2-({4-Chloro-6-[4-(4-chlorobenzoyl)-3-methyl-1-piperazinyl]-2-pyrimidinyl}sulfanyl)-1-(4-ethyl-1-piperazinyl)ethanone

ChemSpider ID: 2803144
Molecular Formula: C₂₄H₃₀Cl₂N₆O₂S
Average mass: 537.505005 Da
Monoisotopic mass: 536.152771 Da
Systematic name

2-({4-Chloro-6-[4-(4-chlorobenzoyl)-3-methyl-1-piperazinyl]-2-pyrimidinyl}sulfanyl)-1-(4-ethyl-1-piperazinyl)ethanone
SMILES and InChIs

SMILES:

Clc1ccc(cc1)C(=O)N4C(C)CN(c2nc(nc(Cl)c2)SCC(=O)N3CCN(CC)CC3)CC4 Copied

Std. InChI:

InChI=1S/C24H30Cl2N6O2S/c1-3-29-8-10-30(11-9-29)22(33)16-35-24-27-20(26)14-21(28-24)31-12-13-32(17(2)15-31)23(34)18-4-6-19(25)7-5-18/h4-7,14,17H,3,8-13,15-16H2,1-2H3 Copied

Std. InChIKey:

OGUXRHICQPGJOS-UHFFFAOYSA-N Copied
Cite this record
CSID:2803144, http://www.chemspider.com/Chemical-Structure.2803144.html (accessed 19:52, May 24, 2013) Copied

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

ACD/LogP:	4.071	# of Rule of 5 Violations:	1
ACD/LogD (pH 5.5):	3.12	ACD/LogD (pH 7.4):	4.03
ACD/BCF (pH 5.5):	81.20	ACD/BCF (pH 7.4):	664.02
ACD/KOC (pH 5.5):	433.68	ACD/KOC (pH 7.4):	3546.48
#H bond acceptors:	8	#H bond donors:	0
#Freely Rotating Bonds:	6	Polar Surface Area:	98.18 Å²
Index of Refraction:	1.663	Molar Refractivity:	141.207 cm³
Molar Volume:	381.023 cm³	Polarizability:	55.979 10^-24cm³
Surface Tension:	71.7870025634766 dyne/cm	Density:	1.411 g/cm³
Flash Point:	389.489 °C	Enthalpy of Vaporization:	105.245 kJ/mol
Boiling Point:	720.409 °C at 760 mmHg	Vapour Pressure:	0 mmHg at 25°C

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Spectra

CIFs

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Publication or Magazine Article	Web-based Article (blog or commentary)
Available Chemicals Databases	Biological Properties
Chemical Reactions	Chemical Safety Data
Drugs or Compounds in Development	Imaging Agents
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Ligand/binding/crystal Structure Databases	Metabolic Pathways
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Substance Vendors	Theoretical Properties
Toxicology/Environmental Databases	Virtual Library

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Pharmacological Links

SimBioSys LASSO

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

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2-({4-Chloro-6-[4-(4-chlorobenzoyl)-3-methyl-1-piperazinyl]-2-pyrimidinyl}sulfanyl)-1-(4-ethyl-1-piperazinyl)ethanone

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2-({4-Chloro-6-[4-(4-chlorobenzoyl)-3-methyl-1-piperazinyl]-2-pyrimidinyl}sulfanyl)-1-(4-ethyl-1-piperazinyl)ethanone

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