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Peptide Powder CAS 108736-35-2 Lanreotide


Pre-sale service
Lanreotide powder
1. Technical consultancy, to help customer know about the properties, features, quality, production and supply of the product they want.
2. Technical information and documents, such as COA, test report, sample etc.
3. Customers are welcome to visit our factory and negotiate with us at any time.
Sales service
1. Sign contract with customer, negotiating price, quality, delivery and other terms.
2.Answer the questions concerning properties, mechanism, application, quality, attention, usage etc. of the product.
3. Production schedule and on time delivery after signing contract.
After-sale service
1. Technical consultancy during use of the product.
2. Customer can return or exchange the merchandise with us if they need to change purchase plan due to some reasonable reasons, on condition that the product is not damaged.
3. If quality problems occur during normal use, please send us written information and documents, and we will respond within 24-48 hours.
Our R&D (research and development) center has around 1,000 square meters synthesis and testing laboratory, meets industrial standards, equipped with first class research facilities and powerful technical team.

Best price Nolvadex tamoxifen tamoxifen citrate powder


1) Product Name: Best price Nolvadex tamoxifen tamoxifen citrate powder
2) Active ingredients: Nolvadex
3) Specification: 99%
4) Test method: HPLC
5) Appearance: White crystals powder
6) Introduction:
Tamoxifen Citrate is a potent and selective inhibitor of PKC (protein kinase C). It is known that Tamoxifen Citrate functions in PKC εtranslocation. Studies suggest that Tamoxifen Citrate functions as an estrogen receptor antagonist in breast tissue. Once bound to the estrogen receptor Tamoxifen Citrate will not allow any other ligand to bind to the receptor. In contrast, Tamoxifen Citrate is an agonist towards this receptor in tissues of the endometrium. Studies indicate Tamoxifen Citrate inhibits DNA synthesis and transcription by recruiting co-repressors, which stop estrogen from interacting with genes. When combined with PAX2, Tamoxifen Citrate can inhibit the proliferation of ERBB2. It is also a high affinity activator of the GPR30 receptor. Tamoxifen Citrate is an activator of Estrogen Receptor.Nolvadex dosage
1. Tamoxifen is an anticancer drug, is given to treat breast cancer.
2. Tamoxifen citrate is an anticancer drug, is given to treat breast cancer. It also has proved effective when cancer has spread to other parts of the body. Tamoxifen citrate is most effective in stopping the kind of breast cancer that thrives on estrogen.
3. Tamoxifen citrateis also prescribed to reduce the risk of invasive breast cancer following surgery and radiation therapy for ductal carcinoma in situ. The drug can also be used to reduce the odds of breast cancer in women at high risk of developing the disease. It does not completely eliminate your chances, but in a five-year study of over 1,500 high-risk women, it slashed the number of cases by 44 percent.

Most important fact about Tamoxifen citrate
Although Tamoxifen citrate reduces the risk of breast cancer, it increases the possibility of developing endometrial (uterine) cancer. Women taking Tamoxifen citrate should have routine gynecological examinations and report any abnormal vaginal bleeding, changes in menstrual periods, change in vaginal discharge, or pelvic pain or pressure to the doctor immediately. Even after Tamoxifen citratetherapy has stopped, any abnormal vaginal bleeding should be reported at once.

Clomiphene Citrate
CAS: 50-41-9
MF: C32H36ClNO8
MW: 598.08
Assay(HPLC): 98.0-101.2%
Other name: clomifene dihydroen citrate,Clomid
Appearance: White or Almost White Crystalline Powder
High quality and competitive price
professional supplier
Functions:
Clomid dosage citrate is the anti-estrogen of choice for improving recovery of naturalproduction after a cycle, improving production of endurance athletes, and is also effective in reducing risk of gynecomastia during a cycle employing aromatizable steroids.
Application

High Purity Clomiphene Citrate/Clomid/CAS No: 50-41-9
Clomid is the anti-estrogen of choice for improving recovery of natural production after a cycle, improving te production of endurance athletes, and is also effective in reducing risk of gynecomastia during a cycle employing aromatizable steroids.

