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Peptide-Based Lung Support
Acts as a bioregulator, targeting lung tissue at the cellular level—enhancing DNA stability, reducing inflammation, and promoting epithelial repair and surfactant production in preclinical studies
Investigated for potential in chronic respiratory conditions like COPD, asthma, and bronchitis—reducing mucus, bronchospasm, and coughing
Anti-Inflammatory & Anti-Aging
May stabilize DNA, reduce inflammatory cytokines, and support healthy lung function—promising for age-related lung decline
Immunomodulation
Proposed to support immune function in the lungs, reducing exacerbations in smokers and older individuals
Bronchogen 20 mg is a promising experimental peptide aimed at improving lung structure and function. While early data—both preclinical and anecdotal—suggest benefits for inflammation and airflow, it remains unapproved and under-researched. If you're exploring respiratory support, consult a medical professional and consider established therapies (e.g., bronchodilators, inhaled steroids).
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USES :-
Anxiety Reduction (Anxiolytic Effect)
Acts on GABA receptors (like benzodiazepines but without sedation or addiction risk)
Reduces symptoms of:
Generalized anxiety
Social anxiety
Stress and tension
Cognitive Enhancement (Nootropic)
Improves:
Focus
Mental clarity
Memory retention and recall
Used for cognitive fatigue and brain fog
Improves Mood & Emotional Stability
Regulates serotonin and dopamine levels in the brain
May help with mild depression and mood swings
Immune System Modulation
Enhances immune system balance without overstimulation
Originally developed in Russia for treating immune-related conditions and infections
Neuroprotection
Protects neurons from oxidative stress and damage
May support recovery after traumatic brain injury or chronic stress
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GHK-Cu (Copper Peptide, 50mg) is a well-known regenerative peptide complex made of glycyl-L-histidyl-L-lysine bound to a copper ion. It naturally occurs in the human body and plays a key role in tissue repair, skin regeneration, inflammation control, and hair growth.
When provided in 50mg lyophilized vials, GHK-Cu is typically used for cosmetic and therapeutic purposes — both topical and injectable (research use only).
💎 1. Skin Regeneration & Anti-Aging
Stimulates collagen and elastin production
Reduces fine lines, wrinkles, and hyperpigmentation
Increases skin firmness and elasticity
Promotes wound healing and reduces scarring
💇 2. Hair Growth Stimulation
Increases size of hair follicles and improves hair thickness
Shown to regrow hair in androgenetic alopecia (male/female pattern baldness)
Often used in microneedling treatments or topical serums
🧫 3. Tissue Repair & Wound Healing
Enhances the body's healing response at cellular level
Promotes angiogenesis (new blood vessel formation)
Reduces inflammation and oxidative stress
🧠 4. Anti-Inflammatory & Antioxidant Effects
Modulates gene expression to suppress pro-inflammatory pathways
Helps protect against oxidative damage in tissues and organs
🧪 5. Stem Cell Activation
Enhances activity of skin and bone marrow stem cells
Supports regeneration in injured or aging tissues
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SS-31 (25mg) :-
SS-31, also known as elamipretide or Bendavia, is a mitochondria-targeting peptide that has shown potential in treating various conditions by improving mitochondrial function. It has been investigated for its antioxidant, anti-inflammatory, and anti-apoptotic properties, particularly in the context of neurodegenerative diseases, inflammatory diseases, and ischemia-reperfusion injury.
SS-31 (also known as Elamipretide) is a synthetic peptide that targets and protects mitochondria, the energy-producing structures in cells. The 25 mg dose is commonly used in clinical trials and experimental protocols.
Use Details
🫀 Heart Disease Improves heart function in heart failure and ischemic heart disease
🧠 Neurodegenerative Diseases May protect brain cells in conditions like Alzheimer’s, Parkinson’s
👁️ Eye Disorders Studied in dry age-related macular degeneration (dry AMD)
💪 Muscle Fatigue Helps with exercise intolerance and mitochondrial myopathy
🧬 Mitochondrial Dysfunction Repairs damaged mitochondria, boosts ATP production
🧫 Kidney Protection May reduce kidney injury in acute or chronic kidney disease
🧓 Age-Related Fatigue Improves mobility and stamina in older adults
How It Works
Targets mitochondria directly
Binds to cardiolipin in the mitochondrial membrane
Prevents oxidative damage
Restores energy production (ATP)
💉 Common Dosage Form
25 mg usually administered subcutaneously (under the skin) once daily in studies.
