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Pentadecapeptide Bpc 157 Human Growth Hormone Supplements Peptide Peptide Drum 137525-51-0

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Pentadecapeptide Bpc 157 Human Growth Hormone Supplements Peptide Peptide Drum 137525-51-0
 
Pentadecapeptide Bpc 157 Basic Info.
 
Product Name: Pentadecapeptide Bpc 157
Alias: Booly Protection Compound 15, Pentadecapeptide, BPC 157;
Sequence: Gly-Glu-Pro-Pro-Pro-Gly- Lys-Pro-Ala-Asp-Asp-Ala-Gly-Leu-Val 
CAS: 137525-51-0 
MF: C62H98N16O22 
MW: 1419.53552 
Purity: 99% 
Specification: 2mg/vial 
Appearance: White Lyophilized Powder 
Standard: USP 
Certification: SGS 
Method of Analysis: HPLC 
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. 
 
Pentadecapeptide Bpc 157 Description:
 
Pentadecapeptide BPC 157, composed of 15 amino acids, is a partial sequence of body protection
compound (BPC) Pentadecapeptide BPC 157, composed of 15 amino acids, is a partial sequence 
of body protection compound (BPC) that is discovered in and isolated from human gastric juice.
The promoting effect of pentadecapeptide BPC 157 on tendon healing involves tendon outgrowth, 
cell survival, and cell migration
 
Stable gastric pentadecapeptide BPC 157 (GEPPPGKPADDAGLV, M.W. 1419) may be the new drug stable in human gastric juice, effective both in the upper and lower GI tract, and free of side effects.
 
BPC 157, in addition to an antiulcer effect efficient in therapy of inflammatory bowel disease (IBD)(PL 14736) so far only tested in clinical phase II, has a very safe profile, and exhibited a particular wound healing effect. It also has shown to interact with the NO-saystem, providing endothelium protection and angiogenic effect, even in severely impaired conditions (i.e., it stimulated expression of early growth response 1 gene responsible for cytokine and factor generation and early extracellular matrix (collagen) formation (but also its repressor nerve factor 1- A binding protein-2)), important to counteract severe complications of advanced and poorly controlled IBD. Hopefully, the lessons from animal studies, particularly advanced intestinal anastomosis healing, reversed short bowel syndrome and fistula healing indicate BPC 157s high significance in further IBD therapy. Also, this supportive evidence (i.e., no toxic effect, limit test negative, LD1 not achieved, no side effect in trials) may counteract the problems commonly exercised in the use of peptidergic agents, particularly those used on a long-term basis
 
Pentadecapeptide Bpc 157 Application:
 
1. BPC 157 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.
 
2. 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.
 
3. 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.
 

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S4 Most Effective Sarm Supplement Andarine Muscle Building Raw Steroids Powder 401900-40-1

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S4 Most Effective Sarm Supplement Andarine Muscle Building Raw Steroids Powder 401900-40-1
 
Andarine Basic Info:
 
Product name: Andarine
Synonyms: Andarine;S4;S-4;GTX-007
CAS No.: 401900-40-1
MF: C19H18F3N3O6
MW: 441.36
Purity: 99.92%
Product categories APIs; Amines; Aromatics; Chiral Reagents; Intermediates & Fine Chemicals; Pharmaceuticals; SARMS
Appearance: White crystalline powder
Natural Bodybuilding SARM Powder Andarine S4 GTX-007 High Purity CAS 401900-40-1
 
Andarine Description:
 
Selective androgen receptor modulators or SARMs are a novel class of androgen receptor ligands. They are intended to have the same kind of effects as androgenic drugs like anabolic steroids but be much more selective in their action, allowing them to be used for many more clinical indications than the relatively limited legitimate uses that anabolic steroids are currently approved for.
 
S-4 is an experimental or investigation-stage proprietary SARM research chemical developed by GTx Inc for treatment of benign prostatic hypertrophy, muscle wasting, and osteoporosis. S-4 is considered a partial agonist of the androgen receptors in target tissue. S-4 has less pronounced anabolic and androgenic compared to other SARMs. In trials treating BPH induced in animal models, S-4 reduced prostate weight as effectively as finasteride and without producing any reduction in muscle mass or other side effects common with androgen receptor binding compounds. Gao et al suggest that by binding to androgen receptors, S-4 prevents DHT from binding and activating, but bypasses the expected anti-androgenic effects that would occur from occupying androgen receptors due to the fact that S-4 itself is a partial agonist of androgen receptors. S-4 has also been shown to prevent bone loss, reduce body fat, and improve muscle strength and body composition in orchidectomized and ovariectomized rats.
 
