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Лейпрорелин
- английское имяLeuprorelin
- CAS №53714-56-0
- CBNumberCB8398455
- ФормулаC59H84N16O12
- мольный вес1209.4
- EINECS633-395-9
- номер MDLMFCD00167544
- файл Mol53714-56-0.mol
химическое свойство
альфа | D25 -31.7° (c = 1 in 1% acetic acid) |
плотность | 1.44±0.1 g/cm3(Predicted) |
температура хранения | −20°C |
растворимость | DMSO (Slightly), Methanol (Slightly), Water (Slightly) |
пка | 9.82±0.15(Predicted) |
Растворимость в воде | Soluble in water at 1mg/ml |
Стабильность | Hygroscopic |
ИнЧИКей | RGLRXNKKBLIBQS-VAZQWRJQNA-N |
Справочник по базе данных CAS | 53714-56-0(CAS DataBase Reference) |
FDA UNII | EFY6W0M8TG |
Код УВД | L02AE02 |
Заявления о безопасности | 22-24/25 |
WGK Германия | 2 |
RTECS | OH6390000 |
Банк данных об опасных веществах | 53714-56-0(Hazardous Substances Data) |
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.
P280:Использовать перчатки/ средства защиты глаз/ лица.
P308+P313:ПРИ подозрении на возможность воздействия обратиться за медицинской помощью.
Лейпрорелин химические свойства, назначение, производство
Химические свойства
Hygroscopic, white or almost white powder.Использование
Gonadotropin releasing hormone (gonadorelin) analogue; treatment of prostate cancer.Определение
ChEBI: An oligopeptide comprising pyroglutamyl, histidyl, tryptophyl, seryl, tyrosyl, D-leucyl, leucyl, arginyl, and N-ethylprolinamide residues joined in sequence. Leuprorelin is a synthetic nonapeptide analogue of gonadotropin-releasi g hormone, and is used as a subcutaneous hydrogel implant (particularly as the acetate salt) for the treatment of prostate cancer and for the suppression of gonadal sex hormone production in children with central precocious puberty.Показания
Leuprolide is a potent LH-RH agonist for the first several days to a few weeks after initiation of therapy, and therefore, it initially stimulates testicular and ovarian steroidogenesis. Because of this initial stimulation of testosterone production, it is recommended that patients with prostatic cancer be treated concurrently with leuprolide and the antiandrogen flutamide (discussed earlier). Leuprolide is generally well tolerated, with hot flashes being the most common side effect.Синтез
The synthesis process of Leuprorelin includes the following steps:(1) Fmoc-Pro-HMPB-AM resin is obtained from Fmoc-Pro-OH and HMPB-AM resin with a substitution degree of 0.2mmol/g~1.2mmol/g as starting materials;
(2) The Fmoc-Pro-HMPB-AM resin was coupled one by one by Fmoc/tBu solid phase method to connect amino acids with protective groups in sequence, and the side chain fully protected leuprolide precursor peptide-HMPB-AM was synthesized Resin;
(3) Cut the side chain fully protected leuprolide precursor peptide-HMPB-AM resin to obtain the side chain fully protected leuprolide precursor peptide;
(4) Fully protected side chain leuprolide precursor peptide undergoes ethylamination to obtain side chain fully protected leuprolide;
(5) Leuprolide is fully protected on the side chain by removing the side chain protecting group to obtain the crude leuprolide peptide;
(6) The crude leuprorelin peptide is separated and purified by a high-pressure liquid phase column and lyophilized to obtain the leuprolide refined peptide.
Лейпрорелин запасные части и сырье
Лейпрорелин поставщик
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