--+8615840669648

Our Products

APIs And Intermediates

Vitamins

Food Ingredients

Personal Care Chemicals

Pharmaceutical Excipients

BPC-157 China

4.0 USD ($)/Piece

Get a Price/Quote

Product Details:

Product Type Peptides
EINECS No 211-519-9
HS Code 2937190099
Ingredients BPC-157
CAS No 137525-51-0
Molecular Formula C62H98N16O22
Properties BPC-157 (Body Protection Compound-157) is a synthetic pentadecapeptide derived from a protective protein found in human gastric juice. Chemical and Physical Properties Amino Acid Sequence: Gly-Glu-Pro-Pro-Pro-Gly-Lys-Pro-Ala-Asp-Asp-Ala-Gly-Leu-Val (15 amino acids) Molecular Formula / Weight: C H N O / 1,419.56 g/mol Solubility & Stability: Freely soluble in water at normal pH. Uniquely stable in human gastric juice and acidic environments (resisting degradation for over 24 hours ex vivo). Pharmacokinetics: Rapid elimination with a plasma half-life under 30 minutes in animal models. Demonstrates variable bioavailability depending on the administration route (e.g., ~14 19% intramuscular in rats; ~45 51% in dogs). Biological and Pharmacological Mechanisms Angiogenesis: Stimulates vascular endothelial growth factor receptor 2 (VEGFR2) and promotes new blood vessel formation. Nitric Oxide (NO) System: Interacts with the L-arginine/NO pathway, stimulating endothelial nitric oxide synthase (eNOS) activity. Growth Factor Signaling: Increases growth hormone receptor (GHR) expression in tendon fibroblasts and amplifies focal adhesion kinase (FAK) paxillin signaling pathways. Cytoprotection: Acts as a stabilizer of the endothelium and counteracts toxic or inflammatory insults (such as NSAID- or alcohol-induced lesions) in the gastrointestinal tract.
Click to View more

Request to Call Back Send Inquiry

Product Details
Product Description

BPC-157 China Price And Quantity

Minimum Order Quantity 10 Piece
Price 4.0 USD ($)/Piece

BPC-157 China Product Specifications

Taste Odorless
Ph Level 3.36 0.10
Refractive Rate 1.575~1.576
Shape other
Storage Freezer
Melting Point >232 C (dec.)
Poisonous NO
Smell Other
Purity Not less than 99.00%
Shelf Life 18 Months
Solubility BPC-157 is highly soluble in water, with a solubility of 100 mg/mL.
Grade Research Grade
Properties BPC-157 (Body Protection Compound-157) is a synthetic pentadecapeptide derived from a protective protein found in human gastric juice. Chemical and Physical Properties Amino Acid Sequence: Gly-Glu-Pro-Pro-Pro-Gly-Lys-Pro-Ala-Asp-Asp-Ala-Gly-Leu-Val (15 amino acids) Molecular Formula / Weight: C H N O / 1,419.56 g/mol Solubility & Stability: Freely soluble in water at normal pH. Uniquely stable in human gastric juice and acidic environments (resisting degradation for over 24 hours ex vivo). Pharmacokinetics: Rapid elimination with a plasma half-life under 30 minutes in animal models. Demonstrates variable bioavailability depending on the administration route (e.g., ~14 19% intramuscular in rats; ~45 51% in dogs). Biological and Pharmacological Mechanisms Angiogenesis: Stimulates vascular endothelial growth factor receptor 2 (VEGFR2) and promotes new blood vessel formation. Nitric Oxide (NO) System: Interacts with the L-arginine/NO pathway, stimulating endothelial nitric oxide synthase (eNOS) activity. Growth Factor Signaling: Increases growth hormone receptor (GHR) expression in tendon fibroblasts and amplifies focal adhesion kinase (FAK) paxillin signaling pathways. Cytoprotection: Acts as a stabilizer of the endothelium and counteracts toxic or inflammatory insults (such as NSAID- or alcohol-induced lesions) in the gastrointestinal tract.
Physical Form Powder
Application Pharmaceutical
Density 1.366 0.06 Gram per cubic centimeter(g/cm3)
Appearance White powder
Usage BPC-157 (Body Protection Compound-157) is an experimental synthetic peptide derived from a protein found in human gastric juice.
Product Type Peptides
EINECS No 211-519-9
HS Code 2937190099
Ingredients BPC-157
CAS No 137525-51-0
Molecular Formula C62H98N16O22

