42 Results for "

Pyrazolo

" in MedChemExpress (MCE) Product Catalog:
Products (42)

42 Results for "Pyrazolo" in MCE Product Catalog:

3
3 Cited Publications
Cat. No.: HY-10520
CAS No.: 522629-08-9
Purity:  98.71%
Target:  

MNK Apoptosis

Research Areas:  

Cancer

CGP 57380 is a cell-permeable pyrazolo-pyrimidine compound that acts as a selective inhibitor of Mnk1 with IC50 of 2.2 μM, but has no inhibitory activity against p38, JNK1, ERK1/2, PKC, or Src-like kinases.
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Cat. No.: HY-78428
CAS No.: 779353-02-5
Target:  

CDK

Research Areas:  

Cancer

CDK-IN-6, a class of pyrazolo[1,5-a]pyrimidine compound, is a CDK inhibitor with anticancer activities .
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Cat. No.: HY-W003486
CAS No.: 57489-77-7
Research Areas:  

Neurological Disease Cancer

5,7-Dichloropyrazolo[1,5-a]pyrimidine is a PDE10A inhibitor with a Ki of 24 μM. 5,7-Dichloropyrazolo[1,5-a]pyrimidine serves as a key intermediate in the synthesis of 5,7-disubstituted pyrazolo[1,5-a]pyrimidine derivatives (HIV-1 non-nucleoside reverse transcriptase inhibitors). 5,7-Dichloropyrazolo[1,5-a]pyrimidine can be used for the research of schizophrenia .
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Cat. No.: HY-48099
CAS No.: 2212021-61-7
Target:  

Drug Intermediate

Research Areas:  

Others

tert-Butyl (S)-2-(4-fluoro-3,5-dimethylphenyl)-4-methyl-3-(2-oxo-2,3-dihydro-1H-imidazol-1-yl)-2,4,6,7-tetrahydro-5H-pyrazolo[4,3-c]pyridine-5-carboxylate is a drug intermediate for synthesis of various active compounds.
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Cat. No.: HY-69077
CAS No.: 875781-17-2
5-Bromo-1H-pyrazolo[3,4-b]pyridine is a drug intermediate that can be used for the synthesis of sulfonamide derivatives.
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Cat. No.: HY-42697
CAS No.: 2135871-21-3
Target:  

Drug Intermediate

Research Areas:  

Others

(R)-Phenyl (5-(2-(2,5-difluorophenyl)pyrrolidin-1-yl)pyrazolo[1,5-a]pyrimidin-3-yl)carbamate is a drug intermediate for synthesis of various active compounds.
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Cat. No.: HY-43029
CAS No.: 1276110-38-3
Target:  

Drug Intermediate

Research Areas:  

Others

(R)-tert-Butyl 3-(4-amino-3-iodo-1H-pyrazolo[3,4-d]pyrimidin-1-yl)piperidine-1-carboxylate is a drug intermediate for synthesis of various active compounds.
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Cat. No.: HY-I0462
CAS No.: 2029205-64-7
Target:  

Drug Intermediate

Research Areas:  

Others

1-(4-Chlorophenyl)-7-oxo-6-(4-(2-oxopiperidin-1-yl)phenyl)-4,5,6,7-tetrahydro-1H-pyrazolo[3,4-c]pyridine-3-carboxamide is a drug intermediate for synthesis of various active compounds.
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Cat. No.: HY-117857
CAS No.: 1401731-54-1
Purity:  99.77%
MRT00033659 is a potent broad-spectrum kinase inhibitor of CK1 (IC50=0.9 μM for CK1δ) and CHK1 (IC50=0.23 μM). MRT00033659, a pyrazolo-pyridine analogue, induces p53 pathway activation and E2F-1 destabilisation .
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Cat. No.: HY-112505
CAS No.: 1776055-29-8
Purity:  ≥98.0%
Target:  

BCRP

Research Areas:  

Cancer

Efflux inhibitor-1 (compound 2) is a pyrazolo[1,5-a]pyrimidine efflux inhibitor. Efflux inhibitor-1 selectively targets toward ABCG2/BCRP over ABCB1 with IC50s of 0.45 μM and 2.17 μM, respectively .
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Cat. No.: HY-W052249
CAS No.: 5334-56-5
1-Methyl-1,5-dihydro-4H-pyrazolo[3,4-d]pyrimidin-4-one is a biochemical reagent that can be used as a biological material or organic compound for life science related research .
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Cat. No.: HY-W002060
CAS No.: 21901-40-6
Synonyms: 2-Amino-5-nitro-4-picoline
Pyridine-3,5-dicarboxylic acid is a drug intermediate that can be used for the synthesis of pyrazolo-pyridine compounds with cytotoxic properties .
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Cat. No.: HY-121682
CAS No.: 61788-27-0
N-(2-Chlorophenyl)-1H-indole-3-carboxamide (Compound 60) is a substituted derivative of the pyrazolo[1,5-a]pyridine core. N-(2-Chlorophenyl)-1H-indole-3-carboxamide does not exhibit EphB3 kinase inhibitory activity and can be used as a negative control compound .
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Cat. No.: HY-W000643
CAS No.: 271-73-8
1H-Pyrazolo[3,4-b]pyridine is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
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Cat. No.: HY-174414
Target:  

EGFR

Research Areas:  

Cancer

EGFR/HER2-IN-18 is a stable EGFR/HER2 dual inhibitor with IC50 values of 0.09 (EGFR) and 0.08 μM (HER2) respectively. EGFR/HER2-IN-18 exhibits broad-spectrum anti-cancer activity. EGFR/HER2-IN-18 induces MCF-7 cells apoptosis and inhibits the cell cycle. EGFR/HER2-IN-18 can be used for the study of breast cancer .
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Cat. No.: HY-148832
CAS No.: 1581714-50-2
Target:  

Btk

Research Areas:  

Inflammation/Immunology Cancer

BTK-IN-20 (compound 283) is a BTK tyrosine kinase inhibitor and a 1H-pyrazolo[3,4-d]pyrimidine derivative. BTK-IN-20 can be used for the research of cancer and inflammation .
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Cat. No.: HY-152408
CAS No.: 124137-35-5
Research Areas:  

Others

2-β-D-Ribofuranosyl-2H-pyrazolo[3,4-d]pyrimidine-4,6-diamine is a purine nucleoside analogue. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc .
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Cat. No.: HY-152828
CAS No.: 70421-30-6
Research Areas:  

Cancer

1-β-D-Ribofuranosyl-1H-pyrazolo[3,4-d]pyrimidine-4,6-diamine is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc .
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Cat. No.: HY-152438
Research Areas:  

Others

6-Amino-3-ethynyl-4-methoxy-1-(β-D-ribofuranosyl)-1H-pyrazolo[3,4-d]pyrimidine is a purine nucleoside analogue. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc . 6-Amino-3-ethynyl-4-methoxy-1-(β-D-ribofuranosyl)-1H-pyrazolo[3,4-d]pyrimidine 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-152398
Research Areas:  

Others

6-Amino-4-methoxy-2-(β-D-ribofuranosyl)-2H-pyrazolo[3,4-d]pyrimidine is a purine nucleoside analogue. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc .
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