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

Muscle Building Steroids Powder Epistane Methyl E 4267-80-5

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Muscle Building Steroids Powder Epistane Methyl E 4267-80-5

Epistane Basic Info.

Product name: Epistane

Alias: Methyl Epitiostanol

Product Categories: Intermediates & Fine Chemicals;Pharmaceuticals;Steroids;Sulfur & Selenium Compounds

CAS: 4267-80-5

M.F.: C20H32OS

Assay: 98%

M.P.: 168-169°C

Appearance: White powder

Package: foil bag

Usage: Epistane is a methylated derivative of the steroid epitiostanol (E588800). Epistane is a readily orally active compound that lacks the 3-ketone common to most anabolic steroids. Epistane greatly incr eases protein synthesis and build up in lean muscle mass

Epistane Description:

Epistane, exhibits a strong, long lasting anti-estrogen effect that is organ tissue specific. This means it works only where you want it to work. Broad range estrogen blockers and aromatase inhibitors can result in system shut down, aching joints, and decreased IGF-I expression. Epistane binds specifically to the 17-estradiol receptor protein in the target tissues. Because of its long lasting and strong effects on specific tissue,

Epistane can significantly reduce and reverse the effects of gynocomastia because not only does Epistane specifically block estrogen in breast tissue but it induces an estrogen-depleted condition which leads to apoptosis or the death of the breast tissue cells. Studies show that small doses of the parent compound, Epitiostanol, at just 10-20mg/week showed a complete disappearance of the mass and pain in 25% of the male patients in the clinical trail, while the other 75% of the patients showed at least a 50% reduction in the mass and complete loss of pain in just 4-8 weeks. Thats results in 100% of the male users with no side effects.

Epistane is more than an anti-estrogen, though, as it also binds to androgen receptors in skeletal muscle. As a PRO-Anabolic compound Epistane promotes increases in strength and lean body mass with an anabolic/androgenic value (Q ratio) of 12. With most powerful androgens there is a high risk of the natural suppression of the gonads. Epistane, unlike other PRO-Anabolic compounds that have recently been released, is relatively mild on the gonads and, due to the anti-estrogenic effects and the fact that Epistane keeps LH levels elevated, post cycle therapy becomes a breeze.

Application Of Epistane:

Epistane is a DHT derived prohormone that was brought to market by RPN with their product "Havoc. " Epistane is an anti-estrogenic dry compound that will aid users in adding lean muscle mass as well as cutting fat. In addition to this, Epistane does not aromatize and is non-progestagenic. This basically means that while on Epistane, estrogen related side effects like gyno and progesterone related side effects like sensitive breast tissue are virtually non-existent. Users will experience little to no side effects while on Epistane, making it an ideal beginner prohormone.

Epistane Function:

Epistane also binds to androgen receptors in skeletal muscle cells and muscle stem cells. This leads to changes in muscle cell function and protein synthesis. In the case of muscle stem cells, which will actually change and fuse with your active adult skeletal muscles increasing the muscles potential for growth and repair. On the opposite side, the presence of androgens actually decreases the ability of stem cells to form new fat cells. So now have increased stem cell conversion to muscle cells and decrease the conversion of stem cells to fat cells, giving you more positive effects of nutrition and training.

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Sarms Powder Steroids Pirfenidone 53179-13-8 Anti Fibrosis

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Sarms Powder Steroids Pirfenidone 53179-13-8 Anti Fibrosis

Pirfenidone Basic information

Product Name: Pirfenidone

Synonyms: 5-methyl-1-phenyl-2(1h)-pyridon;amr-69;PIRFENIDONE;5-METHYL-1-PHENYL-1H-PYRIDIN-2-ONE;5-METHYL-1-PHENYL-2(1H)-PYRIDINONE;5-METHYL-1-PHENYL-2-(1H)-PYRIDONE;5-Methyl-N-phenyl-2-1H-pyridone;Pirfenidone also see 5-Methyl-1-Phenyl-2(1H)-Pyridinone

CAS: 53179-13-8

MF: C12H11NO

MW: 185.22

EINECS: N/A

Melting point: 96-97°C

Storage temp.: Store at RT

Solubility: DMSO: ≥10 mg/mL, Soluble

Chemical Properties: Off-White Solid

Usage: Pirfenidone has demonstrated activity in multiple fibrotic conditions, including those of the lung, kidney and liver

Product Categories: Aromatics Compounds;Aromatics;Heterocycles;Intermediates & Fine Chemicals;Pharmaceuticals;Cytokine signaling;Inhibitors.

