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Pharmaceutical Grade Treatment Of Prostate Cancer Peptide Deslorelin Acetate 57773-65-6

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Pharmaceutical Grade Treatment Of Prostate Cancer Peptide Deslorelin Acetate 57773-65-6
 
Deslorelin Basic Info.:
 
Product Name: Deslorelin
Specification: 50mg*50vials/kit
Synonyms: GLP-HIS-TRP-SER-TYR-D-TRP-LEU-ARG-PRO-NHET;Desorelin;Deslorelin; Deslorelin Acetate; Deslorelin (Human);
CAS: 57773-65-6
MF: C64H83N17O12
MW: 1282.45
Purity: 98%
Storage temp.: −20°C
Product Categories: Peptide;Hormones
Usage: Biochemical research;Clinical used in the treatment of prostate cancer.
 
Deslorelin Description:
 
Deslorelin acetate is an injectable gonadotropin releasing hormone super-agonist (GnRH agonist) also known as an LHRH agonist. It stops the production of sex hormones (and oestrogen). Deslorelin Acetate is marketed by Peptech with the brand name Ovuplant. It is currently approved for use in veterinary medicine and is used to induce ovulation in mares as part of the artificial insemination process. It is also used to stabilize high-risk pregnancies, mainly of livestock. Unlike other GnRH agonists, which are mainly used to inhibit uteinizing hormone and follicle-stimulating hormone by their ultimate downregulation of the pituitary gland, Deslorelin is primarily used for the initial flare effect upon the pituitary, and its associated surge of LH secretion.
 
Deslorelin Application:
 
Deslorelin was successfully trialed in the US and was approved for veterinary use under certain  circumstances. In Europe, it was approved for use in equine assisted reproduction. It is also being trialed in humans to study its efficacy in treatment of breast cancer in women,and in treating  precocious puberty and congenital adrenal hyperplasia in male and female children.
 

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Pharmaceutical Human Growth Hormone Peptide TB-500 Anti Inflammatory

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Pharmaceutical Human Growth Hormone Peptide TB-500 Anti Inflammatory
 
TB 500 Basic Info.:
 
Product Name: TB 500 
Synonyms:TB 500;TB500;Thymosin Beta 500
TB500 Appearance: White powder
TB500 CAS No.: 77591-33-4
TB500 MF: C212H350N56O78S
TB500 MW: 4963.49
TB500 Specification: 2mg/vial,10vials/kit
TB500 Purity (HPLC): 95%min
TB500 Amino Acid Composition: ± 10% of theoretical
TB500 Peptide Content (N%): ≥ 80.0%
TB500 Water Content(Karl Fischer): ≤ 5.0%
TB500 Acetate Content (HPIC): ≤ 15.0%
TB500 Single Impurity (HPLC): 2.0%max
TB500 MS(ESI): Consistent
 
TB 500 Description:
 
TB-500 is a synthetic fraction of the protein thymosin beta-4, which is present in virtually all human 
and animal cells. The main purpose of this peptide is to promote healing. It also promotes creation 
of new blood and muscle cells. The healing effects of TB-500 have been observed in tendons,
ligaments, muscle, skin, heart, and the eyes. Thymosin beta-4 is naturally produced in higher 
concentration where tissue has been damaged. This peptide is also a very potent anti-inflamatory 
agent. 
 
TB-500 is different from other repair factors (growth hormone, IGF-1), because it promotes 
endothelial and keratinocyte migration. It also does not bind to the extracellular matrix and has 
a very low molecular weight. Because of this it can travel long distances through the tissues in the 
human body. 
 
One of TB-500 key mechanisms of action is its ability to regulate the cell-building protein - Actin. 
Of the thousands of proteins present within human cells, actin represents roughly 10% of the total.
It is thus a vital component of cell structure and movement.
 
TB-500 was identified as a gene that was up-regulated four-to-six fold during early blood vessel
formation and found to promote the growth of new blood cells from the existing vessels. This peptide is present in wound fluid and when administered subcutaneously, it promotes wound healing, muscle building and speeds up recovery time of muscles fibres and their cells. An additional key factor of
TB-500 is that it promotes cell migration through a specific interaction with actin in the cell cytoskeleton.
It has been demonstrated that a central small amino acid long-actin binding domain has both blood cell reproduction and wound healing characteristics. These characteristics are uncovered by accelerating
the migration of endothelial cells and keratinocytes. It also increases the production of extracellular matrix-degrading enzymes.
 
