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Nvp-lcq195

HCID 11655534
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Basic information

CAS
902156-99-4
Standard SMILES
CS(=O)(=O)N1CCC(NC(=O)c2[nH]ncc2NC(=O)c2c(Cl)cccc2Cl)CC1
InChIKey
CCUXEBOOTMDSAM-UHFFFAOYSA-N
Molecular formula
C17H19Cl2N5O4S
Average molar mass
460.3 g/mol
Monoisotopic mass
459.0534807

Names & identifiers

Preferred name
Nvp-lcq195
IUPAC
4-[(2,6-dichlorobenzoyl)amino]-N-(1-methylsulfonylpiperidin-4-yl)-1H-pyrazole-5-carboxamide
English name
NVP-LCQ195
Molecular formula
C17H19Cl2N5O4S
Molecular weight
460.33486

Names & synonyms

NVP-LCQ195902156-99-44-[(2,6-dichlorobenzoyl)amino]-N-(1-methylsulfonylpiperidin-4-yl)-1H-pyrazole-5-carboxamide4-(2,6-dichloro-benzoylamino)-1H-pyrazole-3-carboxylic acid (1-methanesulphonyl-piperidin-4-yl)-amideC17H19Cl2N5O4SMFCD12031595NVP-LCQ195?orb1296228SCHEMBL2029686SCHEMBL17252164DTXSID90470112LCQ-195
Show more names
LCQ 195AT 9311NVP-LCQ195 (AT9311Nvp-lcq195 , NVP-LCQ195NVP-LCQ195, 10 mM in DMSONVP-LCQ195 (AT9311LCQ195)NVP LCQ195
CCUXEBOOTMDSAM-UHFFFAOYSA-NGLXC-04412CLB15699AT9311AKOS037645025AT-9311CS-0840NCGC00379060-01

Database identifiers

CAS
902156-99-4
PubChem CID
11655534
DTXSID
DTXSID90470112

Properties

Computed structural properties

XLogP
2.3
Topological polar surface area
133 Ų
Hydrogen bond donors
3
Hydrogen bond acceptors
6
Rotatable bonds
5
Heavy atoms
29
Formal charge
0
Complexity
701

Physicochemical properties

Density
1.57 · 1.57±0.1 g/cm3(Predicted)
storage temp.
-20 °C · Store at -20°C
solubility
2 O; · insoluble in H2O; ≥152.4 mg/mL in DMSO; ≥3.28 mg/mL in EtOH with gentle warming and ultrasonic
form
solid
pka
11.1 · 11.10±0.70(Predicted)
color
White to off-white

Chemistry & industry

Applications · 1 item

UsesNVP-LCQ195 (AT9311; LCQ195) is a small molecule heterocyclic inhibitor of CDK1, CDK2, CDK3 and CDK5 with IC50 of 1-42 nM. IC50 Value: 1 nM(CDK5/p25 and CDK5/p35); 2 nM(CDK1/cyclinB and CDK2/cyclinA); 5 nM(CDK2/cyclinE); 42 nM(CDK3/cyclinE) Target: CDKs LCQ195 induced cell cycle arrest and eventual apoptotic cell death of MM cells, even at sub-lmol/l concentrations, spared non-malignant cells, and overcame the protection conferred to MM cells by stroma or cytokines of the bone marrow milieu. In MM cells, LCQ195 triggered decreased amplitude of transcriptional signatures associated with oncogenesis, drug resistance and stem cell renewal, including signatures of activation of key transcription factors for MM cells e.g. myc, HIF-1a, IRF4. Bortezomib-treated MM patients whose tumours had high baseline expression of genes suppressed by LCQ195 had significantly shorter progression-free and overall survival than those with low levels of these transcripts in their MM cells. These observations provide insight into the biological relevance of multi-targeted CDK inhibition in MM.

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