SS-31, also known as Elamipretide, is a synthetic peptide designed to improve mitochondrial function and reduce oxidative stress. It's primarily used to protect and restore mitochondrial function, specifically by reducing oxidative stress, stabilizing cardiolipin (a mitochondrial phospholipid), and improving mitochondrial energy production. Research suggests it may also be beneficial in conditions like Alzheimer's, brain injury, and kidney disease. The 25mg dosage refers to the amount of SS-31 in a single dose, often administered via injection.
Mitochondrial Target:
SS-31 specifically targets mitochondria, the powerhouses of cells, and is thought to protect and restore their function.
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Name Semaglutide
Purity ≥98% (as tested by HPLC, High-Performance Liquid Chromatography)
CAS Number 910463-68-2
Molecular Formula C₁₈₇H₂₉₁N₄₅O₅₉
Molecular Weight ~4113.58 g/mol
Peptide Sequence Modified GLP-1 (7-37) analog with substitutions to enhance stability
Form Lyophilized powder (freeze-dried)
Content 3mg per vial
Semaglutide is a medication originally developed for type 2 diabetes and obesity treatment. It's a GLP-1 receptor agonist, meaning it mimics the hormone GLP-1, which helps regulate blood sugar and appetite.
Type 2 Diabetes Management
Lowers blood sugar by increasing insulin release and reducing glucagon secretion.
Helps patients achieve better glycemic control.
Weight Loss (Obesity or Overweight with Comorbidities)
Reduces appetite and slows gastric emptying.
FDA-approved under the brand name Wegovy for chronic weight management.
💉 Semaglutide 3mg – Dosing Guide (Research and Clinical Context)
✅ Clinically Approved Dosing (Prescription Use)
Under brand names like Ozempic (for diabetes) and Wegovy (for weight loss), the FDA-approved semaglutide dosing follows this gradual titration to minimize side effects:
Week Dose (Subcutaneous Injection)
Weeks 1–4 0.25 mg once weekly
Weeks 5–8 0.5 mg once weekly
Weeks 9–12 1.0 mg once weekly (maintenance or increase as needed)
Weeks 13+ 1.7 mg – 2.4 mg weekly (Wegovy max) or up to 2.0 mg (Ozempic max)
Route: Subcutaneous injection (abdomen, thigh, or upper arm)
Frequency: Once per week, same day/time
⚠️ Important Notes
Side Effects: Can include nausea, vomiting, diarrhea, abdominal pain, and risk of pancreatitis.
Not for Type 1 Diabetes or Ketoacidosis.
Only certain brands and dosages are approved for specific uses.
The first 29 amino acids of GHRH were discovered to be as equally potent as its full 44 amino acid structure[1][2] This fragment became known as GRF (1-29). However, due to a rapid metabolic clearance analogues of GRF (1-29) were synthesized to enhance the biological activity and reduce the rapidity of metabolic clearance. These analogues were primarily created by substituting amino acids within the peptide structure for amino acids more resistant to enzymatic cleavage. One early analogue substituted the amino acid L-alanine (abbreviated as Ala or A) at the 2nd position of the peptide structure for its optical isomer (mirror image), D-alanine (abbreviated as D-Ala). This substitution resulted in a peptide bond between D-Ala and the 3rd amino acid in the structure aspartic acid (Asp) more able to resist rapid cleavage by the enzyme dipeptidyl peptidase-4, a cleavage which had previously led to an inactive peptide fragment.[3][4] This successful modification prompted the further creation of analogues with additional amino acid substitutions.
Ipamorelin:
A selective growth hormone secretagogue, Ipamorelin stimulates the release of GH by mimicking ghrelin's action on the ghrelin receptor. It is known for its specificity and minimal side effects compared to other GH-releasing peptides.
Mod GRF 1-29 (CJC-1295 without DAC):
This is a modified version of the first 29 amino acids of growth hormone-releasing hormone (GHRH). The modifications extend its half-life and enhance its ability to stimulate the pituitary gland to release GH. It is often used in research to study GH secretion patterns and related metabolic effects.
