Hormone drugs used in treating deficient hormone levels in body, thyroid problems, ovulation

1,4-Androstadienedione Male Sex Enhancement For Cancer Treatment 897-06-3

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1,4-Androstadienedione Male Sex Enhancement For Cancer Treatment 897-06-3

1,4-Androstadienedione Basic Infor.

Product Name: Androsta-1,4-diene-3,17-dione

Synonyms: Delta-1,4-Androstadiene-3,17-Dione;Androstadiendione;Androstadienedione;Androsta-1,4-Diene-3,17-Dione;1-Dehydroandrostenedione;1,4-Androstadien-3,17-Dione;1,4-Androstadiene-3,17-Dione

CAS: 897-06-3

MF: C19H24O2

MW: 284.39

EINECS: 212-977-2

Melting point: 138-139 °C(lit.)

Storage temp.: Refrigerator

Chemical Properties: White Crystalline Powder

Usage: Boldenone related steroid; anabolic androgenic steroid

Product Categories: Pharmaceutical Intermediates;Intermediates & Fine Chemicals;Pharmaceuticals;Steroids

1,4-Androstadienedione Description:

Androsta-1 is used for simplified hormone drugs, from the testis or urine extracted with the role of a male hormone steroid, norethisterone, testosterone propionate in the middle body, is widely used in small rheumatoid arthritis, diuretic, and a variety of contraceptive to control infectious inflammation&period;

Androsta-1 is the precursor to bolde-none, and as of January 4, 2010 is a Schedule III Controlled Substance&period; In 2004 the United States Congress passed the Anabolic Steroid Control Act of 2005 which placed 36 steroids and over the counter pro-hormones into schedule III of the Controlled Substances Act&period;

1,4-Androstadienedione Application:

Simplified hormonal drugs, from the testis or urine extracted with the role of a male hormone steroids, norethisteron.Bol-dione is the precursor to bolde-none, and as of January 4, 2010 is a Schedule III Controlled Substance.In 2004 the United States Congress passed the Anabolic Steroid Control Act of 2005 which placed 36 steroids and over the counter pro-hormones into schedule III of the Controlled Substances Act. In this legislation bolde-none was classified as a controlled substance and bol-dione remained legal.In April 2008 the United States Drug Enforcement Administration published an "Initial Notice of Proposed Rulemaking" concerning the scheduling of three anabolic substances: bol-dione, desoxymethyltestos-terone, and diene-dione. In 2008, at the time of the proposal, these three substances were listed as ingredients in more than 58 dietary supplements which were available for purchase over the counter.

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1-Testosterone Cypionate USP 99%

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Anabolic Steroid Powder 1-Testosterone Cypionate 1-Test Cyp For Muscle Buidling 58-20-8

1-Testosterone Cypionate Basic Info.

Product name: 1-Testosterone Cypionate (Dihydroboldenone)

Synonyms: Dihydroboldenone;1-Test Cyp;1 Test, Dhb;1-Testosterone Cypionate.

Chemical Names: 17Beta-Hydroxyandrost-1-En-3-One;5Alpha-Androst-1-En-3-One,17Beta-Ol.

CAS: 58-20-8

MF: C27H40O3

MW: 412.6

EINECS: 200-368-4

Purity: 95.5%min

Active Life: depends on the ester utilized

Anabolic/Androgenic Ratio: 200/100.

Dosage: 300-400 mg/week to 1000 mg/week.

Melting point: 192~196 °C.

Appearance: Almost white to slight yellow powder

1-Testosterone Cypionate Description:

Dihydroboldenone, most commonly known as 1-testosterone Cypionate , is a 5alpha reduced form of the steroid boldenone. This lack of 5alpha reduction with the compound allows users to administe it without suffering the negative side effects associated with Dihydroboldenone Cypionate chemical reaction but also eliminates the benefits as well. In fact 1-Test Cyp is chemically identical to the Methenolone ( Prima 100) except for the 1-methylation that is apart of Methenolone. Also 1-Test Cyp is structurally similar to GP Bold 200 and less so to 1-Testosterone Cypionate despite the commonly used name for it, 1-Testosterone Cypionate .

For this reason some female athletes may be inclined to use 1-Test Cyp as well. The potential for development of symptoms of virilization still remain but are not as severe as with synthetic Testosterone Steroids or other harsher drugs. This is not to say however that 1-Test Cyp is a mild drug. To simplify the explanation of exactly what the drug is . This would explain why the effects of 1-Test Cyp, both positive and negative.

