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Results for "

cv-1

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    14
    TargetMol | Inhibitors_Agonists
  • Peptide Products
    3
    TargetMol | Peptide_Products
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    1
    TargetMol | PROTAC
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    TargetMol | Natural_Products
  • Recombinant Protein
    4
    TargetMol | Recombinant_Protein
CV-159
T1502186384-98-7
CV-159 is a distinctive dihydropyridine Ca2+ antagonist exhibiting anti-inflammatory properties and possessing anti-calmodulin (CaM) activity.
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6-8 weeks
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CV-1674
NSC 310669,CV 1674
T3111537151-17-0
CV-1674 induced selective coronary vasodilation and had little effect on cardiac hemodynamics.
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6-8 weeks
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HCV-1 e2 Protein (554-569)
T76514290362-31-1
HCV-1 e2 Protein (554-569), a primary antigenic region within the Hepatitis C Virus envelope 2 (e2) protein, contains a putative N-glycosylation site believed to affect immune recognition of e2 [1].
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HCV-1 e2 Protein (484-499)
T76516161012-10-8
HCV-1 e2 Protein (484-499) is a 16-amino acid peptide derived from the envelope 2 protein of the hepatitis C virus, identified in the sera of individuals possessing antibodies to HCV [1].
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HCV-1 e2 Protein (554-569) (TFA)
T80089
HCV-1 e2 Protein (554-569) TFA, an antigenic segment of the hepatitis C virus envelope 2 (e2) protein, contains a potential N-glycosylation site that may influence immune recognition of e2 [1].
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Chloroquinoxaline sulfonamide
NSC-339004, Chloroquinoxaline
T1495397919-22-7In house
Chloroquinoxaline sulfonamide (Chloroquinoxaline) is a topoisomerase II alpha beta toxin with antitumor activity and immunosuppressive properties that inhibits the proliferation of B16 melanoma cells in mice, and can be used to study metastatic colorectal cancer. It can be used to study metastatic colorectal cancer.
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6-8 weeks
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Chlamydia pneumoniae-IN-1
T79088518010-44-1In house
Chlamydia pneumoniae-IN-1 (compound 55), a benzimidazole derivative, exhibits potent antibacterial activity, inhibiting 99% of C. pneumoniae growth at a concentration of 10 μM while maintaining 95% viability of host cells. It effectively inhibits the CV-6 strain of C. pneumoniae with a minimum inhibitory concentration (MIC) of 12.6 μM, demonstrating its antichlamydial efficacy [1].
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6-8 weeks
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S-23
(S)-3-(4-chloro-3-fluorophenoxy)-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide, S23
T207891010396-29-8
S-23 ((S)-3-(4-chloro-3-fluorophenoxy)-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide) is an oral selective androgen receptor modulator (SARM) with a Ki of 1.7 nM. S-23 increases prostate, seminal vesicle, and levator ani muscle weights in castrated rats.
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Rupatadine
UR-12592, UR12592
T36618158876-82-5
Rupatadine (UR-12592, rupatadine) is a potent and orally available dual antagonist of PAF and histamine H1 receptors with Ki values of 0.55 μM and 0.1 μM, respectively, which provides relief of allergic symptoms and anti-inflammatory properties, and is used in allergic rhinitis and chronic urticaria.
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7-10 days
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4′-Hydroxy-2′-methylacetophenone
T36738875-59-2
4′-Hydroxy-2′-methylacetophenone, a red wine aroma compound isolated from the cv. Bobal grape variety, exhibits ciliate toxicity and inhibits T. pyriformis growth with an IC50 of 0.65 mM[1][2].
    7-10 days
    Inquiry
    Desmethyl Bosentan
    T37351253688-61-8
    Desmethyl bosentan, an active metabolite of the endothelin receptor antagonist bosentan, activates the pregnane X receptor (PXR) in CV-1 monkey kidney cells expressing the human receptor in a reporter assay at a concentration of 25 μM.
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    4-Methyl-1-pentanol
    Isohexanol
    T40718626-89-1
    4-Methyl-1-pentanol (Isohexanol), a volatile aroma compound found in red wine from the cv. Kalecik Karası cultivar, enhances the beverage's scent profile.
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    7-10 days
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    Petanin chloride
    T8150869915-09-9
    Petanin (chloride) is a p-coumaroyl anthocyanin extracted from the tuber epidermis of the colored potato variety Solanum tuberosum L. cv 'Jayoung' [1].
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    3′-deoxy Thymidine
    2',3'-Dideoxythymidine
    T849873416-05-5
    d2T, a nucleoside analog of thymidine, exhibits antiviral activity by inhibiting HIV replication in infected human peripheral blood mononuclear cells (PBMCs; EC50 = 0.17 µM). Additionally, 3′-deoxy Thymidine at concentrations of 1, 3, 10, or 30 µM significantly decreases viral plaque formation in CV-1 cells infected with herpes simplex virus 1 (HSV-1).
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    8-10 weeks
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