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ЛОХО-101
- английское имяLOXO-101
- CAS №1223403-58-4
- CBNumberCB53121981
- ФормулаC21H22F2N6O2
- мольный вес428.44
- номер MDLMFCD28902192
- файл Mol1223403-58-4.mol
химическое свойство
плотность | 1.55±0.1 g/cm3(Predicted) |
температура хранения | RT |
растворимость | Soluble in DMSO (up to 5 mg/ml). |
форма | solid |
пка | 8.41±0.40(Predicted) |
цвет | Yellow |
Стабильность | Stable for 1 year from date of purchase as supplied. Solutions in DMSO may be stored at -20° for up to 2 months. |
FDA UNII | PF9462I9HX |
Словарь онкологических терминов NCI | LOXO-101 |
Код УВД | L01EX12 |
рисовальное письмо(GHS)
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рисовальное письмо(GHS)
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сигнальный язык
предупреждение
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вредная бумага
H302:Вредно при проглатывании.
H317:При контакте с кожей может вызывать аллергическую реакцию.
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оператор предупредительных мер
P280:Использовать перчатки/ средства защиты глаз/ лица.
ЛОХО-101 химические свойства, назначение, производство
Описание
LOXO-101 is an inhibitor of the tropomyosin-related kinases TrkA, TrkB, and TrkC (IC50s = 2-20 nM). It is selective for TrkA, -B, and -C over a panel of 226 kinases at 1 μM. LOXO-101 inhibits the growth of CUTO-3.29, KM12, and MO-91 patient-derived cancer cell lines (IC50s = <100, <10, and <10 nM, respectively). In vivo, LOXO-101 (60 and 200 mg/kg) reduces tumor growth in a KM12 mouse xenograft model.Описание
Larotrectinib, also known as LOXO-101 and ARRY-470, is a small molecule that was designed to block the ATP-binding site of the TRKA, TRKB, and TRKC, serving as a highly specific and potent inhibitor of all of the three tropomyosin kinase receptors.Использование
Larotrectinib is a TRK Inhibitor (Tyrosine kinase inhibitor).Имя бренда
VitrakviКлиническое использование
The US Food and Drug Administration (FDA) granted accelerated approval to larotrectinib (Vitrakvi?) on November 26th, 2018, as a treatment for adult and pediatric patients with solid tumors that have NTRK gene fusions without a known acquired resistance mutation, are metastatic or where surgical resection is likely to result in severe morbidity, and have no satisfactory alternative treatments or that have progressed following treatment on. In the approval statement by FDA, a complete response rate of 22% and partial response rate of 53% were cited.ЛОХО-101 запасные части и сырье
запасной предмет
ЛОХО-101 поставщик
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