27 Results for "

NSC11

" in MedChemExpress (MCE) Product Catalog:
Products (27)

27 Results for "NSC11" in MCE Product Catalog:

120
120 Publications Verification
Cat. No.: HY-B0069
CAS No.: 21679-14-1
Synonyms: F-ara-A; NSC 118218
Fludarabine (NSC 118218) is a DNA synthesis inhibitor and a fluorinated purine analogue with antineoplastic activity in lymphoproliferative malignancies. Fludarabine inhibits the cytokine-induced activation of STAT1 and STAT1-dependent gene transcription in normal resting or activated lymphocytes .
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13
13 Cited Publications
Cat. No.: HY-15424
CAS No.: 24386-93-4
Purity:  99.64%
Synonyms: NSC 113939; 5-ITu
Target:  

Adenosine Kinase

Research Areas:  

Cancer

5-Iodotubercidin (NSC 113939), an ATP mimetic, is a potent adenosine kinase inhibitor with an IC50 of 26 nM. 5-Iodotubercidin (NSC 113939) initiates glycogen synthesis in isolated hepatocytes by causing inactivation of phosphorylase and activation of glycogen synthase. 5-Iodotubercidin (NSC 113939) also inhibits CK1, insulin receptor tyrosine kinase, phosphorylase kinase, PKA, CK2, PKC and Haspin .
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9
9 Cited Publications
Cat. No.: HY-B0028
CAS No.: 75607-67-9
Synonyms: NSC 118218 phosphate
Research Areas:  

Cancer

Fludarabine (phosphate) is an analogue of adenosine and deoxyadenosine, which is able to compete with dATP for incorporation into DNA and inhibit DNA synthesis.
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4
4 Cited Publications
Cat. No.: HY-117656
CAS No.: 5184-64-5
Purity:  99.78%
Synonyms: NSC 116966
Target:  

Acyltransferase

ESI-05 is a specific exchange proteins directly activated by cAMP 2 (EPAC2) inhibitor. ESI-05 inhibits cAMP-mediated EPAC2 GEF activity with an IC50 of 0.43 μM. ESI-05 can be used for the research of diabetes, insulin secretion and neurological disorders .
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3
3 Cited Publications
Cat. No.: HY-15345A
CAS No.: 18771-50-1
Purity:  99.89%
Synonyms: THU; NSC-112907
Target:  

DNA/RNA Synthesis

Research Areas:  

Cancer

Tetrahydrouridine dihydrate is potent inhibitor of cytidine deaminase (CDA), which competitively blocks the enzyme's active site more effectively than intrinsic cytidine .
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3
3 Cited Publications
Cat. No.: HY-15345
Purity:  99.79%
Synonyms: THU dihydrate; NSC-112907 dihydrate
Target:  

DNA/RNA Synthesis

Research Areas:  

Cancer

Tetrahydrouridine dihydrate (THU dihydrate) is potent inhibitor of cytidine deaminase (CDA), which competitively blocks the enzyme's active site more effectively than intrinsic cytidine.
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Cat. No.: HY-111285
CAS No.: 138736-73-9
Purity:  99.73%
Synonyms: NSC111847
Target:  

DNA/RNA Synthesis

Research Areas:  

Cancer

HAMNO is a novel protein interaction inhibitor of replication protein A (RPA).
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Cat. No.: HY-D0221
CAS No.: 3682-35-7
Synonyms: NSC 112125; 2,4,6-Tipyidyl-s-tiazie
2,4,6-Tri-2-pyridinyl-1,3,5-triazine (NSC 112125) is a colorimetric reagent for detecting iron. 2,4,6-Tri-2-pyridinyl-1,3,5-triazine forms a complex with Fe (II) and can be quantified as a measure of iron concentration by colorimetric detection at 594 nm .
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Cat. No.: HY-19819
CAS No.: 500363-63-3
Target:  

Phosphatase

Research Areas:  

Inflammation/Immunology

NSC117079 is a novel PHLPP inhibitor.
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Cat. No.: HY-A0161A
CAS No.: 511-13-7
Synonyms: Clofedanol hydrochloride; Calmotusin hydrochloride; NSC 113595 hydrochloride
Target:  

Others

Research Areas:  