⚖️ Dosage and Composition
The 5/5 mg blend indicates that each vial contains 5 mg of Mod GRF 1-29 and 5 mg of Ipamorelin, totaling 10 mg per vial. This combination is designed to provide a balanced stimulation of GH release, potentially offering synergistic effects when used in research protocols.
🔬 Research Applications
In scientific studies, this peptide blend is utilized to:
Study Growth Hormone Dynamics: Investigating the patterns and regulation of GH secretion.
Metabolic Research: Understanding the role of GH in metabolism, including fat metabolism and muscle growth.
Aging and Longevity Studies: Exploring the effects of GH on aging processes and potential therapeutic applications.
Sleep and Recovery Research: Examining how GH influences sleep patterns and recovery processes.
⚠️ Important Considerations
Research Use Only: These peptides are intended strictly for laboratory research and are not approved for human or veterinary use.
Legal Status: The legality of purchasing and possessing these peptides varies by country and jurisdiction. It's essential to consult local regulations before acquiring them.
Storage and Handling: Proper storage conditions are crucial to maintain peptide stability. Typically, lyophilized peptides should be stored at -20°C or colder and protected from light. Reconstitution should be done with appropriate solvents, and solutions should be stored at 4°C and used within a specified timeframe.
Mod GRF 1-29 + Ipamorelin (5/5 mg) is primarily used in scientific research and clinical studies to investigate its effects on human growth hormone (GH) release and related metabolic functions. It is not FDA-approved for general medical use, but here are the commonly researched uses and potential applications:
Stimulation of Growth Hormone (GH) Release
Both peptides work synergistically to enhance the natural pulsatile release of GH from the pituitary gland.
Mod GRF 1-29 initiates GH release, while Ipamorelin amplifies it by mimicking ghrelin.
Anti-Aging Studies
GH has regenerative effects on tissues, so researchers study this combo to explore its potential for:
Improving skin elasticity
Increasing energy levels
Enhancing sleep quality
Muscle Growth and Recovery (in studies)
GH can help stimulate muscle protein synthesis and recovery.
This combo is sometimes researched for its effects on lean muscle mass and exercise recovery.
Fat Loss & Metabolic Support
GH mobilizes stored fat, making this blend of interest in obesity and metabolic syndrome research.
May support lipolysis (fat breakdown) in clinical models.
Bone Density Studies
GH supports bone mineralization. This combo is explored for potential applications in osteopenia/osteoporosis research.
Sleep Improvement
GH release is tied to deep sleep stages; researchers observe whether this combo improves sleep architecture and REM sleep.
Modified GRF (1-29) acts to increase growth hormone production and release by binding to the growth-hormone-releasing hormone receptor (GHRHR) on cells in the anterior pituitary.
Tesamorelin injection is a hormone similar to the one normally released from the hypothalamus gland in the brain. It is used to reduce excess fat (lipodystrophy) in the stomach area in patients with human immunodeficiency virus (HIV) infection.
Tesamorelin + Ipamorelin (6mg/2mg) Blend: Medical Uses & Applications
This peptide combination is primarily used for metabolic, anti-aging, and body composition benefits. Here’s a breakdown of its primary medical and off-label uses:
1. Approved Medical Use (FDA-Approved for HIV Lipodystrophy)
✅ Tesamorelin (6mg)
FDA-approved to treat HIV-associated lipodystrophy (excess belly fat caused by antiretroviral therapy).
Mechanism: Stimulates growth hormone (GH) release, reducing visceral fat.
2. Off-Label & Research-Based Uses
A. Fat Loss & Metabolic Health
Visceral fat reduction (even in non-HIV patients).
Improves insulin sensitivity (potential for metabolic syndrome/type 2 diabetes support).
B. Muscle Growth & Recovery
Ipamorelin (2mg) is a growth hormone secretagogue (GHS) that:
Boosts lean muscle mass.
Enhances post-workout recovery.
C. Anti-Aging & Longevity
Increases collagen production (improves skin elasticity).
May support cognitive function (GH plays a role in brain health).
D. Injury & Tissue Repair
Accelerates healing of tendons/ligaments (used by athletes).
3. Typical Treatment Protocol
Dosage:
Tesamorelin: 1-2mg/day (often 6mg total per week).
Ipamorelin: 200-300mcg/day (2mg total per week).
Administration: Subcutaneous injections (stomach or thigh).
Cycle Length: 8-12 weeks (with breaks to avoid GH desensitization).
