MedKoo Cat#: 584696 | Name: MD 780236

Description:

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

MD 780236 is a monoamine oxidase-B inhibitor.

Chemical Structure

MD 780236
MD 780236
CAS#73423-36-6

Theoretical Analysis

MedKoo Cat#: 584696

Name: MD 780236

CAS#: 73423-36-6

Chemical Formula: C18H19ClN2O3

Exact Mass: 346.1084

Molecular Weight: 346.81

Elemental Analysis: C, 62.34; H, 5.52; Cl, 10.22; N, 8.08; O, 13.84

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
MD 780236; MD780236; MD-780236;
IUPAC/Chemical Name
2-Oxazolidinone, 3-(4-((3-chlorophenyl)methoxy)phenyl)-5-((methylamino)methyl)-
InChi Key
KYXSTSXVEXKFJI-UHFFFAOYSA-N
InChi Code
InChI=1S/C18H19ClN2O3/c1-20-10-17-11-21(18(22)24-17)15-5-7-16(8-6-15)23-12-13-3-2-4-14(19)9-13/h2-9,17,20H,10-12H2,1H3
SMILES Code
O=C1OC(CNC)CN1C2=CC=C(OCC3=CC=CC(Cl)=C3)C=C2
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
>3 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
2934.99.03.00
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 346.81 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: Tipton KF, Fowler CJ, McCrodden JM, Strolin Benedetti M. The enzyme-activated irreversible inhibition of type-B monoamine oxidase by 3-(4-[(3-chlorophenyl)methoxy]phenyl)-5-[(methylamino) methyl]-2-oxazolidinone methanesulphonate (compound MD 780236) and the enzyme-catalysed oxidation of this compound as competing reactions. Biochem J. 1983 Jan 1;209(1):235-42. PubMed PMID: 6847610; PubMed Central PMCID: PMC1154077. 2: Strolin Benedetti M, Dow J. A monoamine oxidase-B inhibitor, MD 780236, metabolized essentially by the A form of the enzyme in the rat. J Pharm Pharmacol. 1983 Apr;35(4):238-45. PubMed PMID: 6133934. 3: Dostert P, Guffroy C, Strolin Benedetti M, Boucher T. Inhibition of semicarbazide-sensitive amine oxidase by monoamine oxidase B inhibitors from the oxazolidinone series. J Pharm Pharmacol. 1984 Nov;36(11):782-5. PubMed PMID: 6150988. 4: Tipton KF, McCrodden JM, Henehan GT, Boucher T, Fowler CJ. The formation of the acidic and alcoholic metabolites of MD 780236. Biochem Pharmacol. 1984 Apr 15;33(8):1377-8. PubMed PMID: 6370268. 5: Dostert P, Strolin Benedetti M, Guffroy C. Different stereoselective inhibition of monoamine oxidase-B by the R- and S-enantiomers of MD 780236. J Pharm Pharmacol. 1983 Mar;35(3):161-5. PubMed PMID: 6132973. 6: Strolin Benedetti M, Dow J, Boucher T, Dostert P. Metabolism of the monoamine oxidase-B inhibitor, MD 780236 and its enantiomers by the A and B forms of the enzyme in the rat. J Pharm Pharmacol. 1983 Dec;35(12):837-40. PubMed PMID: 6141254. 7: Kinemuchi H, Morikawa F, Ueda T, Arai Y. Studies of monoamine oxidase and semicarbazide-sensitive amine oxidase. I. Inhibition by a selective monoamine oxidase-B inhibitor, MD 780236. Jpn J Pharmacol. 1986 Jun;41(2):183-9. PubMed PMID: 3747265. 8: Fuller RW, Wong CJ, Hemrick-Luecke SK. MD 240928 and harmaline: opposite selectivity in antagonism of the inactivation of types A and B monoamine oxidase by pargyline in mice. Life Sci. 1986 Feb 3;38(5):409-12. PubMed PMID: 3945167. 9: Fuller RW, Hemrick-Luecke SK. Influence of selective, reversible inhibitors of monoamine oxidase on the prolonged depletion of striatal dopamine by 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine in mice. Life Sci. 1985 Sep 23;37(12):1089-96. PubMed PMID: 3875779. 10: Turkish S, Yu PH, Greenshaw AJ. Monoamine oxidase-B inhibition: a comparison of in vivo and ex vivo measures of reversible effects. J Neural Transm. 1988;74(3):141-8. PubMed PMID: 3145323. 11: Benedetti MS, Dostert P, Guffroy C, Tipton KF. Partial or total protection from long-acting monoamine oxidase inhibitors (MAOIs) by new short-acting MAOIs of type A MD780515 and type B MD780236. Mod Probl Pharmacopsychiatry. 1983;19:82-104. PubMed PMID: 6408412. 12: Ding CZ, Silverman RB. Transformation of heterocyclic reversible monoamine oxidase-B inactivators into irreversible inactivators by N-methylation. J Med Chem. 1993 Nov 12;36(23):3606-10. PubMed PMID: 8246228.