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Merck
CN

Q3504

Quazinone

powder

Synonym(s):

Ro 13-6438

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About This Item

Empirical Formula (Hill Notation):
C11H10ClN3O
CAS Number:
Molecular Weight:
235.67
UNSPSC Code:
41106305
PubChem Substance ID:
MDL number:
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assay

≥98% (TLC)

form

powder

color

white

solubility

ethanol: 1 mg/mL

SMILES string

C[C@H]1N2Cc3c(Cl)cccc3N=C2NC1=O

InChI

1S/C11H10ClN3O/c1-6-10(16)14-11-13-9-4-2-3-8(12)7(9)5-15(6)11/h2-4,6H,5H2,1H3,(H,13,14,16)/t6-/m1/s1

InChI key

BHZFZYLBVSWUMT-ZCFIWIBFSA-N

Gene Information

Biochem/physiol Actions

Phosphodiesterase III (PDE3) inhibitor.

Features and Benefits

This compound was developed by Roche. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.


Storage Class

13 - Non Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

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M Komajda et al.
Fundamental & clinical pharmacology, 1(6), 459-470 (1987-01-01)
The dose-response for the new cardiotonic agent RO13-6438 was studied in 6 patients with grade III or IV congestive heart failure. Oral doses of 10, 20, or 30 mg of RO 13-6438 were administered on 3 consecutive days in accordance
C A Simonton et al.
Chest, 92(1), 118-123 (1987-07-01)
Survival in severe left ventricular failure is poor but has not been widely assessed since the introduction of several new nonglycosidic, nonsympathomimetic oral inotropic agents for long-term therapy. We examined retrospectively the survival of 82 patients with severe left heart
S Braun et al.
Drugs under experimental and clinical research, 12(5), 381-384 (1986-01-01)
The chemical class 1,5 dihydroimidazo (2,1-6) guinazolin-2(3H)ones has been shown to have positive inotropic activity, some of its members displaying a favourable ratio between positive inotropic and chronotropic activity. This study was designed to determine the cardiovascular properties of Ro