4H-Pyrazolo[3,4-d]pyrimidin-4-one,1,5-dihydro-1,5-dimethyl
![4H-Pyrazolo[3,4-d]pyrimidin-4-one,1,5-dihydro-1,5-dimethyl Structure](https://image.chemsrc.com/caspic/251/5334-54-3.png)
4H-Pyrazolo[3,4-d]pyrimidin-4-one,1,5-dihydro-1,5-dimethyl structure
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Common Name | 4H-Pyrazolo[3,4-d]pyrimidin-4-one,1,5-dihydro-1,5-dimethyl | ||
|---|---|---|---|---|
| CAS Number | 5334-54-3 | Molecular Weight | 164.16500 | |
| Density | 1.43g/cm3 | Boiling Point | 342.9ºC at 760mmHg | |
| Molecular Formula | C7H8N4O | Melting Point | N/A | |
| MSDS | N/A | Flash Point | 161.2ºC | |
| Name | 1,5-dimethylpyrazolo[3,4-d]pyrimidin-4-one |
|---|---|
| Synonym | More Synonyms |
| Density | 1.43g/cm3 |
|---|---|
| Boiling Point | 342.9ºC at 760mmHg |
| Molecular Formula | C7H8N4O |
| Molecular Weight | 164.16500 |
| Flash Point | 161.2ºC |
| Exact Mass | 164.07000 |
| PSA | 52.71000 |
| Index of Refraction | 1.697 |
| InChIKey | PVQKQWMEXZGTMR-UHFFFAOYSA-N |
| SMILES | Cn1cnc2c(cnn2C)c1=O |
|
~37%
4H-Pyrazolo[3,4... CAS#:5334-54-3 |
| Literature: Bulychev, Yu. N.; Preobrazhenskaya, M. N. Chemistry of Heterocyclic Compounds (New York, NY, United States), 1988 , vol. 24, # 11 p. 1265 - 1270 Khimiya Geterotsiklicheskikh Soedinenii, 1988 , vol. 24, # 11 p. 1526 - 1531 |
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~%
4H-Pyrazolo[3,4... CAS#:5334-54-3 |
| Literature: Cheng; Robins Journal of Organic Chemistry, 1956 , vol. 21, p. 1240,1242 |
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4H-Pyrazolo[3,4... CAS#:5334-54-3 |
| Literature: Cheng; Robins Journal of Organic Chemistry, 1956 , vol. 21, p. 1240,1242 |
|
~%
4H-Pyrazolo[3,4... CAS#:5334-54-3 |
| Literature: Cheng; Robins Journal of Organic Chemistry, 1956 , vol. 21, p. 1240,1242 |
|
~%
4H-Pyrazolo[3,4... CAS#:5334-54-3 |
| Literature: Cheng; Robins Journal of Organic Chemistry, 1956 , vol. 21, p. 1240,1242 |
|
~16%
4H-Pyrazolo[3,4... CAS#:5334-54-3
Detail
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| Literature: Lichtenthaler; Cuny Chemische Berichte, 1981 , vol. 114, # 5 p. 1610 - 1623 |
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~%
4H-Pyrazolo[3,4... CAS#:5334-54-3 |
| Literature: Schmidt et al. Helvetica Chimica Acta, 1959 , vol. 42, p. 349,358 |
![2,5-dimethylpyrazolo[3,4-d]pyrimidin-4-one structure](https://image.chemsrc.com/caspic/096/57121-50-3.png)
![1-METHYL-1,5-DIHYDRO-4H-PYRAZOLO[3,4-D]PYRIMIDIN-4-ONE structure](https://image.chemsrc.com/caspic/175/5334-56-5.png)
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Name: Luminescence-based cell-based primary high throughput screening assay to identify ago...
Source: The Scripps Research Institute Molecular Screening Center
Target: mu-type opioid receptor isoform MOR-1 [Homo sapiens]
External Id: OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN
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|
Name: QFRET-based biochemical primary high throughput screening assay to identify exosite i...
Source: The Scripps Research Institute Molecular Screening Center
Target: disintegrin and metalloproteinase domain-containing protein 17 preproprotein [Homo sapiens]
External Id: ADAM17_INH_QFRET_1536_1X%INH PRUN
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|
Name: Fluorescence-based cell-based primary high throughput screening assay to identify ago...
Source: The Scripps Research Institute Molecular Screening Center
Target: muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id: CHRM1_AG_FLUO8_1536_1X%ACT PRUN
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|
Name: qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
Source: NCGC
Target: TDP1 protein [Homo sapiens]
External Id: TDP1100
|
|
Name: qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
Source: NCGC
Target: TDP1 protein [Homo sapiens]
External Id: TDP1101
|
|
Name: Schnurri-3 Inhibitors: specific inducers of adult bone formation Measured in Cell-Bas...
Source: Broad Institute
Target: N/A
External Id: 2134-01_Inhibitor_SinglePoint_HTS_Activity_Set2
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Name: Fluorescence polarization to screen for inhibitor that competite the binding of FadD2...
Source: Broad Institute
Target: FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE)
External Id: 2147-01_Inhibitor_SinglePoint_HTS_Activity
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|
Name: Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfect...
Source: Broad Institute
Target: N/A
External Id: Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfected HEK293 cells Inhibition - 7011-01_Antagonist_SinglePoint_HTS_Activity
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Name: High throughput screen for small molecule inhibitors of a hypoxia-regulated fluoresce...
Source: ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
Target: N/A
External Id: HMS1149-MLP
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Name: qHTS for Inhibitors of AMA1-RON; Towards Development of Antimalarial Drug Lead: Prima...
Source: NCGC
Target: apical membrane antigen 1, AMA1 [Plasmodium falciparum 3D7]
External Id: AMA1100
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| 4,5-Dihydro-1,5-dimethyl-1H-pyrazolo<3,4-d>pyrimidine-4-one |
| 1,5-Dimethyl-1,5-dihydro-4H-pyrazolo[3,4-d]pyrimidin-4-one |
| 1,5-dihydro-1,5-dimethyl-4H-pyrazolo<3,4-d>pyrimidin-4-one |
| 1,5-dimethylallopurinol |
| Allopurinol di-methyl derivative |
| 1,5-dimethylpyrazolo<3,4-d>pyrimidin-4-one |
| 1,5-Dimethyl-4-oxo-4,5-dihydro-pyrazolo<3,4-d>pyrimidin |
| 1,5-Dimethyl-1,5-dihydro-pyrazolo[3,4-d]pyrimidin-4-on |
| 1,5-dimethyl-1,5-dihydro-pyrazolo[3,4-d]pyrimidin-4-one |
| PVQKQWMEXZGTMR-UHFFFAOYSA |