Drug Information
| Drug General Information | |||||
|---|---|---|---|---|---|
| Drug ID |
D01RJV
|
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| Former ID |
DNC011838
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| Drug Name |
4-((2S,3R)-2-Methyl-pyrrolidin-3-yl)-1H-imidazole
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| Drug Type |
Small molecular drug
|
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| Indication | Discovery agent | Investigative | [1] | ||
| Structure |
|
Download2D MOL |
|||
| Formula |
C8H13N3
|
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| Canonical SMILES |
CC1C(CCN1)C2=CN=CN2
|
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| InChI |
1S/C8H13N3/c1-6-7(2-3-10-6)8-4-9-5-11-8/h4-7,10H,2-3H2,1H3,(H,9,11)/t6-,7+/m0/s1
|
||||
| InChIKey |
FLOJCNYYPGNYBP-NKWVEPMBSA-N
|
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| PubChem Compound ID | |||||
| Target and Pathway | |||||
| Target(s) | Histamine H3 receptor | Target Info | Inhibitor | [1] | |
| KEGG Pathway | Neuroactive ligand-receptor interaction | ||||
| Reactome | Histamine receptors | ||||
| G alpha (i) signalling events | |||||
| WikiPathways | Monoamine Transport | ||||
| GPCRs, Class A Rhodopsin-like | |||||
| GPCR ligand binding | |||||
| GPCR downstream signaling | |||||
| References | |||||
| REF 1 | J Med Chem. 1995 May 12;38(10):1593-9.A novel pyrrolidine analog of histamine as a potent, highly selective histamine H3 receptor agonist. | ||||
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