CAS NO.:107868-30-4
Chemical Name: 6-Methylenandrosta-1,4-diene-3,17-dione
Molecular Formula: C20H24O2
Molecular weight: 296.40
Assay: 99%
Appearance: white to almost white powder
Standard: Enterprise Standard
Packing: 1kg/aluminum foil bag
Min. order quantity: 5g
Payment: Western Union, Moneygram
Shipment: EMS, DHL, FeDex
Delivery: safe & timely, around 7days after payment.
Specifications:

Exemestane uses later period breast cancer who have used tamoxifen before. So exemestane is a good choice.
Packaging: as your requirement
using method: you should make exemestane into pills and 25mg/pill. you must use the exemestane pills after meal.
exemestane is chemical name and Aromasin is trade name for exemestane.

An antineoplastic (hormonal), suitable for menopause later period breast cancer who have used tamoxifen before. So exemestane is a good choice.
Packaging & Delivery:

We have the special way can ship 50g to 50kg products at a time. We can offer the melting powder into liquid service.And ship the liquid in the special bottles. According to your request and the quantity what you buy, we have several packaging methods for your choice. safety and quick shipping to you.

Free Sample High quality bpc 157 powder

BPC 157 powder has a strong anti-inflammatory activity in both acute and chronic inflammation models.In fact, preliminary results in clinical trials suggest that BPC 157 may become an important therapeutic tool for the treatment of inflammatory bowel disease.BPC 157 was shown to accelerate wound healing and to have a marked angiogenic effect.In addition, it significantly facilitates the healing of bone fracture in rats.This peptide also exhibits an osteogenic effect significantly improving the healing of segmental bone defect.BPC 157 accelerates the healing of transected rat Achilles tendon and transected rat quadriceps muscle.

FITC-phalloidin staining was able to demonstrate that BPC 157 induces F-actin formation in fibroblasts.
Likewise,Western blot analysis was able to detect the production and activation of paxillin and FAK proteins.The western blot analysis also showed that BPC 157 increases the extent of phosphorylation of paxillin and FAK proteins without affecting the amounts produced.
Quick Details
CAS No.:
137525-51-0
Other Names:
bpc-157 peptides
MF:
C62H98N16O22
EINECS No.:
137525-51-0
Place of Origin:
Guangdong, China
Type:
Auxiliaries and Other Medicinal Chemicals
Grade Standard:
Medicine Grade
Brand Name:
Mall
Model Number:
137525-51-0
Purity:
Min 99%
Product Name:
BPC 157
Appearance:
White Fine Powder
CAS:
137525-51-0
Grade:
Phamaceutical Grade
Assay:
HPLC 99%
Shelf life:
2 Years
Application:
White powder
Color:
White Color
Certificate:
GMP, HSE, ISO 9001, USP
Storage:
Cool dried storage

Lab Supply&Better Price Teriparatide Acetate CAS 52232-67-4

Teriparatide Acetate powder is a recombinant form of parathyroid hormone consisting of the first (N-terminus) 34 amino acids, which is the bioactive portion of the hormone. It is an effective anabolic(i.e., bone growing) agent used in the treatment of some forms of osteoporosis. It is also occasionally used off-label to speed fracture healing. Teriparatide is identical to a portion of human parathyroid hormone (PTH) and intermittent use activates osteoblasts more than osteoclasts, which leads to an overall increase in bone.
Teriparatide is the only anabolic (i.e., bone growing) agent indicated for use in postmenopausal women with osteoporosis at a high risk for fracture or with a history of osteoporotic fracture, patients with multiple risk factors for fracture, and for patients who have failed or are intolerant to other available osteoporosis therapy. It has been FDA-approved since 2002. It is effective in growing bone (e.g., 8% increase in bone density in the spine after one year)[6"> and reducing the risk of fragility fractures. Osteoporosis medications are generally safe, but some side effects of teriparatide include headache, nausea, dizziness, and limb pain.