BPC-157 China Trade Information

FOB Port Shenzhen or Guangzhou
Payment Terms Telegraphic Transfer (T/T), Western Union
Supply Ability 10000 Piece Per Week
Delivery Time 5 Days
Sample Available Yes
Sample Policy Free samples available with shipping and taxes paid by the buyer
Packaging Details 10 Vials per Kit
Main Export Market(s) Western Europe, Asia, Australia, North America
Main Domestic Market All India
Certifications GMP, ISO9001

Product Description

BPC-157 (short for Body Protection Compound-157) is a synthetic peptide fragment consisting of 15 amino acids, originally isolated from proteins found in human gastric juice. In the fitness and biohacking communities, it is often referred to as a "biological Band-Aid."

Key Features and Functions

Tissue Repair: In animal studies and anecdotal reports, it is believed to promote the repair of tendons, ligaments, muscles, bones, skin, and nerves.

Gastrointestinal Protection: It possesses anti-ulcer properties and may offer protective effects for the gastrointestinal mucosa, as well as in conditions like ulcerative colitis.

Anti-inflammatory Mechanism: Research indicates that it can modulate inflammatory factors such as IL-6 and TNF-, thereby reducing localized inflammatory responses in the body.

Tell us about your requirement

Price:

Quantity

Select Unit

50
100
200
250
500
1000+

Additional detail

Mobile number

Other Products in 'Peptide Preparations' category

Tesamorelin 2mg 5mg 10mg 20mg Price : 5.8 USD ($)/Piece Minimum Order Quantity : 10 CAS No : 218949485 Ingredients : Tesamorelin Product Type : Peptides Appearance : White powder Usage : The primary use of Tesamorelin is to treat lipid dystrophism in HIVinfected individuals, specifically by reducing excess visceral fat around the liver. Main Uses and Efficacy: This drug works by mimicking the body natural growth hormonereleasing hormone, stimulating the pituitary gland to secrete growth hormone, thereby specifically regulating lipid metabolism. Multiple clinical studies have confirmed its effectiveness in the following areas: 1) Reducing Visceral Fat: Significantly reduces abdominal visceral fat accumulation (average reduction of approximately 14%18%) and shrinks waist circumference. 2) Improving Liver Fat: Significantly reduces liver fat content, particularly beneficial for patients with HIV and metabolicrelated fatty liver disease. 3) Optimizing Body Composition: While reducing trunk fat, it increases lean body mass (muscle mass) with minimal impact on subcutaneous fat. Application : Pharmaceutical Properties : Tesamorelin is a synthetic growth hormonereleasing hormone analogue primarily used to reduce visceral fat accumulation (lipodystrophy) in HIVinfected individuals. Its core characteristics can be summarized as follows: 1) Pharmacological Properties: Mechanism of Action: It is a growth hormonereleasing factor (GRF) analogue that binds to and activates GRF receptors in the pituitary gland, stimulating the pituitary to secrete endogenous growth hormone (GH) in a pulsatile manner. Subsequently, growth hormone stimulates the liver to produce insulinlike growth factor 1 (IGF1), which mediates most of the biological effects, including reducing visceral fat and regulating metabolism. Hepatic Effects: In clinical trials, tesamorelin did not cause elevated serum transaminases or significant liver damage; on the contrary, it was even associated with lowering existing ALT levels, potentially improving nonalcoholic fatty liver disease. 2) Pharmacokinetic Properties: Absorption and Bioavailability: Administered subcutaneously, the amount absorbed into systemic circulation is very limited, with an absolute bioavailability of less than 4%. Its pharmacokinetic characteristics are similar in HIVinfected individuals and healthy subjects, and are not significantly affected by factors such as age, body size, or race. Distribution and elimination: It has a large volume of distribution, averaging 200 liters; the elimination halflife is very short, approximately 826 minutes in healthy subjects and approximately 38 minutes in HIVinfected individuals. Metabolism and excretion: There are currently no formal human metabolic studies. 3) Clinical Characteristics: Primary indication: For reducing excess abdominal fat in patients with HIVrelated lipodystrophy. It is important to emphasize that this is not a general medication for weight loss. Efficacy: Clinical studies have shown that daily subcutaneous injection of 2 mg for 26 weeks significantly reduces visceral adipose tissue (VAT) (average reduction of approximately 1418%), with no adverse effects on subcutaneous fat in the extremities. It also lowers triglyceride levels. Administration: Once daily, subcutaneous injection. Dosage varies depending on the drug strength. For example, the recommended dose for the 1 mg/vial strength is 2 mg daily; the recommended dose for the 2 mg/vial strength (Egrifta SV) is 1.4 mg daily. 4) Safety Characteristics: Common Side Effects: Primarily include injection site reactions (such as redness, swelling, pain, and itching), arthralgia, muscle pain, and limb pain. Side Effects to Watch Out For: May cause elevated blood sugar (increased risk of glucose intolerance or type 2 diabetes), therefore, caution should be exercised in diabetic patients. In addition, fluid retention (manifested as arthralgia, carpal tunnel syndrome), allergic reactions (such as rash, shortness of breath), and antibody production may occur (occurring in approximately 50% of patients, but usually does not affect efficacy). Contraindications: Contraindicated in patients with hypersensitivity to any of the drug components, those with an active or previous history of malignancy, and patients with pituitaryrelated diseases (such as pituitary tumors). Contraindicated in pregnant women as it may harm the fetus. Drug Interactions: Concomitant use with corticosteroids (such as prednisone) may reduce the efficacy of the latter. No clinically significant interactions were observed when used in combination with simvastatin or ritonavir. It has minimal effect on the hepatic CYP3A enzyme system. 5) Chemical Properties: Chemical Nature: It is a polypeptide composed of 44 amino acids and is a synthetic analog of human natural growth hormonereleasing hormone (GHRH). Its chemical structure is C221H366N72O67S. Structural Modification: The Nterminus of its molecule has been modified (by adding a trans3hexenoyl group) to increase its stability and prolong its duration of action. Appearance: Usually a sterile, preservativefree lyophilized powder, which must be dissolved in the matching diluent before use. Physical Form : Powder Grade : Research Grade Shelf Life : 18 Months Solubility : Soluble in water Purity : 99.0% Poisonous : NO Smell : Other Storage : Freezer Taste : Other Molecular Formula : C221H366N72O67S HS Code : 2937190099 EINECS No : 6038092 Shape : other Molecular Weight : 5135.86 Milligram (mg)