Pirfenidone Description:

Pirfenidone (INN, BAN) is an anti-fibrotic drug for the treatment of idiopathic pulmonary fibrosis (IPF). It works by reducing lung fibrosis through downregulation of the production of growth factors and procollagens I and II.

It is a drug developed by several companies worldwide, including InterMune Inc. (now part of Roche), Shionogi Ltd., and GNI Group Ltd. In 2008, it was first approved in Japan for the treatment of IPF after clinical trials, under the trade name of Pirespa by Shionogi & Co. In October 2010, the Indian Company Cipla launched it as Pirfenex. In 2011, it was approved for use in Europe for IPF; it was approved in Canada in 2012 ; and was approved in the United States in October 2014 under the same name. In September 2011, the Chinese State Food and Drug Administration provided GNI Group Ltd with new drug approval of pirfenidone in China, and later manufacture approval in 2013 under the trade name of Etuary.

In 2014 it was approved in Mexico under the name KitosCell LP, indicated for pulmonary fibrosis and liver fibrosis.There is also a topical form created for the treatment of abnormal wound healing processes.

Pirfenidone Application:

In vitro, pirfenidone can inhibit the uterine flesh tumour cells and leiomyoma cells proliferation. Pirfenidone can inhibit the TGF - beta - 1 inducing fibroblast collagen formation. Inhibition of PDGF, FGF and TGF - beta - 1 inducing fibroblast proliferation. In hamster model, pirfenidone, taken by mouth, that can the prevention and treatment of pulmonary fibrosis . Pirfenidone can prevent the sclerosing peritonitis in rats induced by chemical, can also be keloid grafting for the treatment of nude mice. Pirfenidone 0.01 1 mg/ml can suppress the matrix and dose dependent manner serum stimulate uterine fibroids and leiomyoma cell DNA synthesis, the compound has no cytotoxic effect, has no effect on collagen mRNA level also. Pirfenidone in hamster pulmonary fibrosis model can reduce the disease before the collagen I mRNA level enhancement, reduce the level of the lung hydroxyproline and malondialadehyde and lung preserved ammonia acyl hydroxylase activity.

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Global Hot Sell Anti Aging Coenzyme Q10 / Ubiquinol 303-98-0

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Global Hot Sell Anti Aging Coenzyme Q10 / Ubiquinol 303-98-0

Coenzyme Q10 Basic Info.:

Product Name: Coenzyme Q10

Synonyms: LABOTEST-BB LT00244787;COQ10;COENZYME Q10;Q-10;Q10 COENZYME;UBIDECARENONE;UBIQUINONE;UBIQUINONE-10

CAS: 303-98-0

MF: C59H90O4

MW: 863.34

EINECS: 206-147-9

Chemical Properties Yellow-Orange Crystalline Powder

Usage antioxidant, cardiovascular agent

Usage Antibacterial and antioxidant for preventing and treating cancer.

Usage Antibacterial, antioxidant

Biological Activity Component of the mitochondrial transporter chain that behaves as a powerful antioxidant. Displays neuroprotective activity.

Ubidecarenone Details Of Coenzyme Q10:

Coenzyme Q10 (CoQ10 or ubiquinone) has a low risk of side effects and it is an essential vitamin-like substance with many health benefits.

It is proven helpful in treating heart-related problems such as congestive heart failure and to lower high blood pressure.

Coenzyme Q10 is a quinone, which is a substance that helps provide energy to cells in all oxygen-breathing organisms. Researchers first discovered coenzyme Q10 in 1957, and first named it ubiquinone,

Because it was a quinone that was found in every cell of the body (the prefix ubi means everywhere).

