CAS 204-02-4 | 1H-Perimidine | CAS Number 204-02-4

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204-02-4 | 1H-Perimidine

CAS No: 204-02-4 Catalog No: AG00298S MDL No:

Product Description

Catalog Number:

AG00298S

Chemical Name:

1H-Perimidine

CAS Number:

204-02-4

Molecular Formula:

C11H8N2

Molecular Weight:

168.1946

IUPAC Name:

1H-perimidine

InChI:

InChI=1S/C11H8N2/c1-3-8-4-2-6-10-11(8)9(5-1)12-7-13-10/h1-7H,(H,12,13)

InChI Key:

AAQTWLBJPNLKHT-UHFFFAOYSA-N

SMILES:

c1cc2cccc3c2c(c1)nc[nH]3

Properties

Complexity:

224

Compound Is Canonicalized:

Yes

Covalently-Bonded Unit Count:

Defined Atom Stereocenter Count:

Defined Bond Stereocenter Count:

Exact Mass:

168.069g/mol

Formal Charge:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Hydrogen Bond Donor Count:

Isotope Atom Count:

Molecular Weight:

168.199g/mol

Monoisotopic Mass:

168.069g/mol

Rotatable Bond Count:

Topological Polar Surface Area:

24.4A^2

Undefined Atom Stereocenter Count:

Undefined Bond Stereocenter Count:

XLogP3:

2.1

Literature

Title	Journal
Life span extension of Caenorhabditis elegans by novel pyridoperimidine derivative.	Archives of pharmacal research 20120101
Synthesis and structure of 2-pyransoylperimidines.	Carbohydrate research 20110103
Synthesis and cytotoxic activity of N-[(alkylamino)alkyl]carboxamide derivatives of 7-oxo-7H-benz[de]anthracene, 7-oxo-7H-naphtho[1,2,3-de]quinoline, and 7-oxo-7H-benzo[e]perimidine.	Bioorganic & medicinal chemistry 20050601
The activity of latent benzoperimidine esters to inhibit P-glycoprotein and multidrug resistance-associated protein 1 dependent efflux of pirarubicin from several lines of multidrug resistant tumor cells.	Cancer detection and prevention 20040101
Effect of modification of 6-[(aminoalkyl)amino]-7H-benzo[e]-perimidin-7-ones on their cytotoxic activity toward sensitive and multidrug resistant tumor cell lines. Synthesis and biological evaluation.	Bioorganic & medicinal chemistry 20020401
Transport of new non-cross-resistant antitumor compounds of the benzoperimidine family in multidrug resistant cells.	European journal of pharmacology 20010216