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 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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