Buy artificial human hormones | human hormones manufacturers | human hormones suppliers

chemical-categories

Pharmaceutical Intermediate Powder Peptide Lanreotide For Acromegaly 108736-35-2

Welcome to inquiry!

Email: tony@kafenbio.com

WhatsApp: +8618002259573

Skype: tony_14616

www.pharmhormone.com

 
Pharmaceutical Intermediate Powder Peptide Lanreotide For Acromegaly 108736-35-2 
 
Lanreotide Basic Info.:
 
Product Name: Lanreotide
Synonyms: Lanreotide;Autogel;Bim-23014;Angiopeptin;Ipstyl 
CAS: 108736-35-2
MF: C54H69N11O10S2
MW: 1096.32
Storage temp.: −20°C
Chemical Properties: White to off-white lyophilised powder
Product Categories: hormones
 
Lanreotide Description:
 
Lanreotide (INN) is a medication used in the management of acromegaly and symptoms caused by neuroendocrine tumors, most notably carcinoid syndrome. It is a long-acting analogue of somatostatin, like octreotide. Its sequence is H-D-2Nal-Cys(1)-Tyr-D-Trp-Lys-Val-Cys(1)-Thr-NH2.
 
Lanreotide is used in the treatment of acromegaly, due to both pituitary and non-pituitary growth hormone-secreting tumors, and the management of symptoms caused by neuroendocrine tumors, particularly carcinoid tumors and VIPomas. In the United States and Canada, lanreotide is only indicated for the treatment of acromegaly. In the United Kingdom, it is also indicated in the treatment of thyrotrophic adenoma,a rare tumor of the pituitary gland which secretes TSH.
 
Lanreotide also shows activity against non-endocrine tumors, and, along with other somatostatin analogues, is being studied as a possible general antitumor agent.
 
Lanreotide Indications:
 
Lanreotide is used in the treatment of acromegaly, due to both pituitary and non-pituitary growth hormone-secreting tumors, and the management of symptoms caused by neuroendocrine tumors, particularly carcinoid tumors and VIPomas.  In the United States and Canada, lanreotide is only indicated for the treatment of acromegaly. In the United Kingdom, it is also indicated in the treatment of thyrotrophic adenoma, a rare tumor of the pituitary gland which secretes.
 
Lanreotide also shows activity against non-endocrine tumors, and, along with other somatostatin analogues, is being studied as a possible general antitumor agent.
 
Lanreotide ,In Dec 2014 the US FDA approved lanreotide for the treatment of patients with unresectable, well or moderately differentiated, locally advanced or metastatic gastroenteropancreatic neuroendocrine tumors (GEP-NETs).
 
Lanreotide Side Effects:
 
Lanreotide ,The main side effects of lanreotide treatment are mild to moderate pain at the injection site and gastrointestinal disturbances, such as diarrhea, nausea and vomiting. Isolated cases of gallstone formation have been associated with use of lanreotide, particularly over long periods of time.
 

Properties Suppliers
Pharmaceutical Intermediates Pregabalin For Anti-Epileptic Treatment 148553-50-8

Welcome to inquiry!

Email: tony@kafenbio.com

WhatsApp: +8618002259573

Skype: tony_14616

www.pharmhormone.com

 
Pharmaceutical Intermediates Pregabalin For Anti-Epileptic Treatment 148553-50-8
 
Pregabalin Basic Info.:
 
Product Name: Pregabalin 
Synonym: Pregablin;3-(Aminomethyl)-5-methyl-hexanoic acid
CAS: 148553-50-8
MF: C8H17NO2
MW: 159.23
Assay: 99.5%
Appearance: White Crystal Powder
Payment: T/T, Western Union and Money Gram
Delivery: Within 12hours After Your Payment
Express: EMS, DHL, FedEx, etc(door-to-door)
Usage: New antiepileptic drugs. Used in the treatment of peripheral neuropathy, or partial seizures adjuvant treatment.
 