Andarine Application:
 
S4 Andarine is an orally active partial agonist for androgen receptors. It is less potent in both anabolic and androgenic effects than other SARMs. In an animal model of benign prostatic hypertrophy, andarine was shown to reduce prostate weight with similar efficacy to finasteride, but without producing any reduction in muscle mass or anti-androgenic side effects.
 
Andarine Function:
 
1. 1/3 as androgenic as testosterone in muscle tissue.
2. Anabolic at doses above 50mg.
3. Great for strength.
4. Great for muscle hardness.
5. Great for enhanced vascularity.
6. Great for endurance (aerobic or anaerobic).
7. Accelerated fat loss above 50mg.
8. Joint healing effects.
 

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USP Grade Pharmaceutical Raw Materials 99%Min Idebenone For Cerebral Infarction 58186-27-9

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USP Grade Pharmaceutical Raw Materials 99%Min Idebenone For Cerebral Infarction 58186-27-9
 
Idebenone Basic Info.:
 
Product Name: Idebenone
CAS: 58186-27-9
Chemical name: 6-(10-Hydroxydecyl)-2,3-dimethoxy-5-methyl-1,4-benzoquinone
Molecular formula: C19H30O5
Molecular weight: 338.44
Melting point: (52- 55 °C )
Loss on drying: ≤ 0.5%
Relevant impurities(HPLC ): ≤ 0.8%
Content(HPLC ): ≥ 99.5%
Packing specification: 5Kg / tin, 25Kg / tin
Storage: Sealed and stored at room temperature.
Executive standard:Enterprise standard
Appearance: Orange yellow or orange crystalline powder, odorless, flavorless.
Property: This product is orange yellow or orange crystalline powder, soluble in methanol, ethanol, insoluble in water, odorless, flavorless.
Used for cerebral infarction, cerebral hemorrhage and cerebral artery sclerosis associated with depression, such as language barriers and intelligence impairment, etc.
 
Idebenone Introduction:
 
Idebenone is a kind of new drug for treating senile dementia and improving mental symptom. Also, it is a better antioxidant in cosmetics and health care than Coenzyme Q10 and Vitamin.
 
Idebenone is a modified version of coenzyme Q10 (CoQ10), which is absolutely crucial for metabolic function. Without it, the electron respiratory chain breaks and cells cannot produce energy. It is also the only lipid-soluble antioxidant that is synthesized in our bodies. Natural levels of CoQ10 begin to decrease after age 30.
 
CoQ10 would be a perfect supplement for athletes that expend excessive energy or push the anaerobic envelope were it not for one important detail: under hypoxic conditions (like going anaerobic), CoQ10 becomes pro-oxidative and creates a powerful free radical that can damage DNA, mitochondria, and lipid membranes.
 
There is a synthetic variation of CoQ10 called ubiquinol, also known as idebenone. It has been formulated to have all the advantages of CoQ10 without the pro-oxidative drawback.
 

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High Quality Pharmaceutical Raw Material Conform USP Diethylstilbestrol 56-53-1 / 6898-97-1

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High Quality Pharmaceutical Raw Material Conform USP Diethylstilbestrol 56-53-1 / 6898-97-1
 
Diethylstilbestrol Basic Info.:
 
Product Name: Diethylstilbestrol
Synonyms: Stilbestrol;Diethylstilbesterol;Domestrol;Grafestrol;Estrosyn;Fonatol;LABOTEST-BB LT00233101;
CAS: 56-53-1 / 6898-97-1
MF: C18H20O2
MW: 268.35
EINECS: 200-278-5
Assay: 99%
Melting point: 170-172 °C(lit.)
Storage temp.: 0-6°C
Solubility methanol: 0.1 g/mL, clear, faintly yellow
Stability: Isomerizes rapidly in Benzene, Chloroform, and Ether. Keep Shielded from light.
Water Solubility: Practically insoluble
Chemical Properties: White Solid
Product Categories: Miscellaneous Biochemicals;Intermediates & Fine Chemicals;Pharmaceuticals;STILBESTROL;Other APIs
Usage: Mainly used for low disease and estrogen hormone imbalance caused by functional bleeding, amenorrhea, can also be used before induction of labor stillbirth to increase myometrial oxytocin sensitivity.
 
