Search term: MOLOFVCAASLRTL-CBIDILNWCK (Found by InChIKey (skeleton match))

4-(4-{[5-Amino-4-(1H-benzimidazol-2-yl)-3-oxo-2,3-dihydro-1H-pyrrol-1-yl]carbamoyl}-2-quinolinyl)-1-[3-cyano-3-(1,3-dihydro-2H-benzimidazol-2-ylidene)-2-oxopropyl]pyridinium

ChemSpider ID: 4780740
Molecular Formula: C₃₇H₂₇N₁₀O₃
Average mass: 659.674927 Da
Monoisotopic mass: 659.226196 Da
Systematic name

4-(4-{[5-Amino-4-(1H-benzimidazol-2-yl)-3-oxo-2,3-dihydro-1H-pyrrol-1-yl]carbamoyl}-2-quinolinyl)-1-[3-cyano-3-(1,3-dihydro-2H-benzimidazol-2-ylidene)-2-oxopropyl]pyridinium
SMILES and InChIs

SMILES:

N#C/C(=C2/Nc1ccccc1N2)C(=O)C[n+]3ccc(cc3)c5nc4c(cccc4)c(c5)C(=O)NN8C(\N)=C(\c7nc6ccccc6n7)C(=O)C8 Copied

Std. InChI:

InChI=1S/C37H26N10O3/c38-18-24(35-41-26-9-3-4-10-27(26)42-35)31(48)19-46-15-13-21(14-16-46)30-17-23(22-7-1-2-8-25(22)40-30)37(50)45-47-20-32(49)33(34(47)39)36-43-28-11-5-6-12-29(28)44-36/h1-17,40H,19-20H2,(H4,39,41,42,43,44,45,48,49,50)/p+1 Copied

Std. InChIKey:

MOLOFVCAASLRTL-UHFFFAOYSA-O Copied
Cite this record
CSID:4780740, http://www.chemspider.com/Chemical-Structure.4780740.html (accessed 09:23, May 19, 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:	-3.453	# of Rule of 5 Violations:	3
ACD/LogD (pH 5.5):	-3.54	ACD/LogD (pH 7.4):	-3.30
ACD/BCF (pH 5.5):	1.00	ACD/BCF (pH 7.4):	1.00
ACD/KOC (pH 5.5):	1.00	ACD/KOC (pH 7.4):	1.00
#H bond acceptors:	13	#H bond donors:	6
#Freely Rotating Bonds:	8	Polar Surface Area:	185.8 Å²
Index of Refraction:		Molar Refractivity:	cm³
Molar Volume:	cm³	Polarizability:	10^-24cm³
Surface Tension:	dyne/cm	Density:	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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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
Information Aggregators	Journal Publishers via MeSH
Ligand/binding/crystal Structure Databases	Metabolic Pathways
Molecular Libraries Screening Center Network	Natural Products
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Protein 3D Structures	Spectroscopy Databases
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Pharmacological Links

SimBioSys LASSO

Category	Target	PDB Code	LASSO Score
Kinases	EGFr, epidermal growth factor receptor	1m17	0.97
Kinases	CDK2, cyclindependent kinase 2	1ckp	0.90
Kinases	VEGFr2, vascular endothelial growth factor receptor	1vr2	0.85
Kinases	SRC, tyrosine kinase SRC	2src	0.81
Kinases	PDGFrb, platelet derived growth factor receptor kinase	N/A	0.70
Kinases	FGFr1, fibroblast growth factor receptor kinase	1agw	0.39
Other Enzymes	COX-2, cyclooxygenase-2	1cx2	0.29
Other Enzymes	ALR2, aldose reductase	1ah3	0.23
Nuclear Hormone Receptors	PPARg, peroxisome proliferator activated receptor	1fm9	0.08
Other Enzymes	PARP, poly(ADP-ribose) polymerase	1efy	0.07
Kinases	P38 MAP, P38 mitogen activated protein	1kv2	0.05
Other Enzymes	PNP, purine nucleoside phosphorylase	1b8o	0.04
Other Enzymes	HIVRT, HIV reverse transcriptase	1rt1	0.02
Folate Enzymes	DHFR, dihydrofolate reductase	3dfr	0.02
Other Enzymes	NA, neuraminidase	1a4g	0.02
Serine Proteases	FXa, factor Xa	1f0r	0.02
Other Enzymes	HMGR, hydroxymethylglutaryl-CoA reductase	1hw8	0.01
Serine Proteases	Thrombin	1ba8	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
Nuclear Hormone Receptors	ER, estrogen receptor; antagonist	3ert	0.01
Metalloenzymes	PDE5, phosphodiesterase 5	1xp0	0.01
Other Enzymes	AmpC, AmpC beta-lactamase	1xgj	0.01
Folate Enzymes	GART, glycinamide ribonucleotide transformylase	1c2t	0.00
Nuclear Hormone Receptors	ER, estrogen receptor; agonist	1l2i	0.00
Metalloenzymes	COMT, catechol O-methyltransferase	1h1d	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	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
Other Enzymes	HIVPR, HIV protease	1hpx	0.00
Other Enzymes	COX-1, cyclooxygenase-1	1p4g	0.00
Kinases	TK, thymidine kinase	1kim	0.00
Metalloenzymes	ADA, adenosine deaminase	1stw	0.00
Nuclear Hormone Receptors	AR, androgen receptor	1xq2	0.00
Other Enzymes	AChE, acetylcholinesterase	1eve	0.00
Nuclear Hormone Receptors	GR, glucocorticoid receptor	1m2z	0.00

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4-(4-{[5-Amino-4-(1H-benzimidazol-2-yl)-3-oxo-2,3-dihydro-1H-pyrrol-1-yl]carbamoyl}-2-quinolinyl)-1-[3-cyano-3-(1,3-dihydro-2H-benzimidazol-2-ylidene)-2-oxopropyl]pyridinium

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4-(4-{[5-Amino-4-(1H-benzimidazol-2-yl)-3-oxo-2,3-dihydro-1H-pyrrol-1-yl]carbamoyl}-2-quinolinyl)-1-[3-cyano-3-(1,3-dihydro-2H-benzimidazol-2-ylidene)-2-oxopropyl]pyridinium

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