Product Introduction Of Pregabalin:
 
Pregabalin works by reducing the abnormal electrical activity in the brain. It is taken alongside other medicines for epilepsy. Pregabalin can also be helpful in treating the symptoms of generalised anxiety disorder (GAD), particularly if other medicines which are more often prescribed for people with this condition are not suitable. GAD is a long-term condition where anxiety is a major symptom.
 
Pregabalin, also known as β-isobutyl-γ-Aminobutyric acid (β-isobutyl-GABA) and sold under the trade name Lyrica among others, is a medication used to in the treatment of epilepsy, neuropathic pain, fibromyalgia and generalized anxiety disorder. Its use for epilepsy is as an add-on therapy for partial seizures with or without secondary generalization in adults.
 
Pregabalin is a structural analogue of the neurotransmitter GABA, consequently it belongs to the γ-Aminobutyric acid analogue class of antiepileptic drugs. Its a ion channel modulator that has analgesic, anticonvulsant, sedative, and anxiolytic properties. Pregabalin is a potent gabapentinoid and close analogue of GABOB (β-hydroxy-GABA), baclofen (β-(4-chlorophenyl)-GABA), and phenibut (β-phenyl-GABA).
 
Pregabalin Usage:
 
Pregabalin belongs to a group of medicines known as anti-epileptic medicines, although it is prescribed for the treatment of several different conditions. You may have been prescribed it for the treatment of partial seizures, which is a type of epilepsy. A seizure is a short episode of symptoms which is caused by a burst of abnormal electrical activity in the brain. With a partial seizure, the burst of electrical activity stays in one part of the brain. Therefore, you tend to have localised or 'focal' symptoms. Pregabalin is also prescribed to treat certain types of long-lasting pain caused by damage to nerves. This type of pain, called neuropathic pain, can be caused by a number of different conditions, including diabetes (where it is called diabetic neuropathy) and shingles(where it is called postherpetic neuralgia).
 

Properties Suppliers
Pharmaceutical Powdered Female Sex Hormones Depofemin Fat Burning Steroids 313-06-4

Welcome to inquiry!

Email: tony@kafenbio.com

WhatsApp: +8618002259573

Skype: tony_14616

www.pharmhormone.com

 
Pharmaceutical Powdered Female Sex Hormones Depofemin Fat Burning Steroids 313-06-4
 
Depofemin Basic Info.:
 
Product Name: Depofemin
CAS: 313-06-4
EINECS Number: 206-237-8
Formula: C26H36O3
MW: 396.5622
Density: 1.15g / cm3
Boiling point: 532.8 °C at 760 mmHg
Flash Point: 207.7 °C
Vapor Pressure: 5.73E-12mmHg at 25 °C
Assay:99%
Specification: USP/BP
Appearance: white crystalline powder.
 
Product Description Of Depofemin:
 
Depofemin is a sex hormone that is present in both males and females, and is the most important form of estrogen in humans. In women, it plays a key role in the development and functioning of the reproductive system, as well as in the growth of certain bones. It also governs the distribution of body fat in women and is the main hormone responsible for the fact that women are shorter than men, on average. Both the ovaries and the adrenal glands produce it.
 
The menstrual cycle in women involves predictable variations in the levels of several hormones, with estradiol being one of them. It is involved in the ovulation process and prepares the inner lining of the uterus for implantation, should the egg be fertilized. Certain tests done on baboons and other primates have indicated that his hormone also plays a continual role in maintaining a pregnancy, helping it to last for the full gestation period.
 
As a sex hormone, it also triggers many of the developments of the reproductive system that begin in puberty. It is present throughout the reproductive years, and declines during and after menopause. This decline is precisely what causes many of the symptoms of menopause, such as hot flashes and night sweats, vaginal dryness, and the loss of bone mass that may lead to osteoporosis.
 

Properties Suppliers
Pharmaceutical Raw Material Flutamide For Cancer Treament 13311-84-7

Welcome to inquiry!

