3H-Imidazo[4,5-c]pyridine,4,5,6,7-tetrahydro-4-phenyl
Modify Date: 2025-09-14 07:49:20
![3H-Imidazo[4,5-c]pyridine,4,5,6,7-tetrahydro-4-phenyl Structure](https://image.chemsrc.com/caspic/302/4875-39-2.png)
3H-Imidazo[4,5-c]pyridine,4,5,6,7-tetrahydro-4-phenyl structure
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Common Name | 3H-Imidazo[4,5-c]pyridine,4,5,6,7-tetrahydro-4-phenyl | ||
|---|---|---|---|---|
| CAS Number | 4875-39-2 | Molecular Weight | 199.25200 | |
| Density | 1.185g/cm3 | Boiling Point | 437ºC at 760mmHg | |
| Molecular Formula | C12H13N3 | Melting Point | N/A | |
| MSDS | N/A | Flash Point | 218.1ºC | |
| Name | 4-phenyl-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridine |
|---|---|
| Synonym | More Synonyms |
| Density | 1.185g/cm3 |
|---|---|
| Boiling Point | 437ºC at 760mmHg |
| Molecular Formula | C12H13N3 |
| Molecular Weight | 199.25200 |
| Flash Point | 218.1ºC |
| Exact Mass | 199.11100 |
| PSA | 40.71000 |
| LogP | 1.97360 |
| Index of Refraction | 1.616 |
| InChIKey | SHIJOLLBBCZWON-UHFFFAOYSA-N |
| SMILES | c1ccc(C2NCCc3[nH]cnc32)cc1 |
| HS Code | 2933990090 |
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| HS Code | 2933990090 |
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| Summary | 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. 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: 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: Antibacterial activity against Klebsiella pneumoniae MDR ATCC 70063 (CO-ADD:GN_003); ...
Source: ChEMBL
Target: Klebsiella pneumoniae
External Id: CHEMBL4296186
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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: 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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| 4-phenylspinaceamine |
| 7-Phenyl-4,5,6,7-tetrahydro-imidazo<5,4-c>pyridin |
| 4-phenyl-4,5,6,7-tetrahydroimidazo<4,5-c>pyridine |
| 4-Phenyl-4,5,6,7-tetrahydro-3H-imidazo<4,5-c>pyridin |
| 7-Phenylspinaceamin |