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Vial of GnRH Triptorelin

GnRH (Triptorelin)

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$32.99$49.99

Concentration
100 mcg 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 C70H87ClN16O13
Molecular Weight 1396.0
Monoisotopic Mass 1394.6327046
Polar Area 444
Complexity 2910
XLogP 2.9
Heavy Atom Count 100
Hydrogen Bond Donor Count 14
Hydrogen Bond Acceptor Count 14
Rotatable Bond Count 33
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 GnRH (Triptorelin) Laboratory Chemical Safety Summary

Identifiers

CID 25078174
CAS 74611-71-5
InChI InChI=1S/C70H87ClN16O13/c1-39(2)30-59(67(98)79-51(16-9-27-75-70(73)74)69(100)87-29-11-17-57(87)65(96)78-37-60(72)91)85(4)68(99)55(34-44-36-77-50-15-8-6-13-48(44)50)83-62(93)52(32-42-21-25-46(90)26-22-42)80-64(95)56(38-88)84-63(94)54(33-43-35-76-49-14-7-5-12-47(43)49)81-61(92)53(31-41-19-23-45(71)24-20-41)82-66(97)58-18-10-28-86(58)40(3)89/h5-8, 10, 12-15, 18-26, 35-36, 39, 51-59, 76-77, 88, 90H, 9, 11, 16-17, 27-34, 37-38H2, 1-4H3, (H2, 72, 91)(H, 78, 96)(H, 79, 98)(H, 80, 95)(H, 81, 92)(H, 82, 97)(H, 83, 93)(H, 84, 94)(H4, 73, 74, 75)/t51-, 52-, 53+, 54+, 55+, 56-, 57-, 58-, 59-/m0/s1
InChIKey IAIQAABWXYYEFZ-FNLUPMSMSA-N
Isomeric SMILES CC(C)C[C@@H](C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)NCC(=O)N)N(C)C(=O)[C@@H](CC2=CNC3=CC=CC=C32)NC(=O)[C@H](CC4=CC=C(C=C4)O)NC(=O)[C@H](CO)NC(=O)[C@@H](CC5=CNC6=CC=CC=C65)NC(=O)[C@@H](CC7=CC=C(C=C7)Cl)NC(=O)[C@@H]8C=CCN8C(=O)C
Canonical SMILES CC(C)CC(C(=O)NC(CCCN=C(N)N)C(=O)N1CCCC1C(=O)NCC(=O)N)N(C)C(=O)C(CC2=CNC3=CC=CC=C32)NC(=O)C(CC4=CC=C(C=C4)O)NC(=O)C(CO)NC(=O)C(CC5=CNC6=CC=CC=C65)NC(=O)C(CC7=CC=C(C=C7)Cl)NC(=O)C8C=CCN8C(=O)C
IUPAC Name (2S)-1-acetyl-N-[(2R)-1-[[(2R)-1-[[(2S)-1-[[(2S)-1-[[(2R)-1-[[(2S)-1-[[(2S)-1-[(2S)-2-[(2-amino-2-oxoethyl)carbamoyl]pyrrolidin-1-yl]-5-(diaminomethylideneamino)-1-oxopentan-2-yl]amino]-4-methyl-1-oxopentan-2-yl]-methylamino]-3-(1H-indol-3-yl)-1-oxopropan-2-yl]amino]-3-(4-hydroxyphenyl)-1-oxopropan-2-yl]amino]-3-hydroxy-1-oxopropan-2-yl]amino]-3-(1H-indol-3-yl)-1-oxopropan-2-yl]amino]-3-(4-chlorophenyl)-1-oxopropan-2-yl]-2, 5-dihydropyrrole-2-carboxamide

2D Structure

Generated by Extreme Peptide with Open Babel, version 2.3.1, http://openbabel.org (accessed May 20, 2024)

GnRH (Triptorelin) 2D molecular structure vector generated with oBabel

Description

Gonadotropin releasing hormone (GnRH) is a synthetic, 10 amino acid sequence, which is structurally identical to the naturally occurring anterior pituitary hormone stimulating hypothalamic decapeptide bearing the same name1. Pulses of GnRH from the hypothalamus are responsible for the synthesis and release of gonadotropins like luteinizing hormone (LH) and follicle-stimulating hormone (FSH), which are hormones intimately related to mammalian sexual preparation and response2.

In mammalian males, pulses of GnRH initiate the process of testosterone production and spermatogenesis (sperm production)3. The introduction of endogenous GnRH to animal test subjects has been shown to raise males’ testosterone capacity beyond natural levels, which has demonstrated effects of promoting bursts of intense energy and aggressive behaviour4.

Product Comparison

GnRH analogues have developed in order exercise further control over the release of GnRH, and in following, LH and FSH. A GnRH agonist was synthesized and was meant to be active in promoting the release of GnRH, though this peptide was found only to cause an initial ‘flare’ of GnRH release, followed by downregulation of native GnRH production in animal tests5. Direct administration of synthetic GnRH, assuming reasonable temporal spacing between treatments, has been shown to induce marked increases in LH, FSH, and testosterone levels during tests with young and old male rats6.

Certain GnRH agonists, like Triptorelin, have been found successful in suppressing LH and FSH production while simultaneous promoting the production of testosterone. During in vivo circulation, this GnRH agonist puts forward a constant stimulatory effect on the pituitary gland.

Synonyms:

Gonadotropin Releasing Hormone; Gonadorelin; GnRH; GnRH1; GnRH-1

Peer-Reviewed Sources:

  1. Kakar, Sham S., et al. “Cloning, sequencing, and expression of human gonadotropin releasing hormone (GnRH) receptor.”Biochemical and biophysical research communications 189.1 (1992): 289-295. ↩︎
  2. Brown RM (1994).An introduction to Neuroendocrinology. Cambridge, UK: Cambridge University Press. ISBN 0-521-42665-0. ↩︎
  3. Ehlers K, Halvorson L (2013). “Gonadotropin-releasing Hormone (GnRH) and the GnRH Receptor (GnRHR)”.The Global Library of Women’s Medicine. doi:10.3843/GLOWM.10285. ↩︎
  4. DeVries MS, Winters CP, Jawor JM (Jun 2012). “Testosterone elevation and response to gonadotropin-releasing hormone challenge by male northern cardinals (Cardinalis cardinalis) following aggressive behavior”.Hormones and Behavior 62 (1): 99–105. ↩︎
  5. Padula, A. M. (2005). GnRH analogues—agonists and antagonists. Animal reproduction science,88(1), 115-126. ↩︎
  6. Bruni, J. F., Huang, H. H., Marshall, S., & Meites, J. (1977). Effects of single and multiple injections of synthetic GnRH on serum LH, FSH and testosterone in young and old male rats. Biology of reproduction, 17(3), 309-312. ↩︎

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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