MedKoo Cat#: 564509 | Name: OMDM-188

Description:

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

OMDM-188 is a potent diglyceride lipase (DGL) inhibitor which inhibits collagen-induced p38(MAPK) phosphorylation, but does not inhibit arachidonic acid-induced aggregation or TxA2 synthesis.

Chemical Structure

OMDM-188
OMDM-188
CAS#NONE

Theoretical Analysis

MedKoo Cat#: 564509

Name: OMDM-188

CAS#: NONE

Chemical Formula: C29H53NO5

Exact Mass: 495.3924

Molecular Weight: 495.75

Elemental Analysis: C, 70.26; H, 10.78; N, 2.83; O, 16.14

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
OMDM188; OMDM 188; OMDM-188
IUPAC/Chemical Name
N-Formyl-l-isoleucine-(1S)-1-[[(2S,3S)-3-hexyl-4-oxo-2-oxetanyl]methyl]dodecyl ester
InChi Key
CBHKWVNFZKJLIS-IRGGMKSGSA-N
InChi Code
InChI=1S/C29H53NO5/c1-5-8-10-12-13-14-15-16-17-19-24(34-29(33)27(30-22-31)23(4)7-3)21-26-25(28(32)35-26)20-18-11-9-6-2/h22-27H,5-21H2,1-4H3,(H,30,31)/t23-,24-,25-,26-,27-/m0/s1
SMILES Code
CC[C@H](C)[C@@H](C(O[C@H](C[C@@H]([C@@H]1CCCCCC)OC1=O)CCCCCCCCCCC)=O)NC=O
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 495.75 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: Singh PK, Markwick R, Lu L, Howell FV, Williams G, Doherty P. Assay and Inhibition of the Purified Catalytic Domain of Diacylglycerol Lipase Beta. Biochemistry. 2016 May 17;55(19):2713-21. doi: 10.1021/acs.biochem.6b00221. Epub 2016 May 4. PubMed PMID: 27115711. 2: Bashashati M, Nasser Y, Keenan CM, Ho W, Piscitelli F, Nalli M, Mackie K, Storr MA, Di Marzo V, Sharkey KA. Inhibiting endocannabinoid biosynthesis: a novel approach to the treatment of constipation. Br J Pharmacol. 2015 Jun;172(12):3099-111. doi: 10.1111/bph.13114. Epub 2015 Apr 23. PubMed PMID: 25684407; PubMed Central PMCID: PMC4459026. 3: Jackson EC, Ortar G, McNicol A. The effects of an inhibitor of diglyceride lipase on collagen-induced platelet activation. J Pharmacol Exp Ther. 2013 Dec;347(3):582-8. doi: 10.1124/jpet.113.205591. Epub 2013 Sep 16. PubMed PMID: 24042163. 4: Hashimotodani Y, Ohno-Shosaku T, Tanimura A, Kita Y, Sano Y, Shimizu T, Di Marzo V, Kano M. Acute inhibition of diacylglycerol lipase blocks endocannabinoid-mediated retrograde signalling: evidence for on-demand biosynthesis of 2-arachidonoylglycerol. J Physiol. 2013 Oct 1;591(19):4765-76. doi: 10.1113/jphysiol.2013.254474. Epub 2013 Jul 15. PubMed PMID: 23858009; PubMed Central PMCID: PMC3800453. 5: Min R, Testa-Silva G, Heistek TS, Canto CB, Lodder JC, Bisogno T, Di Marzo V, Brussaard AB, Burnashev N, Mansvelder HD. Diacylglycerol lipase is not involved in depolarization-induced suppression of inhibition at unitary inhibitory connections in mouse hippocampus. J Neurosci. 2010 Feb 17;30(7):2710-5. doi: 10.1523/JNEUROSCI.BC-3622-09.2010. PubMed PMID: 20164355.