MedKoo Cat#: 526149 | Name: Ro 14-7437

Description:

WARNING: This product is for research use only, not for human or veterinary use.

Ro 14-7437 is a GABA-benzodiazepine receptor antagonist.

Chemical Structure

Ro 14-7437
Ro 14-7437
CAS#78756-03-3

Theoretical Analysis

MedKoo Cat#: 526149

Name: Ro 14-7437

CAS#: 78756-03-3

Chemical Formula: C15H15N3O3

Exact Mass: 285.1113

Molecular Weight: 285.30

Elemental Analysis: C, 63.15; H, 5.30; N, 14.73; O, 16.82

Price and Availability

This product is currently not in stock but may be available through custom synthesis. To ensure cost efficiency, the minimum order quantity is 1 gram. The estimated lead time is 2 to 4 months, with pricing dependent on the complexity of the synthesis (typically high for intricate chemistries). Quotes for quantities below 1 gram will not be provided. To request a quote, please click the button below. Note: If this product becomes available in stock in the future, pricing will be listed accordingly.
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Related CAS #
No Data
Synonym
Ro 14-7437; Ro 147437; Ro-14-7437.
IUPAC/Chemical Name
4H-Imidazo(1,5-a)(1,4)benzodiazepine-3-carboxylic acid, 5,6-dihydro-5-methyl-6-oxo-, ethyl ester
InChi Key
HNGRWUCKESPKRC-UHFFFAOYSA-N
InChi Code
InChI=1S/C15H15N3O3/c1-3-21-15(20)13-12-8-17(2)14(19)10-6-4-5-7-11(10)18(12)9-16-13/h4-7,9H,3,8H2,1-2H3
SMILES Code
O=C(C1=C(CN2C)N(C=N1)C3=CC=CC=C3C2=O)OCC
Appearance
Solid powder
Purity
>98% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility
Soluble in DMSO
Shelf Life
>2 years if stored properly
Drug Formulation
This drug may be formulated in DMSO
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.9001
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 285.30 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
1: Harris BD, Moody EJ, Gu ZQ, Skolnick P. Contribution of "diazepam-insensitive" GABAA receptors to the alcohol antagonist properties of Ro 15-4513 and related imidazobenzodiazepines. Pharmacol Biochem Behav. 1995 Sep;52(1):113-8. PubMed PMID: 7501652. 2: Püspök A, Herneth A, Steindl P, Ferenci P. Hepatic encephalopathy in rats with thioacetamide-induced acute liver failure is not mediated by endogenous benzodiazepines. Gastroenterology. 1993 Sep;105(3):851-7. PubMed PMID: 8359654. 3: Basile AS, Gammal SH, Mullen KD, Jones EA, Skolnick P. Differential responsiveness of cerebellar Purkinje neurons to GABA and benzodiazepine receptor ligands in an animal model of hepatic encephalopathy. J Neurosci. 1988 Jul;8(7):2414-21. PubMed PMID: 2854841. 4: Laurent JP. [Pharmacologic bases of the action of benzodiazepine ligands]. Rev Med Suisse Romande. 1987 Sep;107(9):711-5. Review. French. PubMed PMID: 2827289. 5: Nistri A, Berti C. GABA-induced depolarizing responses of the frog spinal cord can be either enhanced or antagonized by the benzodiazepine midazolam and the methylxanthine caffeine. Neurosci Lett. 1984 Jun 29;47(3):277-81. PubMed PMID: 6089044. 6: Krespan B, Springfield SA, Haas H, Geller HM. Electrophysiological studies on benzodiazepine antagonists. Brain Res. 1984 Mar 19;295(2):265-74. PubMed PMID: 6424866. 7: Nistri A, Berti C. Potentiating action of midazolam on GABA-mediated responses and its antagonism by Ro 14-7437 in the frog spinal cord. Neurosci Lett. 1983 Aug 29;39(2):199-204. PubMed PMID: 6605499. 8: Carlen PL, Gurevich N, Polc P. The excitatory effects of the specific benzodiazepine antagonist Ro14-7437, measured intracellularly in hippocampal CA1 cells. Brain Res. 1983 Jul 18;271(1):115-9. PubMed PMID: 6883110.