99 Results for "

TK

" in MedChemExpress (MCE) Product Catalog:
Products (99)

99 Results for "TK" in MCE Product Catalog:

  • Recombinant Proteins Recommended:
14
14 Publications Verification
Cat. No.: HY-N0377
CAS No.: 578-86-9
Synonyms: 4',7-Dihydroxyflavanone
Liquiritigenin, a flavanone isolated from Glycyrrhiza uralensis, is a highly selective estrogen receptor β (ERβ) agonist with an EC50 of 36.5 nM for activation of the ERE tk-Luc.
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9
9 Cited Publications
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-W342664
CAS No.: 55612-21-0
Synonyms: FIRU
Research Areas:  

Cancer

2'-Deoxy-2'-fluoro-5-iodouridine (FIRU) is a nucleoside analog. When labeled with 123I, 2'-Deoxy-2'-fluoro-5-iodouridine accumulates highly selectively in tumors expressing the HSV1-tk gene. Radiolabeled 2'-Deoxy-2'-fluoro-5-iodouridine enables imaging of adenovirus-mediated HSV1-tk suicide gene transfer .
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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-132302
CAS No.: 2360523-76-6
Purity:  99.91%
Research Areas:  

Cancer

Hu7691 is an orally active, selective Akt inhibitor with IC50s of 4.0 nM, 97.5 nM, 28 nM for Akt1, Akt2 and Akt3, respectively. Hu7691 inhibits tumor growth and enables decrease of cutaneous toxicity in mice .
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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-114327
CAS No.: 14689-84-0
Synonyms: R15P
D-Ribose 1,5-diphosphate (R15P) is a metabolic intermediate and enzyme substrate. Purified Tk-E2b2 converts D-Ribose 1,5-diphosphate into Ribulose-1,5-bisphosphate, with a specific activity of 32.3 μmol min -1 mg -1[1] .
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Cat. No.: HY-D2415
CAS No.: 2411845-57-1
BODIPY-FL staurosporine (Compound 8a) is a fluorescence probe based on staurosporine, exhibiting high specificity towards tyrosine kinases (TK) and tyrosine kinase-like (TKL) family kinases. BODIPY-FL staurosporine has the potential to develop binding assays for kinases that are not recommended for use with Kinase Tracer 236, such as PIM3, CDC42BPG, MAP2K7, TXK, and SIK3. BODIPY-FL staurosporine can be a powerful tool for analyzing kinase selectivity in kinase drug discovery .
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Cat. No.: HY-139731
CAS No.: 2763650-87-7
Purity:  99.06%
Target:  

Transketolase Herbicide

Research Areas:  

Others

Transketolase-IN-1 is a transketolase inhibitor and a herbicide. Transketolase-IN-1 inhibits weed growth and exhibits safety for maize and wheat at specified application rates. Transketolase-IN-1 can be used for the research of weed control in wheat and maize fields .
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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-E70075
Synonyms: GDH-TIM; GDH-TPI
Target:  

Transketolase

Research Areas:  

Metabolic Disease

α-Glycerophosphate Dehydrogenase-Triosephosphate (GDH-TIM) is an enzyme mixture composed of glycerol phosphate dehydrogenase (GDH) and triphosphate isomerase (TIM). α-Glycerophosphate Dehydrogenase-Triosephosphate can be used to determine the activity of transketolase (TK) in hemolytic substances of red blood cells to evaluate vitamin B deficiency .
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