TB 500 Application:
 
TB-500 is different from other repair factors because it promotes endothelial and keratinocyte migration. It also does not bind to the extracellular matrix and has a very low molecular weight.Because of this it can travel long distances through the tissues in the human body. 
 
TB-500 is a synthetic fraction of the protein thymosin beta-4, which is present in virtually all human and animal cells. The main purpose of this peptide is to promote healing. It also promotes creation of new blood and muscle cells. The healing effects of TB-500 have been observed in tendons, ligaments, muscle, skin, heart, and the eyes. Thymosin beta-4 is naturally produced in higher concentration where tissue has been damaged. This peptide is also a very potent anti-inflamatory agent.
 

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Pharmaceutical Ingredients Folic Acid for Pregnant Woman 59-30-3 Medical Raw Material

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Pharmaceutical Ingredients Folic Acid for Pregnant Woman 59-30-3 Medical Raw Material
 
Folic Acid Basic Info.:
 
Product Name: Folic Acid
CAS: 59-30-3
MF: C19H19N7O6
MW: 441.4
EINECS: 200-419-0
Chemical Properties orange to yellow crystalline powder
Usage A vitamin needed to synthesize DNA, conduct DNA repair and methylate DNA, it also acts as a cofactor in biological reactions involving folate.
 
Folic Acid Description:
 
Air & Water Reactions Insoluble in water. Aqueous solutions have pHs of 4.0-4.8.
Reactivity Profile Acid solutions of Folic acid are sensitive to heat, but towards neutrality, stability progressively increases. Solutions are inactivated by ultraviolet light and alkaline solutions are sensitive to oxidation. Folic acid is also inactivated by light. Folic acid is incompatible with oxidizing agents, reducing agents and heavy metal ions. Fire Hazard Flash point data for Folic acid are not available; however, Folic acid is probably combustible.
 
Folic Acid Function:
 
Folic Acid is one of the B vitamins and is also known as vitamin B9.It's widely applied to food and feed.We can used it for preventing and treating low blood levels, as well as its complications, including "tired blood" (anemia) and the inability of the bowel to absorb nutrients properly. Women who are pregnant or might become pregnant take folic acid to prevent miscarriage and "neural tube defects," birth defects such as spina bifida that occur when the fetus's spine and back don't close during development.
1. Increasing the appetite.
2. Stimulating the formation of digestive acids.
3. Promoting the formation of red blood cells and mature with vitamin.
5. Necessary for pregnancy.
6. Reduing the risk of nervous system problem in newborn infants.
 

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Pharmaceutical Intermediate Anti-Estrogen Clomiphene Citrate Steroid Hormone Powder Clomid 50-41-9

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Pharmaceutical Intermediate Anti-Estrogen Clomiphene Citrate Steroid Hormone Powder Clomid 50-41-9
Male Anti Estrogenic Clomid for Steroid Cycle Clomiphene
 
Clomid Basic Info.:
 
Product Name: Clomid (Clomiphene Citrate)
Alias: Clomid;Clomifen;Clomiphene;Clomiphene Citrate;Serophene;Pergotime;Clomphid;Clomiphene Citrate Salt.
CAS No: 50-41-9
MF: C32H36ClNO8
MW: 598.09
Einecs No: 200-035-3
Purity: 99%
Melting point: 116.5-118°C
Storage temp.: 2-8°C
Appearance: Crystalline Solid; Odourless.
Product Categories: API;Intermediates & Fine Chemicals;Pharmaceuticals;Amines;Aromatics;Peptides;CLOMID
Usage:
(1)An unducer of ovulation. A gonad-stimulating principle
(2)Synthetic estrogen agonist-antagonist. Gonad-stimulating principle.
(3)A selective estrogen receptor modulator
 
Clomid Description:
 
Clomid is a mixed estrogen agonist/antagonist (activator/blocker) which, when bound to the estrogen receptor, puts it in a somewhat different conformation (shape) than does estradiol. The estrogen receptor requires binding of an estrogen or drug at its binding site and also the binding of any of several cofactors at different sites. Without the binding of the cofactor, the estrogen receptor is inactive. Different tissues use different cofactors. Some of these cofactors are able to bind to the estrogen receptor/Clomid complex, but others are blocked due to the change in shape. The result is that in some tissues Clomid acts as an antagonist - the cofactor used in that tissue cannot bind and so the receptor remains inactive - and in others Clomid acts as an agonist (activator), because the cofactors used in that tissue are able to bind. 
 