Email: tony@kafenbio.com

WhatsApp: +8618002259573

Skype: tony_14616

www.pharmhormone.com

 
Pharmaceutical Raw Material Flutamide For Cancer Treament 13311-84-7
 
Flutamide Basic Info.:
 
Product Name: Flutamide 
Synonyms: Timtec-bb sbb006930;Flutamide;Aurora ka-860
CAS: 13311-84-7 
MF: C11H11F3N2O3 
MW: 276.21 
EINECS: 236-341-9 
Chemical Properties: Light Yellow Solid 
Standard: Enterprise Standard 
Packing: foil bag or as required
Product Categories: Antitumors for Research and Experimental Use;Biochemistry;Amines;Aromatics;Pharmaceutical raw material 
 
Flutamide Usage:
 
Neuroleptic, Flutamide is a nonsteroidal antiandrogen drug, antineoplastic (hormonal). 
 
Flutamide Features:
 
For prostate cancer or benign prostatic hypertrophy. This product with bright prolyl Lee Teuk combination (should also start and at the same time, the continued use of) for the treatment of metastatic prostate
cancer, can significantly increase the efficacy.
 

Properties Suppliers
Pharmaceutical Raw Materials Desonide Used To Treat Atopic Dermatitis 638-94-8

Welcome to inquiry!

Email: tony@kafenbio.com

WhatsApp: +8618002259573

Skype: tony_14616

www.pharmhormone.com

 
Pharmaceutical Raw Materials Desonide Used To Treat Atopic Dermatitis 638-94-8
 
Desonide Basic info:
 
Product Name: Desonide
Synonyms: Prednacinolone;Desonide;D-2083;Steroderm
CAS NO.: 638-94-8
Molecular Formula: C24H32O6
Molecular Weight: 416.51
EINECS: 211-351-6
Assay: 99.5%
Melting point: 272-274°C
Storage temp.: Refrigerator
Appearance: White powder
Product Categories: Chiral Reagents;Intermediates & Fine Chemicals;Pharmaceuticals;Steroids;SPORANOX;Hormone Drugs.
Usage: 
(1)With acetal-based adrenal cortex hormones;
(2)Antifungal;
(3)Anti-inflammatory. Desonide has also been found as an impurity in budesonide (B689490).
How to use desonide topical: Use this medication only on the skin.
 
Desonide Description:
 
Desonide Ointment, 0.05% contains Desonide (Pregna - 1,4 - diene - 3,20 - dione,11,21 - dihydroxy - 16,17 - [(1 - methylethylidene)bis(oxy)] - ,(11β,16α)) a synthetic corticosteroid for topical dermatologic use. The corticosteroids constitute a class of primary synthetic steroids used topically as anti-inflammatory and antipruritic agents.
 
Chemically, Desonide, the active ingredient in Desonide Ointment, 0.05% is C24H32O6. It has the following structural formula:
 
The molecular weight of Desonide is 416.51. It is a white to off-white powder. The solubility of Desonide in distilled water saturated with ether is 184 mg/L.
Each gram of Desonide Ointment, 0.05% contains 0.5 milligram of Desonide microdispersed in a base of white petrolatum.
 
Desonide Application:
 
Desonide belongs to the group of medications known as topical corticosteroids. It is used to Treat various skin conditions, including rashes. It works by reducing inflammation and itching.
 
Endogenous eczema clinical cure rate, the overall curative effect is distinct, and the low Incidence of adverse reactions, is a safe and effective external cortex hormone.
 
Wash your hands. Before applying the medication, clean and dry the affected area. Apply a thin film of the medication to the affected area and gently rub in, usually 2-3 times daily, or as directed by your doctor. If using the gel, apply the gel usually only 2 times daily. Do not bandage, wrap, or cover the area unless you are instructed to do so by your doctor. If used in the diaper area on an infant, do not use tight-fitting diapers or plastic pants.
 
After applying the medication, wash and dry your hands, unless you are using this medication to treat the hands. When applying this medication near the eyes, avoid getting it in the eyes because this may worsen or cause glaucoma, or cause irritation. Also, avoid getting this medication in the nose or mouth. If you get this medication in your eyes, nose, or mouth, rinse immediately with plenty of water.
 

Properties Suppliers
Pharmaceutical Raw Materials Dexamethasone Sodium Phosphate For Acute Disorders 2392-39-4

Welcome to inquiry!

