58 Results for "

TK inhibitor

" in MedChemExpress (MCE) Product Catalog:
Products (58)

58 Results for "TK inhibitor" in MCE Product Catalog:

9
9 Publications Verification
Cat. No.: HY-122903
CAS No.: 1903783-48-1
Purity:  99.84%
Target:  

DNA/RNA Synthesis

Research Areas:  

Cancer

TK216 is an orally active and potent E26 transformation specific (ETS) inhibitor . TK216 directly binds EWS-FLI1 and inhibits EWS-FLI1 protein interactions. TK216 blocks the binding between EWS-FLI1 and RNA helicase A. TK216 has anticancer activity .
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3
3 Cited Publications
Cat. No.: HY-107430
CAS No.: 136-16-3
Purity:  96.28%
Synonyms: Hydroxythiamin
Oxythiamine (Hydroxythiamin), an analogue of anti-metabolite, can suppress the non-oxidative synthesis of ribose and induce cell apoptosis. Oxythiamine is a thiamine antagonist and inhibits transketolase (TK). Oxythiamine inhibits cancer cell apoptosis and inhibits cell proliferation .
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3
3 Cited Publications
Cat. No.: HY-107430A
CAS No.: 614-05-1
Purity:  96.36%
Synonyms: Hydroxythiamine chloride hydrochloride
Oxythiamine (Hydroxythiamine) chloride hydrochloride, an analogue of anti-metabolite, can suppress the non-oxidative synthesis of ribose and induce cell apoptosis. Oxythiamine chloride hydrochloride is a thiamine antagonist and inhibits transketolase (TK). Oxythiamine chloride hydrochloride inhibits cancer cell apoptosis and inhibits cell proliferation .
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2
2 Cited Publications
Cat. No.: HY-16339
CAS No.: 13860-66-7
Synonyms: N3-pyridyl thiamine
Target:  

Transketolase

Research Areas:  

Cancer

N3PT (N3-pyridyl thiamine) is a potent and selective transketolase inhibitor. N3PT is pyrophosphorylated and then binds to transketolase with an Kd value of 22 nM (Apo-TK, transketolase lacking bound thiamine) .
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2
2 Cited Publications
Cat. No.: HY-117143
CAS No.: 1245734-61-5
Purity:  97.05%
Research Areas:  

Inflammation/Immunology

TK05 is a potent and selective inhibitor of leukotriene C4 synthase (LTC4S) with an IC50 of 95 nM .
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1
1 Cited Publications
Cat. No.: HY-112889B
Target:  

Transketolase

Research Areas:  

Metabolic Disease

Oxythiamin diphosphate ammonium is a potent transketolase (TK) inhibitor .
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Cat. No.: HY-W008491
CAS No.: 22423-26-3
Target:  

Phosphorylase

Research Areas:  

Inflammation/Immunology Cancer

TK-112690 is a UPP1 inhibitor. TK-112690 inhibits murine small intestinal uridine phosphorylase (UPase) with an IC50 of 12.5 μM and human small intestinal UPase with an IC50 of 20.0 μM in vitro. TK-112690 increases plasma uridine concentration in mice. TK-112690 can be used for the study of cancer and pulmonary fibrosis .
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Cat. No.: HY-112889
CAS No.: 10497-04-8
Target:  

Transketolase

Research Areas:  

Metabolic Disease

Oxythiamin diphosphate is a potent transketolase (TK) inhibitor .
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Cat. No.: HY-17422S1
CAS No.: 1185179-33-2
Synonyms: Aciclovir-d4; Acycloguanosine-d4
Acyclovir-d4 is the deuterium labeled Acyclovir. Acyclovir (Aciclovir) is a guanosine analogue and an orally active antiviral agent. Acyclovir inhibits HSV-1 (IC50 of 0.85 μM), HSV-2 (IC50 of 0.86 μM) and varicella-zoster virus. Acyclovir can be phosphorylated by viral thymidine kinase (TK), and Acyclovir triphosphate interferes with viral DNA polymerization through competitive inhibition with guanosine triphosphate and obligatory chain termination . Acyclovir prevents bacterial infections during induction therapy for acute leukaemia .
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Cat. No.: HY-151483
CAS No.: 3031476-73-7
Purity:  ≥98.0%
Target:  

Wnt Histone Demethylase

Research Areas:  

Cardiovascular Disease

TK-129 is an orally active, low-toxicity, potent KDM5B inhibitor (with high affinity; IC50=44 nM). TK-129 exerts cardioprotective effects by inhibiting KDM5B and blocking the KDM5B-associated Wnt pathway. TK-129 reduces ang II-induced activation of cardiac fibroblasts in vitro and reduces isoprenaline-induced myocardial remodelling and fibrosis in vivo. TK-129 can be used in studies of cardiovascular disease .
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Cat. No.: HY-151604
CAS No.: 2757552-03-5
Purity:  98.52%
Target:  

Transketolase

Research Areas:  