GMP grade best triptorelin acetate bodybuilding peptide Triptorelin powder

Triptorelin Acetate powder, a decapeptide (pGlu-His-Trp-Ser-Tyr-D-Trp-Leu-Arg-PRO-Gly-NH2), is a gonadotropin-releasing hormone agonist (GnRH agonist) used as the acetate or pamoate salts. By causing constant stimulation of the pituitary, it decreases pituitary secretion of gonadotropins luteinizing hormone (LH) and follicle stimulating hormone (FSH). Like other GnRH agonists, triptorelin may be used in the treatment of hormone-responsive cancers such as prostate cancer or breast cancer, precocious puberty, estrogen-dependent conditions (such as endometriosis or uterine fibroids), and in assisted reproduction. Triptorelin is marketed under the brand names Decapeptyl (Ipsen) and Diphereline and Gonapeptyl (Ferring Pharmaceuticals).
Quick Details
CAS No.:
57773-63-4
Other Names:
Trifluoroacetate-d5
MF:
C66H80F3N18O15
EINECS No.:
N/M
Place of Origin:
Jiangsu, China
Type:
Auxiliaries and Other Medicinal Chemicals
Grade Standard:
Medicine Grade
Usage:
Animal Pharmaceuticals
Brand Name:
EUBO
Model Number:
EUBO-PEP18
Purity:
99%
Product Name:
triptorelin
Appearance:
White Powder
Grade:
Phamaceutical Grade
CAS:
57773-63-4
Assay:
Purity 99%
Certificate:
ISO
Shelf life:
2 Years
Function:
Health Proctect
Package:
in vial
Sample:
Availiable

Best Quality Triptorelin Acetate Peptide Powder 2mg for Muscle Gain

Triptorelin Acetate powder is usually given as an injection at your doctor's office, hospital, or clinic. If you will be
using triptorelin at home, a health care provider will teach you how to use it. Be sure you understandhow to use triptorelin. Follow the procedures you are taught when you use a dose. Contact yourhealth care provider if you have any questions.Triptorelin is injected into the muscle.Rotate the injection site. Do not inject into an area of skin that is red, hard, or bruised, or has scarsr stretch marks.Do not use triptorelin if it contains particles, is cloudy or discolored, or if the vial is cracked or damaged.Keep this product, as well as syringes and needles, out of the reach of children and away from pets.Do not reuse needles, syringes, or other materials. Ask your health care provider how to dispose of these materials after use.

Description :
Triptorelin is a releasing hormone agonist used as the acetate or pamoate salts. By causing constant stimulation of the pituitary, it decreases pituitary secretion of luteinizing hormone and follicle stimulating hormone.
Like other GnRH agonists, triptorelin may be used in the treatment of hormone-responsive cancers such as prostate cancer or breast cancer, precocious puberty, estrogen-dependent conditions, and in assisted reproduction. Triptorelin is marketed under the brand names Decapeptyl and Diphereline and Gonapeptyl.
Application :
Triptorelin may be used in the treatment of hormone-responsive cancers such as prostate cancer or breast cancer, precocious puberty, estrogen-dependent conditions, and in assisted reproduction. Triptorelin is marketed under the brand names Decapeptyl and Diphereline and Gonapeptyl.
In the United States, it is sold by Watson as Trelstar.In Iran Triptorelin is marketed under the brand name Variopeptyl.In India, Dr. Reddy's Laboratories has launched recently Triptorelin under the brand name "Pamorelin LA". During the treatment of prostate cancer it does cause a surge, known as a flare effect. In men a reduction of serum levels into the range normally seen after surgical castration occurs approximately two to four weeks after initiation of therapy.

Basic Info.
CAS:33515-09-2
Sequence:P-Glu-His-Trp-Ser-Tyr-Gly-Leu-Arg-Pro-Gly-NH2
MF:C55-H75-N17-O13
MW:1182
Purity:99%
Specification:2mg/vial, 10mg/vial
Appearance:White Lyophilized Powder
Standard:USP
Storage: Lyophilized peptides although stable at room temperature for 3 months, should be stored desiccated below -18 C. Upon reconstitution of the peptide it should be stored at 4 C between 2-21 days and for future use below -18 C.Gonadorelin Acetate powder,Gonadorelin powder