Later studies showed that ubiquinone acts as a coenzyme in the body, without which the three enzymes that provide energy to the body cannot function.

Coenzyme Q10 Benefits:

1. Anti-Aging As a strong antioxidant Q10 protects cells from chemicals and other harmful factors.

2. Anti-oxidant Q10 naturally prevents our body and cells from free radicals damage and works as a shield against harmful effects.

3. Muscles are also in need of this enzyme, due to its energy boosting quality. Experiments proved that people who had a balanced Q10 level were more energetic and vigorous

4. Heart-related problems It is proven helpful in treating heart-related problems such as congestive heart failure and to lower high blood pressure.

5. Improves immunity and can dramatically slow tumor growth.

Coenzyme Q10 Application:

1. Applied in pharmaceutical field, it can be used for treating cardiovascular disease.

2. Applied in Cosmetics, it can be sued for skin whitening, removing wrinkling and slowing down ageing.

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High Purity Dutasteride Avodart For Bodybuilding 164656-23-9

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Raw Medical Material Powder Priligy / Dapoxetine 119356-77-3

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Raw Medical Material Powder Priligy / Dapoxetine 119356-77-3

Dapoxetine Basic Info:

Product Name: Dapoxetine

Synonyms: Priligy;Dapoxetine;Dapoxetine hydrochloride;Dapoxetine base;D-Dapoxetine HCL

CAS: 119356-77-3

MF: C21H23NO.ClH

MW: 341.88

EINECS: N/A

Purity: 99%

Appearance: White powder, odorless, slightly sweet, soluble in water and alcohol.

Product Categories: Erectile Dysfunction;API;Dapoxetine hydrochloride

Dapoxetine Description:

Premature ejaculation (PE) is the most common male sexual dysfunction. Dapoxetine hydrochloride, belonging to a class of drugs known as selective serotonin reuptake inhibitors or, was the first drug originally approved for the on-demand treatment of men with PE. We aimed to compare the intravaginal ejaculatory latency time (IELT), patient-reported global impression of change (PGIC), and adverse effect (AE) incidence associated with the use of dapoxetine (30 mg and 60 mg) versus placebo, and evaluate the differences in administering 60 mg versus 30 mg as on-demand medical oral therapy for the treatment of PE via a literature review and meta-analysis. Relevant randomized controlled trials (RCTs) were identified from PubMed, EMBASE, and Cochrane Central Register of Controlled Trials (Cochrane Library) databases. Ultimately, a total of seven RCTs with 8039 patients were included. Our meta-analysis demonstrated that dapoxetine (in the 30 mg and 60 mg subgroup) resulted in significantly higher IELT, PGIC, and AE incidence relative to the placebo, with higher proportions observed for 60 mg versus 30 mg of dapoxetine administration. The most common AEs were mild and tolerable. We conclude that dapoxetine (particularly the 60 mg dosage) may be considered a safe and effective drug for patients with PE.

Dapoxetine Application:

Dapoxetine hydrochloride is a drug that is used to treat premature ejaculation in men. It is available by prescription and is taken orally, prior to sexual intercourse. The drug belongs to the class called serotonin reuptake inhibitors (SSRIs), which have mainly been used to treat depression.

Sexual dysfunction, including premature ejaculation, is an extremely common condition worldwide. The cause of premature ejaculation has not been fully elucidated, but may include both psychological and physiological factors. Premature ejaculation refers to a short ejaculation time, which can affect the satisfaction of both partners during sexual intercourse.

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Yk11 Sarm Myostatin Inhibitor Yk-11 For Athletes 431579-34-9

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Yk11 Sarm Myostatin Inhibitor Yk-11 For Athletes 431579-34-9

YK-11 Basic Info.

