SHU 9119
featured

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

Hodoodo CAT#: H597498

CAS#: 168482-23-3

Description: SHU 9119 is an agonist of melanocortin receptor 1 (MC1R) and antagonist of MC4R.


Chemical Structure

img
SHU 9119
CAS# 168482-23-3

Theoretical Analysis

Hodoodo Cat#: H597498
Name: SHU 9119
CAS#: 168482-23-3
Chemical Formula: C54H71N15O9
Exact Mass: 1,073.56
Molecular Weight: 1,074.250
Elemental Analysis: C, 60.38; H, 6.66; N, 19.56; O, 13.40

Price and Availability

Size Price Availability Quantity
1mg USD 310
Bulk inquiry

Synonym: Shu 9119; Shu-9119; Shu9119;

IUPAC/Chemical Name: (2S)-N-((3S,6S,E)-3-((4H-imidazol-4-yl)methyl)-14-((2S)-2-((S)-2-((R)-2-amino-3-(naphthalen-2-yl)propanamido)-5-guanidinopentanamido)-3-(indolin-3-yl)propanamido)-2,5,8,15-tetraoxo-1,4,9-triazacyclopentadec-13-en-6-yl)-2-acetamidohexanamide

InChi Key: ORTUTLYEGOSCRP-ATNXLWBUSA-N

InChi Code: InChI=1S/C54H71N15O9/c1-3-4-15-40(63-31(2)70)48(73)68-45-27-46(71)59-21-10-9-17-41(50(75)69-53(78)44(67-52(45)77)26-36-29-58-30-62-36)65-51(76)43(25-35-28-61-39-16-8-7-14-37(35)39)66-49(74)42(18-11-22-60-54(56)57)64-47(72)38(55)24-32-19-20-33-12-5-6-13-34(33)23-32/h5-8,12-14,16-17,19-20,23,29-30,35-36,38,40,42-45,61H,3-4,9-11,15,18,21-22,24-28,55H2,1-2H3,(H,59,71)(H,63,70)(H,64,72)(H,65,76)(H,66,74)(H,67,77)(H,68,73)(H4,56,57,60)(H,69,75,78)/b41-17+/t35?,36?,38-,40+,42+,43+,44+,45+/m1/s1

SMILES Code: CCCC[C@H](NC(C)=O)C(N[C@H]1CC(NCCC/C=C(NC([C@@H](NC([C@@H](NC([C@H](N)Cc(cc2)cc3c2cccc3)=O)CCCNC(N)=N)=O)CC4CNc5ccccc54)=O)\C(NC([C@H](CC6C=NC=N6)NC1=O)=O)=O)=O)=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:

Biological target:
In vitro activity:
In vivo activity:

Preparing Stock Solutions

The following data is based on the product molecular weight 1,074.25 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
Formulation protocol:
In vitro protocol:
In vivo protocol:

Molarity Calculator

Calculate the mass, volume, or concentration required for a solution.
=
x
x
g/mol

*When preparing stock solutions always use the batch-specific molecular weight of the product found on the vial label and SDS / CoA (available online).

Reconstitution Calculator

The reconstitution calculator allows you to quickly calculate the volume of a reagent to reconstitute your vial. Simply enter the mass of reagent and the target concentration and the calculator will determine the rest.

=
÷

Dilution Calculator

Calculate the dilution required to prepare a stock solution.
x
=
x

1: Grieco P, Cai M, Han G, Trivedi D, Campiglia P, Novellino E, Hruby VJ. Further structure-activity studies of lactam derivatives of MT-II and SHU-9119: their activity and selectivity at human melanocortin receptors 3, 4, and 5. Peptides. 2007 Jun;28(6):1191-6. Epub 2007 Mar 1. PubMed PMID: 17482720; PubMed Central PMCID: PMC1955225.

2: Grieco P, Balse-Srinivasan P, Han G, Weinberg D, MacNeil T, Van der Ploeg LH, Hruby VJ. Extensive structure-activity studies of lactam derivatives of MT-II and SHU-9119: their activity and selectivity at human melanocortin receptors 3, 4, and 5. J Pept Res. 2003 Nov;62(5):199-206. PubMed PMID: 14531843.

