8-(3-Chloro-4-fluorophenyl)-2-{[3-chloro-6-(trifluoromethyl)-2-pyridinyl](methyl)amino}-6-(1-hydroxy-2-naphthyl)-6a-methyl-3a,4,6,6a,9a,10,10a,10b-octahydroisoindolo[5,6-e]isoindole-1,3,7,9(2H,8H)-tet rone

ChemSpider ID: 3663649
Molecular Formula: C₃₈H₂₈Cl₂F₄N₄O₅
Average mass: 767.552307 Da
Monoisotopic mass: 766.137268 Da
Systematic name

8-(3-Chloro-4-fluorophenyl)-2-{[3-chloro-6-(trifluoromethyl)-2-pyridinyl](methyl)amino}-6-(1-hydroxy-2-naphthyl)-6a-methyl-3a,4,6,6a,9a,10,10a,10b-octahydroisoindolo[5,6-e]isoindole-1,3,7,9(2H,8H)-tet rone
SMILES and InChIs

SMILES:

FC(F)(F)c1nc(c(Cl)cc1)N(N5C(=O)C6C/C=C4/C(c3ccc2ccccc2c3O)C7(C(=O)N(C(=O)C7CC4C6C5=O)c8ccc(F)c(Cl)c8)C)C Copied

Std. InChI:

InChI=1S/C38H28Cl2F4N4O5/c1-37-24(34(51)47(36(37)53)18-8-13-27(41)26(40)15-18)16-23-20(30(37)22-9-7-17-5-3-4-6-19(17)31(22)49)10-11-21-29(23)35(52)48(33(21)50)46(2)32-25(39)12-14-28(45-32)38(42,43)44/h3-10,12-15,21,23-24,29-30,49H,11,16H2,1-2H3 Copied

Std. InChIKey:

XLZWBEYWOYRYLO-UHFFFAOYSA-N Copied
Cite this record
CSID:3663649, http://www.chemspider.com/Chemical-Structure.3663649.html (accessed 10:43, Jun 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:	6.499	# of Rule of 5 Violations:	2
ACD/LogD (pH 5.5):	6.50	ACD/LogD (pH 7.4):	6.50
ACD/BCF (pH 5.5):	51157.02	ACD/BCF (pH 7.4):	50682.48
ACD/KOC (pH 5.5):	81696.12	ACD/KOC (pH 7.4):	80938.29
#H bond acceptors:	9	#H bond donors:	1
#Freely Rotating Bonds:	5	Polar Surface Area:	111.12 Å²
Index of Refraction:	1.71	Molar Refractivity:	185.429 cm³
Molar Volume:	474.678 cm³	Polarizability:	73.51 10^-24cm³
Surface Tension:	76.4049987792969 dyne/cm	Density:	1.617 g/cm³
Flash Point:	473.533 °C	Enthalpy of Vaporization:	129.148 kJ/mol
Boiling Point:	859.375 °C at 760 mmHg	Vapour Pressure:	0 mmHg at 25°C

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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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SimBioSys LASSO

Category	Target	PDB Code	LASSO Score
Other Enzymes	COX-2, cyclooxygenase-2	1cx2	0.29
Nuclear Hormone Receptors	PPARg, peroxisome proliferator activated receptor	1fm9	0.05
Kinases	FGFr1, fibroblast growth factor receptor kinase	1agw	0.04
Nuclear Hormone Receptors	AR, androgen receptor	1xq2	0.03
Other Enzymes	HIVRT, HIV reverse transcriptase	1rt1	0.02
Kinases	VEGFr2, vascular endothelial growth factor receptor	1vr2	0.02
Kinases	SRC, tyrosine kinase SRC	2src	0.01
Other Enzymes	HMGR, hydroxymethylglutaryl-CoA reductase	1hw8	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
Other Enzymes	COX-1, cyclooxygenase-1	1p4g	0.01
Other Enzymes	PARP, poly(ADP-ribose) polymerase	1efy	0.01
Nuclear Hormone Receptors	ER, estrogen receptor; antagonist	3ert	0.01
Other Enzymes	HIVPR, HIV protease	1hpx	0.01
Kinases	PDGFrb, platelet derived growth factor receptor kinase	N/A	0.00
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
Serine Proteases	Thrombin	1ba8	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
Nuclear Hormone Receptors	RXRa, retinoic X receptor R	1mvc	0.00
Other Enzymes	InhA, enoyl ACP reductase	1p44	0.00
Other Enzymes	NA, neuraminidase	1a4g	0.00
Kinases	TK, thymidine kinase	1kim	0.00
Other Enzymes	ALR2, aldose reductase	1ah3	0.00
Metalloenzymes	ADA, adenosine deaminase	1stw	0.00
Metalloenzymes	PDE5, phosphodiesterase 5	1xp0	0.00
Other Enzymes	AChE, acetylcholinesterase	1eve	0.00
Kinases	CDK2, cyclindependent kinase 2	1ckp	0.00
Folate Enzymes	GART, glycinamide ribonucleotide transformylase	1c2t	0.00
Kinases	P38 MAP, P38 mitogen activated protein	1kv2	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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8-(3-Chloro-4-fluorophenyl)-2-{[3-chloro-6-(trifluoromethyl)-2-pyridinyl](methyl)amino}-6-(1-hydroxy-2-naphthyl)-6a-methyl-3a,4,6,6a,9a,10,10a,10b-octahydroisoindolo[5,6-e]isoindole-1,3,7,9(2H,8H)-tet rone

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8-(3-Chloro-4-fluorophenyl)-2-{[3-chloro-6-(trifluoromethyl)-2-pyridinyl](methyl)amino}-6-(1-hydroxy-2-naphthyl)-6a-methyl-3a,4,6,6a,9a,10,10a,10b-octahydroisoindolo[5,6-e]isoindole-1,3,7,9(2H,8H)-tet rone

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