ChemicalBook--->CAS DataBase List--->2097523-60-7

2097523-60-7

2097523-60-7 Structure

2097523-60-7 Structure
IdentificationBack Directory
[Name]

CC-90011
[CAS]

2097523-60-7
[Synonyms]

CC-90011
CC-90011 besylate
LSD1-IN-7 benzenesulfote
LSD1-IN-7 benzenesulfonate
CC-90011; CC90011; CC 90011; CC-90011 BESYLATE;
[Molecular Formula]

C30H29F2N5O5S
[MDL Number]

MFCD32644589
[MOL File]

2097523-60-7.mol
[Molecular Weight]

609.65
Chemical PropertiesBack Directory
[solubility ]

DMSO:62.5(Max Conc. mg/mL);102.52(Max Conc. mM)
[form ]

Solid
[color ]

Off-white to light yellow
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P280-P301+P312-P302+P352-P305+P351+P338
Hazard InformationBack Directory
[Uses]

CC-90011 benzenesulfonate is a potent, selective, reversible and orally active inhibitor of lysine specific demethylase-1 (LSD1) with an IC50 of 0.25 nM. CC-90011 benzenesulfonate is less enzymatic inhibition against LSD2, MOA-A, and MAO-B. CC-90011 benzenesulfonate induces acute myeloid leukemia (AML) and small cell lung cancer (SCLC) cells differentiation and has potent anticancer activity[1].
[in vivo]

CC-90011 (5 mg/kg; oral administration; daily; for 30 days) treatment inhibits tumor growth in patient-derived xenograft SCLC models[1].
CC-90011 (once a day; for 4 days) treatment results in robust downregulation of GRP mRNA levels at 2.5 mg/kg and maximum suppression of GRP at 5 mg/kg in a SCLC human tumor xenograft (H1417) mice[1].
After i.v. administration, CC-90011 (Compound 11; 5 mg/kg) has systemic clearance of 32.4 mL/min/kg, elimination half-life of 2 h, and a high volume of distribution of 7.5 L/kg. CC-90011 (Compound 11; 5 mg/kg) is readily absorbed after oral administration with an AUC0-24h of 1.8 μM·h, C/sub>max of 0.36 μM, and oral bioavailability of 32%[1].

Animal Model:BALB/c nude mice bearing small cell lung carcinoma (SCLC)[1]
Dosage:5 mg/kg
Administration:Oral administration; daily; for 30 days
Result:Showed a tumor growth inhibition (TGI) of 78% at 5 mg/kg with no body weight loss.
[IC 50]

KDM1/LSD1
[References]

[1] Toufike Kanouni, et al. Discovery of CC-90011: A Potent and Selective Reversible Inhibitor of Lysine Specific Demethylase 1 (LSD1). J Med Chem. 2020 Dec 10;63(23):14522-14529. DOI:10.1021/acs.jmedchem.0c00978
Spectrum DetailBack Directory
[Spectrum Detail]

CC-90011(2097523-60-7)1HNMR
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