Email: tony@kafenbio.com

WhatsApp: +8618002259573

Skype: tony_14616

www.pharmhormone.com

 
Pharmaceutical Raw Materials Dexamethasone Sodium Phosphate For Acute Disorders 2392-39-4
 
Dexamethasone Sodium Phosphate Quick Detail:
 
Product name: Dexamethasone Phosphate Sodium
Synonyms: Dexamethasone sodium phosphate; Dexamethasone Phosphate Sodium; dexamethasone 21-(disodium phosphate); Dexamethasone Sodium Phosphate; Dexamethasone Phosphate Disodium
CAS: 2392-39-4
M.F.: C22H28FNa2O8P 
M.W.: 516.4
Usage : pharmaceutical raw materials, the hormone
Assay: 99%
Packaging Details: Foil bag or as requirement 
Payment Terms: T/T, Western Union, MoneyGram
Shipping way: EMS, HKEMS, DHL, Fedex, UPS (you can choose the fastest and your favourite)
 
Description of Dexamethasone Sodium Phosphate:
 
Dexamethasone sodium phosphate, a corticosteroid, is similar to a natural hormone produced by your adrenal glands. It often is used to replace this chemical when your body does not make enough of it. It relieves inflammation (swelling, heat, redness, and pain) and is used to treat certain forms of arthritis; skin, blood, kidney, eye, thyroid, and intestinal disorders (e.g., colitis); severe allergies; and asthma. Dexamethasone sodium phosphate is also used to treat certain types of cancer.
 
Dexamethasone sodium phosphate comes as a tablet and a solution to take by mouth. Your doctor will prescribe a dosing schedule that is best for you. Follow the directions on your prescription label carefully, and ask your doctor or pharmacist to explain any part you do not understand. Take Dexamethasone sodium phosphate exactly as directed. Do not take more or less of it or take it more often than prescribed by your doctor.
 
Applications of Dexamethasone Sodium Phosphate:
 
Do not stop taking Dexamethasone sodium phosphate without talking to your doctor. Stopping the drug abruptly can cause loss of appetite, upset stomach, vomiting, drowsiness, confusion, headache, fever, joint and muscle pain, peeling skin, and weight loss. If you take large doses for a long time, your doctor probably will decrease your dose gradually to allow your body to adjust before stopping the drug completely. Watch for these side effects if you are gradually decreasing your dose and after you stop taking the tablets or oral liquid, even if you switch to an inhalation corticosteroid medication. If these problems occur, call your doctor immediately. You may need to increase your dose of tablets or liquid temporarily or start taking them again.
 

Properties Suppliers
Pharmaceutical Raw Materials Elubiol Dichlorophenylimidazoldioxolan 67914-69-6

Welcome to inquiry!

Email: tony@kafenbio.com

WhatsApp: +8618002259573

Skype: tony_14616

www.pharmhormone.com

 
Pharmaceutical Raw Materials Elubiol Dichlorophenylimidazoldioxolan 67914-69-6
 
Elubiol Basic Info.:
 
Product Name: Elubiol (Dichlorophenylimidazoldioxolan)
Synonyms: Elubiol; Dichlorophenylimidazoldioxolan
CAS: 67914-69-6
Molecular formula: C27H30Cl2N4O5
Molecular weight: 561.46
Quantity: 500Kgs stock inventory. 10 tons per month
Appearance white to off white crystalline powder
Identification of HPLC
Loss on drying 0.50%max
The heavy metal 20ppmmax
The purity of (HPLC) 99.00%min
Content (titrimetric) 99.0%-101.0%
Package: 25kg paperboard barrel
 
Elubiol Description:
 
New posaconazole is a novel imidazole fungicides could inhibit the fungal sterol biosynthesis, wheat, and other components of the changes of cell membrane lipid compounds. Killing of Candida albicans, Histoplasma, Blastomyces dermatitidis and Coccidioides immitis, to dandruff, sterilization and regulate the skin grease in the washing products.
 
