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" in TargetMol Product Catalog
  • Inhibitors & Agonists
    69
    TargetMol | Inhibitors_Agonists
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    7
    TargetMol | Peptide_Products
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    TargetMol | Dye_Reagents
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    TargetMol | PROTAC
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    TargetMol | Natural_Products
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    TargetMol | Recombinant_Protein
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    5
    TargetMol | Antibody_Products
Trametinib
JTP-74057, GSK1120212
T2125871700-17-3
Trametinib (GSK1120212) is a MEK inhibitor that inhibits MEK1 and MEK2 (IC50=0.7 0.9 nM) with ATP non-competitive and oral activity. Trametinib activates autophagy and induces apoptosis.
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CIA-1 (Free base)
CIA-1(Free base)
T71534L452087-38-6
CIA-1 (Free base) is a nuclear receptor COUP-TFII inhibitor with IC50 values ranging from 1.2 μM to 7.6 μM in prostate cancer cell lines. CIA-1 (Free base) inhibits tumor growth in a mouse model of prostate cancer xenografts.
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Trametinib (DMSO solvate)
Trametinib DMSO solvate, Trametinib dimethyl sulfoxide, JTP-74057 (DMSO solvate), GSK-1120212 (DMSO solvate)
T58571187431-43-1
Trametinib (DMSO solvate) (GSK-1120212 (DMSO solvate)) is a highly potent and selective MEK inhibitor that specifically inhibits MEK1 2 (IC50: 2 nM).
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CIA-1 hcl(452087-38-6 Free base)
T715341049691-47-5
CIA-1 inhibits the nuclear receptor COUP-TFII, with IC50s ranging from 1.2 μM to 7.6 μM in prostate cancer cell lines.CIA-1 inhibits the growth of a variety of prostate cancer cell lines in vitro and inhibits COUP-TFII activity to regulate its target genes.CIA-1 in vivo exhibits tumor growth inhibitory effects in a mouse model of prostate cancer xenografts. inhibitory effect on tumor growth in a xenograft mouse model of prostate cancer in vivo.
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1-2 weeks
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TargetMol
Cianopramine
Ro112465, Ro-11-2465, Ro 112465, Ro-112465, Cyanimipramine
T2524866834-24-0In house
Cianopramine (Ro 112465) is a selective 5-hydroxytryptamine uptake inhibitor and a tricyclic antidepressant used in the study of neurological disorders.
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6-8 weeks
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Ciamexon
Ciamexone, BM-41332, BM41332, BM 41332
T6804375985-31-8In house
Ciamexon (Ciamexone) is a novel immunomodulator that has shown promising results in experimental models of autoimmune disease with little demonstrated cytotoxicity.Ciamexon can be used to study endocrine ophthalmopathies and diabetes mellitus, with slight improvement in ophthalmic disease following short-term administration.
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Sciadopitysin
T5S2129521-34-6
Sciadopitysin may prevent the development of diabetic osteopathy, it exerts its therapeutic effects via upregulation of mitochondrial biogenesis.Sciadopitysin shows protective effects on antimycin A-induced toxicity in osteoblastic MC3T3-E1 cells, it may
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GnRH Associated Peptide (1-13) Acetate(human)
GnRH Associated Peptide (GAP) (1-13), human Acetate (100111-07-7 Free base), GnRH Associated Peptide (1-13), Acetate(human) (100111-07-7 Free base)
T21649L
GnRH Associated Peptide (GAP) (1-13), human Acetate was found to be a potent inhibitor of prolactin secretion and to stimulate the release of gonadotropins. Active immunization with peptides corresponding to GAP sequences led to greatly increased prolacti
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m-Ciaamp
3-Carboxyphenyl((N-((4-iodophenyl)acetyl)amino)methyl)phosphonate
T29390156483-88-4
3-Carboxyphenyl((N-((4-iodophenyl)acetyl)amino)methyl)phosphonate is a bioactive chemical.
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    cIAP1 ligand 2
    E3 ligase Ligand 11
    T178692357114-70-4
    cIAP1 ligand 2, a derivative of LCL161, is an IAP ligand that can be connected to the ABL ligand for protein via a linker, resulting in the formation of SNIPER.