Diethylstilbestrol Description:
 
Diethylstilbestrol (DES, former BAN stilboestrol) is a synthetic nonsteroidal estrogen that was first synthesized in 1938. It is also classified as an endocrine disruptor. Human exposure to DES occurred through diverse sources, such as dietary ingestion from supplemented cattle feed and medical treatment for certain conditions, including breast and prostate cancers.:)
 
From about 1940 to 1971, DES was given to pregnant women in the mistaken belief it would reduce the risk of pregnancy complications and losses.:)
 
In 1971, DES was shown to cause a rare vaginal tumor in girls and women who had been exposed to this drug in utero. The United States Food and Drug Administration subsequently withdrew DES from use in pregnant women. Follow-up studies have indicated that DES also has the potential to cause a variety of significant adverse medical complications during the lifetimes of those exposed.:)
 
The United States National Cancer Institute recommends women born to mothers who took DES undergo special medical exams on a regular basis to screen for complications as a result of the drug. Individuals who were exposed to DES during their mothers' pregnancies are commonly referred to as "DES daughters" and "DES sons".
 
Diethylstilbestrol Application:
 
A synthetic, nonsteroidal estrogen. Recomended solvents are DMSO, DMF and ethanol, even in these solvents do not store in solution for any prolonged period of time.
 

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98% Pharmaceutical Anabolic Weight Loss Steroids Raw Powder Halodrol-50 Turinadiol 2446-23-3

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98% Pharmaceutical Anabolic Weight Loss Steroids Raw Powder Halodrol-50 Turinadiol 2446-23-3
 
Halodrol Basic Info.:
 
Product Name: Halodrol (Turinadiol)
Chemical Name: Halodrol-50; Turinadiol; Turinabol-oral; 4-Chlorodehydromethyltestosterone; 4-Chlorodehydrone Thyltestosterone;Oral turinabol;4-ChlordehydroMethyl Testosterone
CAS Number: 2446-23-3
Molecular Formula: C20H31CLO2
Molecular Weight: 336.8960
Assay: 99.5%
Appearance: White powder
 
Halodrol Description:
 
Halodrol also known as 4-chloro-17a-methyl-androst-1,4-diene-3b,17b-diol, or HD is an excellent compound for adding lean hard muscles as well as strength gains. Halodrol is good for improved vascularity, dry gains with only a small to no amount of water retention.
 
Halodrol exhibits an extremely high anabolic to androgenic ratio translating into hard and consistent muscle gains with No aromatization. These gains are notably extremely lean and dry in nature, making this a favorite for the pre-contest athlete, or as an anabolic addition to many stacks. Mainly used to increase muscle mass most particularly in the abdomen region and will increase muscle endurance and decrease your recovery time after workouts.
 
Halodrol Application:
 
1. It is common for Halodrol users to see strength and size gains within the first 1-2 weeks.
2. Halodrol provides exactly that, lean, hard, dry gains as well as strength gains.
 

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Pharmaceutical Trenbolone Steroids Parabolan Trenbolone Enanthate For Weight Loss 10161-33-8

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Pharmaceutical Trenbolone Steroids Parabolan Trenbolone Enanthate For Weight Loss 10161-33-8
 
Trenbolone Enanthate Basic Info.
 
Product Name: Trenbolone Enanthate
Alias: Trenbolone Enanthate;Parabolan;Tren E;10161-33-8;Primobolan-depot;Primobolan-depot
CAS No.: 10161-33-8
Molecular Formula: C25H34O3
Molecular weight: 382.54
Assay: 99.02%
Appearance: pale yellow or yellow crystalline powder
Usage: Trenbolone Enanthate is only available from underground labs and was not designed for human consumption, although it is considered to be an ideal drug for bodybuilders who want to burn fat and gain muscle, although its long ester makes unwise for professional athletes who undergo testing to use.
 
Trenbolone Enanthate Description:
    
Trenbolone Enanthate also shines is in its ability to greatly preserve lean muscle tissue.When we diet, in-order to lose body fat, not weight but body fat we must be in a caloric deficit; we must burn more calories than we consume. As a result, as the body fights change with a desire to hang onto stored body fat due to its survival nature lean muscle tissue is often sacrificed in-order to meet its energy needs. As we lose more lean muscle tissue, this slows down the metabolic rate, and of course, it makes the physique look worse; Trenbolone Enanthate will prevent this. Of course, it gets even better; through its traits, Trenbolone Enanthate will provide the ultimate in visual conditioning effects.
 
Trenbolone Enanthate is a steroid that will greatly increase muscular endurance, more work can be done and you will not tire out as fast and it will also play an important role in recovery and healing.
 
Trenbolone Enanthate Applications:
 
Trenbolone is notably more potent than testosterone, and has an effect that is as much as three times as strong on a milligram for milligram basis. Likewise we can expect to see some level of androgenic side effects with use of this compound. Oily skin, aggressive behavior, acne and hair loss are therefore not uncommon during a cycle with this steroid. The androgenic nature of this drug of course makes it a very risky item for women to use, the chance for virilization symptoms extremely high with such a potent androgen.
 
Trenbolone is also much more potent than testosterone at suppressing endogenous androgen production. This makes clear the fact that estrogen is not the only culprit with negative feedback inhibition, as here there is no buildup of this hormone to report here. There is however some activity as a progestin inherent in this compound, as trenbolone is a 19-nortestosterone (nandrolone) derivative (a trait characteristic of these compounds).
 

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Yellow to Light Orange Pharmaceutical Raw Materials Tretinoin for Dermatology Drugs 302-79-4

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Yellow to Light Orange Pharmaceutical Raw Materials Tretinoin for Dermatology Drugs 302-79-4
 
Tretinoin Basic Info.:
 
Product Name: Tretinoin
CAS: 302-79-4
Molecular Formula: C20H27O2
Specification: USP32
Appearance: Yellow or pale orange crystalline powder
Content: 98.0--102.5%: 
Melting point: 179-186 º C
Boiling point: 462.8 ° Cat 780 mmHg
Water soluble: Insoluble
Categories: Tretinoin is a derivative of Vitamin A and is used to treat comedonal acne, or whiteheads and blackheads. It works by affecting the growth of skin cells. It also prevents the formation of new comedones. Tretinoin is also the only topical medication that has been proven to improve wrinkles.
 
Tretinoin Usage:
 
Tretinoin is commonly used in dermatology drugs, which is the department of vitamin A (Victoria methanol) metabolic intermediates.It mainly affects the growth of bones and epithelial metabolism, can promote epithelial cell proliferation and updates, and can inhibit the proliferation and differentiation of keratinocytes, so hyperkeratosis can be back to normal. Therefore many complete or incomplete keratosis, hyperkeratosis of diseases have a certain therapeutic effect, treat a variety of skin diseases. The use of the drug can penetrate topical skin quickly, enable significantly increased epithelial cell turnover. This class of drugs has strong and rapid inhibition on the secretion of the sebaceous glands, can reduce sebum secretion. In addition, the product also has anti-tumor, promote wound healing and anti-inflammatory effects.
 

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Acidic fibroblast growth factor intracellular-binding protein isoform a (169-179) LAB GRADE 97%

Creative peptides is specialized in the process development and the manufacturing of bioactive peptides. We offer custom peptide synthesis, process development, GMP manufacturing as well as catalog products. We supply Acidic fibroblast growth factor intracellular-binding protein isoform a (169-179).http://www.creative-peptides.com/product/acidic-fibroblast-growth-factor-intracellular-binding-protein-isoform-a-item-ta-148-9080.html

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Corticosteroid Drug Fluocinolone Acetate Fluocinolone Acetonide For Anti-inflammatory 67-73-2

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Corticosteroid Drug Fluocinolone Acetate Fluocinolone Acetonide For Anti-inflammatory 67-73-2
 
Fluocinolone Acetate Basic Info.:
 
Product Name: Fluocinolone Acetonide
Synonyms: dermalar; fluocinolone16,17-acetonide; Fluocinoloneacetate; Fluocinolone acetonide; Fluocinoloneacetate
CAS: 67-73-2
MF: C24H30F2O6
MW: 452.49
EINECS: 200-668-5
Product Categories: Organics;Alkaloids;Biochemistry;Quinoline Alkaloids;Intermediates & Fine Chemicals;Pharmaceuticals;Steroids;RETISERT;Hormone Drugs
Melting point: 267-269 °C(lit.)
refractive index: 103°(C=1, MeOH)
storage temp.: Refrigerator
Chemical Properties: Crystalline Solid
Uses: It is suitable in the treatment of eczema, neurodermatitis, skin pruritus, contact dermatitis, psoriasis, dermatitis and other diseases, Glucocorticoid; anti-inflammatory.
 