Clomid Applications:
 
Steroids Hormone Clomiphene Citrate/Clomid powders/CAS No: 50-41-9
Clomid is the anti-estrogen of choice for improving recovery of natural testosterone production after a cycle, improving testosterone production of endurance athletes, and is also effective in reducing risk of gynecomastia during a cycle employing aromatizable steroids. 
 

 

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

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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.
 

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

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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).
 

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

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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.
 

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

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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.
 

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Pharmaceutical Raw Material For Vitamin C Ascorbic Acid 50-81-7

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Pharmaceutical Raw Material For Vitamin C Ascorbic Acid 50-81-7
 
Vitamin C Basic Info.:
 
Product Name: Vitamin C
Synonyms: L-Ascorbic Acid, Free Acid; Vitamin C; L-(+)-Ascorbic acid; VC; Ascorbic acid; Vita C BP2005; Vitamine C;
Assay: 98%
CAS No.: 50-81-7
EINECS No.: 200-066-2
Molecular Formula: C6H8O6
Molecular Weight: 176.12
Melting point: 190-194 ° C (DEC. )
Boiling point: 552.672° C at 760 mmHg
Flashing point: 238.199° C
Water solubility: 333 g/L (20º C)
Appearance: White crystalline powder
Packing: 25KG/Drum
Application: To cure Scurvy
 
Vitamin C Description:
 
Vitamin C or L-ascorbic acid, or simply ascorbate (the anion of ascorbic acid), is an essential nutrient for humans and certain other animal species. Vitamin C refers to a number of vitamers that have vitamin C activity in animals, including ascorbic acid and its salts, and some oxidized forms of the molecule like dehydroascorbic acid. Ascorbate and ascorbic acid are both naturally present in the body when either of these is introduced into cells, since the forms interconvert according to pH.
 
Vitamin C is a cofactor in at least eight enzymatic reactions, including several collagen synthesis reactions that, when dysfunctional, cause the most severe symptoms of scurvy. [1] In animals, these reactions are especially important in wound-healing and in preventing bleeding from capillaries. Ascorbate may also act as an antioxidant against oxidative stress. [2] However, the fact that the enantiomer D-ascorbate (not found in nature) has identical antioxidant activity to L-ascorbate, yet far less vitamin activity, [3] underscores the fact that most of the function of L-ascorbate as a vitamin relies not on its antioxidant properties, but upon enzymic reactions that are stereospecific. "Ascorbate" without the letter for the enantiomeric form is always presumed to be the chemical L-ascorbate.
 
Vitamin C Application:
 
Scurvy is an avitaminosis resulting from lack of vitamin C, since without this vitamin, the synthesized collagen is too unstable to perform its function. Scurvy leads to the formation of brown spots on the skin, spongy gums, and bleeding from all mucous membranes. The spots are most abundant on the thighs and legs, and a person with the ailment looks pale, feels depressed, and is partially immobilized. In advanced scurvy there are open, suppurating wounds and loss of teeth and, eventually, death. The human body can store only a certain amount of vitamin C, [41] and so the body stores are depleted if fresh supplies are not consumed. The time frame for onset of symptoms of scurvy in unstressed adults on a completely vitamin C free diet, however, may range from one month to more than six months, depending on previous loading of vitamin C.
 

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Pharmaceutical Raw Material Griseofulvin For Health Skin Tinea Inhibition 126-07-8

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Pharmaceutical Raw Material Griseofulvin For Health Skin Tinea Inhibition 126-07-8 
 
Griseofulvin Basic Info.:
 
Product Name: Griseofulvin
Synonyms: (+)-GRISEOFULVIN;GRISEOFULVIN;
CAS: 126-07-8 
MF: C17H17ClO6 
MW: 352.77 
EINECS: 204-767-4 
Chemical Properties: Crystalline Solid 
 
(+)-Griseofulvin Usage:
 
1.Adrenegic blocker, Ca channel blocker, coronary vasodilator, antiarrhythmic. 
2.Antifungal, inhibits mitosis in metaphase.
3.Griseofulvin is a spirobenzofuran produced by a number of Penicillium species, first isolated in the 1930s by Raistrick's group. Griseofulvin is a selective antifungal agent used to treat skin infections in animals and humans. Griseofulvin acts by binding to fungal tubulin and inhibiting the mitotic spindle. Griseofulvin's ability to bind to keratin is considered an important aspect of the metabolite's access to dermatophytic fungi. More recently, griseofulvin has become an important phenotypic marker in Penicillium taxonomy. 
4.It is an antifungal drug. It is used both in animal and in humans, to treat rigworm infections of the skin and nails. It is derived from the mold Penicillium griseofulvum.
 

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