Hexarelin – 2mg
$29.99 $19.99
2 mg per vial
- 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 |
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Molecular Weight | 887.0 |
Monoisotopic Mass | 886.46022862 |
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 | Clear Liquid |
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 |
Identifiers
CID | 6918297 |
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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 |
Description
Description – Hexarelin
Product Comparison – Hexarelin
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, it 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:
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
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