1-Test Cyp, while not overly androgenic, is a potent anabolic. 1-Test Cyp has been demonstrated that the drug binds extremely well and selectively to the androgen receptor and stimulates androgen receptor transactivation of dependent reporter genes. This equates to a drug that possesses the ability to stimulate significant muscle growth while not producing androgenic side effects. 1-Test Cyp has been shown to be by far more anabolic then such compounds and even Testosterone Steroids itself. Obviously this is of great benefit to many athletes and bodybuilders.

Anecdotally some users have indicated that post-injection pain with 1-Test Cyp can become an issue for some. Diluting the drug with either another injectable drug or some other type of sterile oil seems to alleviate at least some of this discomfort. The type of ester used does not appear to negate this pain for the users that experience it however.

1-Testosterone Cypionate Usage:

As for the duration with which 1-Test Cyp can be run, due to the mild nature of the drug extended use of the compound can be completed with little in the way of serious complications arising. There are no major issues with hepatoxicity or severe kidney stress and the effect it has on other vital health markers such as blood pressure is slight in the majority of users.

As for specific dosages used with this drug, the low end is primarily thought to be 300-400 mg per week for male users. Like all drugs this number will vary from user to user and also depends on how much of a dramatic effect a user will want to achieve with 1-Test Cyp. As for the highest doses that would be worthwhile for users to attempt, this again depends on a number of variables. Doses of one gram per week are not uncommon for some users with others attempting doses in excess of this. It will always come back to how much one is willing to administer and at what point do the positives of increasing your doses begin to be outweighed by the negatives.

For females the usual rules apply with 1-Test Cyp as they do with other drugs. If side effects begin to become too severe discontinuation of the drug can begin immediately and low doses should be administered at the beginning of the cycle and can be increased once the tolerance of the user is gauged. Anywhere from 25 to 100 mg per week would be a good starting point for the majority of female users who have little to moderate experience with anabolic steroids.

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1-Testosterone USP 99%

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Pharmaceuticals 1-Testosterone Steroid Hormone 65-065

1-Testosterone Basic info:

Product name: 1-Testosterone

Synonyms: 1-Testosterone;1-Dehydroandrostanolone;1-Testosteroneseries;Androstendolone;

CAS: 65-06-5

MF: C19H28O2

MW: 288.42

Purity: 99% min.

Melting point: 157-159°C

Storage temp.? Controlled Substance, -20°C Freezer

Chemical Properties? White Solid

Customized: Yes

Suitable for: Adult

HS Code: 29061310

Origin: China

Certification: SGS, GMP, ISO 9001, USP, BP

Product Categories: Intermediates & Fine Chemicals;Pharmaceuticals;Steroids;Steroid and Hormone.

Usage? Testosterone (T155000) derivative. It is a potent androgen with anabolic properties. Since the begining of the year 2005, the use of steroid precursors (prohormones) is illegal in the United States.

1-Testosterone Function:

1-Testosterone is a potent androgen with anabolic properties. Since the begining of the year 2005, the use of steroid precursors (prohormones) is illegal in the United States.

Intermediates & Fine Chemicals;Pharmaceuticals;Steroids;Steroid and Hormone.

(Δ1-dihydrotestos-terone, 17β-hydroxy-5α-androst-1-en-3-one, 1-Testo, 1-T) is an androgen and anabolic steroid that differs from testos-terone by having a 1,2-double bond instead of a 4,5-double bond in its A ring. It was legally sold as a prohormone in the United States until 2005, when it was reclassified as a Schedule III drug.

1-Testosterone Dosage:

1-Testosterone is best to start out with at least a week at a dose of 5-10 mg to see how one reacts. Many users find this range to be effective, while others feel the ideal amount is 20-40 mg. It comes down to the experience, goals, and individual reaction. Many find a lower dose to be just as effective as a higher one, but with less side effects. With a compound such as this, it is generally best to err on the side of caution, especially for those that are less experienced with steroids. Most seem to find their ideal dose to be in the 10-30 mg range. Cycle length should be kept short, in the range of 1-4 weeks. Finally, it is especially important to take adequate time off after each cycle with this substance to allow the body to recover.

