98 Results for "

TK

" in MedChemExpress (MCE) Product Catalog:
Products (98)

98 Results for "TK" in MCE Product Catalog:

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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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Cat. No.: HY-122903A
CAS No.: 1903783-78-7
Purity:  99.45%
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. (-)-TK216 has anti-cancer activity .
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Cat. No.: HY-169436
Target:  

PD-1/PD-L1

Lon-TK is a glycolysis inhibitor + linker conjugate of LTB (HY-169434). LTB is an intelligent responsive prodrug that connects Lonidamine (Lon) (HY-B0486) and a PD-L1 inhibitor (BMS-1, HY-19991) through a thioketal linker. It significantly inhibits the glycolytic metabolism of tumor cells and blocks the PD-1/PD-L1 immune escape pathway. Lon-TK shows potential for application in photodynamic-enhanced immunotherapy research .
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Cat. No.: HY-P3633
CAS No.: 126985-98-6
Synonyms: Lom-TK II
Target:  

Inhibitory Antibodies

Research Areas:  

Neurological Disease

Locustatachykinin II (Lom-TK II) is an insect neuropeptide with homology to peptides of the vertebrate tachykinin family. Locustatachykinin II can be used for the research of insect endocrine .
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Cat. No.: HY-P1768
CAS No.: 149097-03-0
Synonyms: Uru-TK I
Target:  

Bacterial

Research Areas:  

Infection

Urechistachykinin I (Uru-TK I), an invertebrate tachykinin-related peptides (TRPs) isolated from echiuroid worms, shows antimicrobial activities without a hemolytic effect .
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Cat. No.: HY-RS23490
Research Areas:  

Others

Tk1 Rat Pre-designed siRNA Set A contains three designed siRNAs for Tk1 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-146471
CAS No.: 2418549-32-1
Target:  

EGFR Apoptosis

Research Areas:  

Cancer

EGFR-IN-51 (Compound 6) is a potent EGFR inhibitor with IC50 values of 0.493, 102.60 and 461.63 µM against EGFR, EGFR L858R-TK and EGFR T790M-TK, respectively. EGFR-IN-51 shows cytotoxic activity against cancer cell lines and induces apoptosis .
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Cat. No.: HY-144445
CAS No.: 24909-18-0
Target:  

EGFR

Research Areas:  

Cancer

NSC114126 is a potent and orally active inhibitor of EGFR tyrosine kinase (EGFR-TK). NSC114126 has strong antiproliferative activities. NSC114126 has the potential for the research of cancer diseases .
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Cat. No.: HY-178442
CAS No.: 3078678-28-8
Target:  

EGFR

Research Areas:  

Cancer

EGFR-IN-179 (Compound 8d) is an EGFR inhibitor (IC50: 0.068 μM for EGFR L858R/T790M/C797S; 2.56 μM for EGFR-WT-TK). EGFR-IN-179 has anticancer activity against non-small cell lung cancer .
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Cat. No.: HY-149022
CAS No.: 2490468-31-8
Target:  

HSV Orthopoxvirus

Research Areas:  

Infection

HSV-1/HSV-2-IN-1 (compound 7d) is a HSV-1 and HSV-2 inhibitor, with EC50s of 7.6, 7.6, 4, and 12 μM for HSV-1 (KOS), HSV-2 (G), HSV-1 TK - KOS ACV r and vaccinia virus in human embryonic lung fibroblast cell cultures .
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Cat. No.: HY-118304
CAS No.: 1175017-90-9
Target:  

FLT3 Apoptosis Caspase

Research Areas:  

Cancer

AKN-028, 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 inhibits FLT3 autophosphorylation. AKN-028 induces dose-dependent cytotoxic response (mean IC50=1 μM). AKN-028 induces apoptosisby activation of caspase 3. AKN-028 can be used in research of acute myeloid leukemia (AML) .
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Cat. No.: HY-173573
Target:  

Apoptosis SHP2

Research Areas:  

Cancer

TK-684 is a potent and selective allosteric SHP2 inhibitor with IC50 values of 2.1, >1000 nM for SHP2 WT, SHP22 PTP, respectively. TK-684 inhibits cell proliferation and induces apoptosis. TK-684 decreases the protein expression of p-AKT, p-ERK .
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Cat. No.: HY-158762
CAS No.: 2765183-10-4
Target:  

SHP2

Research Areas:  

Cancer

TK-642 is a highly active, selective, orally activity SHP2 inhibitor based on pyrazole and pyrazine (IC50=2.7 nmol/L). TK-642 can effectively inhibit the proliferation of esophageal carcinoma cells and induce cell apoptosis. TK-642 can be used in the study of esophageal cancer .
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Cat. No.: HY-126218
CAS No.: 111687-37-7
Target:  

HSV

Research Areas:  

Cancer

HSV-TK substrate is a substrate for HSV-TK, and induces multi-log cytotoxicity in HSV-TK-expressing and bystander cells. HSV-TK substrate shows antitumor activity .
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Cat. No.: HY-161927
CAS No.: 3053485-72-3
Target:  

EGFR Apoptosis

Research Areas:  

Cancer

EGFR-TK-IN-4 (compound 10k) is a potent and selective EGFR-TK inhibitor. EGFR-TK-IN-4 can induce apoptosis . EGFR-TK-IN-4 has antitumor activity .
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Cat. No.: HY-169435
CAS No.: 861587-94-2
Target:  

Drug Intermediate

Research Areas:  

Cancer

TK-OH is the linker of LTB (HY-169434). TK-OH can be used for the research of cancers .
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