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4-Thiazolidinone, 3-(2-methoxyethyl)-5-[[3-[4-(3-methylbutoxy)phenyl]-1-phenyl-1H-pyrazol-4-yl]methylene]-2-thioxo-, (5Z)-

ChemSpider ID: 4878611
Molecular Formula: C₂₇H₂₉N₃O₃S₂
Average mass: 507.667511 Da
Monoisotopic mass: 507.165039 Da
Systematic name

(5Z)-3-(2-Methoxyethyl)-5-({3-[4-(3-methylbutoxy)phenyl]-1-phenyl-1H-pyrazol-4-yl}methylene)-2-thioxo-1,3-thiazolidin-4-one
SMILES and InChIs

SMILES:

S=C1S/C(C(=O)N1CCOC)=C\c3cn(nc3c2ccc(OCCC(C)C)cc2)c4ccccc4 Copied

Std. InChI:

InChI=1S/C27H29N3O3S2/c1-19(2)13-15-33-23-11-9-20(10-12-23)25-21(18-30(28-25)22-7-5-4-6-8-22)17-24-26(31)29(14-16-32-3)27(34)35-24/h4-12,17-19H,13-16H2,1-3H3/b24-17- Copied

Std. InChIKey:

IVYVIMBPIGZGOD-ULJHMMPZSA-N Copied
Cite this record
CSID:4878611, http://www.chemspider.com/Chemical-Structure.4878611.html (accessed 17:24, Jun 19, 2013) Copied

Names and Identifiers

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Data supplied by datasources and users.

Experimental Physico-chemical Properties
- Experimental LogP:
  
  5.69 Vitas-M STK703121

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

ACD/LogP:	5.69	# of Rule of 5 Violations:	2
ACD/LogD (pH 5.5):	5.69	ACD/LogD (pH 7.4):	5.69
ACD/BCF (pH 5.5):	12430.95	ACD/BCF (pH 7.4):	12430.95
ACD/KOC (pH 5.5):	29677.99	ACD/KOC (pH 7.4):	29677.99
#H bond acceptors:	6	#H bond donors:	0
#Freely Rotating Bonds:	10	Polar Surface Area:	113.98 Å²
Index of Refraction:	1.631	Molar Refractivity:	145.965 cm³
Molar Volume:	409.829 cm³	Polarizability:	57.865 10^-24cm³
Surface Tension:	45.6720008850098 dyne/cm	Density:	1.239 g/cm³
Flash Point:	349.912 °C	Enthalpy of Vaporization:	96.463 kJ/mol
Boiling Point:	654.967 °C at 760 mmHg	Vapour Pressure:	0 mmHg at 25°C

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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
Molecular Libraries Screening Center Network	Natural Products
NIH Substance Repository	Physical Properties (including SAR/QSAR databases)
Protein 3D Structures	Spectroscopy Databases
Substance Vendors	Theoretical Properties
Toxicology/Environmental Databases	Virtual Library

Category	Target	PDB Code	LASSO Score
Kinases	PDGFrb, platelet derived growth factor receptor kinase	N/A	0.07
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
Nuclear Hormone Receptors	RXRa, retinoic X receptor R	1mvc	0.02
Serine Proteases	FXa, factor Xa	1f0r	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
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
Nuclear Hormone Receptors	ER, estrogen receptor; antagonist	3ert	0.01
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
Kinases	VEGFr2, vascular endothelial growth factor receptor	1vr2	0.00
Serine Proteases	Trypsin	1bju	0.00
Other Enzymes	GPB, glycogen phosphorylase	1a8i	0.00
Folate Enzymes	GART, glycinamide ribonucleotide transformylase	1c2t	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
Metalloenzymes	COMT, catechol O-methyltransferase	1h1d	0.00
Kinases	CDK2, cyclindependent kinase 2	1ckp	0.00
Other Enzymes	ALR2, aldose reductase	1ah3	0.00
Other Enzymes	NA, neuraminidase	1a4g	0.00
Kinases	TK, thymidine kinase	1kim	0.00
Other Enzymes	COX-1, cyclooxygenase-1	1p4g	0.00
Metalloenzymes	ADA, adenosine deaminase	1stw	0.00
Kinases	P38 MAP, P38 mitogen activated protein	1kv2	0.00
Nuclear Hormone Receptors	AR, androgen receptor	1xq2	0.00
Nuclear Hormone Receptors	GR, glucocorticoid receptor	1m2z	0.00
Other Enzymes	InhA, enoyl ACP reductase	1p44	0.00
Kinases	HSP90, human heat shock protein 90	1uy6	0.00
Kinases	EGFr, epidermal growth factor receptor	1m17	0.00

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4-Thiazolidinone, 3-(2-methoxyethyl)-5-[[3-[4-(3-methylbutoxy)phenyl]-1-phenyl-1H-pyrazol-4-yl]methylene]-2-thioxo-, (5Z)-

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4-Thiazolidinone, 3-(2-methoxyethyl)-5-[[3-[4-(3-methylbutoxy)phenyl]-1-phenyl-1H-pyrazol-4-yl]methylene]-2-thioxo-, (5Z)-

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