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11-Keto Testosterone USP 99%

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Safe Anabolic Steroid Powder 11-Keto-Testosterone 564-35-2

11-Keto Testosterone Basic Info.:

Product Name: 11-Ketotestosterone

Synonyms: 4-Androsten-17Beta-Ol-3,11-Dione;11-Ketotestosterone;11-Oxotestosterone

CAS: 564-35-2

MF: C19H26O3

MW: 302.41

Product Categories: Intermediates & Fine Chemicals;Metabolites & Impurities;Pharmaceuticals;Steroids.

Usage: A metabolite of Adrenosterone.

How To Storage 11-Keto Testosterone?

1.Avoid mixing with heterogeneous odor items stored.

2.Keep the drug away from direct sunlight, heat and moistrue.

3.Do not let the drug at the sight and reach of children.

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17 Alpha-Estradiol / Estradiol For Skin Absorption Agent CAS 57-91-0

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17 Alpha-Estradiol / Estradiol For Skin Absorption Agent CAS 57-91-0

17 Alpha-Estradiol Basic Info.:

Product Name: 17 Alpha-Estradiol

Synonyms: Alpha-estradiol; 17A-estradiol

CAS: 57-91-0

EINECS: 200-354-8

Molecular Formula: C18H24O2

Molecular Weight: 272.39

Appearance :hite or off-white crystalline powder

Assay :99%min.

Melting range:216-224 oC

Specific rotation:+52o to +60o

Loss on drying :3.5%MAX

Monor impurity :0.2%MAX

Total impurities:1.0% max

17 Alpha-Estradiol Description:

Estradiol (called α - estradiol or 17α - estradiol) for human breast cancer cells in tissue culture biologically active estrogen. Not part of the 17- and selective estrogen receptor (ER-X) traditional hormone / receptor of the endocrine system, but an important autocrine / paracrine function of the system is part of the growth in the adult brain. In menopause, and neurodegenerative diseases (eg Alzheimer's disease and ischemic stroke) treatment, 17- estradiol may have important implications for hormone replacement therapy thing.

The development of secondary sex characteristics in women is driven by estrogens, to be specific, estradiol. These changes are initiated at the time of puberty, most are enhanced during the reproductive years, and become less pronounced with declining estradiol support after the menopause. Thus, estradiol enhances breast development, and is responsible for changes in the body shape, affecting bones, joints and fat deposition. Fat structure and skin composition are modified by estradiol.

17 Alpha-Estradiol Applications:

This medication is a female hormone. It is used by women to help reduce symptoms of menopause (such as hot flashes, vaginal dryness). These symptoms are caused by the body making less estrogen. If you are using this medication to treat symptoms only in and around the vagina, products applied directly inside the vagina should be considered before medications that are taken by mouth, absorbed through the skin, or injected.

Certain estrogen products may also be used by women after menopause to prevent bone loss (osteoporosis). However, there are other medications (such as bisphosphonates including alendronate) that are also effective in preventing bone loss and may be safer. These medications should be considered for use before estrogen treatment.

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6-Oxo Muscle Building Steroids 4-Androstene-3 to Increase Muscle Mass 2243-06-3

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6-Oxo Muscle Building Steroids 4-Androstene-3 to Increase Muscle Mass 2243-06-3

6-OXO Basic Info.

Product Name: 6-OXO

Alias: 4-androstene-3, 6, 17- trione; Androst-4-ene-3, 6, 17-trione; 4-Androstenetrione; 4-Androstenetriol

CAS: 2243-06-3

Molecular Weight: 300.39

Molecular Formula: C19H24O3

Melting Point: 223-224° C

Package: Foil bag or tin, or as you require

Properties: White powder

Usage: Steroid drug intermediates. Low Estrogen Levels.

Payment: T/T, Western Union and Money Gram

Delivery: Within 12hours After Your Payment

Express: EMS, DHL, FedEx, etc(door-to-door)

6-OXO Description:

6 OXO refer to the same chemical compound that is a steroidal testosterone booster/anti-aromatase agent. First identified in cow adrenal glands it was further found to be a natural metabolite of androstenedione metabolism in humans and most mammals. This makes 6 OXO a perfectly legal dietary supplement under the current DSHEA law and since it is not androgenic, not at all an anabolic steroid. What 6 OXO does is reduce an enzyme in the body that turns your testosterone into estrogen. By blocking this enzyme two major things happen, first it causes you to keep more of your testosterone and second, the body senses a lack of estrogen and causes the testes to release more testosterone.

