洛美曲索
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- CAS号:
- 106400-81-1
- 英文名:
- Lometrexol
- 英文别名:
- LY 264618;Lometrexol;Lometrexolum;LY 264618 hydrate;Lometrexol hydrate;Lometrexol(LY 264618);Lometrexolum [inn-latin];(6R)-5,10-Dideaza-5,6,7,8-tetrahydrofolic acid;N-[4-[2-[[(R)-2-Amino-4-oxo-1,4,5,6,7,8-hexahydropyrido[2,3-d]pyrimidin]-6-yl]ethyl]benzoyl]-L-glutamic acid;L-Glutamic acid, N-(4-(2-((6R)-2-amino-1,4,5,6,7,8-hexahydro-4-oxopyrido(2,3-D)pyrimidin-6-yl)ethyl)benzoyl)-
- 中文名:
- 洛美曲索
- 中文别名:
- 洛美曲索;洛美曲索水合物;化合物 T15826
- CBNumber:
- CB81179064
- 分子式:
- C21H25N5O6
- 分子量:
- 443.45
- MOL File:
- 106400-81-1.mol
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洛美曲索化学性质
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密度:
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1.56±0.1 g/cm3(Predicted)
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储存条件:
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2-8°C
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溶解度:
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DMSO: ≥5mg/mL
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酸度系数(pKa):
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3.60±0.10(Predicted)
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形态:
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powder
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颜色:
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white to light yellow
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稳定性:
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Hygroscopic
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洛美曲索性质、用途与生产工艺
Lometrexol hydrate (DDATHF hydrate) 是一种抗嘌呤类抗叶酸 (antifolate) 药，可抑制甘氨酰胺核糖核苷酸甲酰基转移酶 (GARFT) 的活性，但不会引起可检测水平的 DNA 链断裂。Lometrexol hydrate 可以进一步抑制嘌呤从头合成，导致异常的细胞增殖，凋亡 (apoptosis) 和细胞周期停滞。Lometrexol hydrate 具有抗癌活性。Lometrexol hydrate 还是一种有效的人丝氨酸羟甲基转移酶 1/2 (hSHMT1/2) 抑制剂。
Lometrexol hydrate (DDATHF hydrate) binds tightly to GART, resulting in a rapid and prolonged depletion of intracellular purine ribonucleotides.
Lometrexol hydrate (1-30 μM; 2-10 hours) induces rapid and complete growth inhibition in L1210 cells.
Lometrexol hydrate (1 μM; 2-24 hours) induces cell cycle arrest in murine leukemia L1210 cells.
Lometrexol hydrate induces abnormal proliferation and apoptosis exist in neural tube defects (NTDs).
Cell Viability Assay
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Cell Line:
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Mouse leukemia L1210 cells
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Concentration:
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1, 30 μM
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Incubation Time:
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2, 4, 6, 8, 10 hours
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Result:
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Induced rapid and complete growth inhibition.
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Cell Cycle Analysis
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Cell Line:
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L1210 cells
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Concentration:
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1 μM
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Incubation Time:
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2, 4, 8, 12, 24 hours
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Result:
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Caused a rapid loss of the G2/M phase population of cells and an early S phase accumulation of cells by 8 hours. By 24 h, the S phase population appeared to be slowly shifting to higher DNA content, and hence, from mid-to-late S phase.
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Lometrexol hydrate (DDATHF hydrate; i.p.; 15-60 mg/kg; on gestation day 7.5) increases the rate of embryonic resorption and growth retardation in a dose-dependent manner.
Lometrexol hydrate (i.p.; 40 mg/kg) maximally inhibits GARFT activity after at 6 hours and thereafter gradually increases with time but remains significantly lower than control even at 96 hours. Levels of ATP, GTP, dATP and dGTP of NTDs embryonic brain tissue decreases significantly at 6 h, and more significantly over time.
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Animal Model:
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C57BL/6 mice (7-8 week, 18-20 g)
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Dosage:
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15, 30, 35, 40, 45 and 60 mg/kg
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Administration:
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Intraperitoneal injection; on gestation day 7.5
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Result:
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Increased the rate of embryonic resorption and growth retardation in a dose-dependent manner.
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洛美曲索
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下游产品
| 更新日期 | 产品编号 | 产品名称 | CAS编号 | 包装 | 价格 |
|---|
| 2024/04/30 | HY-14521 | 洛美曲索
Lometrexol | 106400-81-1 | 1mg | 1000元 |
| 2024/04/30 | HY-14521 | 洛美曲索
Lometrexol | 106400-81-1 | 10mM * 1mLin DMSO | 2750元 |
106400-81-1, 洛美曲索 相关搜索:
- Pharmaceuticals
- Intermediates & Fine Chemicals
- Heterocycles
- Chiral Reagents
- Aromatics
- 化合物 T15826
- 洛美曲索水合物
- 洛美曲索
- 106400-81-1
- L-Glutamic acid, N-[4-[2-[(6R)-2-amino-3,4,5,6,7,8-hexahydro-4-oxopyrido[2,3-d]pyrimidin-6-yl]ethyl]benzoyl]-
- Lometrexol(LY 264618)
- N-[4-[2-[(6R)-2-amino-3,4,5,6,7,8-hexahydro-4-oxopyrido[2,3-d]pyrimidin-6-yl]ethyl]benzoyl]-L-glutamic acid hydrate
- LY 264618 hydrate
- Lometrexol hydrate
- LY 264618
- Lometrexolum [inn-latin]
- Lometrexolum
- L-Glutamic acid, N-(4-(2-(2-amino-1,4,5,6,7,8-hexahydro-4-oxopyrido(2,3-D)pyrimidin-6-yl)ethyl)benzoyl)-, (R)-
- L-Glutamic acid, N-(4-(2-((6R)-2-amino-1,4,5,6,7,8-hexahydro-4-oxopyrido(2,3-D)pyrimidin-6-yl)ethyl)benzoyl)-
- N-[4-[2-[[(R)-2-Amino-4-oxo-1,4,5,6,7,8-hexahydropyrido[2,3-d]pyrimidin]-6-yl]ethyl]benzoyl]-L-glutamic acid
- N-[4-[2-[[(6R)-2-Amino-3,4,5,6,7,8-hexahydro-4-oxopyrido[2,3-d]pyrimidin]-6-yl]ethyl]benzoyl]-L-glutamic acid
- (6R)-5,10-Dideaza-5,6,7,8-tetrahydrofolic acid
- Lometrexol