MedKoo Cat#: 532871 | Name: UK-356618
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Description:

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

UK-356618 is a selective antagonist of the CB1 receptor (cannabinoid receptor 1), which is part of the endocannabinoid system involved in regulating various physiological processes, including appetite, pain, mood, and memory. By inhibiting CB1 receptor activity, UK-356618 can reduce the effects of cannabinoids, such as appetite stimulation and the euphoric feeling associated with cannabis use. It has been investigated for its potential in the treatment of obesity and metabolic disorders, as well as in neurological conditions where CB1 activation may contribute to disease pathology. UK-356618 is a part of ongoing research into cannabinoid-based therapies that target specific receptors to avoid side effects related to broader endocannabinoid system modulation.

Chemical Structure

UK-356618
UK-356618
CAS#230961-08-7

Theoretical Analysis

MedKoo Cat#: 532871

Name: UK-356618

CAS#: 230961-08-7

Chemical Formula: C34H43N3O4

Exact Mass: 557.3254

Molecular Weight: 557.74

Elemental Analysis: C, 73.22; H, 7.77; N, 7.53; O, 11.47

Price and Availability

Size Price Availability Quantity
5mg USD 350.00 2 Weeks
10mg USD 600.00 2 Weeks
25mg USD 950.00 2 Weeks
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Related CAS #
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Synonym
UK-356618, UK356618, UK356618
IUPAC/Chemical Name
(2R)-N-[(2S)-3,3-dimethyl-1-oxo-1-[[(1R)-1-phenylethyl]amino]butan-2-yl]-N'-hydroxy-2-[3-(3-methyl-4-phenylphenyl)propyl]butanediamide
InChi Key
JJHRUUKMPWUYIB-HVOSOHGQSA-N
InChi Code
InChI=1S/C34H43N3O4/c1-23-21-25(19-20-29(23)27-16-10-7-11-17-27)13-12-18-28(22-30(38)37-41)32(39)36-31(34(3,4)5)33(40)35-24(2)26-14-8-6-9-15-26/h6-11,14-17,19-21,24,28,31,41H,12-13,18,22H2,1-5H3,(H,35,40)(H,36,39)(H,37,38)/t24-,28-,31-/m1/s1
SMILES Code
O=C(N[C@@H](C(C)(C)C)C(N[C@@H](C1=CC=CC=C1)C)=O)[C@H](CCCC2=CC=C(C3=CC=CC=C3)C(C)=C2)CC(NO)=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
>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 557.74 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
Matsuura, T., Li, X. H., Tao, C., & Zhuo, M. (2019). Effects of matrix metalloproteinase inhibitors on N-methyl-D-aspartate receptor and contribute to long-term potentiation in the anterior cingulate cortex of adult mice. Molecular Pain, 15, 1744806919842958. Brzdak, P., Lebida, K., & Mozrzymas, J. W. (2019). Matrix metalloproteinase 3 critically affects postsynaptic long-term potentiation at GABAergic synapses in the mouse hippocampal CA1 region. Acta Neurobiologiae Experimentalis, 79(Suppl. 1). Chang, C. H., Lin, Y. L., Tyan, Y. S., Chiu, Y. H., Liang, Y. H., Chen, C. P., ... & Wang, H. S. (2021). Interleukin-1β-induced matrix metalloproteinase-3 via ERK1/2 pathway to promote mesenchymal stem cell migration. PLoS One, 16(5), e0252163. Hafez, S., Abdelsaid, M., El-Shafey, S., Johnson, M. H., Fagan, S. C., & Ergul, A. (2016). Matrix metalloprotease 3 exacerbates hemorrhagic transformation and worsens functional outcomes in hyperglycemic stroke. Stroke, 47(3), 843-851. Abe, H., Hisaoka-Nakashima, K., Kajitani, N., Okada-Tsuchioka, M., Yano, R., Itagaki, K., ... & Takebayashi, M. (2016). The expression of glial cell line-derived neurotrophic factor mRNA by antidepressants involves matrix metalloproteinase-9 activation in rat astroglial cells. Biochemical and biophysical research communications, 479(4), 907-912.