6 OXO has been well studied in men and the original manufacturer of 6 OXO, Ergopharm Inc actually paid for quite a few studies in both men and rats. The most telling one was done by Incledon, which studied 6 OXO in doses of 300mg in healthy men, then measured the effects. The Incledon study found a boost of testosterone of about 200% with a slight reduction in estradiol, which means it was very effective at boosting testosterone while reducing estrogen. This was the first really well tested testosterone booster on the market.

Applications Of 6-OXO:

Study delivered a dose of 50 mg of 1-DHEA for 10 months with no serious adverse events reported.

1-DHEA was administered at a dose of 200 mg/day for 24 weeks with slight androgenic effects noted.

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98% Androstene Safe Steroids 11-Oxo For Muscle Building 382-45-6

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98% Androstene Safe Steroids 11-Oxo For Muscle Building 382-45-6

11-Oxo Basic Info.:

Product Name: 11-Oxo

Synonyms: Androst-4-ene-3,11,17-trione

CAS Number: 382-45-6

Molecular Formula: C19H24O3

Molecular Weight: 300.3921

Density: 1.18g/cm3

Appearance: white crystalline powder

Package: 1kg/ Aluminum foil bag

Payment: T/T, Western Union and Money Gram

Delivery: Within 12hours After Your Payment

Express: EMS, DHL, FedEx, etc(door-to-door)

11-Oxo Description:

Adrenosterone is a steroid hormone with weak androgenic effect first isolated in 1936 from the adrenal cortex. Adrenosterone occurs in trace amounts in humans as well as most mammals and in larger amounts in fish, where it is a precursor to the primary androgen, 11-ketotestosterone. Adrenosterone has shown to be converted into 11-ketotestosterone in humans, which contributes to adrenosterone's androgenic effects.

11-Oxo Applications:

Adrenosterone's main action is it lowers cortisol levels. Cortisol is the main catabolic (muscle-eating) hormone and it also promotes fat gain. Cortisol and testosterone also work in an inverse relationship, so high cortisol levels lower testosterone. Adrenosterone acts as a competitive inhibitor, preventing cortisone from attaching to the 11b-hydroxysteroid dehydrogenase type I reductase. By competing at the receptor, it keeps cortisone from attaching and converting to cortisol through the enzyme. Adrenosterone is found naturally in the body and is released by the adrenal glands. The body uses it as a way to help regulate cortisol levels.

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98% Injectable Polypeptide Hormones Eptifibatide Raw Steroid Powders 148031-34-9

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98% Injectable Polypeptide Hormones Eptifibatide Raw Steroid Powders 148031-34-9

Eptifibatide Basic Info.

Product Name: Eptifibatide

Synonyms: Human Eptifibatide; Eptifitide

Sequence: Mpr-Har-Gly-Asp-Trp-Pro-Cys-NH2

Cas No.: 148031-34-9

Molecular Formula: C35H49N11O9S2

Molecular Weight: 831.96

Appearance: White slightly yellwish powder.

Specific Rotation[20/D]: -75.0~-95.0°(C=1,1%HAc)

Amino Acids composition: ± 10%

Peptide Purity (By HPLC): >98% by area integration.

Related Substance (By HPLC): Total Impurities (%)<2.0%;Largest Single Impurity (%)< 1.0%

Water Content (Karl Fischer): <8.0%

Peptide Content(N determination): >80%

Acetate Content: <15%

IR spectrum: in accordance

Grade : Pharmaceutical Grade

Storage: Closed, below 2 ~ 8ºC preservation

Usage : Platelet glycoprotein receptor antagonist model, the third generation of antiplatelet drugs. For acute coronary syndrome (including unstable angina or non Q wave myocardial infarction) or percutaneous coronary interventional therapy (including angioplasty or atheromatous plaque excision).

Description Of Eptifibatide:

Eptifibatide (Integrilin, Millennium Pharmaceuticals, also co-promoted by Schering-Plough/Essex), is an antiplatelet drug of the glycoprotein IIb/IIIa inhibitor class.[1] Eptifibatide is a cyclic heptapeptide derived from a protein found in the venom of the southeastern pygmy rattlesnake (Sistrurus miliarius barbouri). It belongs to the class of the so-called arginin-glycin-aspartat-mimetics and reversibly binds to platelets. Eptifibatide has a short half-life. The drug is the third inhibitor of GPIIb/IIIa that has found broad acceptance after the specific antibody abciximab and the non-peptide tirofiban entered the global market.

