Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C14H20N2 |
| Molecular Weight | 216.322 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)(C)CCC#C[C@H]1C[C@@H]1C2=CNC=N2
InChI
InChIKey=CVKJAXCQPFOAIN-RYUDHWBXSA-N
InChI=1S/C14H20N2/c1-14(2,3)7-5-4-6-11-8-12(11)13-9-15-10-16-13/h9-12H,5,7-8H2,1-3H3,(H,15,16)/t11-,12-/m0/s1
| Molecular Formula | C14H20N2 |
| Molecular Weight | 216.322 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| G protein-dependent pharmacology of histamine H3 receptor ligands: evidence for heterogeneous active state receptor conformations. | 2005-07 |
|
| Characteristics of recombinantly expressed rat and human histamine H3 receptors. | 2002-10-18 |
|
| Differential in vivo effects of H3 receptor ligands in a new mouse dipsogenia model. | 2002-06 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:51:24 GMT 2025
by
admin
on
Mon Mar 31 22:51:24 GMT 2025
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| Record UNII |
D65M9I0R5X
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| Record Status |
Validated (UNII)
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| Record Version |
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D65M9I0R5X
Created by
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DTXSID201167209
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223420-11-9
Created by
admin on Mon Mar 31 22:51:24 GMT 2025 , Edited by admin on Mon Mar 31 22:51:24 GMT 2025
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10512919
Created by
admin on Mon Mar 31 22:51:24 GMT 2025 , Edited by admin on Mon Mar 31 22:51:24 GMT 2025
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| Related Record | Type | Details | ||
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ACTIVE MOIETY |