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    cIAP1 Ligand-Linker Conjugates 3
    E3 ligase Ligand-Linker Conjugates 40
    T178942222354-20-1
    cIAP1 Ligand-Linker Conjugates 3 are chemical compounds comprising an IAP ligand designed specifically for the E3 ubiquitin ligase and a PROTAC linker. These conjugates, denoted as cIAP1 Ligand-Linker Conjugates 3, find utility in the design of SNIPERs, short for Specific and Non-genetic IAP-dependent Protein Erasers [1].
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    cIAP1 Ligand-Linker Conjugates 7
    E3 ligase Ligand-Linker Conjugates 44
    T17898
    cIAP1 Ligand-Linker Conjugates 7 is a chemical compound that combines an IAP ligand for the E3 ubiquitin ligase with a PROTAC linker. It is utilized in the design of SNIPERs[1].
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    cIAP1 Ligand-Linker Conjugates 11 Hydrochloride
    E3 ligase Ligand-Linker Conjugates 33 Hydrochloride
    T178841239866-59-1
    cIAP1 Ligand-Linker Conjugates 11 Hydrochloride is a chemical compound comprising an IAP ligand that targets the E3 ubiquitin ligase and a PROTAC linker, mainly used in the development of SNIPERs for targeted protein degradation[1].
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    cIAP1 Ligand-Linker Conjugates 15 hydrochloride
    E3 ligase Ligand-Linker Conjugates 34 hydrochloride
    T178861225383-36-7
    cIAP1 Ligand-Linker Conjugates 15 hydrochloride is a chemical compound that combines an IAP ligand for the E3 ubiquitin ligase and a PROTAC linker, useful in the development of SNIPERs [1].
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    cIAP1 Ligand-Linker Conjugates 1
    E3 ligase Ligand-Linker Conjugates 41
    T178952357114-75-9
    cIAP1 Ligand-Linker Conjugates 1 is composed of an IAP ligand for the E3 ubiquitin ligase and a PROTAC linker. This compound, cIAP1 Ligand-Linker Conjugates 1, is particularly useful in the development of SNIPERs[1].
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    cIAP1 Ligand-Linker Conjugates 16
    cIAP1 Ligand-Linker Conjugates 16
    T396092143956-63-0
    cIAP1 Ligand-Linker Conjugates 16 refers to a specific type of ligase ligand-linker conjugate, possessing the ability to engage with E3 ligases, which finds application in the synthesis of PROTACs.
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    Pegulicianine
    T2025022230217-17-9
    Pegulicianine is an imaging agent utilized to detect residual cancer cells in the tumor bed of female patients undergoing breast-conserving surgery (BCS).
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    xiap/ciap1 antagonist-1
    T64302
    XIAP cIAP1 antagonist-1 is a potent, orally active XIAP cIAP1 antagonist with an EC50 of 5.1 nM for XIAP and 0.32 nM for cIAP1, and dose-dependently inhibits tumor growth in vivo.
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    10-14 weeks
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    Kaempferol 3-O-vicianoside
    T126403110352-79-9
    Kaempferol 3-O-vicianoside is a useful organic compound for research related to life sciences. The catalog number is T126403 and the CAS number is 110352-79-9.
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    cIAP1 Ligand-Linker Conjugates 9
    E3 ligase Ligand-Linker Conjugates 45
    T17899
    cIAP1 Ligand-Linker Conjugates 9 feature an IAP ligand specifically targeting the E3 ubiquitin ligase, along with a PROTAC linker. It is valuable tools for developing SNIPERs[1].
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    Cianopramine hydrochloride
    Ro-11-2465 hydrochloride, Ro 112465 hydrochloride, Cianopramine HCl
    T3092966834-20-6
    Cianopramine hydrochloride is a bio-active chemical.
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    Passitrifasciatin
    T3388997564-60-8
    Passitrifasciatin is a cyclopentanoid cyanohydrin glycoside isolated from Passiflora trifasciata.
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    Helicianeoide A
    TN4195496066-82-1
    Helicianeoide A is a natural product for research related to life sciences. The catalog number is TN4195 and the CAS number is 496066-82-1.
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    Boscialin
    TN5364129277-03-8
    Boscialin can inhibit signal transducer and activator of transcription 1 translocation at a concentration of 10 uM.
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