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Results for "

c 215

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    14
    TargetMol | All_Pathways
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    1
    TargetMol | Peptide_Products
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    3
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    TargetMol | Antibody_Products
C-215
T8411912780-51-9
C-215 is a novel inhibitor of mycobacterial membrane protein large 3 (MmpL3).
  • $30
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TargetMol | Inhibitor Sale
Antibiotic 2158
T125527
Antibiotic 2158 is a useful organic compound for research related to life sciences and the catalog number is T125527.
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Tepotinib
MSC2156119, EMD-1214063
T61211100598-32-0
Tepotinib (EMD-1214063) is a c-MET tyrosine kinase inhibitor (IC50=3 nM) that is selective, orally active, and ATP-competitive. Tepotinib has antitumor effect and is used in the treatment of non-small cell lung cancer.
  • $30
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TargetMol | Citations Cited
Thymidine
Thymidin, NSC 21548, DThyd, Doxribtimine, Deoxyribothymidine, 5-Methyldeoxyuridine
TWP291150-89-5
Thymidine (DThyd) is a cell synchronizing agent and a specific precursor of deoxyribonucleic acid. Thymidine inhibits DNA synthesis and can cause cell cycle arrest in the G1/S phase.
  • $45
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TargetMol | Citations Cited
Osajin
NSC 21565, CID 95168
T16407482-53-1
Osajin is the major bioactive iso avone present in the fruit of Maclura pomifera. It has antitumor, antioxidant, and anti-inflammatory activities.
  • $649
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(R)-FTY720-OMe
T708161382486-90-9
(R)-FTY720-OMe is a structural analogue of FTY720 which acts as a specific competitive inhibitor of sphingosine kinase 2 (SK2). Furthermore, (R)-FTY720-OMe does not inhibit sphingosine kinase 1 (SK1) activity.
  • $1,520
6-8 weeks
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TC-2153
T708181381769-23-8
TC-2153 is a selective inhibitor of striatal-enriched protein tyrosine phosphatase (STEP), exhibiting psychotropic activity and low acute toxicity. It enhances the expression of brain-derived neurotropic factor (BDNF) in the brain, reduces mRNA levels of MAOA and 5-HT1A receptors in the midbrain, and inhibits 5-HT2A receptor-mediated signaling.
  • $570
6-8 weeks
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Roxadustat-13C2-15N
TMIH-0507
Roxadustat-13C2-15N is 13C and 15N labeled Roxadustat.
  • $857
7-10 days
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Vadadustat-13C2-15N
TMIH-0591
Vadadustat-13C2-15N is 13C and 15N labeled Vadadustat. Vadadustat has a CAS number of 1000025-07-9. Vadadustat is a novel, titratable, oral hypoxia-inducible factor prolyl hydroxylase (HIF-PH) inhibitor in development for the treatment of anemia.
  • $857
7-10 days
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Glutathione-(glyucine-13C2-15N) Trifluoroacetate
TMIJ-0165
Glutathione-(glyucine-13C2-15N) Trifluoroacetate is the 13C and 15N labeled compound of Glutathione Trifluoroacetate.
  • Inquiry Price
20 days
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Tranexamic Acid-13C2-15N
TMIJ-03111292837-95-6
Tranexamic Acid-13C2-15N is the 13C and 15N labeled compound of Tranexamic Acid. Tranexamic Acid has a CAS number of 1197-18-8. Tranexamic acid is an Antifibrinolytic Agent. The physiologic effect of tranexamic acid is by means of Decreased Fibrinolysis.
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20 days
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Glyphosate-13C2-15N
TMIJ-04481185107-63-4
Glyphosate-13C2-15N is the 13C and 15N labeled compound of Glyphosate. Glyphosate has a CAS number of 1071-83-6. Glyphosate is an herbicide. It also is a possible carcinogen to humans.
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20 days
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1,3,6,8-Pyrenetetrasulfonic Acid (sodium salt hydrate)
T383571771776-02-3
1,3,6,8-Pyrenetetrasulfonic acid is an intermediate in the synthesis of the color additive pyranine.1It has been used to stabilize intermolecular interactions for the crystallization ofL. mexicanapyruvate kinase.2 1.Jitian, S., White, S.R., Yang, H.-H.W., et al.Conventional high-performance liquid chromatography versus derivative spectrophotometry for the determination of 1,3,6-pyrenetrisulfonic acid trisodium salt and 1,3,6,8-pyrenetetrasulfonic acid tetrasodium salt in the color additive D&C Green No. 8 (Pyranine)J. Chromatogr. A1324238-241(2014) 2.Morgan, H.P., McNae, I.W., Hsin, K.-Y., et al.An improved strategy for the crystallization of Leishmania mexicana pyruvate kinaseActa Crystallogr. Sect. F Struct. Biol. Cryst. Commun.66(Pt 3)215-218(2010)
  • $198
35 days
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SP-A (196-215) (human) TFA
Surfactant Protein A, SPA4
T83847
Surfactant protein A (SP-A) (196-215) is a synthetic peptide derived from the C-terminal carbohydrate recognition domain of human SP-A, specifically amino acids 196-215. This peptide suppresses LPS-induced TNF-α release in JAWSII mouse dendritic cells at 1 and 10 µM concentrations and promotes phagocytosis of P. aeruginosa at a 75 µM concentration. Furthermore, intratracheal administration of SP-A (196-215) at a dose of 50 µg per animal reduces disease severity and lung colony-forming units in mice infected with P. aeruginosa.
  • $105
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