2-Cyclohexyl-4-[(4-methyl-2-quinolinyl)amino]-3,5-bis(trifluoromethyl)benzamide

ChemSpider ID: 16066107
Molecular Formula: C₂₅H₂₃F₆N₃O
Monoisotopic mass: 495.17453 Da
Systematic name

2-Cyclohexyl-4-[(4-methyl-2-quinolinyl)amino]-3,5-bis(trifluoromethyl)benzamide
SMILES and InChIs

SMILES:

FC(F)(F)c4c(C1CCCCC1)c(cc(c4Nc2cc(C)c3ccccc3n2)C(F)(F)F)C(N)=O Copied

Std. InChI:

InChI=1S/C25H23F6N3O/c1-13-11-19(33-18-10-6-5-9-15(13)18)34-22-17(24(26,27)28)12-16(23(32)35)20(21(22)25(29,30)31)14-7-3-2-4-8-14/h5-6,9-12,14H,2-4,7-8H2,1H3,(H2,32,35)(H,33,34) Copied

Std. InChIKey:

CMADFPHEURUGED-UHFFFAOYSA-N Copied

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Predicted data is generated using the ACD/Labs’ ACD/PhysChem Suite, for more information see their website.

ACD/LogP:	8.543	# of Rule of 5 Violations:	1
ACD/LogD (pH 5.5):	8.52	ACD/LogD (pH 7.4):	8.54
ACD/BCF (pH 5.5):	1000000.00	ACD/BCF (pH 7.4):	1000000.00
ACD/KOC (pH 5.5):	995720.60	ACD/KOC (pH 7.4):	1057439.00
#H bond acceptors:	4	#H bond donors:	3
#Freely Rotating Bonds:	3	Polar Surface Area:	68.01 Å²
Index of Refraction:	1.576	Molar Refractivity:	121.138 cm³
Molar Volume:	366.015 cm³	Polarizability:	48.023 10^-24cm³
Surface Tension:	41.939998626709 dyne/cm	Density:	1.354 g/cm³
Flash Point:	229.945 °C	Enthalpy of Vaporization:	71.658 kJ/mol
Boiling Point:	456.601 °C at 760 mmHg	Vapour Pressure:	0 mmHg at 25°C

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Spectra

CIFs

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SimBioSys LASSO

Category	Target	PDB Code	LASSO Score
Other Enzymes	HIVRT, HIV reverse transcriptase	1rt1	0.95
Kinases	P38 MAP, P38 mitogen activated protein	1kv2	0.94
Nuclear Hormone Receptors	AR, androgen receptor	1xq2	0.89
Kinases	SRC, tyrosine kinase SRC	2src	0.60
Other Enzymes	COX-2, cyclooxygenase-2	1cx2	0.29
Nuclear Hormone Receptors	GR, glucocorticoid receptor	1m2z	0.06
Kinases	FGFr1, fibroblast growth factor receptor kinase	1agw	0.04
Nuclear Hormone Receptors	PPARg, peroxisome proliferator activated receptor	1fm9	0.03
Kinases	VEGFr2, vascular endothelial growth factor receptor	1vr2	0.02
Other Enzymes	HMGR, hydroxymethylglutaryl-CoA reductase	1hw8	0.01
Kinases	HSP90, human heat shock protein 90	1uy6	0.01
Nuclear Hormone Receptors	MR, mineralocorticoid receptor	2aa2	0.01
Nuclear Hormone Receptors	PR, progesterone receptor	1sr7	0.01
Other Enzymes	COX-1, cyclooxygenase-1	1p4g	0.01
Nuclear Hormone Receptors	ER, estrogen receptor; antagonist	3ert	0.01
Other Enzymes	PARP, poly(ADP-ribose) polymerase	1efy	0.01
Metalloenzymes	PDE5, phosphodiesterase 5	1xp0	0.01
Other Enzymes	PNP, purine nucleoside phosphorylase	1b8o	0.00
Kinases	PDGFrb, platelet derived growth factor receptor kinase	N/A	0.00
Other Enzymes	AmpC, AmpC beta-lactamase	1xgj	0.00
Other Enzymes	ALR2, aldose reductase	1ah3	0.00
Serine Proteases	Thrombin	1ba8	0.00
Nuclear Hormone Receptors	ER, estrogen receptor; agonist	1l2i	0.00
Folate Enzymes	DHFR, dihydrofolate reductase	3dfr	0.00
Metalloenzymes	ACE, angiotensin-converting enzyme	1o86	0.00
Other Enzymes	GPB, glycogen phosphorylase	1a8i	0.00
Serine Proteases	Trypsin	1bju	0.00
Other Enzymes	HIVPR, HIV protease	1hpx	0.00
Other Enzymes	InhA, enoyl ACP reductase	1p44	0.00
Other Enzymes	SAHH, S-adenosyl-homocysteine hydrolase	1a7a	0.00
Nuclear Hormone Receptors	RXRa, retinoic X receptor R	1mvc	0.00
Kinases	EGFr, epidermal growth factor receptor	1m17	0.00
Other Enzymes	NA, neuraminidase	1a4g	0.00
Kinases	TK, thymidine kinase	1kim	0.00
Kinases	CDK2, cyclindependent kinase 2	1ckp	0.00
Metalloenzymes	ADA, adenosine deaminase	1stw	0.00
Folate Enzymes	GART, glycinamide ribonucleotide transformylase	1c2t	0.00
Serine Proteases	FXa, factor Xa	1f0r	0.00
Other Enzymes	AChE, acetylcholinesterase	1eve	0.00
Metalloenzymes	COMT, catechol O-methyltransferase	1h1d	0.00

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2-Cyclohexyl-4-[(4-methyl-2-quinolinyl)amino]-3,5-bis(trifluoromethyl)benzamide

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Std. InChI:

Std. InChIKey:

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2-Cyclohexyl-4-[(4-methyl-2-quinolinyl)amino]-3,5-bis(trifluoromethyl)benzamide

SMILES:

Std. InChI:

Std. InChIKey:

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Properties

Spectra

CIFs

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Pharmacological Links

SimBioSys LASSO

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