Product Name: YK11/ YK-11

Full Name: (17a,20E)-17,20-[(1-Methoxyethylidene)bis(oxy)]-3-oxo-19-norpregna- 4,20-diene-21-carboxylic Acid Methyl Ester

Synonyms: (17a,20E)-17,20-[(1-Methoxyethylidene)bis(oxy)]-3-oxo-19-norpregna- 4,20-diene-21-carboxylic Acid Methyl Ester;YK11 ((17α,20E)-17,20-[(1-methoxyethylidene)bis-(oxy)]-3-oxo-

CAS: 431579-34-9; 366508-78-3

Standard: In-house Standard

Appearance: White powder

Purity: 98.6 %

Shelf life: 2 years

Dosage: Daily dosage of YK11 is 4 mg once a day for hardcore users max 8 mg

YK-11 Description:

S.A.R.M. "YK-11" is one of the most powerful S.A.R.M.S (Selective Androgen Receptor Modulator) on the market today. It is used to achieve Anabolic Steroid type results, but without the negative side effects and legality issues.

This particular SARM "YK-11" is for helping the user Gain Lean Muscle Tissue and Lose Fat simultaneously.

Taking a Moderate dose (4mg - 8mg per day, 2 to 4 capsules per day) of "YK-11" the user can expect to get a more Aesthetic Physique (Lean, Hard and Strong).

Taking a Large dose (18mg - 22mg per day, 9 to 11 capsules) of "YK-11" the user will experience Gaining More Muscle Tissue and maintaining Extreme Muscle Fullness (The "Pumped" Look) 24/7. This is attributed to the abilities of "YK-11" inducing the muscle cells to produce more Follistatin (even more than DHT Steroids), which helps inhibit the production of Myostatin (Myostatin - limits muscle growth). This S.A.R.M. has the potential for being as good as Testosterone in term of Muscle Strengthening, but without the negative side effects.

YK-11 Introduction:

YK11 attaches itself to the AR (androgen receptor), but only inducts methods that lead to the traditional side effects of androgens such as growth of body hair and prostate and enhanced aggression - to a restricted degree.

Kanno tested C2C12 muscle cells and not lab animals or humans. It has been discovered that muscle cells produce more anabolic factors if exposed to 500 nmol (nanomoles) YK11 than if you expose the same muscle cells to 500 nmol DHT.

YK11 induces muscle cells to make more follistatin (more than DHT does) - a strong myostatin inhibitor.

YK-11 Functions:

Sarm YK-11 is a powerful SARM supplement promoting massive lean muscle gains which is a great benefit for those wanting to have an aesthetic and shredded physique!

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99% Purity Peptide Triptorelin For Muscle Building 57773-63-4

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99% Purity Peptide Triptorelin For Muscle Building 57773-63-4

Triptorelin Basic Info.

Product Name: Triptorelin

Synonyms: PGLU-HIS-TRP-SER-TYR-D-TRP-LEU-ARG-PRO-GLY-NH2;PYROGLU-HIS-TRP-SER-TYR-D-TRP-LEU-ARG-PRO-GLY NH2;PYR-HIS-TRP-SER-TYR-D-TRP-LEU-ARG-PRO-GLY-NH2;PYR-HIS-TRP-SER-TYR-D-TRP-LEU-ARG-PRO-GLY-NH2 PAMOATE SALT;Triptorelin Pamoate;Triptorelin Acetate;Triptorelin Amide;Triptorelin, [Dtrp6]-Lh-Rh, Amide

CAS: 57773-63-4

MF: C64H82N18O13

MW: 1311.45

Usage: promoting ovulation

Description Of Triptorelin:

Triptorelin is a gonadotropin-releasing hormone agonist (GnRH agonist) used as the acetate or pamoate salts.

Triptorelin raises testosterone levels 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.

Application Of Triptorelin:

Triptorelin is used to treat advanced prostate cancer in men. It is not a cure. Mosttypes of prostate cancer need the male hormone testosterone to grow and spread.

Triptorelin works by reducing the amount of testosterone that the body makes. This effect helps slow or stop the growth of cancer cells and helps relieve symptoms such as painful/difficult urination.

This medication is similar to a natural substance made by the body (luteinizing hormone releasing hormone-LHRH).