Send Inquiry

Cathelicidin LL-37 (Human) Price : 8.6 USD ($)/Piece Minimum Order Quantity : 100 CAS No : 154947667 Ingredients : LL37 Product Type : Lyophilized Powder Appearance : White powder Usage : 1) New Drugs: Low expression of TLR2 and LL37 and low level of serum LL37 in children with atopic dermatitis (AD) suggest that AD has problems such as innate immunity and skin barrier function defects. Vitamin D may activate vitamin D receptors and promote LL37 expression through the TLR2 pathway, thereby protecting AD. Perhaps in the future, LL37related drugs can be designed to assist vitamin D in combating atopic dermatitis. Neonatal sepsis is mainly caused by infection. With the emergence of drugresistant bacteria, antibiotic selection has become increasingly difficult, so it is particularly important to improve one's own resistance. Studies have shown that vitamin D can increase the expression of the body's antimicrobial peptide LL37, thereby improving the body's ability to defend against infection and providing strong protection for antibiotic treatment. This will provide ideas for designing drugs that replace antibiotics. 2) Animal Feed Additives: LL37 has a broad antibacterial spectrum and high antibacterial activity, bacteria are not easy to develop drug resistance, it can also neutralize endotoxins and can be regarded as a new alternative to antibiotics. Therefore, choosing a suitable expression template to express LL37 analogs will promote the production of animal feed additives with high antibacterial efficiency and high nutrition, making it have certain economic benefits. 3) Preservatives: LL37 and CP1 are produced on a large scale through genetic engineering, they have strong antibacterial activity, small relative molecular mass, high antibacterial activity when heated at 121 for 30 minutes, good water solubility, safe and nontoxic, and not easy to develop drug resistance. Adding an appropriate amount of antimicrobial peptides to milk has a certain preservation effect on storage. Application : Pharmaceutical Properties : 1) Antimicrobial: As an important member of the natural immune system, LL37 has strong antimicrobial activity both in vivo and in vitro, including Grampositive bacteria (such as Staphylococcus aureus, Streptococcus, etc.), Gramnegative bacteria (such as Salmonella, Escherichia coli, etc.), fungi and viruses. Moreover, LL37 also has a certain selective killing effect on some fungi, viruses, tumor cells and protozoa. 2) Regulate the Release of Immune and Inflammatory Mediators: LL37 can cause immune cell differentiation and chemotaxis, induce cell differentiation, cytokine release, neutralize endotoxins and antitumor, etc., and enhance the body's ability to resist harmful microorganisms. Advantages: Compared with traditional antibiotics, Antimicrobial Peptide LL37 human can kill pathogens, is not easy to produce drug resistance, and is not easy to produce immune rejection reactions. It is an important effector molecule of the natural immune system. Physical Form : Powder Grade : Reagent Grade Shelf Life : 24 Months Solubility : Soluble in water or acidic buffer (such as 0.1% acetic acid) Purity : 99.0% Poisonous : NO Smell : Other Storage : Freezer Taste : Other Molecular Formula : C205H340N60O53 EINECS No : 2115199 Shape : other Molecular Weight : 4493.74 Grams (g)