Integrilin is sold in two strengths, globally: vials containing 2 mg/ml (20 mg totally) and 0.75 mg/ml (75 mg totally).

Application Of Eptifibatide:

Eptifibatide is used to reduce the risk of acute cardiac ischemic events (death and/or myocardial infarction) in patients with unstable angina or non-ST-segment-elevation (e.g., non-Q-wave) myocardial infarction (i.e., non-ST-segment elevation acute coronary syndromes) both in patients who are to receive non surgery (conservative) medical treatment and those undergoing percutaneous coronary intervention (PCI).

The drug is usually applied together with aspirin or clopidogrel and (low molecular weight or unfractionated) heparin. Additionally, the usual supportive treatment consisting of applications of nitrates, beta-blockers, opioid analgesics and/or benzodiazepines should be employed as indicated. Angiographic evaluation and other intensive diagnostic procedures may be considered a first line task before initiating therapy with eptifibatide.

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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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98% Purity Aicar 2627-69-2 Sarms White Solid Raw Material

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98% Purity Aicar 2627-69-2 Sarms White Solid Raw Material

Aicar Basic Info:

Product Name: Aicar

CAS: 2627-69-2

MF: C9H14N4O5

MW: 258.23

EINECS: 220-097-5

Assay: 99%

Product Categories: Carbohydrates & Derivatives;Nucleotides;Protein Kinase;Cardiovascular;

Chemical Properties: White or off-white solid

Product Description Of Aicar:

Aicar is a peptide whose technical name is 5-Aminoimidazole-4-carboxamide ribonucleotide.

It can also be known as AICA ribonucleotide, ZMP, or Acadesine. It is an intermediate contained in the generation of inosine monophosphate. It primarily functions as an AMP-activated protein kinase agonist, meaning that it has the ability to promote the operation of nutrient stores for energy production. It has a molecular mass of 338.211, and it has a molecular formula of C9H15N4O8P.

Aicar is an adenosine analog that selectively activates AMP-activated protein kinase (AMPK). AMPK regulates lipid and glucose metabolism to maintain cellular energy homeostasis (Hardie and Carling).

Aicar can play a hand in boosting these processes because it contains the ability to penetrate cardiac

cells and block the production of enzymes tied to regulating glucose intake and energy expulsion. With these regulatory enzymes inhibited, the affected cells can in turn boost the amount of glucose that can be received, and it can also increase its level of energy conversion. Additionally, the peptide’s presence has been determined to aid in lowering programmed cell death, a process that is also known as apoptosis.

Aicar Application:

Glucose uptake stimulant; AMPK activator.AICAR is a nucleoside analogue that is able to enter

nucleoside pools and is able to significantly increase levels of adenosine during periods of ATP

breakdown. Adenosine-regulating agents (ARAs) hav e been recognized for therapeutic potential

in myocardial ischemia. Cardioprotective.

Aicar is a nucleoside analogue that is able to enter nucleoside pools and is able to significantly increase levels of adenosine during periods of ATP breakdown. Adenosine-regulating agents (ARAs) hav e been recognized for therapeutic potential in myocardial ischemia. Cardioprotective.

Biological Activity Cell-permeable, allosteric activator of AMP-activated protein kinase (AMPK). Augments proliferation, differentiation and mineralization of osteoblastic MC3T3-EI cells and attenuates psychosine-induced expression of proinflammatory cytokines and iNOS in astrocytes.

Aicar is a peptide whose technical name is 5-Aminoimidazole-4-carboxamide ribonucleotide. It can also be known as AICA ribonucleotide, ZMP, or Acadesine. It is an intermediate contained in the generation of inosine monophosphate. It primarily functions as an AMP-activated protein kinase agonist, meaning that it has the ability to promote the operation of nutrient stores for energy production. It has a molecular mass of 338.211, and it has a molecular formula of C9H15N4O8P.

Aicar Function:

Aicar is an adenosine analog that selectively activates AMP-activated protein kinase (AMPK). AMPK regulates lipid and glucose metabolism to maintain cellular energy homeostasis (Hardie and Carling).

Aicar can play a hand in boosting these processes because it contains the ability to penetrate cardiac cells and block the production of enzymes tied to regulating glucose intake and energy expulsion. With these regulatory enzymes inhibited, the affected cells can in turn boost the amount of glucose that can be received, and it can also increase its level of energy conversion. Additionally, the peptide's presence has been determined to aid in lowering programmed cell death, a process that is also known as apoptosis.

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