4H-1-Benzopyran-4-one,2-(4-pyridinyl) structure
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Common Name | 4H-1-Benzopyran-4-one,2-(4-pyridinyl) | ||
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| CAS Number | 3034-16-0 | Molecular Weight | 223.22700 | |
| Density | 1.294g/cm3 | Boiling Point | 392.5ºC at 760mmHg | |
| Molecular Formula | C14H9NO2 | Melting Point | N/A | |
| MSDS | N/A | Flash Point | 191.2ºC | |
| Name | 2-pyridin-4-ylchromen-4-one |
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| Synonym | More Synonyms |
| Density | 1.294g/cm3 |
|---|---|
| Boiling Point | 392.5ºC at 760mmHg |
| Molecular Formula | C14H9NO2 |
| Molecular Weight | 223.22700 |
| Flash Point | 191.2ºC |
| Exact Mass | 223.06300 |
| PSA | 43.10000 |
| LogP | 2.85500 |
| Index of Refraction | 1.641 |
| InChIKey | WTKMIKUCGVSMDD-UHFFFAOYSA-N |
| SMILES | O=c1cc(-c2ccncc2)oc2ccccc12 |
| HS Code | 2934999090 |
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~96%
4H-1-Benzopyran... CAS#:3034-16-0 |
| Literature: RESVERLOGIX CORP.; JOHANSSON, Jan, O.; HANSEN, Henrik, C.; CHIACCHIA, Fabrizio, S.; WONG, Norman, C.W. Patent: WO2007/16525 A2, 2007 ; Location in patent: Page/Page column 60 ; WO 2007/016525 A2 |
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4H-1-Benzopyran... CAS#:3034-16-0 |
| Literature: Dyrager, Christine; Moellers, Linda Nilsson; Kjaell, Linda Karlsson; Alao, John Patrick; Diner, Peter; Wallner, Fredrik K.; Sunnerhagen, Per; Grotil, Morten Journal of Medicinal Chemistry, 2011 , vol. 54, # 20 p. 7427 - 7431 |
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4H-1-Benzopyran... CAS#:3034-16-0 |
| Literature: Springsteel, Mark F.; Galietta, Luis J. V.; Ma, Tonghui; By, Kolbot; Berger, Gideon O.; Yang, Hong; Dicus, Christopher W.; Choung, Wonken; Quan, Chao; Shelat, Anang A.; Guy, R. Kiplin; Verkman; Kurth, Mark J.; Nantz, Michael H. Bioorganic and Medicinal Chemistry, 2003 , vol. 11, # 18 p. 4113 - 4120 |
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4H-1-Benzopyran... CAS#:3034-16-0 |
| Literature: Springsteel, Mark F.; Galietta, Luis J. V.; Ma, Tonghui; By, Kolbot; Berger, Gideon O.; Yang, Hong; Dicus, Christopher W.; Choung, Wonken; Quan, Chao; Shelat, Anang A.; Guy, R. Kiplin; Verkman; Kurth, Mark J.; Nantz, Michael H. Bioorganic and Medicinal Chemistry, 2003 , vol. 11, # 18 p. 4113 - 4120 |
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~%
4H-1-Benzopyran... CAS#:3034-16-0 |
| Literature: Dyrager, Christine; Moellers, Linda Nilsson; Kjaell, Linda Karlsson; Alao, John Patrick; Diner, Peter; Wallner, Fredrik K.; Sunnerhagen, Per; Grotil, Morten Journal of Medicinal Chemistry, 2011 , vol. 54, # 20 p. 7427 - 7431 |
| HS Code | 2934999090 |
|---|---|
| Summary | 2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
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Name: Primary cell-based high-throughput screening assay for identification of compounds th...
Source: Johns Hopkins Ion Channel Center
Target: regulator of G-protein signaling 4 isoform 2 [Homo sapiens]
External Id: JHICC_RGS_Act_HTS
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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: Luminescence Cell-Free Homogeneous Counter Screen to Identify Inhibitors of ADP-glo R...
Source: Broad Institute
Target: N/A
External Id: 2046-03_INHIBITORS_DOSE-TITRATION_MLPCN-CHERRYPICK
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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: uHTS identification of small molecule activators of the adaptive arm of the Unfolded ...
Source: Burnham Center for Chemical Genomics
Target: N/A
External Id: BCCG-A405-UPR-XBP1-PrimaryAgonist-Assay
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Name: A screen for compounds that inhibit the activity of LtaS in Staphylococcus aureus
Source: ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id: HMS979
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Name: High throughput fluorescence intensity-based biochemical assay to screen for small mo...
Source: University of Pittsburgh Molecular Library Screening Center
Target: furin (paired basic amino acid cleaving enzyme), isoform CRA_a [Homo sapiens]
External Id: MH080376 Biochemical HTS for Inhibitors of the Proprotein Convertase Furin.
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Name: Luminescence Cell-Free Homogeneous Dose Retest to Identify Inhibitors of Glycogen Syn...
Source: Broad Institute
Target: glycogen synthase kinase 3 beta isoform 1 [Homo sapiens]
External Id: 2046-02_INHIBITORS_DOSE-TITRATION_MLPCN-CHERRYPICK
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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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| 2-<4-Pyridyl>-chromon |