ChemicalBook--->CAS DataBase List--->1403859-14-2

1403859-14-2

1403859-14-2 Structure

1403859-14-2 Structure
IdentificationBack Directory
[Name]

CC-90001
[CAS]

1403859-14-2
[Synonyms]

CC90001
CC-90001
CC90001 free base
CC90001,kinase,IPF,JNK,c-Jun,idiopathic,JNK1,Inhibitor,N-terminal,inhibit,CC-90001,CC 90001,fibrosis,pulmonary
[Molecular Formula]

C16H27N5O2
[MDL Number]

MFCD33029314
[MOL File]

1403859-14-2.mol
[Molecular Weight]

321.42
Chemical PropertiesBack Directory
[Boiling point ]

549.5±60.0 °C(Predicted)
[density ]

1.224±0.06 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMSO : 250 mg/mL (777.80 mM; Need ultrasonic)
[form ]

Solid
[pka]

14.17±0.50(Predicted)
[color ]

White to yellow
Hazard InformationBack Directory
[Uses]

CC-90001 is a potent, selective and orally active inhibitor of c-Jun N-terminal kinase (JNK). CC-90001 shows 12.9-fold selectivity for JNK1 over JNK2 in a cell-based model. CC-90001 can be used for the research of idiopathic pulmonary fibrosis[1][2].
[in vivo]

CC-90001 (3 mg/kg b.i.d.) reduces the development of fibrosis, as evidenced by a 48% reduction in collagen and a 53% reduction in α-smooth muscle actin (α-SMA) in a steatohepatitis model[1].
CC-90001 decreases multiple measures of lung collagen and reduces disease induced increases in α-SMA to nearly baseline levels in a house dust mite model of lung fibrosis[1].

[IC 50]

JNK1; JNK2
[storage]

Store at -20°C
[References]

[1] Bennett B, et, al. CC-90001, a Second Generation Jun N-Terminal Kinase (JNK) Inhibitor for the Treatment of Idiopathic Pulmonary Fibrosis. American Journal of Respiratory and Critical Care Medicine 2017; 195:A5409.
[2] Kolb M, et, al. Therapeutic targets in idiopathic pulmonary fibrosis. Respir Med. 2017 Oct;131:49-57. DOI:10.1016/j.rmed.2017.07.062
Spectrum DetailBack Directory
[Spectrum Detail]

CC-90001(1403859-14-2)1HNMR
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