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1. 5-Amino-1MQ 10mg
2. 5-Amino-1MQ 50mg
3. ACE-031 1mg
4. ACTH 1-39 5mg
5. Adamax 5mg
6. AHK-Cu 50mg
7. AICAR 50mg
8. AICAR 100mg
9. AOD-9604 5mg
10. AOD-9604 10mg
11. Alprostadil 20mcg
12. Amylin 5mg
13. Angiotensin (1–7) 5mg
14. ARA-290 10mg
15. Bimagrumab 5mg
16. Botulinum Toxin 100IU
17. BPC-157 10mg
18. BPC-157 20mg
19. BPC-157 5mg + TB-500 5mg
20. BPC-157 10mg + TB-500 10mg
21. Bronchogen 20mg
22. Cagrilintide 10mg
23. Cagrilintide 20mg
24. Cardiogen 20mg
25. Cartalax 20mg
26. CBL-514 10mg
27. CBL-514 20mg
28. CBL-514 30mg
29. Cerebrolysin 60mg
30. Cerlankin 2mg
31. CGRP (Calcitonin Gene-Related Peptide) 1mg
32. CJC-1295 with DAC 5mg
33. CJC-1295 with DAC 10mg
34. CJC-1295 with DAC 5mg + Ipamorelin 5mg
35. CJC-1295 without DAC 5mg
36. CJC-1295 without DAC 10mg
37. CJC-1295 without DAC 5mg + Ipamorelin 5mg
38. Chonluten 20mg
39. Cortagen 20mg
40. Crystagen 20mg
41. CT-1 Cardiotrophin-1 5mg
42. Dermorphin 5mg
43. Dihexa 5mg
44. DSIP 5mg
45. Dulaglutide 5mg
46. Elabela Apelin 5mg
47. Enfuvirtide 90mg
48. Epithalon 5mg
49. Epithalon 40mg
50. Epithalon 50mg
51. EPO 3000IU
52. FGF21 10mg
53. Follistatin-344 1mg
54. FOXO4 10mg
55. GHK-Cu 50mg
56. GHK-Cu 100mg
57. Ghrelin 10mg
58. GHRP-2 5mg
59. GHRP-6 5mg
60. Glucagon 1mg
61. Glutathione 1500mg
62. Gonadorelin Acetate 2mg
63. Goserelin 10mg
64. GLOW BPC-157 10mg + GHK-Cu 50mg + TB-500 10mg
65. HGH 191AA 15IU
66. HGH 191AA 36IU
67. HGH Fragment 176-191 10mg
68. HGH Fragment 176-191 15mg
69. HMG (Human Menopausal Gonadotropin) 75IU
70. Humanin 10mg
71. Hyaluronic Acid 5mg
72. Hexarelin Acetate 2mg
73. Hexarelin Acetate 5mg
74. IGF-1 LR3 1mg
75. Ipamorelin 5mg
76. Ipamorelin 10mg
77. Kisspeptin-10 5mg
78. Kisspeptin-10 10mg
79. KLOW BPC-157 10mg + GHK-Cu 50mg + TB-500 10mg + KPV 10mg
80. KPV 10mg
81. Leuprolide Acetate 10mg
82. Liraglutide 5mg
83. Livagen 20mg
84. LL-37 5mg
85. Lysyl Oxidase 30mg
86. Matrixyl 10mg
87. Mazdutide 10mg
88. Melanotan I 10mg
89. Melanotan II 10mg
90. Melatonin 10mg
91. MGF 2mg
92. MOTS-c 10mg
93. MOTS-c 40mg
94. NAD+ 100mg
95. NAD+ 500mg
96. NAD+ 1000mg
97. Nesiritide 5mg
98. Neuropeptide Y (NPY) 10mg
99. Ovagen 20mg
100. Oxytocin Acetate 5mg
101. Oxytocin Acetate 10mg
102. P21 5mg
103. P21 10mg
104. PACAP 5mg
105. Pancragen 20mg
106. PE 22-28 10mg
107. PEG-MGF 2mg
108. Pinealon 5mg
109. Pinealon 10mg
110. Pinealon 20mg
111. PNC-27 5mg
112. PNC-27 10mg
113. Prostamax 20mg
114. PT-141 10mg
115. PTH Fragments 10mg
116. Relamorelin 5mg
117. Retatrutide 10mg
118. Retatrutide 20mg
119. Retatrutide 30mg
120. Retatrutide 40mg
121. Retatrutide 60mg
122. Retatrutide 5mg + Cagrilintide 5mg
123. Selank 5mg
124. Selank 10mg
125. Semaglutide 5mg + Cagrilintide 5mg
126. Semax 5mg
127. Sermorelin 5mg
128. SLU-PP-332 10mg
129. SNAP-8 10mg
130. SS-31 10mg
131. SS-31 50mg
132. Survodutide 10mg
133. TB-500 10mg
134. TB-500 (FRAG) 10mg
135. Teduglutide 5mg
136. Teriparatide 10mg
137. Tesamorelin 5mg
138. Tesamorelin 10mg
139. Tesamorelin 20mg
140. Tesamorelin 5mg + Ipamorelin 5mg
141. Tesofensine 1mg
142. Testagen 20mg
143. Thymalin 10mg
144. Thymosin Alpha-1 5mg
145. Thymosin Alpha-1 10mg
146. Treprostinil 5mg
147. Vesugen 20mg
148. VIP 5mg
149. VIP 10mg
150. Vilon 20mg

