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- 6 of 6 defined stereocentres

(3aS,6R,6aS,9aR,10aS,10bR)-8-(Bromomethyl)-6a,9a-dichloro-6-(2-hydroxy-5-methoxyphenyl)-1,3,7,9-tetraoxo-3,3a,4,6,6a,7,8,9,9a,10,10a,10b-dodecahydroisoindolo[5,6-e]isoindole-2(1H)-carboxamide

ChemSpider ID: 5075431
Molecular Formula: C₂₃H₂₀BrCl₂N₃O₇
Average mass: 601.230774 Da
Monoisotopic mass: 598.986145 Da
Systematic name

(3aS,6R,6aS,9aR,10aS,10bR)-8-(Bromomethyl)-6a,9a-dichloro-6-(2-hydroxy-5-methoxyphenyl)-1,3,7,9-tetraoxo-3,3a,4,6,6a,7,8,9,9a,10,10a,10b-dodecahydroisoindolo[5,6-e]isoindole-2(1H)-carboxamide
SMILES and InChIs

SMILES:

O=C1N(C(=O)N)C(=O)[C@@H]2[C@H]5C(=C/C[C@H]12)\[C@H](c3cc(OC)ccc3O)[C@]4(Cl)C(=O)N(C(=O)[C@]4(Cl)C5)CBr Copied

Std. InChI:

InChI=1S/C23H20BrCl2N3O7/c1-36-9-2-5-14(30)12(6-9)16-10-3-4-11-15(18(32)29(17(11)31)21(27)35)13(10)7-22(25)19(33)28(8-24)20(34)23(16,22)26/h2-3,5-6,11,13,15-16,30H,4,7-8H2,1H3,(H2,27,35)/t11-,13+,15-,16+,22+,23-/m0/s1 Copied

Std. InChIKey:

HDCZUWFZPFFXFI-ZEOVBVLXSA-N Copied
Cite this record
CSID:5075431, http://www.chemspider.com/Chemical-Structure.5075431.html (accessed 02:10, May 24, 2013) Copied

Names and Identifiers

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

ACD/LogP:	-1.722	# of Rule of 5 Violations:	2
ACD/LogD (pH 5.5):	-1.72	ACD/LogD (pH 7.4):	-1.72
ACD/BCF (pH 5.5):	1.00	ACD/BCF (pH 7.4):	1.00
ACD/KOC (pH 5.5):	2.76	ACD/KOC (pH 7.4):	2.75
#H bond acceptors:	10	#H bond donors:	3
#Freely Rotating Bonds:	4	Polar Surface Area:	147.31 Å²
Index of Refraction:	1.721	Molar Refractivity:	129.543 cm³
Molar Volume:	327.746 cm³	Polarizability:	51.355 10^-24cm³
Surface Tension:	89.4339981079102 dyne/cm	Density:	1.834 g/cm³
Flash Point:	410.25 °C	Enthalpy of Vaporization:	113.844 kJ/mol
Boiling Point:	754.736 °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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NIH Substance Repository	Physical Properties (including SAR/QSAR databases)
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Substance Vendors	Theoretical Properties
Toxicology/Environmental Databases	Virtual Library

Patents

Pharmacological Links

SimBioSys LASSO

Category	Target	PDB Code	LASSO Score
Kinases	FGFr1, fibroblast growth factor receptor kinase	1agw	0.04
Nuclear Hormone Receptors	PPARg, peroxisome proliferator activated receptor	1fm9	0.03
Kinases	SRC, tyrosine kinase SRC	2src	0.01
Other Enzymes	HMGR, hydroxymethylglutaryl-CoA reductase	1hw8	0.01
Kinases	TK, thymidine kinase	1kim	0.01
Other Enzymes	HIVPR, HIV protease	1hpx	0.01
Nuclear Hormone Receptors	MR, mineralocorticoid receptor	2aa2	0.01
Other Enzymes	COX-1, cyclooxygenase-1	1p4g	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	GR, glucocorticoid receptor	1m2z	0.00
Metalloenzymes	ACE, angiotensin-converting enzyme	1o86	0.00
Nuclear Hormone Receptors	ER, estrogen receptor; agonist	1l2i	0.00
Nuclear Hormone Receptors	PR, progesterone receptor	1sr7	0.00
Folate Enzymes	DHFR, dihydrofolate reductase	3dfr	0.00
Kinases	VEGFr2, vascular endothelial growth factor receptor	1vr2	0.00
Other Enzymes	GPB, glycogen phosphorylase	1a8i	0.00
Other Enzymes	ALR2, aldose reductase	1ah3	0.00
Other Enzymes	NA, neuraminidase	1a4g	0.00
Other Enzymes	SAHH, S-adenosyl-homocysteine hydrolase	1a7a	0.00
Kinases	CDK2, cyclindependent kinase 2	1ckp	0.00
Metalloenzymes	PDE5, phosphodiesterase 5	1xp0	0.00
Nuclear Hormone Receptors	AR, androgen receptor	1xq2	0.00
Other Enzymes	AChE, acetylcholinesterase	1eve	0.00
Other Enzymes	COX-2, cyclooxygenase-2	1cx2	0.00
Folate Enzymes	GART, glycinamide ribonucleotide transformylase	1c2t	0.00
Kinases	PDGFrb, platelet derived growth factor receptor kinase	N/A	0.00
Other Enzymes	PARP, poly(ADP-ribose) polymerase	1efy	0.00
Kinases	HSP90, human heat shock protein 90	1uy6	0.00
Other Enzymes	InhA, enoyl ACP reductase	1p44	0.00
Kinases	P38 MAP, P38 mitogen activated protein	1kv2	0.00
Other Enzymes	HIVRT, HIV reverse transcriptase	1rt1	0.00
Nuclear Hormone Receptors	RXRa, retinoic X receptor R	1mvc	0.00
Serine Proteases	Thrombin	1ba8	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
Metalloenzymes	ADA, adenosine deaminase	1stw	0.00
Serine Proteases	Trypsin	1bju	0.00

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(3aS,6R,6aS,9aR,10aS,10bR)-8-(Bromomethyl)-6a,9a-dichloro-6-(2-hydroxy-5-methoxyphenyl)-1,3,7,9-tetraoxo-3,3a,4,6,6a,7,8,9,9a,10,10a,10b-dodecahydroisoindolo[5,6-e]isoindole-2(1H)-carboxamide

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CIFs

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SimBioSys LASSO

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(3aS,6R,6aS,9aR,10aS,10bR)-8-(Bromomethyl)-6a,9a-dichloro-6-(2-hydroxy-5-methoxyphenyl)-1,3,7,9-tetraoxo-3,3a,4,6,6a,7,8,9,9a,10,10a,10b-dodecahydroisoindolo[5,6-e]isoindole-2(1H)-carboxamide

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