Dosage And Suggestion:

Triptorelin injection comes as a powder to be mixed with sterile water and injected into the muscle of either buttock by a doctor or nurse in a medical office or clinic.

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99.72% Purity Anesthetic Pharma Raw Powder Lidocaine 137-58-6

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99.72% Purity Anesthetic Pharma Raw Powder Lidocaine 137-58-6

Lidocaine Basic Info.:

Product Name: Lidocaine

CAS No.: 137-58-6

Molecular Formula: C14H22N2O

Molecular Weight: 234.34 g/mol

EINECS: 205-302-8

Density: 1.026 g/cm3

Melting Point: 66-69 °C

Boiling Point: 350.8 °C at 760 mmHg

Flash Point: 166 °C

Application: It is a common local anesthetic and antiarrhythmic drug.

Solubility: Soluble in water

Lidocaine Descroptions:

Lidocaine Hydrochloride Injection, USP is indicated for production of local or regional anesthesia by infiltration techniques such as percutaneous injection and intravenous regional anesthesia by peripheral nerve block techniques such as brachial plexus and intercostal and by central neural techniques such as lumbar and caudal epidural blocks, when the accepted procedures for these techniques as described in standard textbooks are observed.

Lidocaine Application and Function:

A- For block anesthesia and epidural anesthesia.

B- Also used for ventricular arrhythmias caused by myocardial infarction, digitalism, glucantime poisoning, surgery and so on. Such as ventricular tachycardia, frequent ventricular premature beat, ventricular fibrillation.

C- As painkillers of injection in the medicament.

D- Also used in suppository and ointment preparation, etc.

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Mk-677 Oral Grow Hormone Sarm Ibutamoren Mesylate 159752-10-0

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Mk-677 Oral Grow Hormone Sarm Ibutamoren Mesylate 159752-10-0

MK-677 Basic Info.:

Product Name: Ibutamoren Mesylate ( MK-677 )

Synonyms: MK-677; Crescendo; IbutaMoren Mesylate; MK-667; IBUTAMORIN; Nutrobal

CAS: 159752-10-0

MF: C27H36N4O5S.CH4O3S

MW: 624.776

Purity: 99%

Boiling Point: 868.9°C at 760 mmHg

Appearance: white powder

Storage temp.: 2-8°C

Product Categories: SARMs(Selective androgen receptor modulator)

Application: active growth secretagpgie, mk-677 Effective for age -related fraity Active.

MK-677 Description:

Nutrobal (Mk-677) is an orally administrated growth hor secretagogue originally developed by Reverse Pharmacology. A secretagogue is the term for a substance that chemically signals for the pituitary gland to secrete growth hor . In other words, Nutrobal could be compared to peptides like GHRP-6 or Ipamorelin, only it doesn't require any injections nor does it have any side effects like GHRP-6. This GHS (Growth Hormone Secretagogue) was developed in an aim to combat such conditions as muscle wasting, obesity and osteoporosis. It was also targeted towards treatment of elderly hip fracture patients, so there are a myriad of studies done on safety.

Ibutamoren (MK-677, L-163,191) is a drug which acts as a potent, orally active secretagogue,mimicking the GH stimulating action of the endogenous hormone ghrelin.It has been demonstrated to increase the release of, and producessustained increases in plasma levels of several hormones including , but without affecting cortisol levels.

It is currently under development as a potential treatment for reduced levels of these hormones, such as

in deficient children or elderly adults, and human studies have shown it to increase both muscle mass

and bone mineral density, making it a promising therapy for the treatment of frailty in the elderly.It also

alters metabolism of body fat and so may have application in the treatment of obesity.Some mk-677 study shows the suggested mk-677 dosage is 25mgs-50mgs when it is the oral.

MK-677 Application:

Produced by Reverse Pharmacology, MK 677 (Nutrobal) is an orally administered growth hormone secretagogue that is designed to stimulate the pituitary gland to release growth hormones. In case you're

wondering, "secretagogue" is basically a natural substance that causes another substance to be

secreted, such as gastrin.