Tesamorelin 10mg

Reduces visceral fat / decreases abdominal fat via GH

Tesamorelin is a 44‑amino‑acid synthetic analog of growth hormone–releasing hormone (GHRH) that demonstrates significant efficacy in stimulating pituitary secretion of endogenous growth hormone, making it a valuable compound for investigating the physiological mechanisms of the growth hormone axis.

R$1.368,00

10 in stock

Warning — For Research Use Only

Scientific content intended for research laboratories only. It is not a clinical, therapeutic, or diagnostic recommendation. Use is restricted to qualified professionals. Consult specialists before purchasing or using. Biopelabs reinforces its commitment to ethical and responsible use.

Description

Tesamorelin is a synthetic peptide analog of GHRH, with a trans‑3‑hexenoic acid group attached to the N‑terminus of its 44‑amino‑acid sequence, conferring greater stability compared with endogenous GHRH. The compound stimulates pituitary secretion of growth hormone and, consequently, increases levels of insulin‑like growth factor‑1 (IGF‑1) and insulin‑like growth factor–binding protein 3 (IGFBP‑3) in laboratory models.

 

Important Information

Property Value
Molecular formula C₂₂₃H₃₇₀N₇₂O₆₉S
Molecular weight 5196 g/mol
Synonyms Tesamorelin acetate, 901758‑09‑6, TH9507, UNII‑LGW5H38VE3, Tesamorelin acetate [USAN]

  

Main structure of the peptide Tesamorelin

Tesamorelin

Source: PubChem

 

Lyophilized Peptides

Peptides undergo a lyophilization process, a technique that contributes to greater stability and extended shelf life, while preserving purity and molecular structure during storage. It is important to note that no fillers are used during this procedure.

Intended Use

Biopelabs states: this material is provided exclusively as a chemical input for research purposes. Its use is restricted to in vitro assays and experimental activities in laboratory environments. The information presented is strictly for informational and educational purposes. Handling must be carried out only by properly qualified professionals. This product is not classified as a medication, food, or cosmetic, and must not be used, marketed, or described as such.

Research

Scientific Research and Metabolic Effects of Tesamorelin

Tesamorelin is a stabilized GHRH analog with significant influence on metabolism via the growth hormone/IGF‑1 axis. In research models, this compound demonstrates the ability to affect visceral adipose tissue metabolism, triglyceride levels, and lipid profiles, combining anabolic and lipolytic mechanisms without substantially impacting glycemic homeostasis under controlled conditions.

