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Pyrimido(5,4-d)pyrimidine, ethanol deriv.

HCID 124165
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Basic information

CAS
54093-30-0
Standard SMILES
CCN(CC)c1nc(N(CCO)CCOC)nc2c(N(CC)CC)nc(N(CCO)CCOC)nc12
InChIKey
ROFXYKJBKWRUBS-UHFFFAOYSA-N
Molecular formula
C24H44N8O4
Average molar mass
508.7 g/mol
Monoisotopic mass
508.34855191

Overview

has central hypertensive properties; structure

Names & identifiers

Preferred name
Pyrimido(5,4-d)pyrimidine, ethanol deriv.
IUPAC
2-[[4,8-bis(diethylamino)-2-[2-hydroxyethyl(2-methoxyethyl)amino]pyrimido[5,4-d]pyrimidin-6-yl]-(2-methoxyethyl)amino]ethanol
English name
RA 642
Molecular formula
C24H44N8O4
Molecular weight
508.66

Names & synonyms

RA 64254093-30-0RA-642DTXSID902024302,2'-((4,8-Bis(diethylamino)pyrimido(5,4-d)pyrimidine-2,6-diyl)bis((2-methoxyethyl)imino))bisethanolRefChem:930379DTXCID90124921Pyrimido(5,4-d)pyrimidine, ethanol deriv.RA6422-[[4,8-bis(diethylamino)-2-[2-hydroxyethyl(2-methoxyethyl)amino]pyrimido[5,4-d]pyrimidin-6-yl]-(2-methoxyethyl)amino]ethanol(2,2'-(4,8-bis(diethylamino)pyrimido(5,4-d)pyrimidine-2,6-diyl)di(2-methoxyethyl)imino)diethanol2,2'-((4,8-bis(diethylamino)pyrimido[5,4-d]pyrimidine-2,6-diyl)bis((2-methoxyethyl)azanediyl))bis(ethan-1-ol)
Show more names
RXRA-642RA-642BS2,2'-[4,8-Bis(diethylamino)pyrimido[5,4-d]pyrimidine-2,6-diyl]bis[(2-methoxyethyl)imino]bisethanolEthanol, 2,2'-[[4,8-bis(diethylamino)pyrimido[5,4-d]pyrimidine-2,6-diyl]bis[(2-methoxyethyl)imino]]bis-
RA 642BSRXRA 642orb1701733SCHEMBL9668239SCHEMBL30066743AKOS040747340Ethanol, 2,2'-((4,8-bis(diethylamino)pyrimido(5,4-d)pyrimidine-2,6-diyl)bis((2-methoxyethyl)imino))bis-CS-0077547

Properties

Computed structural properties

XLogP
1.5
Topological polar surface area
123 Ų
Hydrogen bond donors
2
Hydrogen bond acceptors
12
Rotatable bonds
18
Heavy atoms
36
Formal charge
0
Complexity
524

Chemistry & industry

Applications · 2 items

DescriptionRA 642 is a PDE-inhibitor.

UsesRA642 is a compound with vasodilatory and hypertensive effects, with the activity of increasing arterial blood pressure, enhancing cerebral blood flow, reducing cerebrovascular resistance and peripheral resistance, and having a papaverine-like relaxant effect on smooth muscle in anesthetized animals.

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On this pageBasic informationOverviewNames & identifiersPropertiesChemistry & industryRelated reactionsCompound notes

Database identifiers

CAS
54093-30-0
PubChem CID
124165
DTXSID
DTXSID90202430
Nikkaji
J23.734E