Zhongshan Latterson Biotechnology Co., Ltd.

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Bicalutamide Powder CAS: 90357-06-5 Treatment For Prostate Cancer China Factory

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Other Hot-Sale Products (Raw Powder)
Model Number : 90357-06-5
Certification : GMP, SGS , ISO 9001:2008 , KOSHER
Place of Origin : China
MOQ : 10g
Price : Negotiable ( Discounts For Big Order )
Payment Terms : Western Union, MoneyGram, Bank Transfer, Bitcoin
Supply Ability : 200 KG/Month
Delivery Time : Within 7 Working Days
Packaging Details : Stealth And Discreet Packaging
Product Name : Bicalutamide
CAS : 90357-06-5
MF : C18H14F4N2O4S
MW : 430.37
Melting point : 191-193°C
Appearance : Off-white crystalline powder
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  • Specifications

Bicalutamide Powder CAS: 90357-06-5 Treatment For Prostate Cancer China Factory

Superiority

Zhongshan Latterson Biotechnology Co., Ltd., is a comprehensive pharmaceutical enterprise, which specialized in bio-pharmaceutical technology over 7 years. The company is located in Zhongshan City, Guangdong Province , China.
Our factory covers an area of 33500 square meters, with clean environment and nice layout. There are several large or medium workshops and QA and research center with advanced equipment. At present, our main products are Anabolic Steroid series, Peptide series, Local Anesthetic series. Our products reach the advanced standard of domestic market, many of which reach the international standard, certificates contain: KOSHER , ISO 9001:2008 , GMP , SGS.

