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Hexarelin

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Concentration
2 mg per vial
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This product is prepared for LABORATORY RESEARCH USE ONLY and may not be used for other purposes.

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Properties

Molecular Formula C47H58N12O6
Molecular Weight 887.0
Monoisotopic Mass 886.46022762
Polar Area 301
Complexity 1600
XLogP 2.3
Heavy Atom Count 65
Hydrogen Bond Donor Count 11
Hydrogen Bond Acceptor Count 9
Rotatable Bond Count 23
Physical Appearance Fine White Lyophilized Powder
Stability Lyophilized protein is to be stored at -20°C. It is recommended to aliquot the reconstituted (dissolved) protein into several discrete vials in order to avoid repeated freezing and thawing. Reconstituted protein can be stored at 4°C
PubChem LCSS Hexarelin Laboratory Chemical Safety Summary

Identifiers

CID 6918297
CAS 140703-51-1
InChI InChI=1S/C47H58N12O6/c1-27-34(33-15-7-9-17-37(33)54-27)23-41(58-44(62)35(49)22-31-25-51-26-53-31)45(63)55-28(2)43(61)57-40(21-30-24-52-36-16-8-6-14-32(30)36)47(65)59-39(20-29-12-4-3-5-13-29)46(64)56-38(42(50)60)18-10-11-19-48/h3-9, 12-17, 24-26, 28, 35, 38-41, 52, 54H, 10-11, 18-23, 48-49H2, 1-2H3, (H2, 50, 60)(H, 51, 53)(H, 55, 63)(H, 56, 64)(H, 57, 61)(H, 58, 62)(H, 59, 65)/t28-, 35-, 38-, 39+, 40-, 41+/m0/s1
InChIKey RVWNMGKSNGWLOL-GIIHNPQRSA-N
Isomeric SMILES CC1=C(C2=CC=CC=C2N1)C[C@H](C(=O)N[C@@H](C)C(=O)N[C@@H](CC3=CNC4=CC=CC=C43)C(=O)N[C@H](CC5=CC=CC=C5)C(=O)N[C@@H](CCCCN)C(=O)N)NC(=O)[C@H](CC6=CN=CN6)N
Canonical SMILES CC1=C(C2=CC=CC=C2N1)CC(C(=O)NC(C)C(=O)NC(CC3=CNC4=CC=CC=C43)C(=O)NC(CC5=CC=CC=C5)C(=O)NC(CCCCN)C(=O)N)NC(=O)C(CC6=CN=CN6)N
IUPAC Name (2S)-6-amino-2-[[(2R)-2-[[(2S)-2-[[(2S)-2-[[(2R)-2-[[(2S)-2-amino-3-(1H-imidazol-5-yl)propanoyl]amino]-3-(2-methyl-1H-indol-3-yl)propanoyl]amino]propanoyl]amino]-3-(1H-indol-3-yl)propanoyl]amino]-3-phenylpropanoyl]amino]hexanamide

2D Structure

Generated by Extreme Peptide with Open Babel, version 2.3.1, http://openbabel.org (accessed June 28, 2022)

Hexarelin 2D molecular structure vector generated with oBabel

Description

Hexarelin is a growth hormone (GH) releasing peptide (GHRP) analog comprised of 6 amino acid residues and having a methylated ‘Trp’ terminus in order to enhance structural stability and to prolong residence time in the bloodstream1. Earning it the classification of a GH secretagogue (GHS), Hexarelin has been found to promote the production of GH by binding to the GHS (ghrelin) receptor within the pituitary gland and the hypothalamus2.

Hexarelin is reported to be a potent agent for the stimulation of GH production, which has been shown to be a promoter of enhanced muscle strength, increased muscle mass, improved joint health, quickened wound healing3, and damage protection threatened by cardiac dysfunction4. Animal testing has demonstrated that Hexarelin stimulates also significant secretion of IGF-1, PRL, ACTH, and cortisol5, while not to inducing appetite and gastric emptying, which is a property of other GHRP analogs6.

Product Comparison

The regular administration of endogenous, synthetic GH has the potential to cause a parallel reduction of natural GH production as a result of modulation by somatostatin5, which may run counter to desired research outcomes. Rather than using synthetic GH to substitute production of the naturally occurring agent, Hexarelin promotes natural GH production alongside normal, systemic production.

Hexarelin and GHRP-6 are noted to have similar capabilities in stimulating sustained GH release, but, as mentioned above, Hexarelin lacks GHRP-6’s appetite inducing properties6.

Synonyms:

Hexarelin Acetate, HEX, Examorelin


Peer-Reviewed Sources:

  1. Torsello, A., Luoni, M., Schweiger, F., Grilli, R., Guidi, M., Bresciani, E., … & Locatelli, V. (1998). Novel hexarelin analogs stimulate feeding in the rat through a mechanism not involving growth hormone release. European journal of pharmacology, 360(2), 123-129. ↩︎
  2. Deghenghi, R., Cananzi, M. M., Torsello, A., Battisti, C., Muller, E. E., & Locatelli, V. (1994). GH-releasing activity of hexarelin, a new growth hormone releasing peptide, in infant and adult rats. Life sciences, 54(18), 1321-1328. ↩︎
  3. Acosta, J. B., Vera, D. C., Herrera, D. G. D. B., Nieto, G. E. G., Alba, J. S., Mola, E. L., & Castillo, M. V. (2011). Pharmaceutical Composition Containing GHRP-6 To Prevent And Eliminate Fibrosis And Other Pathological Deposits In Tissues. U.S. Patent Application 13/150,526. ↩︎
  4. Locatelli, V., Rossoni, G., Schweiger, F., Torsello, A., De Gennaro Colonna, V., Bernareggi, M., & Berti, F. (1999). Growth Hormone-Independent Cardioprotective Effects of Hexarelin in the Rat 1. Endocrinology, 140(9), 4024-4031. ↩︎
  5. Arvat, E., Maccario, M., Di Vito, L., Broglio, F., Benso, A., Gottero, C., & Ghigo, E. (2001). Endocrine activities of ghrelin, a natural growth hormone secretagogue (GHS), in humans: comparison and interactions with hexarelin, a nonnatural peptidyl GHS, and GH-releasing hormone 1. The Journal of Clinical Endocrinology & Metabolism, 86(3), 1169-1174. ↩︎
  6. Schmid, D. A., Held, K., Ising, M., Uhr, M., Weikel, J. C., & Steiger, A. (2005). Ghrelin stimulates appetite, imagination of food, GH, ACTH, and cortisol, but does not affect leptin in normal controls. Neuropsychopharmacology, 30(6), 1187-1192. ↩︎

All literature, information, and data, provided on this website are for informational and educational purposes only.

Accurate research is our priority.

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