Methyl 2-{[3-({4-chloro-1-[4-(ethoxycarbonyl)phenyl]-2,5-dioxo-2,5-dihydro-1H-pyrrol-3-yl}amino)benzoyl]amino}-4-methyl-1,3-thiazole-5-carboxylate

ChemSpider ID: 1347433
Molecular Formula: C₂₆H₂₁ClN₄O₇S
Average mass: 568.985474 Da
Monoisotopic mass: 568.08197 Da
Systematic name

Methyl 2-{[3-({4-chloro-1-[4-(ethoxycarbonyl)phenyl]-2,5-dioxo-2,5-dihydro-1H-pyrrol-3-yl}amino)benzoyl]amino}-4-methyl-1,3-thiazole-5-carboxylate
SMILES and InChIs

SMILES:

O=C(Nc1nc(c(s1)C(=O)OC)C)c4cccc(NC\3=C(/Cl)C(=O)N(c2ccc(C(=O)OCC)cc2)C/3=O)c4 Copied

Std. InChI:

InChI=1S/C26H21ClN4O7S/c1-4-38-24(35)14-8-10-17(11-9-14)31-22(33)18(27)19(23(31)34)29-16-7-5-6-15(12-16)21(32)30-26-28-13(2)20(39-26)25(36)37-3/h5-12,29H,4H2,1-3H3,(H,28,30,32) Copied

Std. InChIKey:

JASRQUVTIYDYDR-UHFFFAOYSA-N Copied
Cite this record
CSID:1347433, http://www.chemspider.com/Chemical-Structure.1347433.html (accessed 08:08, May 20, 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:	4.019	# of Rule of 5 Violations:	2
ACD/LogD (pH 5.5):	4.00	ACD/LogD (pH 7.4):	3.34
ACD/BCF (pH 5.5):	635.39	ACD/BCF (pH 7.4):	138.40
ACD/KOC (pH 5.5):	3483.25	ACD/KOC (pH 7.4):	758.71
#H bond acceptors:	11	#H bond donors:	2
#Freely Rotating Bonds:	9	Polar Surface Area:	172.24 Å²
Index of Refraction:	1.678	Molar Refractivity:	140.519 cm³
Molar Volume:	372.707 cm³	Polarizability:	55.706 10^-24cm³
Surface Tension:	77.0619964599609 dyne/cm	Density:	1.527 g/cm³
Flash Point:	°C	Enthalpy of Vaporization:	kJ/mol
Boiling Point:	°C at 760 mmHg	Vapour Pressure:	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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Toxicology/Environmental Databases	Virtual Library

Patents

Pharmacological Links

SimBioSys LASSO

Category	Target	PDB Code	LASSO Score
Nuclear Hormone Receptors	PPARg, peroxisome proliferator activated receptor	1fm9	0.08
Other Enzymes	HIVRT, HIV reverse transcriptase	1rt1	0.02
Serine Proteases	FXa, factor Xa	1f0r	0.02
Kinases	SRC, tyrosine kinase SRC	2src	0.01
Other Enzymes	HMGR, hydroxymethylglutaryl-CoA reductase	1hw8	0.01
Kinases	VEGFr2, vascular endothelial growth factor receptor	1vr2	0.01
Nuclear Hormone Receptors	MR, mineralocorticoid receptor	2aa2	0.01
Nuclear Hormone Receptors	PR, progesterone receptor	1sr7	0.01
Nuclear Hormone Receptors	ER, estrogen receptor; antagonist	3ert	0.01
Other Enzymes	HIVPR, HIV protease	1hpx	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	ALR2, aldose reductase	1ah3	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
Folate Enzymes	GART, glycinamide ribonucleotide transformylase	1c2t	0.00
Kinases	FGFr1, fibroblast growth factor receptor kinase	1agw	0.00
Nuclear Hormone Receptors	RXRa, retinoic X receptor R	1mvc	0.00
Kinases	PDGFrb, platelet derived growth factor receptor kinase	N/A	0.00
Kinases	TK, thymidine kinase	1kim	0.00
Metalloenzymes	COMT, catechol O-methyltransferase	1h1d	0.00
Kinases	CDK2, cyclindependent kinase 2	1ckp	0.00
Other Enzymes	NA, neuraminidase	1a4g	0.00
Other Enzymes	SAHH, S-adenosyl-homocysteine hydrolase	1a7a	0.00
Metalloenzymes	ADA, adenosine deaminase	1stw	0.00
Nuclear Hormone Receptors	AR, androgen receptor	1xq2	0.00
Other Enzymes	COX-2, cyclooxygenase-2	1cx2	0.00
Other Enzymes	PARP, poly(ADP-ribose) polymerase	1efy	0.00
Kinases	HSP90, human heat shock protein 90	1uy6	0.00
Kinases	P38 MAP, P38 mitogen activated protein	1kv2	0.00
Serine Proteases	Thrombin	1ba8	0.00
Other Enzymes	AChE, acetylcholinesterase	1eve	0.00
Kinases	EGFr, epidermal growth factor receptor	1m17	0.00

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Methyl 2-{[3-({4-chloro-1-[4-(ethoxycarbonyl)phenyl]-2,5-dioxo-2,5-dihydro-1H-pyrrol-3-yl}amino)benzoyl]amino}-4-methyl-1,3-thiazole-5-carboxylate

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Std. InChI:

Std. InChIKey:

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SimBioSys LASSO

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Methyl 2-{[3-({4-chloro-1-[4-(ethoxycarbonyl)phenyl]-2,5-dioxo-2,5-dihydro-1H-pyrrol-3-yl}amino)benzoyl]amino}-4-methyl-1,3-thiazole-5-carboxylate

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