3: do Carmo JM, da Silva AA, Rushing JS, Hall JE. Activation of the central melanocortin system contributes to the increased arterial pressure in obese Zucker rats. Am J Physiol Regul Integr Comp Physiol. 2012 Mar 1;302(5):R561-7. doi: 10.1152/ajpregu.00392.2011. Epub 2011 Dec 28. PubMed PMID: 22204957; PubMed Central PMCID: PMC3311523.

4: Kabra DG, Pfuhlmann K, García-Cáceres C, Schriever SC, Casquero García V, Kebede AF, Fuente-Martin E, Trivedi C, Heppner K, Uhlenhaut NH, Legutko B, Kabra UD, Gao Y, Yi CX, Quarta C, Clemmensen C, Finan B, Müller TD, Meyer CW, Paez-Pereda M, Stemmer K, Woods SC, Perez-Tilve D, Schneider R, Olson EN, Tschöp MH, Pfluger PT. Hypothalamic leptin action is mediated by histone deacetylase 5. Nat Commun. 2016 Feb 29;7:10782. doi: 10.1038/ncomms10782. PubMed PMID: 26923837; PubMed Central PMCID: PMC4773494.

5: Turcic P, Stambuk N, Konjevoda P, Kelava T, Gabricevic M, Stojkovic R, Aralica G. Modulation of γ2-MSH hepatoprotection by antisense peptides and melanocortin subtype 3 and 4 receptor antagonists. Med Chem. 2015;11(3):286-95. PubMed PMID: 25219927.

6: do Carmo JM, da Silva AA, Rushing JS, Pace B, Hall JE. Differential control of metabolic and cardiovascular functions by melanocortin-4 receptors in proopiomelanocortin neurons. Am J Physiol Regul Integr Comp Physiol. 2013 Aug 15;305(4):R359-68. doi: 10.1152/ajpregu.00518.2012. Epub 2013 Jul 10. PubMed PMID: 23842677; PubMed Central PMCID: PMC3833394.

7: do Carmo JM, da Silva AA, Hall JE. Role of hindbrain melanocortin-4 receptor activity in controlling cardiovascular and metabolic functions in spontaneously hypertensive rats. J Hypertens. 2015 Jun;33(6):1201-6. doi: 10.1097/HJH.0000000000000530. PubMed PMID: 25668357; PubMed Central PMCID: PMC4748968.

8: Shi Z, Brooks VL. Leptin differentially increases sympathetic nerve activity and its baroreflex regulation in female rats: role of oestrogen. J Physiol. 2015 Apr 1;593(7):1633-47. doi: 10.1113/jphysiol.2014.284638. Epub 2014 Dec 22. PubMed PMID: 25398524; PubMed Central PMCID: PMC4386963.

9: Carotenuto A, Merlino F, Cai M, Brancaccio D, Yousif AM, Novellino E, Hruby VJ, Grieco P. Discovery of Novel Potent and Selective Agonists at the Melanocortin-3 Receptor. J Med Chem. 2015 Dec 24;58(24):9773-8. doi: 10.1021/acs.jmedchem.5b01285. Epub 2015 Dec 16. PubMed PMID: 26599352; PubMed Central PMCID: PMC5070805.

10: Zheng H, Patterson LM, Rhodes CJ, Louis GW, Skibicka KP, Grill HJ, Myers MG Jr, Berthoud HR. A potential role for hypothalamomedullary POMC projections in leptin-induced suppression of food intake. Am J Physiol Regul Integr Comp Physiol. 2010 Mar;298(3):R720-8. doi: 10.1152/ajpregu.00619.2009. Epub 2010 Jan 13. PubMed PMID: 20071607; PubMed Central PMCID: PMC2838656.

11: Maranon RO, Lima R, Mathbout M, do Carmo JM, Hall JE, Roman RJ, Reckelhoff JF. Postmenopausal hypertension: role of the sympathetic nervous system in an animal model. Am J Physiol Regul Integr Comp Physiol. 2014 Feb 15;306(4):R248-56. doi: 10.1152/ajpregu.00490.2013. Epub 2013 Dec 31. PubMed PMID: 24381180; PubMed Central PMCID: PMC3921310.