MK 677 (Nutrobal) was originally formulated to keep health problems like osteoporosis, obesity and

muscle wasting, but has been seen to promote an increase in lean body mass as well as a boost in

IGF-1 serum concentration during clinical runs.

Moreover, here are the positive effects of MK 677 (Nutrobal) in terms of improving growth hormone

pulse intensity:Inhibits the signaling of somatostatin receptors.Slows down the activity of somastostatin in the system.Improves somatotroph signaling in growth hormone releasing hormones (GHRH).Amplifies and increases the overall production and release of GHRH.

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Steroids Hormone Female Use Estrone Estrogen Steroids 53-16-7

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Steroids Hormone Female Use Estrone Estrogen Steroids 53-16-7

Estrone Basic Info.

Product Name: Estrone

Related Products: Ethisterone, Estradiol, Estriol, Formestane, Norethisterone

Purity: 99%

Molecular Formula: C18H22O2

Molecular Weigh: 270.371

CAS No: 53-16-7

EINECS: 200-164-5

Appearance: White or almost white powder

Solubility: Water: 0.03 g/L

Function: Hormones and Regulation of Endocrine Function of Drug

Storage: Shading, Confined Preservation

Package: Discreet Packing ways for your choice.

Delivery: Deliver out within 24 hours after payment.

Payment: West Union, Money Gram.T/T

Estrone Description:

Estrogen is a female hormone produced by the ovaries and placenta. Adrenal cortex also produces a

small number of estrogen.

Female children after puberty, the ovaries begin to secrete estrogen to promote the vagina, uterus,

fallopian tubes and ovaries own development, while endometrial hyperplasia produce menstruation.

Estrogen can promote the accumulation of subcutaneous fat, plump; Hyperplasia, nipple and areola

become darker in color, and produces sexuality; Promote sodium and water retention in the body, such as bone calcium deposition.

Estrogen is a steroid compounds have a wide range of biological activity, it is not only to promote and

maintain the female reproductive organs and secondary sexual characteristics of the physiological role, and the endocrine system, the cardiovascular system, the body's metabolism, bone growth and

maturation, skin and other aspects have a significant impact.

Due to the secretion of estrogen, can nourish the skin, beautiful hair, and promote breast development

increased, reflecting the graceful curve of the body. So estrogen for women to maintain their youth and

women second feature essential trace elements. In addition to the beauty estrogen plays an important

role, and human health are closely linked.

Menopausal syndrome, arteriosclerosis, cerebral vascular obstruction, osteoporosis, Alzheimer's disease, weary, back pain, sore shoulders, sex, irregular menstruation, irregular menstruation, amenorrhea, infertility, breast dysplasia, dry skin, yellowish, rough, loss of elasticity, wrinkles, melasma, etc., and the body is low estrogen secretion lead to endocrine disorders. As noted above, estrogen for women is a very important trace elements. But the body's secretion of estrogen declining with age. And in vitro estrogen can not be supplemented by food, this is because estrogen in the human or animal body can build

yourself.

Estrone Application:

Estrone (E1, and also oestrone) is an estrogenic hormone secreted by the ovary as well as adipose tissue with the chemical name of 3-hydroxyestra-1,3,5(10)-triene-17-one and the chemical formula C18H22O2. Estrone is an odorless, solid crystalline powder, white in color with a melting point of 254.5 °C and a specific gravity of 1.23. Estrone is one of several natural estrogens, which also include estriol and estradiol. Estrone is the least abundant of the three hormones; estradiol is present almost always in the reproductive female body, and estriol is abundant primarily duringpregnancy.

Estrone is known to be a carcinogen for human females as well as cause breast tenderness or pain, nausea, headache, hypertension, and leg cramps. In men, estrone has been known to cause anorexia, nausea, vomiting, and erectile dysfunction.Estrone is relevant to health and disease states because of its conversion to estrone sulfate, a long-lived derivative. Estrone sulfate acts as a reservoir that can be converted as needed to the more active estradiol. It is the predominant estrogen in postmenopausal women.

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