中文名 | ML-18 |
英文名 | ML-18 |
别名 | 化合物ML 18 ML-18游离态 (S)-3-(1H-吲哚-3-基)-N-((1-(4-甲氧基苯基)环己基)甲基)-2-(3-(4-硝基苯基)脲基)丙酰胺 |
英文别名 | ML18 ML 18 ML-18 1422269-30-4 BRS-3 ANTAGONIST BRS-3 antagonist (S)-3-(1H-Indol-3-yl)-N-((1-(4-methoxyphenyl)cyclohexyl)methyl)-2-(3-(4-nitrophenyl)ureido)propanamide (2S)-3-(1H-INDOL-3-YL)-N-{[1-(4-METHOXYPHENYL)CYCLOHEXYL]METHYL}-2-{[(4-NITROPHENYL)CARBAMOYL]AMINO}PROPANAMIDE |
CAS | 1422269-30-4 |
化学式 | C32H35N5O5 |
分子量 | 569.66 |
密度 | 1.291±0.06 g/cm3(Predicted) |
沸点 | 821.8±65.0 °C(Predicted) |
溶解度 | DMSO: ≥ 100 mg/mL |
酸度系数 | 11.99±0.46(Predicted) |
存储条件 | 2-8°C |
体外研究 | ML-18 inhibits specific 125 I-BA1 (DTyr-Gln-Trp-Ala-Val-βAla-His-Phe-Nle-NH2)BB6-14 binding to NCI-H1299 lung cancer cells stably transfected with BRS-3 with IC 50 values of 4.8 μM. ML-18 binds with lower affinity to the GRPR and NMBR with IC 50 values of 16 and more than 100 μM, respectively. ML-18 at 16 μM inhibits the ability of 10 nM BA1 to elevate cytosolic Ca 2+ in a reversible manner using lung cancer cells loaded with FURA2-AM. ML-18 at 16 μM inhibits the ability of 100 nM BA1 to cause tyrosine phosphorylation of the EGFR and ERK in lung cancer cells. It inhibits the proliferation of lung cancer cells. |
1mg | 5mg | 10mg | |
---|---|---|---|
1 mM | 1.755 ml | 8.777 ml | 17.555 ml |
5 mM | 0.351 ml | 1.755 ml | 3.511 ml |
10 mM | 0.176 ml | 0.878 ml | 1.755 ml |
5 mM | 0.035 ml | 0.176 ml | 0.351 ml |
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