Efficacy in Visceral Adipose Tissue Reduction

Tesamorelin has shown efficacy in reducing visceral adipose tissue (VAT) in individuals with HIV‑associated lipodystrophy. In two well‑designed, randomized, placebo‑controlled trials, a significant reduction in VAT was observed, whereas subcutaneous adipose tissue remained clinically unchanged. This VAT reduction was maintained over a prolonged period in patients who continued therapy, although VAT tended to accumulate again after discontinuation.
In addition, tesamorelin improved body‑composition measures, including reductions in trunk fat and waist circumference, as well as improvements in body‑image perception.

Impact on Non‑alcoholic Fatty Liver Disease (NAFLD)

Promising results have been observed with tesamorelin in reducing hepatic fat and limiting fibrosis progression in patients with HIV‑related NAFLD. In a placebo‑controlled trial, tesamorelin decreased hepatic fat fraction and improved gene‑expression scores associated with fibrosis, indicating a potential therapeutic role in NAFLD management in this population.
The peptide influences hepatic genetic pathways by increasing oxidative phosphorylation and reducing expression of inflammatory genes.

Effects on Adipose Tissue Quality

Beyond reducing total fat mass, tesamorelin has been shown to improve adipose tissue quality. Trials assessing fat density reported increases in the density of both subcutaneous adipose tissue and VAT, suggesting an improvement in fat quality independent of changes in absolute fat amount.

Cardiovascular and Metabolic Outcomes

The effect of tesamorelin on cardiovascular disease (CVD) risk has also been investigated, with data indicating a modest reduction in atherosclerotic risk factors over a 10‑year period. This reduction was primarily attributed to lower total‑cholesterol levels, even among participants who were already on lipid‑lowering therapy.
Tesamorelin was well tolerated, with no significant differences in glycemic parameters between treatment and placebo groups.

Neurocognitive and Health‑related Considerations

Although tesamorelin reduced waist circumference, its effects on neurocognitive impairment in obese individuals with HIV did not differ significantly from standard care, suggesting limited cognitive benefit. However, the peptide’s ability to increase IGF‑1 levels may open avenues for additional experimental applications that warrant further investigation.

References

  • Falutz, J., et al. (2010). Effects of tesamorelin (TH9507), a growth hormone–releasing hormone analog, in HIV‑infected patients with excess abdominal fat: a pooled analysis of two multicenter, double‑blind, placebo‑controlled, phase 3 trials with safety‑extension data. The Journal of Clinical Endocrinology and Metabolism, 95(9), 4291–4304.
  • Fourman, L., et al. (2020). Effects of tesamorelin on hepatic transcriptomic signatures in HIV‑associated NAFLD. JCI Insight, 5.
  • Lake, J., et al. (2021). Tesamorelin improves fat quality independent of changes in fat quantity. AIDS, 35, 1395–1402.
  • Grinspoon, S., et al. (2025). Impact of tesamorelin on cardiovascular risk‑prediction scores in phase‑3 trials: a subanalysis. Open Forum Infectious Diseases, 12.
  • Ellis, R., et al. (2025). Effects of tesamorelin on neurocognitive impairment in abdominally obese individuals with HIV. The Journal of Infectious Diseases.

Scientific Reviewer

The content was reviewed by Dr. Ky H. Le, MD. Dr. Ky H. Le is a family physician in Aiea, Hawaii. He received his medical degree from St. George’s University School of Medicine and has practiced for over 20 years. He has expertise in the treatment of obesity, diabetes, hypertension, and high blood pressure, among other conditions. Dr. Ky H. Le accepts Medicare, Aetna, Humana, Blue Cross, and United Healthcare.

Ref.: https://health.usnews.com/doctors/ky-le-371599#expertise

COAs

LAL Endotoxin Test Report

Certificate of Analysis (Including Product Images)

Certificate of Analysis (General / Physicochemical)

Certificate of Analysis (Analytical Method Details) ✅

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Additional information

Weight 40 g
Dimensions 7 × 3,6 × 8 cm

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