MedKoo Cat#: 532786 | Name: SR120819A

Description:

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

SR120819A is an orally-active and selective neuropeptide Y Y1 receptor antagonist.

Chemical Structure

SR120819A
SR120819A
CAS#NA

Theoretical Analysis

MedKoo Cat#: 532786

Name: SR120819A

CAS#: NA

Chemical Formula: C43H54N6O4S

Exact Mass: 750.3927

Molecular Weight: 751.00

Elemental Analysis: C, 68.77; H, 7.25; N, 11.19; O, 8.52; S, 4.27

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.
Bulk Inquiry
Related CAS #
No Data
Synonym
SR120819A; SR 120819A; SR-120819A.
IUPAC/Chemical Name
(R)-N-((R)-3-(4-((Z)-N'-(((1s,4S)-4-((dimethylamino)methyl)cyclohexyl)methyl)carbamimidoyl)phenyl)-1-oxo-1-(pyrrolidin-1-yl)propan-2-yl)-2-(naphthalene-2-sulfonamido)-3-phenylpropanamide
InChi Key
GKKPXBHNFVDHAQ-GWOGJWAKSA-N
InChi Code
InChI=1S/C43H54N6O4S/c1-48(2)30-34-16-14-33(15-17-34)29-45-41(44)36-20-18-32(19-21-36)27-40(43(51)49-24-8-9-25-49)46-42(50)39(26-31-10-4-3-5-11-31)47-54(52,53)38-23-22-35-12-6-7-13-37(35)28-38/h3-7,10-13,18-23,28,33-34,39-40,47H,8-9,14-17,24-27,29-30H2,1-2H3,(H2,44,45)(H,46,50)/t33-,34+,39-,40-/m1/s1
SMILES Code
O=C(N[C@H](CC1=CC=C(/C(N)=N/C[C@H]2CC[C@@H](CN(C)C)CC2)C=C1)C(N3CCCC3)=O)[C@H](NS(=O)(C4=CC=C5C=CC=CC5=C4)=O)CC6=CC=CC=C6
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 751.00 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: Sjödin P, Holmberg SK, Akerberg H, Berglund MM, Mohell N, Larhammar D. Re-evaluation of receptor-ligand interactions of the human neuropeptide Y receptor Y1: a site-directed mutagenesis study. Biochem J. 2006 Jan 1;393(Pt 1):161-9. Erratum in: Biochem J. 2006 Sep 15;398(3):613. PubMed PMID: 16097949; PubMed Central PMCID: PMC1383674. 2: Holmberg SK, Mikko S, Boswell T, Zoorob R, Larhammar D. Pharmacological characterization of cloned chicken neuropeptide Y receptors Y1 and Y5. J Neurochem. 2002 May;81(3):462-71. PubMed PMID: 12065655. 3: Berglund MM, Lundell I, Cabrele C, Serradeil-Le Gal C, Beck-Sickinger AG, Larhammar D. Binding properties of three neuropeptide Y receptor subtypes from zebrafish: comparison with mammalian Y1 receptors. Biochem Pharmacol. 2000 Dec 15;60(12):1815-22. PubMed PMID: 11108796. 4: Serradeil-Le Gal C, Lafontan M, Raufaste D, Marchand J, Pouzet B, Casellas P, Pascal M, Maffrand JP, Le Fur G. Characterization of NPY receptors controlling lipolysis and leptin secretion in human adipocytes. FEBS Lett. 2000 Jun 16;475(2):150-6. PubMed PMID: 10858507. 5: Sun L, Philipson LH, Miller RJ. Regulation of K+ and Ca++ channels by a family of neuropeptide Y receptors. J Pharmacol Exp Ther. 1998 Feb;284(2):625-32. PubMed PMID: 9454807.