12: Iemolo A, Ferragud A, Cottone P, Sabino V. Pituitary Adenylate Cyclase-Activating Peptide in the Central Amygdala Causes Anorexia and Body Weight Loss via the Melanocortin and the TrkB Systems. Neuropsychopharmacology. 2015 Jul;40(8):1846-55. doi: 10.1038/npp.2015.34. Epub 2015 Feb 4. PubMed PMID: 25649277; PubMed Central PMCID: PMC4839508.

13: Tala SR, Schnell SM, Haskell-Luevano C. Microwave-assisted solid-phase synthesis of side-chain to side-chain lactam-bridge cyclic peptides. Bioorg Med Chem Lett. 2015 Dec 15;25(24):5708-11. doi: 10.1016/j.bmcl.2015.10.095. Epub 2015 Oct 31. PubMed PMID: 26555357; PubMed Central PMCID: PMC4654418.

14: Bassi M, Nakamura NB, Furuya WI, Colombari DS, Menani JV, do Carmo JM, da Silva AA, Hall JE, Colombari E. Activation of the brain melanocortin system is required for leptin-induced modulation of chemorespiratory function. Acta Physiol (Oxf). 2015 Apr;213(4):893-901. doi: 10.1111/apha.12394. Epub 2014 Sep 30. PubMed PMID: 25207799; PubMed Central PMCID: PMC4362918.

15: Xu L, Wang Q, Guo F, Pang M, Sun X, Gao S, Gong Y. Nesfatin-1 signaling in the basom edial amygdala modulates the gastric distension-sensitive neurons discharge and decreases gastric motility via melanocortin 3/4 receptors and modified by the arcuate nucleus. Eur J Pharmacol. 2015 Oct 5;764:164-72. doi: 10.1016/j.ejphar.2015.07.002. Epub 2015 Jul 3. PubMed PMID: 26144374.

16: Shi Z, Cassaglia PA, Gotthardt LC, Brooks VL. Hypothalamic Paraventricular and Arcuate Nuclei Contribute to Elevated Sympathetic Nerve Activity in Pregnant Rats: Roles of Neuropeptide Y and α-Melanocyte-Stimulating Hormone. Hypertension. 2015 Dec;66(6):1191-8. doi: 10.1161/HYPERTENSIONAHA.115.06045. Epub 2015 Oct 19. PubMed PMID: 26483343; PubMed Central PMCID: PMC4824187.

17: Guzmán-Ruiz MA, Ramirez-Corona A, Guerrero-Vargas NN, Sabath E, Ramirez-Plascencia OD, Fuentes-Romero R, León-Mercado LA, Basualdo Sigales M, Escobar C, Buijs RM. Role of the Suprachiasmatic and Arcuate Nuclei in Diurnal Temperature Regulation in the Rat. J Neurosci. 2015 Nov 18;35(46):15419-29. doi: 10.1523/JNEUROSCI.1449-15.2015. PubMed PMID: 26586828.

18: da Silva AA, Kuo JJ, Hall JE. Role of hypothalamic melanocortin 3/4-receptors in mediating chronic cardiovascular, renal, and metabolic actions of leptin. Hypertension. 2004 Jun;43(6):1312-7. Epub 2004 May 3. PubMed PMID: 15123576.

19: Cerritelli S, Hirschberg S, Hill R, Balthasar N, Pickering AE. Activation of Brainstem Pro-opiomelanocortin Neurons Produces Opioidergic Analgesia, Bradycardia and Bradypnoea. PLoS One. 2016 Apr 14;11(4):e0153187. doi: 10.1371/journal.pone.0153187. eCollection 2016. PubMed PMID: 27077912; PubMed Central PMCID: PMC4831707.

20: Iemolo A, Seiglie M, Blasio A, Cottone P, Sabino V. Pituitary adenylate cyclase-activating polypeptide (PACAP) in the central nucleus of the amygdala induces anxiety via melanocortin receptors. Psychopharmacology (Berl). 2016 Sep;233(17):3269-77. doi: 10.1007/s00213-016-4366-y. Epub 2016 Jul 4. PubMed PMID: 27376948; PubMed Central PMCID: PMC4982769.