9 Results for "

fR2

" in MedChemExpress (MCE) Product Catalog:
Products (9)

9 Results for "fR2" in MCE Product Catalog:

1
1 Cited Publications
Cat. No.: HY-N3009
CAS No.: 58822-47-2
Secoxyloganin is an orally effective iridoid derivative. Secoxyloganin can be isolated from the flower buds of L. japonica. Secoxyloganin induces Apoptosis by inhibiting the expression of Bcl-2. Secoxyloganin potently inhibits the proliferation of breast cancer cells, while exerting weak activity against normal mammary epithelial cells. Secoxyloganin inhibits the decrease in tail vein blood flow associated with allergic reactions [2].
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Cat. No.: HY-107367A
CAS No.: 2071195-74-7
Purity:  98.15%
Synonyms: S-22611 hydrochloride
Target:  

EGFR

Research Areas:  

Cancer

Epertinib (S-22611) hydrochloride is a potent, orally active, reversible, and selective tyrosine kinase inhibitor of EGFR, HER4 and HER2, with IC50s of 1.48 nM, 2.49 nM and 7.15 nM, respectively. Epertinib hydrochloride shows potent antitumor activity [2]. Epertinib (hydrochloride) is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
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Cat. No.: HY-P2317
CAS No.: 125667-96-1
Research Areas:  

Infection

Cecropin P1, porcine is an antibacterial peptide that can be isolated from the upper part of the small intestine of the pig. Cecropin P1, porcine shows antibacterial activity against Gram-negative bacteria. Cecropin P1, porcine shows antiviral activity and inhibits PRRSV infection [2].
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Cat. No.: HY-107367
CAS No.: 908305-13-5
Synonyms: S-22611
Target:  

EGFR

Research Areas:  

Cancer

Epertinib (S-22611) is a potent, orally active, reversible, and selective tyrosine kinase inhibitor of EGFR, HER4 and HER2, with IC50s of 1.48 nM, 2.49 nM and 7.15 nM, respectively. Epertinib shows potent antitumor activity [2]. Epertinib is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
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Cat. No.: HY-146103
CAS No.: 2497687-47-3
Research Areas:  

Cancer

Antiproliferative agent-7 (compound 8f) is a potent anti-proliferative agent. Antiproliferative agent-7 has antiproliferative activity against cancer cell lines MCF-7, MDA-MB-231, HCT-116 and FR-2 with IC50s of 3.5 μM, 15.54 μM, 30.43 μM and 34.8 μM, respectively. Antiproliferative agent-7 can increase ROS production and induce apoptosis .
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P12FR2 sodium
0 Images
RNA,(5'-GGGCGfUGfCfUGGGfCfCfUGfUAAAfUAfCAfCGfCAfUfCGfUAfUfCfUfCGAfUfUfCGfCAfUfCfCfCfUGAfCfUfCAfUAAfCfCfCAGAGGfUfCGAfUG-3') sodium salt, (All C and U are 2'-fluoro-pyrimidine modified nucleic acids.)
Cat. No.: HY-164185
P12FR2 sodium is an aptamer targeting human pancreatic adenocarcinoma up-regulated factor (PAUF). P12FR2 specifically binds to human PAUF with an estimated apparent KD of 77 nM. P12FR2 inhibits PAUF-induced PANC-1 cell migration and pancreatic cancer xenograft growth.
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Cat. No.: HY-160061
Research Areas:  

Cancer

P12FR2 aptamer sodium is a 2'-fluoropyrimidine-modified RNA aptamer targeting human PAUF with an estimated apparent KD of 77 nM. P12FR2 aptamer sodium inhibits PAUF-induced migration of PANC-1 (human pancreatic cancer cells) in wound healing assays and suppresses tumor growth in a mouse CFPAC-1 pancreatic cancer model .
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Cat. No.: HY-107367AR
CAS No.: 2071195-74-7
Synonyms: S-22611 hydrochloride (Standard)
Research Areas:  

Cancer

Epertinib hydrochloride (Standard) (S-22611 hydrochloride (Standard)) is the analytical standard of Epertinib (hydrochloride) (HY-107367A). This product is intended for research and analytical applications. Epertinib (S-22611) hydrochloride is a potent, orally active, reversible, and selective tyrosine Kinase inhibitor of EGFR, HER4 and HER2, with IC50s of 1.48 nM, 2.49 nM and 7.15 nM, respectively. Epertinib hydrochloride shows potent antitumor activity [2]. Epertinib (hydrochloride) is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
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Cat. No.: HY-P71919
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: 6-bisphosphatase TIGAR; C12ORF5; chromosome 12 open reading fRame 5; fR2BP; fRuctose-2,6-bisphosphatase TIGAR; fRuctose-2,6-bisphosphate 2-phosphatase; Probable fRuctose 2,6 bisphosphatase TIGAR; Probable fRuctose-2; tigar; TIGAR_HUMAN; TP53 induced glycolysis and apoptosis regulator; TP53 induced glycolysis regulatory phosphatase; TP53-induced glycolysis and apoptosis regulator; Transactivated by NS3TP2 protein
Species:  
Source:  
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