Send Inquiry

SLU-PP-332 China Price : 10.0 USD ($)/Unit Minimum Order Quantity : 10 CAS No : 303760603 Ingredients : SLUPP332 Product Type : Peptides Appearance : White powder Usage : Obesity and weight management research: It can activate specific receptors within cells, tricking the body into thinking it's engaged in highintensity exercise, thereby promoting fatty acid burning and reducing body fat accumulation without suppressing appetite. Type 2 diabetes and metabolic diseases: Researchers are using it to explore how to improve insulin sensitivity, lower blood sugar and lipids, and thus improve metabolic syndrome. Improvement of muscle atrophy and aging: This compound can increase oxidized skeletal muscle fibers (endurance muscle), and is used to study how to alleviate muscle weakness and atrophy caused by aging, disease, or prolonged bed rest. Improvement of exercise endurance research: In animal experiments, it can significantly enhance the function of mitochondria within cells, increasing the running distance and time of mice on a treadmill by 50% to 70%. Application : Pharmaceutical Properties : PanERR Agonist: It is an agonist of the estrogen receptorassociated receptor (ERR). It can activate three receptors simultaneously, with the strongest effect on ERR . Affinity Values: According to data from MedChemExpress, its EC values for the three receptors are 98 nM (ERR ), 230 nM (ERR ), and 430 nM (ERR ). NonToxic Small Molecule: In laboratory tests, it exhibits characteristics of a cellsafe, nontoxic compound. Physical Form : Powder Grade : Research Grade Shelf Life : 24 Months Solubility : Soluble in water Purity : 99% Poisonous : NO Smell : Other Storage : Freezer Taste : Other Molecular Formula : C18H14N2O2 HS Code : 2937190099 EINECS No : N/A Shape : other

Send Inquiry

China Melanotan 2 Acetate (MT-2) 10mg Price : 7.0 USD ($)/Piece Minimum Order Quantity : 10 CAS No : 121062086 Ingredients : MT2 Product Type : Peptides Appearance : White powder Usage : Promotes skin tanning: By binding to melanin receptors, it stimulates melanin production, promoting skin pigmentation without requiring excessive UV exposure. Regulates sexual function: It can act on the central nervous system, and in relevant laboratory studies, it has been observed to enhance libido and improve erectile function. Metabolism and appetite control: It can act on the hypothalamus, showing the potential to suppress appetite, reduce energy intake, and promote lipolysis. Application : Pharmaceutical Properties : Promotes pigmentation (tanning): By activating MC1 receptors in the skin, it stimulates melanin production, thus darkening the skin without excessive UV exposure. Regulates metabolism and appetite: By acting on MC4 receptors in the hypothalamus, it has a certain anorexia effect, inducing weight loss and reducing food intake. Improves sexual function: One of its initial development goals was to treat erectile dysfunction and female sexual dysfunction. It triggers and enhances erectile activity through a central nervous system mechanism (activation of MC3 and MC4 receptors). Neuro and antiinflammatory properties: In some animal models, it has shown potential to promote peripheral nerve regeneration and provide neuroprotection. Physical Form : Powder Grade : Research Grade Shelf Life : 24 Months Solubility : Soluble in water Purity : 99% Poisonous : NO Smell : Other Storage : Freezer Taste : Other Molecular Formula : C50H69N15O9 HS Code : 2937190099 EINECS No : N/A Shape : other

Send Inquiry

SEND INQUIRY CALL ME FREE

Quick Inquiry

Quick Links

Contact Details

DALIAN HANDOM CHEMICALS CO.,LTD.

RM702, Unit 1, Building 21, Liuhe Road, Ganjingzi Dist,Dalian - 116091, Liaoning, China

Phone :--+8615840669648

Mr John Wang (Manager)

Mobile :+8615840669648

Send Inquiry

E-mail us : export@handom-chem.com