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8-methoxy-5-phenyl-1,3-dihydrobenzo[e][1,4]diazepin-2-one is a complex organic compound belonging to the class of benzodiazepines. This molecule features a benzene ring fused to a diazepine ring, with a 1,3-dihydro structure indicating the presence of a single bond between the two carbons in the diazepine ring. The compound is characterized by a methoxy group at the 8-position and a phenyl group at the 5-position, which are both substituents attached to the benzene ring. The 2-one functional group indicates the presence of a carbonyl group at the 2-position of the diazepine ring. This chemical structure is significant in medicinal chemistry, as benzodiazepines are known for their anxiolytic, sedative, hypnotic, anticonvulsant, and muscle relaxant properties. The specific arrangement of functional groups in 8-methoxy-5-phenyl-1,3-dihydrobenzo[e][1,4]diazepin-2-one may confer unique pharmacological properties, making it a subject of interest for potential therapeutic applications.

5358-30-5

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5358-30-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5358-30-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,5 and 8 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5358-30:
(6*5)+(5*3)+(4*5)+(3*8)+(2*3)+(1*0)=95
95 % 10 = 5
So 5358-30-5 is a valid CAS Registry Number.

5358-30-5Relevant academic research and scientific papers

Novel benzo[1,4]diazepin-2-one derivatives as endothelin receptor antagonists

Bolli, Martin H.,Marfurt, Judith,Grisostomi, Corinna,Boss, Christoph,Binkert, Christoph,Hess, Patrick,Treiber, Alexander,Thorin, Eric,Morrison, Keith,Buchmann, Stephan,Bur, Daniel,Ramuz, Henri,Clozel, Martine,Fischli, Walter,Weller, Thomas

, p. 2776 - 2795 (2007/10/03)

Since its discovery in 1988 by Yanagisawa et al., endothelin (ET), a potent vasoconstrictor, has been widely implicated in the pathophysiology of cardiovascular, cerebrovascular, and renal diseases. Many research groups have embarked on the discovery and development of ET receptor antagonists for the treatment of such diseases. While several compounds, e.g., ambrisentan 2, are in late clinical trials for various indications, one compound (bosentan, Tracleer) is being marketed to treat pulmonary arterial hypertension. Inspired by the structure of ambrisentan 2, we designed a novel class of ET receptor antagonists based on a 1,3,4,5-tetrahydro-1H-benzo[e][1,4]diazepin-2-one scaffold. Here, we report on the preparation as well as the in vitro and in vivo structure-activity relationships of these derivatives. Potent dual ET A/ETB receptor antagonists with affinities in the low nanomolar range have been identified. In addition, several compounds efficiently reduced arterial blood pressure after oral administration to Dahl salt sensitive rats. In this animal model, the efficacy of the benzo[e] [1,4]diazepin-2-one derivative rac-39au was superior to that of racemic ambrisentan, rac-2.

Cyclic nucleotide phosphodiesterase inhibitors, preparation and uses thereof

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Page/Page column 25, (2010/02/08)

The invention concerns novel benzodiazepine derivatives and their uses in the field of therapeutics particularly for treating pathologies involving the activity of a cyclic nucleotide phosphodiesterase. It also concerns methods for preparing them and novel synthesis intermediates. The inventive compounds more particularly correspond to general formula (I):

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