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ChemicalBook--->CAS DataBase List--->1422269-30-4

1422269-30-4

1422269-30-4 Structure

1422269-30-4 Structure
IdentificationBack Directory
[Name]

ML 18
[CAS]

1422269-30-4
[Synonyms]

ML 18
ML18, >98%
BRS-3 antagonist
ML18;ML-18;ML 18;BRS-3 ANTAGONIST;1422269-30-4
(2S)-3-(1H-INDOL-3-YL)-N-{[1-(4-METHOXYPHENYL)CYCLOHEXYL]METHYL}-2-{[(4-NITROPHENYL)CARBAMOYL]AMINO}PROPANAMIDE
[Molecular Formula]

C32H35N5O5
[MOL File]

1422269-30-4.mol
[Molecular Weight]

569.65
Chemical PropertiesBack Directory
[Boiling point ]

821.8±65.0 °C(Predicted)
[density ]

1.291±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,2-8°C
[solubility ]

DMSO: soluble
[form ]

A solid
[pka]

11.99±0.46(Predicted)
[color ]

White to yellow
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Hazard InformationBack Directory
[Description]

ML-18 is a non-peptide bombesin receptor subtype 3 (BB3) antagonist that inhibits [125I]BA1 binding to NCI-H1299 lung cancer cells transfected with human BB3 receptors (IC50 = 4.8 μM). It is selective for BB3 over the gastrin releasing peptide receptor (GRPR) and the neuromedin B receptor (NMBR) with IC50 values of 16 and >100 μM, respectively, in a radioligand binding assay. ML-18 (16 μM) reversibly inhibits BA1-induced increases in cytosolic calcium in NCI-H1299 cells. It also inhibits BA1-induced phosphorylation of ERK and EGFR and reduces proliferation of NCI-H1299 cells.
[Uses]

ML-18 is a non-peptide bombesin receptor subtype-3 antagonist. It also inhibits lung cancer growth.
[storage]

Store at -20°C
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