The main structure and the new azole ketoconazole are exactly the same, only at the end of keto ester instead of ketoconazole in. The Pityrosporum ovale of dandruff, two is the most potent inhibitor. The new azole included in the INCI directory, list the EU cosmetics ingredients and the Ministry of "health standard Chinese names of raw materials of Cosmetics International Directory", can be legally used in cosmetics.
 

Properties Suppliers
Pharmaceutical Raw Materials Female Steroids Raw Hormone Powders Mifepristone 84371-65-3

Welcome to inquiry!

Email: tony@kafenbio.com

WhatsApp: +8618002259573

Skype: tony_14616

www.pharmhormone.com

 
Pharmaceutical Raw Materials Female Steroids Raw Hormone Powders Mifepristone 84371-65-3
 
Mifepristone Basic Info.:
 
Product Name: Mifepristone (R38486)
Synonyms: 11-(4-(dimethylamino)phenyl)-17-hydroxy-17-(1-propynyl)-estra-9-dien-3-one;11beta-[4-(n,n-dimethylamino)phenyl]-17alpha-(prop-1-ynyl)-delta4,9-estradiene;r38486
CAS Number: 84371-65-3
Molecular Formula: C29H35NO2
Molecular Weight: 429.65
Assay: 99%
Melting Point: 195-198 °C
Storage temp.: 2-8°C
Appearance: Light yellowish powder
Product Categories: Steroids;Hormone;Acetylenes;Biochemistry;Functionalized Acetylenes;Hydroxyketosteroids;Chiral Reagents;Intermediates & Fine Chemicals;Pharmaceuticals;Intracellular receptor;Nuclear Receptors;Steroid and Hormone;API;Hormone Drugs.
Uses: It is a novel anti-progestin and has anti-glucocorticoid activity without the activity of progesterone, estrogen, androgen and anti-estrogen. It has a progesterone receptor affinity five times as high as progesterone. It is used for anti-pregnancy, inducing menstruation and terminating pregnancy, intrauterine inducer labor for dead fetal.
 
Mifepristone Description:
 
Mifepristone is a synthetic steroid compound with both antiprogesterone and antiglucocorticoid properties. The compound is a 19-nor steroid with substitutions at positions C11 and C17 (17 beta-hydroxy-11 beta-[4-dimethylamino phenyl] 17 alpha-[1-propynyl]estra-4, 9-dien-3-one), which antagonizes cortisol action competitively at the receptor level.
 
Mifepristone is a progesterone receptor antagonist used as an abortifacient in the first months of pregnancy, and in smaller doses as an emergency contraceptive. It is also a powerful glucocorticoid receptor antagonist.
 
Mifepristone Applications:
 
Mifepristone is used alone or in combination with misoprostol (Cytotec) to end an early pregnancy. Early pregnancy means it has been 49 days or less since your last menstrual period began. Mifepristone is in a class of medications called antiprogestational steroids. It works by blocking the activity of progesterone, a substance your body makes to help continue pregnancy.
 
Mifepristone is also available as another product (Korlym), which is used to control hyperglycemia (high blood sugar) in people with a certain type of Cushing's Syndrome in which the body makes too much of the hormone cortisol. This monograph only gives information about mifepristone (Mifeprex), which is used alone or in combination with another medication to end an early pregnancy. If you are using mifepristone to control hyperglycemia caused by Cushing's syndrome, read the monograph entitled mifepristone (Korlym) that has been written about this product.
 
Mifepristone (or RU-486) is a synthetic steroid compound with both antiprogesterone and antiglucocorticoid properties. The compound is a 19-nor steroid with substitutions at positions C11 and C17 (17 beta-hydroxy-11 beta-[4-dimethylamino phenyl] 17 alpha-[1-propynyl]estra-4, 9-dien-3-one), which antagonizes cortisol action competitively at the receptor level.
 
Mifepristone is a progesterone receptor antagonist used as an abortifacient in the first months of pregnancy, and in smaller doses as an emergency contraceptive. It is also a powerful glucocorticoid receptor antagonist, and has occasionally been used in refractory Cushing's syndrome (due to ectopic/neoplastic ACTH/cortisol secretion).
Mifepristone was the first antiprogestin to be developed and it has been evaluated extensively for its use as an abortifacient.
 

