Company Name: |
3B Pharmachem (Wuhan) International Co.,Ltd.
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Tel: |
821-50328103-801 18930552037 |
Email: |
3bsc@sina.com |
Products Intro: |
Product Name:Devazepide;N-[(3S)-2,3-Dihydro-1-Methyl-2-oxo-5-phenyl-1H-1,4-benzodiazepin-3-yl]-1H-indole-2-carboxaMide CAS:103420-77-5 Purity:99% HPLC Package:1Mg ; 5Mg;10Mg ;100Mg;250Mg ;500Mg ;1g;2.5g ;5g ;10g
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Company Name: |
Sigma-Aldrich
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Tel: |
021-61415566 800-8193336 |
Email: |
orderCN@merckgroup.com |
Products Intro: |
Product Name:Devazepide CAS:103420-77-5 Purity:>=98% (HPLC) Package:5mg, 25mg Remarks:D3821
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Company Name: |
EMMX Biotechnology LLC
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Tel: |
888-539-0666 |
Email: |
info@emmx.com |
Products Intro: |
Product Name:Devazepide CAS:103420-77-5 Purity:98% HPLC Package:5mg;10mg;25mg;50mg;100mg;250mg;500mg;1g
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| DEVAZEPIDE Basic information |
Product Name: | DEVAZEPIDE | Synonyms: | N-[(3S)-2,3-DIHYDRO-1-METHYL-2-OXO-5-PHENYL-1H-1,4-BENZODIAZEPIN-3-YL]-1H-INDOLE-2-CARBOXAMIDE;DEVAZEPIDE;EVAZEPIDE, PANOS;(3S)-1-Methyl-3-[(1H-indol-2-yl)carbonylamino]-5-phenyl-1H-1,4-benzodiazepin-2(3H)-one;L-364718;MK-329;(S)-N-(2,3-Dihydro-1-methyl-2-oxo-5-phenyl-1H-1,4-benzodiazepin-3-yl)indole-2-carboxamide;1H-Indole-2-carboxamide, N-[(3S)-2,3-dihydro-1-methyl-2-oxo-5-phenyl-1H-1,4-benzodiazepin-3-yl]- | CAS: | 103420-77-5 | MF: | C25H20N4O2 | MW: | 408.45 | EINECS: | | Product Categories: | | Mol File: | 103420-77-5.mol | |
| DEVAZEPIDE Chemical Properties |
Boiling point | 758.6±60.0 °C(Predicted) | density | 1.31±0.1 g/cm3(Predicted) | storage temp. | 2-8°C | solubility | DMSO: >5mg/mL | pka | 13.25±0.40(Predicted) | form | powder | color | white to off-white |
Hazard Codes | T+ | Risk Statements | 28 | Safety Statements | 28-36/37-45 | RIDADR | UN 2811 6.1 / PGI | WGK Germany | 3 | RTECS | NL5994460 |
| DEVAZEPIDE Usage And Synthesis |
Uses | Antagonist (cholecystokinin). | Uses | Devazepide has been used as a cholecystokinin receptor 1 (CCK1R) antagonist in human embryonic kidney 293T cells and in human pancreatic slices. | Definition | ChEBI: An indolecarboxamide obtained by formal condensation of the carboxy group of indole-2-carboxylic acid with the exocyclic amino group of (3S)-3-amino-1-methyl-5-phenyl-1,3-dihydro-1,4-benzodiazepin-2-one. A cholecystokinin antagonist used f
r treatment of gastrointestinal disorders. | General Description | Devazepide is derived from asperlicin by chemical modification and has the benzodiazepine backbone. | Biochem/physiol Actions | Devazepide is a CCK1 (CCK-A) receptor antagonist and a CCK8 antagonist. | storage | Store at +4°C |
| DEVAZEPIDE Preparation Products And Raw materials |
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