Infection

Chlophedianol (Clofedanol) hydrochloride is an orally active and potent antitussive agent. Chlophedianol hydrochloride can be used for the research of acute cough due to upper respiratory tract infections (URIs) .
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Cat. No.: HY-114502
CAS No.: 10453-89-1
Purity:  99.08%
Synonyms: NSC 11779
Chrysanthemic acid (NSC 11779) is an organic compound that is associated with a variety of natural and synthetic insecticides for the prevention of insect-borne diseases, among others .
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Cat. No.: HY-15424R
CAS No.: 24386-93-4
Synonyms: NSC 113939 (Standard); 5-ITu (Standard)
Research Areas:  

Cancer

5-Iodotubercidin (Standard) is the analytical standard of 5-Iodotubercidin. This product is intended for research and analytical applications. 5-Iodotubercidin (NSC 113939), an ATP mimetic, is a potent adenosine kinase inhibitor with an IC50 of 26 nM. 5-Iodotubercidin (NSC 113939) initiates glycogen synthesis in isolated hepatocytes by causing inactivation of phosphorylase and activation of glycogen synthase. 5-Iodotubercidin (NSC 113939) also inhibits CK1, insulin receptor tyrosine kinase, phosphorylase kinase, PKA, CK2, PKC and Haspin .
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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-B0028R
CAS No.: 75607-67-9
Synonyms: NSC 118218 phosphate (Standard)
Fludarabine (phosphate) (Standard) is the analytical standard of Fludarabine (phosphate). This product is intended for research and analytical applications. Fludarabine (phosphate) is an analogue of adenosine and deoxyadenosine, which is able to compete with dATP for incorporation into DNA and inhibit DNA synthesis.
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Cat. No.: HY-B0069R
CAS No.: 21679-14-1
Synonyms: F-ara-A (Standard); NSC 118218 (Standard)
Fludarabine (Standard) is the analytical standard of Fludarabine. This product is intended for research and analytical applications. Fludarabine (NSC 118218) is a DNA synthesis inhibitor and a fluorinated purine analogue with antineoplastic activity in lymphoproliferative malignancies. Fludarabine inhibits the cytokine-induced activation of STAT1 and STAT1-dependent gene transcription in normal resting or activated lymphocytes .
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Cat. No.: HY-122101
CAS No.: 17392-79-9
Target:  

JAK Apoptosis

Research Areas:  

Cancer

NSC114792 is a selective JAK3 inhibitor. NSC114792 induces apoptosis. NSC114792 decreases the protein expression of p-JAK3 and p-STAT5 .
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Cat. No.: HY-153719
CAS No.: 40420-48-2
Target:  

SARS-CoV

Research Areas:  

Infection

NSC111552 is a potent SARS-CoV-2 NSP14 MTase inhibitor. NSC111552 inhibits the FL-NAH binding to the SARS-CoV-2 NSP14 MTase with an IC50 of 5.1 μM .
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Cat. No.: HY-28099
CAS No.: 3431-16-1
Synonyms: NSC 11435
Target:  

Endogenous Metabolite

Research Areas:  

Cancer

VEC6 (NSC 11435) is an inhibitor of VEZF1–DNA interaction and has the activity to recapitulate RhoB loss in ischemic retinopathy. VEC6 reduces pathological angiogenesis and promotes lymphangiogenesis. VEC6 plays a unique role in angiogenesis and lymphangiogenesis by regulating the expression of different sets of genes in endothelial cells. VEC6 has an inhibitory effect on VEZF1-mediated transcriptional activity, thereby affecting the proliferation and sprouting of endothelial cells .
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Cat. No.: HY-A0161
CAS No.: 791-35-5
Synonyms: Clofedanol; Calmotusin; NSC 113595
Target:  

Others

Research Areas:  

Infection

Chlophedianol (Clofedanol) is an orally active and potent antitussive agent. Chlophedianol can be used for the research of acute cough due to upper respiratory tract infections (URIs) .
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Cat. No.: HY-15345AR
CAS No.: 18771-50-1
Synonyms: THU (Standard); NSC-112907 (Standard)
Research Areas:  

Cancer

Tetrahydrouridine (Standard) is the analytical standard of Tetrahydrouridine. This product is intended for research and analytical applications. Tetrahydrouridine dihydrate is potent inhibitor of cytidine deaminase (CDA), which competitively blocks the enzyme's active site more effectively than intrinsic cytidine .
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