Properties Suppliers
Pharmaceutical Raw Materials Mitotan Used to Antineoplastic Agent 53-19-0

Welcome to inquiry!

Email: tony@kafenbio.com

WhatsApp: +8618002259573

Skype: tony_14616

www.pharmhormone.com

 
Pharmaceutical Raw Materials Mitotan Used to Antineoplastic Agent 53-19-0
 
Mitotane Basic Info.:
 
Product Name: Mitotane
CAS:53-19-0
MF:C14H10Cl4
MW:320.04
EINECS:200-166-6
Air & Water Reactions:Insoluble in water.
Chemical Properties:White Crystalline Solid
Usage:insecticide, antineoplastic. treatment of osteoporosis and Paget's bone disease. Used as an adrenolytic agent
 
Mitotane Description:
 
Mitotane Simple aromatic halogenated organic compounds are very unreactive; halogenated aliphatic compounds are moderately or very reactive. For both subgroups, reactivity generally decreases with increased degree of substitution of halogen for hydrogen atoms. Materials in this group are incompatible with strong oxidizing and reducing agents. Also, they are incompatible with many amines, nitrides, azo/diazo compounds, alkali metals, and epoxides.
 
Mitotane Avail:
 
Mitotane structure and pharmacological action insecticide DDT (DDT) and DDD similar, it selectively adrenal zona fasciculata and reticularis cells atrophy, necrosis, but does not affect the zona, aldosterone secretion and therefore will not be affected. Blood and urine cortisol and its metabolites rapidly reduced after treatment, the body adrenocorticotropic hormone and metabolism products decreased rapidly, for the treatment of inoperable, functional and non-functional adrenal cortical carcinoma, adrenal tumor, adrenal gland cruzi induced hyperplasia syndrome, adrenal hyperplasia, cortical cancer adjuvant therapy and tumor-induced Cushing's syndrome.
 

Properties Suppliers
Pharmaceutical Raw Materials Natural Steroid Hormones Powder Methyldienedione 5173-46-6

Welcome to inquiry!

Email: tony@kafenbio.com

WhatsApp: +8618002259573

Skype: tony_14616

www.pharmhormone.com

 
Pharmaceutical Raw Materials Natural Steroid Hormones Powder Methyldienedione 5173-46-6
 
Methyldienedione Basic Info.:
 
Product Name: Methyldienedione
Alias: Estra-4,9-diene-3,17-dione
CAS register number: 5173-46-6
Molecular Formula: C18H22O2
Molecular Weight: 270.37
Melting Point: 131-134°C
Assay: 98%min
Grade: Pharmaceutical Grade
Storage: Shading, confined preservation
Packing: 1kg/foil bag. 25kg/drum
Character: White crystalline powder.
Usage: A potential metabolitie of STS 557 (Dienogest). A steroid with antiglucocorticoid activity.
 
Methyldienedione Description:
 
Estra-4,9-diene-3,17-dione is a powerful pro-steroid chemically similar to the anabolic agent Trenbolone.
When in the body, estra-4,9-diene-3,17-dione completes the conversion to Trenbolone. Trenbolone is a potent anabolic steroid, which binds to specific receptors present in reproductive tissue, muscle and fat.
 
Estra Diene Dione (estra-4,9-diene-3,17-dione) is an anabolic steroid and a precursor to Estra Diene Dione. It became a controlled substance in the US on January 4, 2010, and is classified as a Schedule III anabolic steroid under the United States Controlled Substances Act. Previous to this, it was sold as a bodybuilding supplement within the United States, and often mistakenly marketed as a prohormone for trenbolone, a veterinary steroid. Prior to its scheduling, it was part of a number of supplements that were seized during FDA enforcement for selling unapproved new drugs. The actual target steroid, Estra Diene Dione has some structural similarity to trenbolone, but lacks the 11-carbon -ene bond.
 
Methyldienedione Applications:
 
1. Protection from gynomastia,
2. Increased sex drive/libido,
3. Enhanced intensity & focus,
4. Estrogen control,
5. Positive effects on strength & lean mass.
 

Properties Suppliers