Description
Gonadorelin is responsible for the release of follicle stimulating hormone and leutinizing hormone from the anterior pitutitary. In the pituitary GnRH stimulates synthesis and release of FSH and LH, a process that is controlled by the frequency and amplitude of GnRH pulses, as well as the feedback of androgens and estrogens. The pulsatility of GnRH secretion has been seen in all vertebrates, and it is necessary to ensure a correct reproductive function. Thus a single hormone, GnRH, controls a complex process of follicular growth, ovulation, and corpus luteum maintenance in the female, and spermatogenesis in the male. Its short half life requires infusion pumps for its clinical use.
Gonadorelin USAGE

For evaluating the functional capacity and response of the gonadotropes of the anterior pituitary also for evaluating residual gonadotropic function of the pituitary following removal of a pituitary tumor by surgery and/or irradiation.
Gonadorelin is responsible for the release of follicle stimulating hormone and leutinizing hormone from the anterior pitutitary. In the pituitary GnRH stimulates synthesis and release of FSH and LH, a process that is controlled by the frequency and amplitude of GnRH pulses, as well as the feedback of androgens and estrogens. The pulsatility of GnRH secretion has been seen in all vertebrates, and it is necessary to ensure a correct reproductive function. Thus a single hormone, GnRH, controls a complex process of follicular growth, ovulation, and corpus luteum maintenance in the female, and spermatogenesis in the male. Its short half life requires infusion pumps for its clinical use
Systemic - Like naturally occurring releasing hormone (GnRH), gonadorelin primarily stimulates the synthesis and release of luteinizing hormone (LH) from the anterior pituitary gland. Follicle-stimulating hormone (FSH) production and release is also increased by gonadorelin, but to a lesser degree. In prepubertal females and some gonadal function disorders, the FSH response may be greater than the LH response. For the treatment of amenorrhea, delayed puberty, and infertility the administration of gonadorelin is used to simulate the physiologic release of GnRH from the hypothalamus in treatment of delayed puberty, treatment of infertility caused by hypogonadotropic hypogonadism, and induction of ovulation in those women with hypothalamic amenorrhea. This results in increased levels of pituitary LH and FSH, which subsequently stimulate the gonads to produce reproductive steroids.

Metenolone enanthate, or methenolone enanthate, is a dihydrotestosterone (DHT)-based anabolic steroid. It is an ester derivative of methenolone sold commonly under the brand names Primobolan (tablet form) or Primobolan Depot (injectable). When it interacts with the aromatase enzyme it does not form any estrogens.[medical citation needed] It is used by people who are very susceptible to estrogenic side effects, having lower estrogenic properties than nandrolone. Methenolone, in form of enanthate and acetate, is available as an injection or as an oral formulation. The injection is regarded as having a higher bioavailability. It is an enanthate ester which is quite long-acting. Because it by-passes hepatic breakdown on the first pass, it also has a higher survival rate. The tablets are in a short-lived acetate form. Methenolone is not 17-alpha-alkylated, but 1-methylated for oral bioavailability. This reduces the stress on the liver, but also the availability. In doses of 200 mg per week or less (intramuscular) blood pressure is rarely altered.Test E (Test P) dosage

Methenolone can be suppressive of the hypothalamic-pituitary-gonadal axis.

Application :

Methenolone enanthate is a very popular option particularly for athletes leaning out and attempting to maintain as much muscle as possible during calorie restriction. Many competitive bodybuilders would not consider a pre-contest stack with out the addition of methenolone. It is an anabolic steroid , widely used in the new metabolism , prevention of osteoporosis and so on .

Protein assimilatio , the protein hormone assimilation strong activity of the liver, and the small toxicity . Methenolone Enanthate is a dihydrotestosterone based anabolic steroid , Methenolone Enanthate is an ester derivative of methenolone sold commonly under the brand name primobolan , Methenolone Enanthate is used by people who are very susceptible to estrogenic aide effect , having lower estrogenic properities than nandrolone, methenolone , in form of enanthate and acetate , Methenolone has no estrogenic side effects and its effects on cholesterol , Methenolone is also not overly suppressive of the HPTA axis , for this reason , mang bodybuilder use Methenolone in between steroid cycles .