Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C19H24N2O2 |
| Molecular Weight | 312.4061 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC(OC(C)CNC(=N)CC2=CC=CC(C)=C2)=CC=C1
InChI
InChIKey=JRYTUFKIORWTNI-UHFFFAOYSA-N
InChI=1S/C19H24N2O2/c1-14-6-4-7-16(10-14)11-19(20)21-13-15(2)23-18-9-5-8-17(12-18)22-3/h4-10,12,15H,11,13H2,1-3H3,(H2,20,21)
| Molecular Formula | C19H24N2O2 |
| Molecular Weight | 312.4061 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| 5-HT activates vagal afferent cell bodies in vivo: role of 5-HT2 and 5-HT3 receptors. | 2006-11-17 |
|
| Differential effects of nitroblue tetrazolium on the hemodynamic responses elicited by activation of alpha1-adrenoceptors and 5-HT2 receptors in conscious rats. | 2006-03-27 |
|
| Serotonin 2A receptors modulate tail-skin temperature in two rodent models of estrogen deficiency-related thermoregulatory dysfunction. | 2004-12-03 |
|
| Role of central 5-HT2 receptors in mediating head bobs and body shakes in the rabbit. | 2004-03 |
|
| Neurogenic dural protein extravasation induced by meta-chlorophenylpiperazine (mCPP) involves nitric oxide and 5-HT2B receptor activation. | 2003-03 |
|
| Central and peripheral injections of the 5-HT2 agonist, 1-(2,5-dimethoxy-4-iodophenyl)-2-aminopropane, modify cardiovascular function through different mechanisms. | 1991-12 |
|
| Effects of xylamidine on peripheral 5-hydroxytryptamine-induced anorexia. | 1989-12 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:38:16 GMT 2025
by
admin
on
Mon Mar 31 18:38:16 GMT 2025
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| Record UNII |
NY0PC84NZK
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| Record Status |
Validated (UNII)
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| Record Version |
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-
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Preferred Name | English | ||
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Common Name | English | ||
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Systematic Name | English |
| Code System | Code | Type | Description | ||
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6443-50-1
Created by
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22951
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C005894
Created by
admin on Mon Mar 31 18:38:16 GMT 2025 , Edited by admin on Mon Mar 31 18:38:16 GMT 2025
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NY0PC84NZK
Created by
admin on Mon Mar 31 18:38:16 GMT 2025 , Edited by admin on Mon Mar 31 18:38:16 GMT 2025
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DTXSID90863843
Created by
admin on Mon Mar 31 18:38:16 GMT 2025 , Edited by admin on Mon Mar 31 18:38:16 GMT 2025
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XYLAMIDINE
Created by
admin on Mon Mar 31 18:38:16 GMT 2025 , Edited by admin on Mon Mar 31 18:38:16 GMT 2025
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PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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ENANTIOMER -> RACEMATE | |||
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SALT/SOLVATE -> PARENT | |||
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ENANTIOMER -> RACEMATE | |||
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SALT/SOLVATE -> PARENT |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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ACTIVE MOIETY |