4-[2-(4-Chlorophenyl)-4-hydroxy-1-piperidinyl]-1-(4-fluorophenyl)-1-butanone

ChemSpider ID: 10728213
Molecular Formula: C₂₁H₂₃ClFNO₂
Monoisotopic mass: 375.140137 Da
Systematic name

4-[2-(4-Chlorophenyl)-4-hydroxy-1-piperidinyl]-1-(4-fluorophenyl)-1-butanone
SMILES and InChIs

SMILES:

Fc1ccc(cc1)C(=O)CCCN3CCC(O)CC3c2ccc(Cl)cc2 Copied

Std. InChI:

InChI=1S/C21H23ClFNO2/c22-17-7-3-15(4-8-17)20-14-19(25)11-13-24(20)12-1-2-21(26)16-5-9-18(23)10-6-16/h3-10,19-20,25H,1-2,11-14H2 Copied

Std. InChIKey:

CJDQPIDDTUWTSD-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:	3.26	# of Rule of 5 Violations:	0
ACD/LogD (pH 5.5):	1.01	ACD/LogD (pH 7.4):	2.71
ACD/BCF (pH 5.5):	1.00	ACD/BCF (pH 7.4):	49.66
ACD/KOC (pH 5.5):	8.02	ACD/KOC (pH 7.4):	397.07
#H bond acceptors:	3	#H bond donors:	1
#Freely Rotating Bonds:	7	Polar Surface Area:	40.54 Å²
Index of Refraction:	1.578	Molar Refractivity:	101.107 cm³
Molar Volume:	304.848 cm³	Polarizability:	40.082 10^-24cm³
Surface Tension:	46.8419990539551 dyne/cm	Density:	1.233 g/cm³
Flash Point:	276.562 °C	Enthalpy of Vaporization:	85.228 kJ/mol
Boiling Point:	533.684 °C at 760 mmHg	Vapour Pressure:	0 mmHg at 25°C

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Spectra

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SimBioSys LASSO

Category	Target	PDB Code	LASSO Score
Other Enzymes	AChE, acetylcholinesterase	1eve	0.04
Nuclear Hormone Receptors	PPARg, peroxisome proliferator activated receptor	1fm9	0.03
Other Enzymes	HIVRT, HIV reverse transcriptase	1rt1	0.02
Kinases	P38 MAP, P38 mitogen activated protein	1kv2	0.02
Kinases	VEGFr2, vascular endothelial growth factor receptor	1vr2	0.02
Other Enzymes	InhA, enoyl ACP reductase	1p44	0.02
Kinases	SRC, tyrosine kinase SRC	2src	0.01
Serine Proteases	Thrombin	1ba8	0.01
Other Enzymes	HMGR, hydroxymethylglutaryl-CoA reductase	1hw8	0.01
Other Enzymes	HIVPR, HIV protease	1hpx	0.01
Kinases	HSP90, human heat shock protein 90	1uy6	0.01
Metalloenzymes	PDE5, phosphodiesterase 5	1xp0	0.01
Nuclear Hormone Receptors	MR, mineralocorticoid receptor	2aa2	0.01
Nuclear Hormone Receptors	PR, progesterone receptor	1sr7	0.01
Other Enzymes	PARP, poly(ADP-ribose) polymerase	1efy	0.01
Kinases	PDGFrb, platelet derived growth factor receptor kinase	N/A	0.00
Other Enzymes	PNP, purine nucleoside phosphorylase	1b8o	0.00
Other Enzymes	AmpC, AmpC beta-lactamase	1xgj	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
Serine Proteases	Trypsin	1bju	0.00
Other Enzymes	GPB, glycogen phosphorylase	1a8i	0.00
Other Enzymes	SAHH, S-adenosyl-homocysteine hydrolase	1a7a	0.00
Kinases	FGFr1, fibroblast growth factor receptor kinase	1agw	0.00
Other Enzymes	COX-2, cyclooxygenase-2	1cx2	0.00
Nuclear Hormone Receptors	RXRa, retinoic X receptor R	1mvc	0.00
Nuclear Hormone Receptors	AR, androgen receptor	1xq2	0.00
Kinases	TK, thymidine kinase	1kim	0.00
Other Enzymes	NA, neuraminidase	1a4g	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
Kinases	EGFr, epidermal growth factor receptor	1m17	0.00
Kinases	CDK2, cyclindependent kinase 2	1ckp	0.00
Metalloenzymes	COMT, catechol O-methyltransferase	1h1d	0.00

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4-[2-(4-Chlorophenyl)-4-hydroxy-1-piperidinyl]-1-(4-fluorophenyl)-1-butanone

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4-[2-(4-Chlorophenyl)-4-hydroxy-1-piperidinyl]-1-(4-fluorophenyl)-1-butanone

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Std. InChI:

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Properties

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