR |
TTAC-0001 | ||
Olinvacimab (TTAC-0001) is a fully human anti-VEGFR2 monoclonal antibody. Olinvacimab inhibits VEGF binds to KDR with a Kd value of 0.23 nM. Olinvacimab has antiangiogenic activity. Olinvacimab can be used for the research of recurrent glioblastoma and breast cancer. | ||
M25181 | Upanovimab | Others |
SCTA01 | ||
Upanovimab (SCTA01) is a monoclonal antibody. | ||
M25429 | Rezafungin acetate | Anti-infection |
Biafungin acetate; CD101 acetate; SP-3025 acetate | ||
Rezafungin acetate is a novel echinocandin-based antifungal agent with potent antifungal activity against Candida, Aspergillus and Pneumocystis. | ||
M28233 | Caficrestat | Aldose Reductase |
Aldose reductase-IN-1; AT-001 | ||
Caficrestat (Aldose reductase-IN-1) is a inhibitor of aldose reductase with IC50 of 28.9 pM. | ||
M29393 | Inolitazone | PPAR |
Efatutazone; CS-7017; RS5444 | ||
Inolitazone a novel high-affinity PPARγ agonist that is dependent upon PPARγ for its biological activity with IC50 of 0.8 nM for growth inhibition. | ||
M52383 | Tau Peptide (301-315) | Tau Protein |
Tau Peptide (301-315) is a polypeptide that can be found by peptide screening. |
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