Bicalutamide

Product Name: Bicalutamide
Synonyms: (+-)–2-hydroxy-2-methyl;propanamide,n-(4-cyano-3-(trifluoromethyl)phenyl)-3-((4-fluorophenyl)sulfonyl);ICI-176334;CASODEX;BICALUTAMIDE;N-[(4-CYANO-3-TRIFLUOROMETHYL)PHENYL]-3-[(4-FLUOROPHENYL)SULFONYL]-2-HYDROXY-2-METHYLPROPANAMIDE;N-[4-CYANO-3-(TRIFLUOROMETHYL)PHENYL]-3-[(4-FLUOROPHENYL)SULFONYL]-2-HYDROXY-2-METHYLPROPIONANILIDE;Bicalutamide (Subject to patent free)
CAS: 90357-06-5
MF: C18H14F4N2O4S
MW: 430.37
EINECS:
Product Categories: Active Pharmaceutical Ingredients;Antiandrogen;Antineoplastic (Hormonal);anti-neoplastic;Aromatics;Intermediates & Fine Chemicals;Pharmaceuticals;Sulfur & Selenium Compounds;API’s;API;MODRASTANE
Mol File: 90357-06-5.mol
Bicalutamide Structure
Bicalutamide Chemical Properties
Melting point 191-193°C
storage temp. Store at RT
solubility DMSO: >5mg/mL
λmax 270nm(CH3CN)(lit.)
Merck 14,1200
CAS DataBase Reference 90357-06-5(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36-24/25
RIDADR 3077
RTECS TX1413500
HazardClass 9
PackingGroup III
HS Code 29242995
Hazardous Substances Data 90357-06-5(Hazardous Substances Data)
MSDS Information
Provider Language
Bicalutamide English
Bicalutamide Usage And Synthesis
Bicalutamide Solubility soluble in dimethyl formamide; dissolved in tetrahydrofuran; slightly soluble in ethyl acetate and methanol; insoluble in water.
Determination of the content of Bicalutamide tablets by high performance liquid chromatography (HPLC) Using SHIMADZU CLC-ODS (150mm´6.0mm, 5μ) column. 0.1% potassium dihydrogen phosphate solution-acetonitrile (50:50) as the mobile phase, detecting at 272nm wavelength. Result: bicalutamide had a good linear relationship (r=0.9995) when the concentration in the range of 0.05mg*ml-1~0.20mg*ml-1. The average recovery was 99.5%, and RSD=0.9% (n=9 ) Conclusion: The method is simple, good accuracy and high precision.
Bicalutamide tablets Bicalutamide tablet is a non-steroidal androgen antagonist, which competes androgen receptor with the androgen, blocks cellular uptake of androgen, and inhibits the binding of androgens to the target organ. It binds with the androgen receptor that forms receptor complex, which enters the nucleus and combined with the nucleoprotein, consequently inhibiting tumor cell growth. It can be as a first-line drug for palliative treatment of advanced prostate cancer.
Dosage and administration:
Adult: adult males including the elderly: one (50mg), once a day. The treatment should be started simultaneously with LHRH analogue therapy or surgical orchiectomy.
Children: This product is contraindicated in children.
Renal impairment: The patients with renal impairment don’t need dose adjustment.
Hepatic impairment: The patients with mild liver damage don’t need dose adjustment, while the patients with severe liver damage may occur drug accumulation (see precautions).
Precautions:
This product is widely metabolized in the liver. Data show that patients with severe liver damage may slow down drug clearance, which may lead to accumulation. So the patients with moderate and severe liver injury should use it with caution.
The patients may appear liver changes by using it, so it should be considered regular liver function tests. The main changes generally appear within the first 6 months of treatment using this product.
Severe changes in liver function are rarely visible in the treatment of the product (see Adverse Reactions). If there is a serious change in treatment using this product, it should be discontinued.
This product is shown to inhibit the activity of cytochrome P450 (CYP3A4). When combined with drugs metabolised mainly by CYP3A4, the patients should be caution (see Contraindications and Drug Interactions).
Pregnancy and lactation: This product is contraindicated in women, especially for pregnant women or nursing mothers.
Effect on driving and operating machinery ability: This product does not affect the ability of patients of driving and operating the machine.
The above information is edited by the chemicalbook of Kui Ming.
Adverse reaction Pharmacological effects of this product caused certain expected reactions, including flushing, itching, in addition to breast tenderness and feminization of male breast, which can alleviate with orchiectomy. This product may also cause diarrhea, nausea, vomiting, fatigue and dry skin.
Liver function changes (elevated levels of transaminases, jaundice) have been observed in clinical trials of this product, but there were rare serious changes. These changes are often short-lived. The changes then gradually subsided or improved whether to continue treatment or discontinuation of treatment. Patients receiving treatment of this product were very rare liver failure, and its causal relationship has not been established. Regularly check liver function should be considered. (See precautions).
During clinical studies, using this product with LHRH analogues, the following side effects were also observed (clinical investigaters thought it may be related to it and drug-related incidence greater than 1%). Side effects associated with the use of these drugs are no causal relationship, and some of them are daily inherent in the elderly.
Cardiovascular system: heart failure
Digestive system: anorexia, dry mouth, indigestion, constipation, flatulence.
Central nervous system: dizziness, insomnia, somnolence, decreased sexual drive.
Respiratory system: dyspnea.
Urogenital system: impotence, nocturia.
Hematology: anemia.
Skin and its appendages: alopecia, rash, sweating, hirsutism.
Metabolism and nutrition: diabetes, hyperglycemia, peripheral edema, increased or decreased body weight.
Torso: abdominal pain, chest pain, headaches, pelvic pain, chills.
Contraindications:
Contraindicated in women and children.
Can not be used in patients with allergy to the chemicals.
This product can’t use combination with terfenadine, astemizole, or cisapride.
Chemical properties Crystallization from 1: 1 (by volume) of ethyl acetate and petroleum ether. Melting point is 191~193 ℃.
Uses V1 taking anti-androgens drug. Prostate cancer therapeutic agents for the treatment of advanced prostate cancer.
Producing method methyl methacrylate epoxidized to form epoxide,and then in the presence of sodium hydride reacted with fluorothiophenol to form the compound ,followed by oxidation to form compound. Then hydrolyzed to the acid,with thionyl chloride chloride as acid chloride.And finally condensation with 4-cyano-3-trifluoromethyl-aniline to obtain the product.
Chemical Properties Off-White Crystalline Solid
Uses adrenocortical suppressant, antineoplastic, steroid biosynthesis inhibitor
Uses Non-steroidal peripherally active antiandrogen. Used as an antiandrogen, antineoplastic (hormonal)
Definition ChEBI: A sulfone that is an oral non-steroidal antiandrogen used in the treatment of prostate cancer and hirsutism.
Biological Activity Orally active non-steroidal androgen receptor antagonist (IC 50 = 190 nM). Displays peripheral selectivity and does not effect serum levels of LH and testosterone. Exhibits potent anticancer activity in vivo .
Bicalutamide Preparation Products And Raw materials
Raw materials Methyl methacrylate–>4-Fluorothiophenol–>Expoxide–>4-Aminobenzonitrile

Our service

1.100% reshipment policy is our business basic.100% reshipment immediately if your parcel stays Customs for 4 days and doesn’t get updated.
2.Total refund for 15 days of dissatisfaction with quality.
3.We can provide free samples.
4.We have a special packing ,It can be easily passed through the customs.It will be more safe.
5.Our company have a long term cooperate with DHL.EMS.Fedex and so on .It can be sent to your hand more quickly. Parcel photo should be offered within 12hours after receiving your steroid payment.
6.If you have a chance to come to China. I can show you our lab.
7.Our company has WU, MG, TT, and Bitcoin payment ways in advance.You can pay 95% for the peptides cost at first for order, the rest can offer us in your next order;

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