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Details

Stereochemistry RACEMIC
Molecular Formula C19H24N2O2.C7H8O3S
Molecular Weight 484.608
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of XYLAMIDINE TOSYLATE ANHYDROUS

SMILES

CC1=CC=C(C=C1)S(O)(=O)=O.COC2=CC=CC(OC(C)CNC(=N)CC3=CC=CC(C)=C3)=C2

InChI

InChIKey=FRJLUWKYXWADTA-UHFFFAOYSA-N
InChI=1S/C19H24N2O2.C7H8O3S/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;1-6-2-4-7(5-3-6)11(8,9)10/h4-10,12,15H,11,13H2,1-3H3,(H2,20,21);2-5H,1H3,(H,8,9,10)

HIDE SMILES / InChI

Molecular Formula C7H8O3S
Molecular Weight 172.202
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

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 ( + / - )

Xylamidine is a peripherally-restricted antagonist of 5HT2A and 5HT1A receptor. It is used to study the role of the serotonin receptors in the regulation of food intake, cardiovascular function, and regulation of body temperature.

Approval Year

PubMed

PubMed

TitleDatePubMed
Effects of xylamidine on peripheral 5-hydroxytryptamine-induced anorexia.
1989 Dec
Central and peripheral injections of the 5-HT2 agonist, 1-(2,5-dimethoxy-4-iodophenyl)-2-aminopropane, modify cardiovascular function through different mechanisms.
1991 Dec
Neurogenic dural protein extravasation induced by meta-chlorophenylpiperazine (mCPP) involves nitric oxide and 5-HT2B receptor activation.
2003 Mar
Serotonin 2A receptors modulate tail-skin temperature in two rodent models of estrogen deficiency-related thermoregulatory dysfunction.
2004 Dec 3
Role of central 5-HT2 receptors in mediating head bobs and body shakes in the rabbit.
2004 Mar
Differential effects of nitroblue tetrazolium on the hemodynamic responses elicited by activation of alpha1-adrenoceptors and 5-HT2 receptors in conscious rats.
2006 Mar 27
5-HT activates vagal afferent cell bodies in vivo: role of 5-HT2 and 5-HT3 receptors.
2006 Nov 17
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:34:47 GMT 2023
Edited
by admin
on Fri Dec 15 17:34:47 GMT 2023
Record UNII
4ZF9UZ56C7
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
XYLAMIDINE TOSYLATE ANHYDROUS
Common Name English
XYLAMIDE TOSILATE
Common Name English
N-(2-(M-METHOXYPHENOXY)PROPYL)-2-M-TOLYLACETAMIDINE MONO-P-TOLUENESULFONATE
Common Name English
XYLAMIDINE TOSILATE
INN  
INN  
Official Name English
XYLAMIDINE TOSYLATE
USAN  
USAN  
Official Name English
XYLAMIDINE TOSYLATE [USAN]
Common Name English
XYLAMIDINE TOSILATE ANHYDROUS
Common Name English
xylamidine tosilate [INN]
Common Name English
N-(2-(M-METHOXYPHENOXY)PROPYL)-2-M-TOLYLACETAMIDINE MONO-P-TOLUENESULPHONATE
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C66885
Created by admin on Fri Dec 15 17:34:47 GMT 2023 , Edited by admin on Fri Dec 15 17:34:47 GMT 2023
Code System Code Type Description
NCI_THESAURUS
C152937
Created by admin on Fri Dec 15 17:34:47 GMT 2023 , Edited by admin on Fri Dec 15 17:34:47 GMT 2023
PRIMARY
ChEMBL
CHEMBL2110630
Created by admin on Fri Dec 15 17:34:47 GMT 2023 , Edited by admin on Fri Dec 15 17:34:47 GMT 2023
PRIMARY
INN
2313
Created by admin on Fri Dec 15 17:34:47 GMT 2023 , Edited by admin on Fri Dec 15 17:34:47 GMT 2023
PRIMARY
CAS
6443-40-9
Created by admin on Fri Dec 15 17:34:47 GMT 2023 , Edited by admin on Fri Dec 15 17:34:47 GMT 2023
PRIMARY
SMS_ID
100000079381
Created by admin on Fri Dec 15 17:34:47 GMT 2023 , Edited by admin on Fri Dec 15 17:34:47 GMT 2023
PRIMARY
FDA UNII
4ZF9UZ56C7
Created by admin on Fri Dec 15 17:34:47 GMT 2023 , Edited by admin on Fri Dec 15 17:34:47 GMT 2023
PRIMARY
EVMPD
SUB00119MIG
Created by admin on Fri Dec 15 17:34:47 GMT 2023 , Edited by admin on Fri Dec 15 17:34:47 GMT 2023
PRIMARY
EPA CompTox
DTXSID00983001
Created by admin on Fri Dec 15 17:34:47 GMT 2023 , Edited by admin on Fri Dec 15 17:34:47 GMT 2023
PRIMARY
PUBCHEM
22950
Created by admin on Fri Dec 15 17:34:47 GMT 2023 , Edited by admin on Fri Dec 15 17:34:47 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
SOLVATE->ANHYDROUS
Related Record Type Details
ACTIVE MOIETY