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ch 1

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    14
    TargetMol | Inhibitors_Agonists
  • PROTAC Products
    1
    TargetMol | PROTAC
  • Recombinant Protein
    9
    TargetMol | Recombinant_Protein
  • Antibody Products
    1
    TargetMol | Antibody_Products
NIOCH 14
NIOCH14
T618241268015-38-8In house
NIOCH 14 is an orally available antiviral compound that inhibits external keratovirus, poxvirus, and smallpox virus.
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6-8 weeks
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Sch 18099
Sch-18099, Sch18099
T3456728953-25-5
Sch 18099 showed anthelmintic activity.
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CH 102
Chinoin 102,CH-102,CH102,Chinoin-102
T3085855393-37-8
CH 102 is an isoquinoline derivative that inhibits platelet aggregation.
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6-8 weeks
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CH 150
CH150,CH-150
T3086070381-44-1
CH 150 is a bio-active chemical.
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CH 141
CH-141,Pthiqdo,CH141
T3085978279-88-6
CH 141 is a new type of peripheral vasodilator.
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6-8 weeks
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Sch 13835
Sch13835,Sch-13835
T28704150519-34-9
Sch 13835 is an inhibitor of platelet derived growth factor.
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6-8 weeks
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Notch 1 TFA
T19483
Notch 1 TFA encodes a member of the NOTCH family of proteins.
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Sch 12223
Sch12223,Sch-12223
T3456689109-20-6
SCH 12223 is a unique drug that protects the stomach and intestinal epithelium from harmful irritation.
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6-8 weeks
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D-Lactate dehydrogenase
T761469028-36-8
D-Lactate dehydrogenase (D-LDH), an oxidoreductase, catalyzes the oxidation of D-lactate to pyruvate leveraging NAD+ or NADP+ as acceptors and acting on the donor CH-OH group. Predominantly found in bacteria and fungi, it is frequently utilized in biochemical research [1].
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ch-0793076 tfa
T73672
CH-0793076 (TP3076) TFA, a hexacyclic camptothecin analog, is active drug and major metabolite of TP300. CH-0793076 TFA inhibits DNA topoisomerase I with an IC 50 of 2.3 μM. CH-0793076 TFA is efficacious against cells expressing BCRP (breast cancer resistance protein) [1] .
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Ch55-O-C3-NH2
RAR ligand 1
T18650144298-98-6
Ch55-O-C3-NH2, also known as RAR ligand 1, is a ligand derived from the Ch55 compound that specifically targets RAR. Through a linker, Ch55-O-C3-NH2 interacts with cIAP1 ligand Bestatin to form SNIPER[1].
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CHIKV nsP2 protease-IN-1
T200505
CHIKV nsP2 protease-IN-1 (compound J13) is an orally active inhibitor of non-structural protein 2 protease (non-structural protein 2protease), exhibiting an EC50 value of 0.39 μM against CH S27. This compound is utilized in the research of Chikungunya virus.
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SU 4029 dihydrochloride
SU-4029 diHCl. hexahydro-1-azepinepropionamidoxime HCl, RTECS CH2520000
T347333194-36-3
SU 4029 dihydrochloride is a bioactive chemical.
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tubulin/hdac-in-1
T615242413587-26-3
Tubulin HDAC-IN-1 is a dual inhibitor of tubulin and HDAC8, interacting with tubulin via CH π interactions and with HDAC8 through hydrogen bonds. It effectively inhibits tubulin polymerization and selectively targets HDAC8 with an IC50 of 150 nM. Additionally, Tubulin HDAC-IN-1 demonstrates cytotoxicity against various human cancer cells, induces cell cycle arrest in the G2 M phase, and triggers cell apoptosis, making it valuable for studying hematologic and solid tumors, including neuroblastoma and leukemia [1].
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6-8 weeks
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