4. Key Benefits vs. Other Peptides
Peptide Primary Use Pros Cons
Tesamorelin FDA-approved fat loss Targets stubborn belly fat Expensive, requires prescri
Final Verdict
This blend is best for:
✔ Men/women targeting stubborn fat (especially abdominal).
✔ Athletes seeking muscle recovery & anti-aging benefits.
✔ Those wanting a safer alternative to synthetic GH.
4. Typical Dosage & Protocol
Tesamorelin: 1-2mg/day (or 6mg/week).
Ipamorelin: 200-300mcg/day (or 2mg/week).
Administration: Subcutaneous injection (stomach/thigh).
Cycle Length: 8-12 weeks (followed by a break to avoid GH resistance).
3. How It Works
Tesamorelin → Stimulates pituitary GH release → Reduces visceral fat.
5. Expected Results & Timeline
📌 4-6 Weeks: Reduced belly fat, improved energy.
📌 8-12 Weeks: Visible muscle definition, better skin elasticity.
📌 Beyond 3 Months: Enhanced recovery, potential cognitive benefits.
5. Expected Results & Timeline
📌 4-6 Weeks: Reduced belly fat, improved energy.
📌 8-12 Weeks: Visible muscle definition, better skin elasticity.
📌 Beyond 3 Months: Enhanced recovery, potential cognitive benefits.
5. Expected Results & Timeline
📌 4-6 Weeks: Reduced belly fat, improved energy.
📌 8-12 Weeks: Visible muscle definition, better skin elasticity.
📌 Beyond 3 Months: Enhanced recovery, potential cognitive benefits.
(Best when combined with diet + exercise) .
Rare (serious):
Increased blood sugar (caution for diabetics).
Carpal tunnel syndrome (high doses).
Final Verdict
✅ Best for:
Men/women struggling with belly fat.
Athletes seeking muscle recovery + anti-aging.
Those wanting GH benefits without synthetic HGH risks.
❌ Not for: Quick fixes – requires consistent use for 2-3 months
Tesamorelin, known for reducing abdominal fat in HIV patients with lipodystrophy, together with Ipamorelin, a growth hormone-releasing peptide, can enhance overall body composition improvements. Furthermore, both substances may work synergistically to boost muscle growth, fat loss, recovery, and anti-aging effects, maximizing the benefits of each peptide when used in tandem.
Before taking this medicine
You should not use tesamorelin if you are allergic to it, or if you have:
cancer;
a pituitary gland disorder;
a history of pituitary gland tumor or surgery;
a history of head injury or radiation treatment; or
if you are pregnant.
To make sure you can safely take tesamorelin, tell your doctor if you have any of these other conditions:
a history of cancer or any tumor (either benign or malignant);
heart disease, high blood pressure;
kidney disease;
diabetes, eye problems caused by diabetes;
epilepsy
asthma;
migraine headaches;
adrenal gland disorder;
if you have ever had open heart surgery; or
if you have any major illness, a recent trauma, or a medical emergency.
FDA pregnancy category X. This medication can harm an unborn baby or cause birth defects. Do not use tesamorelin if you are pregnant. Tell your doctor right away if you become pregnant during treatment.
Women with HIV or AIDS should not breastfeed a baby. Even if your baby is born without HIV, the virus may be passed to the baby in your breast milk.
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Erectile Dysfunction (ED)
Designed to treat ED by inhibiting PDE‑5, which boosts cGMP levels, relaxing penile blood vessels, and improving erection firmness upon arousal.
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Tadalafil may help relax prostate and bladder neck muscles, easing urinary symptoms in BPH.
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Chewable tablet: Chew thoroughly before swallowing, for faster absorption—typically works within 15–30 minutes, or up to 30–60 minutes
Timing: Take about 30–60 min before sex; effects may last up to 36 hours
Frequency: Only once every 24 hours.
Food and drink: Can be taken with/without food. Avoid high-fat meals, alcohol, grapefruit juice for best effect.
Special note: Some sources erroneously say “place under tongue,” but chew is standard; tablets shouldn’t be swallowed whole.
Vidalista Ct 20 mg is a class PDE5 inhibitor medication which is used to treat erectile dysfunction (ED) or impotence in men.
Most men have the complaint of dissatisfied sexual intercourse due to a softer erection which even leads to breakups.
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