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Results for "

683 m hydrochloride

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    15
    TargetMol | Inhibitors_Agonists
  • Peptide Products
    3
    TargetMol | Peptide_Products
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    1
    TargetMol | Inhibitory_Antibodies
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    1
    TargetMol | PROTAC
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    7
    TargetMol | Recombinant_Protein
Oxolamine hydrochloride
Oxolamine HCl, AF 438 hydrochloride, 683 M hydrochloride
T0768L1219-20-1
Oxolamine hydrochloride is a cough suppressant which may be useful in the treatment of pediatric asthma.
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2-4 weeks
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MAK-683 hydrochloride
T96812170606-94-5In house
MAK683 hydrochloride embryonic ectodermal development (EED) inhibitor, also a potent PRC2 inhibitor, blocked cancer cell proliferation (IC50=1.014nM), with IC50 values of 59, 26, and 89 nM measured in EED Alphascreen, ELISA, and LC-MS assays, respectively.
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TargetMol | Inhibitor Hot
Selisistat
SEN0014196, EX-527
T611149843-98-3
Selisistat (EX-527) is a potent and specific inhibitor of the deacetylase SIRT1 (IC50 = 38 nM) and can be utilized in the study of neurological disorders such as Huntington's chorea.
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TargetMol | Citations Cited
MAK683
T152011951408-58-4In house
MAK683 is an inhibitor of embryonic ectoderm development (EED) (IC50s: 59, 89, 26 nM in EED Alphascreen binding, LC-MS and ELISA assay).
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TargetMol | Citations Cited
Ripazepam
Pyrazapon,CI-683,CCRIS 552,BRN 0819726,Cl-68
T2853926308-28-1
Ripazepam has anxiolytic effects.
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6-8 weeks
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AHN-683
T23675143934-15-0
AHN-683 is a fluorescent ligand. It was used for peripheral-type benzodiazepine receptors.
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3-6 months
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TAK-683
TP2156L872719-49-8
TAK-683 is an effective full KISS1 receptor agonist (IC50=170 pM). TAK-683 is a nonapeptide metastin analog, shows agonistic activities to KISS1R (EC50: 0.96 nM and 1.6 nM for human and rat, respectively).
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Carbazomycin A
T3753675139-39-8
Carbazomycin A is a bacterial metabolite that has been found in Streptomyces and has diverse biological activities.1,2It is active againstS. aureus,T. asteroides, andT. mentagrophytes(MIC = 12.5 μg ml for all), as well as the plant pathogenic fungusP. oryzae(MIC = 25 μg ml). Carbazomycin A is cytotoxic to MCF-7, KB, NCI H187, and Vero cells (IC50s = 26.2, 30.1, 18.4, and 32.6 μg ml, respectively).2 1.Sakano, K.-I., Ishimaru, K., and Nakamura, S.New antibiotics, carbazomycins A and B. I. Fermentation, extraction, purification and physico-chemical and biological propertiesJ Antibiot. (Tokyo)33(7)683-689(1980) 2.Intaraudom, C., Rachtawee, P., Suvannakad, R., et al.Antimalarial and antituberculosis substances from Streptomyces sp. BCC26924Tetrahedron67(39)7593-7597(2011)
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MK6-83
MK683
T244771062271-24-2
MK6-83 is the transient receptor potential channel ML3 agonist.
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MAK683-CH2CH2COOH
T137652639882-68-9
MAK683-CH2CH2COOH binds to EED (embryonic ectoderm development protein) and, together with a VHL ligand for the E3 ubiquitin ligase, has been used to design EED-Targeted PROTACs, specifically EED degrader-1 and PROTAC EED degrader-2 [1].
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8-10 weeks
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Anti-HER3/ERBB3 Antibody (2Y512)
T9901A-683
Anti-HER3 ERBB3 Antibody (2Y512) is a mouse (varialbe region) human (kappa IgG1 constant) chimeric monoclonal antibody targeting Human HER3 ERBB3.
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7-10 days
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TAK-683 TFA (872719-49-8 free base)
TAK-683 TFA
TP2156
TAK-683 TFA is a potent full agonist of the KISS1 receptor (KISS1R; IC50: 170 pM) with improved metabolic stability. It shows agonistic activities to KISS1R (EC50s: 0.96 nM and 1.6 nM for human and rat).
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2,2-Dichloroacetamide
T67290683-72-7
2,2-Dichloroacetamide is a useful organic compound for research related to life sciences. The catalog number is T67290 and the CAS number is 683-72-7.
    7-10 days
    Inquiry
    TAK-683 acetate
    T76048
    TAK-683 acetate is a nonapeptide metastin analog and a potent full agonist of the KISS1 receptor (KISS1R), exhibiting IC 50 =170 pM and enhanced metabolic stability. This compound shows agonistic activities towards KISS1R, with EC 50 values of 0.96 nM and 1.6 nM for human and rat KISS1R, respectively. TAK-683 acetate effectively depletes GnRH in the hypothalamus and reduces plasma levels of FSH, LH, and testosterone in vivo, showcasing its potential for hormone-dependent prostate cancer research.
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