Others

Transketolase-IN-3 is a potent transketolase (TK) inhibitor. Transketolase-IN-3 has herbicidal activity and has inhibitory effects against Digitaria sanguinalis (DS) and Amaranthus retroflexus (AR). Transketolase-IN-3 can be used for the research of herbicides .
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Cat. No.: HY-122903B
CAS No.: 1903783-77-6
Purity:  99.91%
Target:  

DNA/RNA Synthesis

Research Areas:  

Cancer

(+)-TK216 is an enantiomer of TK216 (HY-122903). TK216 is an orally active and potent E26 transformation specific (ETS) inhibitor .
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Cat. No.: HY-P1079
CAS No.: 158484-42-5
Target:  

Calcium Channel

Research Areas:  

Neurological Disease

ω-Agatoxin TK, a peptidyl toxin of the venom of Agelenopsis aperta, is a potent and selective P/Q type Ca 2+ channel blocker. ω-Agatoxin TK inhibits the high K + depolarisation-induced rise in internal Ca 2+ in cerebral isolated nerve endings with an IC50 of of 60 nM. ω-Agatoxin TK has no effect on L-type, N-type, or T-type calcium channels .
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Cat. No.: HY-128710
CAS No.: 122799-38-6
Purity:  99.07%
Synonyms: 2'-​Deoxy-​2'-​fluoro-​5-​Methyluridine
Research Areas:  

Cancer

2'-Fluorothymidine (2'-Fluoro-2'-deoxythymidine) is a nucleoside analog and hCNT inhibitor, with an IC50 of 1.1 μM against hCNT1 and an IC50 of 9.7 μM against hCNT3. 2'-Fluorothymidine undergoes phosphorylation by cytosolic thymidine kinase (TK1) and mitochondrial thymidine kinase (TK2). 2'-Fluorothymidine acts as a backbone stabilizer in oligonucleotide synthesis and can also form radiolabeled candidates. 2'-Fluorothymidine is applicable in tumor-related research .
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Cat. No.: HY-118304B
Purity:  99.95%
Target:  

FLT3 Apoptosis Caspase

Research Areas:  

Cancer

AKN-028 acetate, a novel tyrosine kinase (TK) inhibitor, is a potent, orally active FMS-like receptor tyrosine kinase 3 (FLT3) inhibitor with an IC50 value of 6 nM. AKN-028 acetate inhibits FLT3 autophosphorylation. AKN-028 acetate induces dose-dependent cytotoxic response (mean IC50=1 μM). AKN-028 acetate induces apoptosisby activation of caspase 3. AKN-028 acetate can be used in research of acute myeloid leukemia (AML).
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Cat. No.: HY-122903S
CAS No.: 3034816-36-6
TK216-d4 is the deuterium labeled TK216 (HY-122903). TK216 is an orally active and potent E26 transformation specific (ETS) inhibitor . TK216 directly binds EWS-FLI1 and inhibits EWS-FLI1 protein interactions. TK216 blocks the binding between EWS-FLI1 and RNA helicase A. TK216 has anticancer activity .
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Cat. No.: HY-107430B
CAS No.: 582-36-5
Synonyms: Hydroxythiamine chloride
Target:  

Apoptosis

Research Areas:  

Cancer

Oxythiamine (Hydroxythiamine) chloride, an analogue of anti-metabolite, can suppress the non-oxidative synthesis of ribose and induce cell apoptosis. Oxythiamine is a thiamine antagonist and inhibits transketolase (TK). Oxythiamine chloride inhibits cancer cell apoptosis and inhibits cell proliferation .
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Cat. No.: HY-173571
Target:  

SHP2 Apoptosis

Research Areas:  

Cancer

TK-685 is an orally active, selective, and allosteric SHP2 inhibitor with an IC50 of 2.1 nM. TK-685 inhibits esophageal cancer cell proliferation and induced apoptosis by targeting SHP2-mediated AKT and ERK signaling pathways .
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Cat. No.: HY-151259
CAS No.: 2232890-81-0
Target:  

JAK

Research Areas:  

Cancer

TK4b is a dual JAK2/3 inhibitor with human JAK2 and JAK3 IC50s of 19.40 nM and 18.42 nM, respectively. TK4b can be used for the research of leukemia and myelofibrosis .
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Cat. No.: HY-107430AR
CAS No.: 614-05-1
Synonyms: Hydroxythiamine chloride hydrochloride (Standard)
Oxythiamine chloride hydrochloride (Standard) is the analytical standard of Oxythiamine chloride hydrochloride (HY-107430A). This product is intended for research and analytical applications. Oxythiamine (Hydroxythiamine) chloride hydrochloride, an analogue of anti-metabolite, can suppress the non-oxidative synthesis of ribose and induce cell apoptosis. Oxythiamine chloride hydrochloride is a thiamine antagonist and inhibits transketolase (TK). Oxythiamine chloride hydrochloride inhibits cancer cell apoptosis and inhibits cell proliferation .
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