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Details

Stereochemistry ACHIRAL
Molecular Formula C20H19N7O2
Molecular Weight 389.4106
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SCH-442416

SMILES

COC1=CC=C(CCCN2N=CC3=C2N=C(N)N4N=C(N=C34)C5=CC=CO5)C=C1

InChI

InChIKey=AEULVFLPCJOBCE-UHFFFAOYSA-N
InChI=1S/C20H19N7O2/c1-28-14-8-6-13(7-9-14)4-2-10-26-18-15(12-22-26)19-23-17(16-5-3-11-29-16)25-27(19)20(21)24-18/h3,5-9,11-12H,2,4,10H2,1H3,(H2,21,24)

HIDE SMILES / InChI

Molecular Formula C20H19N7O2
Molecular Weight 389.4106
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

SCH-442416 is a selective antagonist of the adenosine A2a receptor with a Ki of 0.48 nM. It was first designed and developed as an [11C] radioisotope for PET imaging and has seen some use as an investigational and diagnostic tool, including one human study (see: SCH-442416 C-11). The non-radiolabeled compound has garnered less interest. SCH-442416 has been investigated in rats as a treatment for learned cocaine addiction; However, another study in rats indicates that SCH-442416 upregulates expression of glutamate synthase (GS) and glutamate aspartate transporter (GAST) in Muller Cells which can exacerbate conditions such as Ocular Hypertension.

CNS Activity

Curator's Comment: CNS activity was demonstrated in rats.

Originator

Curator's Comment: SCH-442416 was first designed and developed as an [11C] PET imaging label, which is annotated under its own entry SCH-442416 C-11.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: P29274
Gene ID: 135.0
Gene Symbol: ADORA2A
Target Organism: Homo sapiens (Human)
0.48 nM [Ki]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
Diagnostic
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Protective roles of adenosine A1, A2A, and A3 receptors in skeletal muscle ischemia and reperfusion injury.
2007 Dec
Brain adenosine A2A receptor occupancy by a novel A1/A2A receptor antagonist, ASP5854, in rhesus monkeys: relationship to anticataleptic effect.
2008 Jul
Synthesis and evaluation of 1,2,4-triazolo[1,5-c]pyrimidine derivatives as A2A receptor-selective antagonists.
2010 Oct 1
Patents

Sample Use Guides

Rats were allowed to self-administer cocaine on a fixed daily ratio over a period of 3 weeks (learning to push a button to receive cocaine). After one week of withdrawal, the effect of SCH-442416 on adenosine receptor modulation was tested against reinstatement to cocaine seeking induced by cues, cocaine, and the dopamine D2 receptor agonist, quinpirole. SCH-442416 was dissolved in dissolved in 33% DMSO and 66% ddH20 and administered by intraperitoneal injection as a dose of 0.3 mg/kg, 1 mg/kg, and 3 mg/kg and administered prior to each extinction training session. Administration of SCH 442416 had no direct effects on the extinction of learned behavior but did produce a dose-dependent persistent impairment of cocaine- and quinpirole-induced seeking.
Route of Administration: Intraperitoneal
Rat retinal Müller cells were treated with 0.1, 1, 10 uM SCH-442416 for 24 hours at hydrostatic pressures of 0, 20, 40, 60, 80 mmHg. Expression of glutamine synthetase (GS) and glutamate aspartate transporter (GLAST) was monitored using real-time PCR and Western Blotting. A significant increase in expression of GS and GLAST was observed at 40 mmHg pressure and expression was further enhanced by treatment with 10 uM SCH-442416 at 40 mmHg pressure.
Substance Class Chemical
Created
by admin
on Sat Dec 16 07:09:33 GMT 2023
Edited
by admin
on Sat Dec 16 07:09:33 GMT 2023
Record UNII
ZMC4G1W59S
Record Status Validated (UNII)
Record Version
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Name Type Language
SCH-442416
Common Name English
SCH-442,416
Code English
7H-PYRAZOLO(4,3-E)(1,2,4)TRIAZOLO(1,5-C)PYRIMIDIN-5-AMINE, 2-(2-FURANYL)-7-(3-(4-METHOXYPHENYL)PROPYL)-
Systematic Name English
Code System Code Type Description
PUBCHEM
10668061
Created by admin on Sat Dec 16 07:09:33 GMT 2023 , Edited by admin on Sat Dec 16 07:09:33 GMT 2023
PRIMARY
EPA CompTox
DTXSID70443263
Created by admin on Sat Dec 16 07:09:33 GMT 2023 , Edited by admin on Sat Dec 16 07:09:33 GMT 2023
PRIMARY
WIKIPEDIA
SCH-442,416
Created by admin on Sat Dec 16 07:09:33 GMT 2023 , Edited by admin on Sat Dec 16 07:09:33 GMT 2023
PRIMARY
FDA UNII
ZMC4G1W59S
Created by admin on Sat Dec 16 07:09:33 GMT 2023 , Edited by admin on Sat Dec 16 07:09:33 GMT 2023
PRIMARY
CAS
316173-57-6
Created by admin on Sat Dec 16 07:09:33 GMT 2023 , Edited by admin on Sat Dec 16 07:09:33 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY