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Steroid Hormone Powder Eplerenone For Lowering Blood Press 107724-20-9

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Steroid Hormone Powder Eplerenone For Lowering Blood Press 107724-20-9
 
Eplerenone Basic Info.:
 
Product Name: Eplerenone
Chemical Name: Pregn-4-ene-7,21-dicarboxylic acid 9,11-epoxy-17-hydroxy-3-oxo gamma-
lactone methyl ester
CAS No.: 107724-20-9
Molecular Formula: C24H30O6
Molecular weight: 414.49
Appearance: white crystalline powder; slightly soluble in water.
Standard: Enterprise Standard
 
Eplerenone Description:
 
Eplerenone (INN) /plrnon/ is an aldosterone antagonist used as an adjunct in the management of chronic heart failure. It is similar to the diuretic spironolactone, though it is much more selective for the mineralocorticoid receptor in comparison (i.e., does not possess any antiandrogen, progestogen, or estrogenic effects), and is specifically marketed for reducing cardiovascular risk in patients following myocardial infarction. It was marketed byPfizer under the trade name Inspra but is now only available as a generic in every country except the United Kingdom. Eplerenone is a potassium-sparing diuretic, meaning that it helps the body get rid of water but still keep potassium.
 
Eplerenone Application:
 
Eplerenone is specifically indicated for the reduction of risk of cardiovascular death in people with heart failure andleft ventricular dysfunction within 3-14 days of an acute myocardial infarction, in combination with standard therapies and as treatment against hypertension. It appears equivalent to spironolactone but is much more expensive.
 

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99% Pharmaceutical Sarms Powder Ostarine Enobosarm Mk-2866 1202044-20-9

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99% Pharmaceutical Sarms Powder Ostarine Enobosarm Mk-2866 1202044-20-9
 
MK-2866 (Ostarine) Basic Info.:
 
Product Name: MK-2866
Synonyms: Ostarine
CAS: 1202044-20-9
MF: C19H10D4F3N3O3
Product Categories: Aromatics;Intermediates & Fine Chemicals;Pharmaceuticals;Hormone Drugs
Recommended maximum dose OSTARINE about 25 mg once a day for men, females and 12.5 mg. It has a half-life of 24 hours a day.Improve the minimum recommended dose aesthetic constitution (means) male is 12.5 mg. Low dose may produce little results notification clause or muscle growth, but it will help to health. Women's minimum recommended dose, and for those who seek to improve health, 5 mg per day, it should be noted that therapeutic doses as low as 3 mg a day have been reported in the gender is good.
 
MK-2866 (Ostarine) Description:
 
Ostarine (MK-2866) is a SARM developed by GTx for the prevention and treatment of muscle wasting. It may eventually be a medical prescription for the prevention of cachexia, atrophy and sarcopenia as well as for Hormone or Testosterone Replacement Therapy.
As a research chemical, Ostarine belongs to a class of chemicals know as SARMS or selective androgen receptor modulators. SARMS create selective anabolic activity at certain androgen receptors. In comparison to testosterone and other anabolic steroids, the advantage of SARMS, is they do not have androgenic activity in non-skeletal muscle tissues. Ostarine is effective in maintaining and increasing lean body mass.
Ostarine is a potent and tissue-selective androgen receptor modulator (SARM) for treatment of conditions such as muscle wasting and osteoporosis. These patent products for research purposes only use. Ostarine (GTx-024, MK-2866, Enobosarm, S-22) is an orally bioavailable nonsteroidal selective androgen receptor modulator. Therefore, ostarine can be used for treatment of conditions such as muscle wasting and osteoporosis.
 
MK-2866 (Ostarine) Application:
 
Selective androgen receptor modulators may be used by athletes to assist in training and increase physical stamina and fitness, potentially producing effects similar to anabolic steroids.
Ostarine is a potent and tissue-selective androgen receptor modulator (SARM) for treatment of conditions such as muscle wasting and osteoporosis. These patent products for research purposes only use. Ostarine (GTx-024, MK-2866, Enobosarm, S-22) is an orally bioavailable nonsteroidal selective androgen receptor modulator. Therefore, ostarine can be used for treatment of conditions such as muscle wasting and osteoporosis.
 
MK-2866 (Ostarine) Function:
 
1.Enobosarm (Ostarine, MK-2866, GTx-024) - affects both muscle and bone, intended mainly for osteoporosis but also general treatment for andropause and reversing muscle sarcopenia in the elderly and for cachexia in cancer patients
2.Nonsteroidal selective androgen receptor modulator (SARM) used in the treatment of osteoporosis and muscle wasting in animal models. A potential compound for the treatment of hypoactive sexual desire disorder.
 

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99% Purity Cancer Treatment Steroids Formestane For Breast CAS 566-48-3

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99% Purity Cancer Treatment Steroids Formestane For Breast CAS 566-48-3
 
Formestane Basic Info.:
 
Product name: Formestane
Other name: Formestane; Lentaron; Formestqne; Hydroxyandrostenedione
CAS Registry Number: 566-48-3
Assay: 98%Packing: 1kg/aluminum foil bag
Molecular Formula: C19H26O3
Molecular Weight: 302.41
Appearance: White crystalline powder
 
Product Description Of Formestane:
 
Formestane was the first selective, type I, steroidal aromatase inhibitor used in the treatment of estrogen-receptor positive breast cancer in post-menopausal women. Formestane suppresses estrogen production from anabolic steroids or prohormones. It also acts as a prohormone to 4-hydroxytestosterone, an active steroid which displays weak androgenic activity in addition to acting as a mild aromatase inhibitor. It is listed as a prohibited substance by the World Anti-Doping Agency for use in athletes. 
 
Formestane has poor oral bioavailability, and thus must be administered forthnightly (bi-weekly) by intramuscular injection. Some clinical data has suggested that the clinically recommended dose of 250mg was too low. With the discovery of newer, non-steroidal and steroidal, aromatase inhibitors which were orally active and less expensive than formestane, formestane lost popularity. 
 
Currently, formestane (categorized as an anti-estrogenic agent) is prohibited from use in sports in accordance to the regulations of the World Anti-Doping Agency. It is not US FDA approved, and the intramuscular injection form of formestane (Lentaron) which was approved in Europe has been withdrawn. 
 
Formestane (Lentaron) is a type I, steroidal aromatase inhibitor. It is used in the treatment of estrogen-receptor positive breast cancer in post-menopausal women. It is available as an intramuscular depot injection.
 
Formestane is often used to suppress estrogen production from anabolic steroids or prohormones. It also acts as a prohormone to 4-hydroxytestosteron, an active steroid which displays weak androgenic activity in addition to acting as a mild aromatase inhibitor.
 
Formestane has poor oral bioavailability and as such is no longer popular as many orally active aromatase inhibitors have been identified.
 
Formestane Applications:
 
Formestane is a second generation, irreversible, steroidal aromatase inhibitor. It inhibits the aromatase enzyme responsible for converting androgens to estrogens, thereby preventing estrogen production. Breast cancer may be estrogen sensitive or insensitive. A majority of breast cancers are estrogen sensitive. Estrogen sensitive breast cancer cells depend on estrogen for viability. Thus removal of estrogen from the body can be an effective treatment for hormone sensitive breast cancers. Formestane has been targeted specifically for the treatment of postmenopausal women. Unlike premenopausal women who produce most estrogen in the ovaries, postmenopausal women produce most estrogen in peripheral tissues with the help of the aromatase enzyme. Formestane, an aromatase inhibitor, can thus help to decrease the local production of estrogen by blocking the aromatase enzyme in peripheral tissues (ie. Adispose tissue of the breast) to treat hormone sensitive breast cancer.
 

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BK-MDMA, Methylone, Ethylone, MDA, Methadone Hcl, 3-HO-PCP LAB GRADE >95%

Cathy
Email: sales2 at huanyingchem.com
Skype:live:b95d7624e9243df7
Website: www dot huanyingchem dot com 
 
Other High quality pharmaceutical intermediates:
BK-MDMA, Methylone, Ethylone, MDA, Methadone Hcl, 3-HO-PCP, A-Methylfentanyl, AMMI, Alfentanyl Hcl, Allylescaline, MDDM, MR-2096, AM-1222, AM-1241, AM-1243, AM-356, AM-404, EAM-2201, JWH-098, JWH-098, 4-MEC, 5F-AM678, A-PPP, AM2201, ETHYL-ONE, N.N-DMMC, 3-MMC, 4-BMC, A-PVP, 4-DME-PVP, 4-FMA, 3-FA, 4-CAB, 4-MEPBP, 4-FPD, 4F-PBP, 4F-PV9, 6-APB, A-PBT, PV-7, PV-4, Pmma, 4-MEPPP, A9, Eg-018, MOPPP, MPHP, PVB, CC1, M2, PV1-3, Dibutylone, 2nmc ,2a1mp.
 
 
Product advantage
 
1. We can guarantee the quality of the product. 
2. Fast and safe delivery by TNT,UPS,DHL,EMS. 
3. We can provide competitive price for you. The more you buy , the lower the price will be.
4. We are an experienced enterprise of manufacturing various kind of Organic intermediates, Our customers come from all parts of the world, had a very good cooperation between us.Customer very pleased with our products.
 
We can provide you stable quality, high purity, good packaging at most competitive price.
 
The products can be sent to USA, Brazil, The Czech republic...with special package
The or shipping way which can ensure high success rate of customs.

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C-Jun-amino-terminal kinase-interacting protein 2 (683-692) 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 C-Jun-amino-terminal kinase-interacting protein 2 (683-692).http://www.creative-peptides.com/product/c-jun-amino-terminal-kinase-interacting-protein-item-ta-068-2619.html

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FAST kinase domain-containing protein 1 isoform 1 (497-514) 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 FAST kinase domain-containing protein 1 isoform 1 (497-514).http://www.creative-peptides.com/product/fast-kinase-domain-containing-protein-isoform-item-ta-149-9082.html

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Fibronectin type III domain-containing protein 3B (292-300) 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 Fibronectin type III domain-containing protein 3B (292-300).http://www.creative-peptides.com/product/fibronectin-type-iii-domain-containing-protein-3b-item-ta-205-13735.html

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Healthy Muscle Building Steroids Injectable Rip Cut 175 175mg/Ml Liquid

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Healthy Muscle Building Steroids Injectable Rip Cut 175 175mg/Ml Liquid
 
Rip Cut 175 Basic Info.:
 
Product Name: 
Each 1 ml of Rip Cut 175 contains:
75 mg of Testosterone Propionate;
50 mg of Trenbolone Acetate;
50 mg of Drostanolone Propionate
 
Rip Cut 175 Description:
 
Masteron (drostanolone propionate) is a moderately anabolic steroid that promotes increases in hardness, lean body mass and strength which has a positive effect on the potential for fat loss. Masteron does not possess any estrogenic activity and therefore water retention is highly unlikely. In fact, Masteron is often described as anti-estrogenic. This DHT derivative actually competes with other aromatizable substrates for binding to the aromatase enzyme. Masteron is not only a moderate anabolic but also a mild anti-estrogen which is very useful when stacking with low doses of other aromatizing steroids such as Testosterone.
 
Testosterone Propionate is a powerful mass building drug that is able to rapidly add gains in muscle size and strength. It's the only aromatizing steroid in this stack but at reasonable doses aromatization is moderate. I'm convinced there's almost no other traditional injectable stack that's as potent and versatile as Testosterone and Trenbolone. It's a simple stack with enormous potential to harden muscle, promote fat loss and add raw strength. The addition of Masteron adds even more to this synergy as it acts as an anti estrogen to control aromatization of Testosterone. If Testosterone doses are higher an aromatase inhibitor may be needed.
 
Trenbolone Acetate is at least 3 times more anabolic and androgenic than Testosterone or Nandrolone. Trenbolone binds to androgen receptors (ARs) with approximately three times the affinity of testosterone and has been shown to augment skeletal muscle mass and bone growth and reduce adiposity! tren is one potent weapon in the bodybuilder's arsenal. Trenbolone is a nonestrogenic steroid so water retention is highly unlikely. Stacking with complimentary steroids such as Testosterone maximizes Trenbolones potential and also reduces side effects such as loss of libido.
 

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Lose Weight Fast Fat Burning Steroids Synephrine No Side Effect 94-07-5

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Lose Weight Fast Fat Burning Steroids Synephrine No Side Effect 94-07-5
 
Synephrine Basic Info.
 
Product Name: Synephrine
Synonyms: Oxedrine;Synephrine;AKOS NCG1-0008;AURORA KA-6561
CAS: 94-07-5
MF: C9H13NO2
MW: 167.21
EINECS: 202-300-9
Assay: 99.2%
Appearance: White powder
Package: 25kg/drum
Storage:Keep away from fire and heat source, hermetically deposit, keep in shady, cool and dry condition, protect against the tide.
 
Synephrine Description:
 
Citrus aurantium extract synephrine as standard has been recommended. 4-20mg daily dose of synephrine is as bitter orange extract containing 200-600mg standard products (3-6% synephrine) typical dose.
 
Synephrine Use:
 
Synephrine is lime fruits of the main active ingredient, which can effectively prevent excess energy (heat accumulation), by the wind qi, warm the stomach stimulates the appetite and speeds up metabolism. It is also a mild fragrance expectorant agent, a neurological tranquilizers and laxative treatment of constipation. Users can expect variable effects include consumption of excess calories, reduce appetite and increase satiety, these are likely to lead to weight loss.
 

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Melanotan II Polypeptide Hormones Melanotan 2 Human Growth Hormone MT-2

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Melanotan II Polypeptide Hormones Melanotan 2 Human Growth Hormone MT-2
 
Basic Info.
 
Product Name: 
Melanotan 2; MT2; Melanotan-II; Melanotan2
CAS: 121062-08-6
Molecular Formula: C50H69N15O9
Molecular weight: 1024.2
Purity (by HPLC): 99.00%
Appearance: White Powder
Sequence: Ac-Nle-Asp-His-D-Phe-Arg-Trp-Lys-NH2
Storage Condition: away from light, cold storage (2-8 degree)
Usage: prevention sunlight-induce skin cancer; Sexual Dysfunction & Fat Decomposition
 
What is Melanotan 2 ?
Melanotan 2  Tanning Injections (otherwise known as MT2) was first synthesized at the University of Arizona.  Researches there knew that onc of the best defenses against skin cancer was melanin activated in the skin, a tan.  They hypothesized that an effective way to reduce skin cancer rates in people would be to induce the body's natural pigmentary system to produce a protective tan prior to UV exposure.  The body's naturally occuring hormone MSH causes melanogenesis, a process by which the skin's pigment cells (melanocytes) produce the skin's pigment (melanin).  They tested to see if administering this endogenous hormone to the body directly could be an effective method to cause sunless tanning.  What they found was that while it appeared to work, natural MSH had too short a half life in the body to be practical as a therapeutic drug.  So they decided to find a more potent and stable alternative, one that would be more practical.
 
After synthesizing and screening hundreds of molecules, the researchers headed by Victor J. Hruby and Mac E. Hadley, found a peptide, [Nle4, D-Phe7] MSH, that was approimately 1,000 times more potent than the natural MSH.  They dubbed this new peptide molecule, "Melanotan" (later Melanotan-1, now know as afamelanotide).  They subsequently developed another analog, Ac-Nle-cyclo[Asp-His-D-Phe-Arg-Trp-Lys]-NH2), which they called "Melanotan" Tanning Injections.  The scientists hoped to use these peptides to combat melanoma by stimulating the body's natural pigmentary mechanism to create a tan without first needing exposure to harmful levels of UV radiation.  This in turn, they hypothesized, could reduce the potential for skin damage that can eventually lead to skin cancer.
 
A pilot phase I clinical trial conducted on three males by the College of Medacine, Pharmacology Department, University of Arizona in Tuscon, Arizona pulished in 1996 reported that, "Melanotan" Tanning Injections has tanning activity in humans given only 5 low doses every other day by subcutaneous injection."  The side effects reported were mild nausea and a "stretching and yawning complex" that correlated with spontaneous penile erections.
 
The Department of Pharmacology, University of Arizona College of Medacin published in 1998 that involved 10 men who suffered from psychogenic erectile dysfunction.  Their trial concluded that, "Melanotan" Tanning Injections is a potent initiator of erections in men with pyschogenic erectile dydfunction and has manageable side effects at a dose of 0.025mg/kg.
 
A clinical study published in 2000 of 20 men with psychogenic and organic erectile dysfunction conducted at the Section of Urology of The University of Arizona College of Medacin concluded, "that Melanotan II Tanning Injections is a potent initiator of penile erection in men with ecrectile dysfunction.
 
How to use Melanotan 2 Mixing the solutionv:
 
Flip off the cap from the Melanotan 2 Tanning Injection vial.
Wipe the surface of the top of the vial with the enclosed alcohol wipe and discard the wipe.
Wipe the surface of the injectable water tube (or glass water vial depending on the pack ordered) with the enclosed alcohol wipe and discard the wipe.
Remove the enclosed syringe from the packaging. Making sure the injectable water tube is upright, insert the needle of the syringe into the sidewall of the water.
Now pull back the plunger of the syringe so you withdraw 1ml of water and slowly pull the syringe out.
Insert the syringe into the Melanotan 2 Tanning Injection vial and depress the plunger so you completely empty the syringe of the water and slowly remove the syringe from the vial.  Do not shake the solution.
Place the Melanotan 2 solution in the fridge for storage until ready for use.
Make sure you put the syringe caps on and carefully dispose of it.
You have now mixed your Melanotan 2 Tanning Injection solution. Please store the solution in the fridge.
 
How to use Melanotan II for tanning?
 
Melanotan II is typically provided in vials containing 10 mg of lyophilized (freeze-dried) powder. The vials are reconstituted with a convenient amount of bacteriostatic or sterile water, added to the vial by syringe. An example convenient amount of water is 2.5 mL. When this amount of water is used, the resulting solution contains 4 mg of MT-II per mL. If for example wishing to take a dose of 1 mg, a volume of 0.25 mL, or "25 IU" as marked on an insulin syringe, would be taken by injection. Injection may be subcutaneous, intramuscular, or intravenous, according to personal preference.
 
Injection typically is only once per day, but where a person is first trying the drug and judging tolerance, injection may be divided into two smaller amounts per day.
Typical dosage range is 0.5 to 2.0 mg/day, with a preferred range of 0.5 to 1.0 mg/day. However, it's best to first assess tolerance with lower dosing of 0.25 mg at a time.
After reconstitution, a Melanotan II vial should preferably be consumed entirely within 30 days. Prior to reconstitution, MT-II should be stored in the refrigerator or freezer, but it's acceptable for it to be shipped without refrigeration.
 
Use generally should be discontinued if MT-II, in the individual case, causes problems with increased growth, number, or darkness of moles.
 
Melanotan II's effect is fairly long-lasting. It can even be the case that it takes a year or more for a cycle's effect to largely disappear. Use of maintenance cycles can maintain effect indefinitely. As a rule of thumb, maintenance typically requires about 2 to 3 times as much MT-II per year as was needed for the first cycle. This can be taken either as a total of 2 to 3 cycles per year done in the same way as the initial cycle, or any more frequent dosing pattern providing this total amount of MT-II per year.
 

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