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Форместан
- английское имяFormestane
- CAS №566-48-3
- CBNumberCB6251183
- ФормулаC19H26O3
- мольный вес302.41
- EINECS625-331-3
- номер MDLMFCD00057814
- файл Mol566-48-3.mol
химическое свойство
Температура плавления | 199-202°C |
альфа | D20 +181° (c = 7.7 in chloroform) |
Температура кипения | 383.44°C (rough estimate) |
плотность | 1.1189 (rough estimate) |
показатель преломления | 1.4200 (estimate) |
температура хранения | 2-8°C |
растворимость | Chloroform (Slightly), Methanol (Slightly) |
форма | solid |
пка | 9.31±0.60(Predicted) |
цвет | White to Off-White |
Биологические источники | rabbit |
InChI | InChI=1S/C19H26O3/c1-18-10-8-15(20)17(22)14(18)4-3-11-12-5-6-16(21)19(12,2)9-7-13(11)18/h11-13,22H,3-10H2,1-2H3/t11-,12-,13-,18+,19-/m0/s1 |
ИнЧИКей | OSVMTWJCGUFAOD-KZQROQTASA-N |
SMILES | C1(=O)C(O)=C2[C@](C)(CC1)[C@]1([H])[C@]([H])([C@@]3([H])[C@@](CC1)(C)C(=O)CC3)CC2 |
Справочник по базе данных CAS | 566-48-3(CAS DataBase Reference) |
FDA UNII | PUB9T8T355 |
Словарь наркотиков NCI | formestane |
Код УВД | L02BG02 |
UNSPSC Code | 12352203 |
NACRES | NA.41 |
больше
Коды опасности | T |
Заявления о рисках | 60 |
Заявления о безопасности | 53-36/37/39-45 |
WGK Германия | 3 |
RTECS | BV8152500 |
рисовальное письмо(GHS)
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рисовальное письмо(GHS)
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сигнальный язык
опасность
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вредная бумага
H360:Может отрицательно повлиять на способность к деторождению или на неродившегося ребенка.
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оператор предупредительных мер
P201:Беречь от тепла, горячих поверхностей, искр, открытого огня и других источников воспламенения. Не курить.
P308+P313:ПРИ подозрении на возможность воздействия обратиться за медицинской помощью.
Форместан химические свойства, назначение, производство
Описание
Formestane is a potent aromatase inhibitor launched in the UK as a second-line endocrine treatment for breast cancer. As a synthetic derivative of androstanedione, the natural substrate for the biosynthesis of estrogen by the enzyme aromatase, formastane selectively inhibits aromatase and binds to its steroid receptor site to cause a rapid and sustained fall in circulating estrogen level and, therefore, inhibits tumor growth. In patients with existing bulky primary tumors, formestane effectively reduces the size of the tumors. Formastane has apparent tolerability advantages and less side effects than other agents such as aminoglutethimide.Химические свойства
NeedlesОпределение
ChEBI: A 17-oxo steroid that is androst-4-ene-3,17-dione in which the hydrogen at position 4 is replaced by a hydroxy group. Formestane was the first selective, type I steroidal aromatase inhibitor, suppressing oestrogen production from anabolic steroids or proho mones. It was formerly used in the treatment of oestrogen-receptor positive breast cancer in post-meopausal women. As it has poor oral bioavailability, it had to be administered by (fortnightly) intramuscular injection. It fell out of use with the subseque t development of cheaper, orally active aromatase inhibitors. Formestane is listed by the World Anti-Doping Agency as a substance prohibited from use by athletes.Механизм действия
Aromatase inhibitors such as formestane and letrozole reduce plasma estradiol levels by inhibiting the conversion of testosterone to estrogen. This compound was first described as a competitive inhibitor, but subsequent evidence proved that its binding to aromatase was irreversible. Hence, it is a suicide inhibitor. In the dog, but not rodents, this results in Leydig cell hypertrophy and hyperplasia. This is thought to be due to the differential sensitivity of the pituitary feedback mechanism to estrogens and androgens in the different species[1-2].Форместан запасные части и сырье
Форместан поставщик
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