Fluocinolone Acetate Description:
 
Fluocinolone acetonide is a corticosteroid primarily used in dermatology to reduce skin inflammation and relieve itching. It is a synthetic hydrocortisone derivative. The fluorine substitution at position 9 in the steroid nucleus greatly enhances its activity. It was first synthesized in 1959 in the Research Department of Syntex Laboratories S.A. Mexico City. Preparations containing it were first marketed under the name Synalar. A typical dosage strength used in dermatology is 0.01-0.025%. One such cream is sold under the brand name Flucort-N and includes the antibioticneomycin.
Fluocinolone acetonide was also found to strongly potentiate TGF-β-associated chondrogenesis of bone marrow mesenchymal stem/progenitor cells, by increasing the levels of collagen type II by more than 100 fold compared to the widely used dexamethasone.
 
Fluocinolone Acetate Application:
 
Fluocinolone acetonide is used to decrease inflammation in the skin. 
It is a corticosteroid, sometimes known as a steroid. 
In general this drug is used to treat inflammatory skin disorders such aseczema and psoriasis. 
Benefits of being on this drug can include reduction of inflammation and relief of itch. 
Listed below are the typical uses of fluocinolone acetonide. 
 

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White Crystal Pharmaceutical Intermediates Hydrochloride Procaine HCL For Pain Relief 51-05-8

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White Crystal Pharmaceutical Intermediates Hydrochloride Procaine HCL For Pain Relief 51-05-8
 
Procaine HCL Basic Info.:
 
Product Name: Procaine Hydrochloride (Procaine HCL)
Synonyms: Aminocaine;Anadolor;Anesthesol;Anestil;Atoxicocaine;Bernocaine
CAS: 51-05-8
MF: C13H21ClN2O2
MW: 272.77
EINECS: 200-077-2
Melting point: 155-156 °C(lit.)
Boiling point: 195-196°C 17mm
Fp: 195-196°C/17mm
storage temp.: room temp
Water Solubility: soluble
Sensitive: Air Sensitive
Merck: 14,7757
Stability: Stable. Incompatible with strong oxidizing agents.
Chemical Properties: White crystalline powder
Product Categories: Pharmaceutical;Sodium channel;APIS;Anesthetics;Pharmaceutical intermediate
Usage: Local anesthesic;Na+ channel blocker;Procaine is a local anesthetic of the amino ester group that is primarily used as a topical anesthetic. Procaine is also used to control the pain of intramuscular injection of penicillin as well as in dentistry;Non Caine local anesthetic.
 
Procaine HCL Product description: 
 
Procaine HCl is a local anesthetic drug of the amino ester group. It is used primarily to reduce the pain of intramuscular injection of penicillin, and it is also used in dentistry. It acts mainly by being a sodium channel blocker. Today it is used therapeutically in some countries due to its sympatholytic, anti-inflammatory, perfusion enhancing, and mood enhancing effects.
 
Procaine HCl is indicated for the production of local or regional analgesia and anesthesia by local infiltration and peripheral nerve block techniques.
 
The routes of administration and concentrations are: For local infiltration use 0.25% to 0.5% (via dilution) and for peripheral nerve blocks use 0.5% (via dilution), 1%, and 2%. (See DOSAGE AND ADMINISTRATION for additional information. )
 
Procaine HCL Application:
 
Procaine HCl is a local anesthetic drug of the amino ester group. It is used primarily to reduce the pain of intramuscular injection of penicillin, and it is also used in dentistry. Owing to the ubiquity of the trade name Novocain, in some regions procaine is referred to generically . It acts mainly by being a sodium channel blocker. Today it is used therapeutically in some countries due to its sympatholytic, anti-inflammatory, perfusion enhancing, and mood enhancing effects.
 
Procaine HCl is indicated for the production of local or regional analgesia and anesthesia by local infiltration and peripheral nerve block techniques.
 
Application of procaine leads to the depression of neuronal activity. The depression causes the nervous system to become hypersensitive producing restlessness and shaking, leading to minor to severe convulsions. Studies on animals have shown the use of procaine LED to the increase of dopamine and serotonin levels in the brain. Other issues may occur because of varying individual tolerance to procaine dosage. Nervousness and dizziness can arise from the excitation of the central nervous system, which may lead to respiratory failure if overdosed. Procaine may also induce weakening of the myocardium leading to cardiac arrest.
 
Procaine can also cause allergic reactions causing the individuals to have problems with breathing, rashes, and swelling. Allergic reactions to procaine are usually not in response to procaine itself, but to its metabolite PABA. About one in 3000 people have an atypical form of pseudocholinesterase, [citation needed] which does not hydrolyze ester anesthetics such as procaine, resulting in a prolonged period of high levels of the anesthetic in the blood and increased toxicity.
 

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