U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C6H5N5O2
Molecular Weight 179.1362
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of XANTHOPTERIN

SMILES

NC1=NC2=C(NC(=O)C=N2)C(=O)N1

InChI

InChIKey=VURKRJGMSKJIQX-UHFFFAOYSA-N
InChI=1S/C6H5N5O2/c7-6-10-4-3(5(13)11-6)9-2(12)1-8-4/h1H,(H,9,12)(H3,7,8,10,11,13)

HIDE SMILES / InChI

Molecular Formula C6H5N5O2
Molecular Weight 179.1362
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Cytotoxicity of xanthopterin and isoxanthopterin in MCF-7 cells.
2005 May 10
Abstracts of papers presented at the 2007 pittsburgh conference.
2007
Effect of methyl substitution in a ligand on the selectivity and binding affinity for a nucleobase: a case study with isoxanthopterin and its derivatives.
2009 Jan 1
Xanthopterin in the Oriental hornet (Vespa orientalis): light absorbance is increased with maturation of yellow pigment granules.
2009 Jul-Aug
Conformational heterogeneity and quasi-static self-quenching in DNA containing a fluorescent guanine analogue, 3MI or 6MI.
2009 Sep 22
[Determination of isoxanthopterin in human urine by solid phase extraction-high performance anion-exchange chromatography coupled with integrated pulsed amperometric detection].
2010 Apr
Substance Class Chemical
Created
by admin
on Fri Dec 15 18:44:57 GMT 2023
Edited
by admin
on Fri Dec 15 18:44:57 GMT 2023
Record UNII
V66551EU1R
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
XANTHOPTERIN
MART.   MI   WHO-DD  
INCI  
Official Name English
XANTHOPTERIN [MI]
Common Name English
XANTHOPTERIN [MART.]
Common Name English
NSC-41836
Code English
Xanthopterin [WHO-DD]
Common Name English
2-AMINO-4,6-DIHYDROXYPTERIDINE
Systematic Name English
Classification Tree Code System Code
LOINC 80183-7
Created by admin on Fri Dec 15 18:44:57 GMT 2023 , Edited by admin on Fri Dec 15 18:44:57 GMT 2023
LOINC 80184-5
Created by admin on Fri Dec 15 18:44:57 GMT 2023 , Edited by admin on Fri Dec 15 18:44:57 GMT 2023
LOINC 80185-2
Created by admin on Fri Dec 15 18:44:57 GMT 2023 , Edited by admin on Fri Dec 15 18:44:57 GMT 2023
Code System Code Type Description
SMS_ID
100000076729
Created by admin on Fri Dec 15 18:44:57 GMT 2023 , Edited by admin on Fri Dec 15 18:44:57 GMT 2023
PRIMARY
ECHA (EC/EINECS)
204-325-0
Created by admin on Fri Dec 15 18:44:57 GMT 2023 , Edited by admin on Fri Dec 15 18:44:57 GMT 2023
PRIMARY
MESH
D014976
Created by admin on Fri Dec 15 18:44:57 GMT 2023 , Edited by admin on Fri Dec 15 18:44:57 GMT 2023
PRIMARY
FDA UNII
V66551EU1R
Created by admin on Fri Dec 15 18:44:57 GMT 2023 , Edited by admin on Fri Dec 15 18:44:57 GMT 2023
PRIMARY
NSC
41836
Created by admin on Fri Dec 15 18:44:57 GMT 2023 , Edited by admin on Fri Dec 15 18:44:57 GMT 2023
PRIMARY
MERCK INDEX
m11532
Created by admin on Fri Dec 15 18:44:57 GMT 2023 , Edited by admin on Fri Dec 15 18:44:57 GMT 2023
PRIMARY Merck Index
EVMPD
SUB15734MIG
Created by admin on Fri Dec 15 18:44:57 GMT 2023 , Edited by admin on Fri Dec 15 18:44:57 GMT 2023
PRIMARY
PUBCHEM
135403800
Created by admin on Fri Dec 15 18:44:57 GMT 2023 , Edited by admin on Fri Dec 15 18:44:57 GMT 2023
PRIMARY
EPA CompTox
DTXSID70152282
Created by admin on Fri Dec 15 18:44:57 GMT 2023 , Edited by admin on Fri Dec 15 18:44:57 GMT 2023
PRIMARY
CAS
119-44-8
Created by admin on Fri Dec 15 18:44:57 GMT 2023 , Edited by admin on Fri Dec 15 18:44:57 GMT 2023
PRIMARY
WIKIPEDIA
XANTHOPTERIN
Created by admin on Fri Dec 15 18:44:57 GMT 2023 , Edited by admin on Fri Dec 15 18:44:57 GMT 2023
PRIMARY