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- Double-bond stereo
- 0 of 10 defined stereocentres

3-Benzyl-5,6,12-trihydroxy-4,5,10,12-tetramethyl-1,11-dioxo-2,3,3a,4,5,6,6a,9,10,11,12,15-dodecahydro-1H-cycloundeca[d]isoindol-15-yl acetate

ChemSpider ID: 2820
Molecular Formula: C₃₀H₃₉NO₇
Average mass: 525.633179 Da
Monoisotopic mass: 525.272644 Da
Systematic name

3-Benzyl-5,6,12-trihydroxy-4,5,10,12-tetramethyl-1,11-dioxo-2,3,3a,4,5,6,6a,9,10,11,12,15-dodecahydro-1H-cycloundeca[d]isoindol-15-yl acetate
SMILES and InChIs

SMILES:

O=C1NC(C3C(C(O)(C(O)C2C=CCC(C(=O)C(O)(C=CC(OC(=O)C)C123)C)C)C)C)Cc4ccccc4 Copied

Std. InChI:

InChI=1S/C30H39NO7/c1-17-10-9-13-21-26(34)29(5,37)18(2)24-22(16-20-11-7-6-8-12-20)31-27(35)30(21,24)23(38-19(3)32)14-15-28(4,36)25(17)33/h6-9,11-15,17-18,21-24,26,34,36-37H,10,16H2,1-5H3,(H,31,35) Copied

Std. InChIKey:

KPIFCQLJNVZJNN-UHFFFAOYSA-N Copied
Cite this record
CSID:2820, http://www.chemspider.com/Chemical-Structure.2820.html (accessed 14:43, May 25, 2012) Copied

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

ACD/LogP:	2.061	# of Rule of 5 Violations:	1
ACD/LogD (pH 5.5):	2.06	ACD/LogD (pH 7.4):	2.06
ACD/BCF (pH 5.5):	21.68	ACD/BCF (pH 7.4):	21.68
ACD/KOC (pH 5.5):	314.72	ACD/KOC (pH 7.4):	314.71
#H bond acceptors:	8	#H bond donors:	4
#Freely Rotating Bonds:	7	Polar Surface Area:	133.16 Å²
Index of Refraction:	1.603	Molar Refractivity:	141.795 cm³
Molar Volume:	412.574 cm³	Polarizability:	56.212 10^-24cm³
Surface Tension:	58.6580009460449 dyne/cm	Density:	1.274 g/cm³
Flash Point:	385.397 °C	Enthalpy of Vaporization:	109.529 kJ/mol
Boiling Point:	713.642 °C at 760 mmHg	Vapour Pressure:	0 mmHg at 25°C

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Spectra

CIFs

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Pharmacological Links

SimBioSys LASSO

Category	Target	PDB Code	LASSO Score
Metalloenzymes	ACE, angiotensin-converting enzyme	1o86	0.03
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
Other Enzymes	HIVPR, HIV protease	1hpx	0.01
Metalloenzymes	PDE5, phosphodiesterase 5	1xp0	0.01
Nuclear Hormone Receptors	MR, mineralocorticoid receptor	2aa2	0.01
Serine Proteases	Thrombin	1ba8	0.01
Kinases	HSP90, human heat shock protein 90	1uy6	0.01
Other Enzymes	PARP, poly(ADP-ribose) polymerase	1efy	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
Nuclear Hormone Receptors	RXRa, retinoic X receptor R	1mvc	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
Serine Proteases	Trypsin	1bju	0.00
Other Enzymes	GPB, glycogen phosphorylase	1a8i	0.00
Other Enzymes	SAHH, S-adenosyl-homocysteine hydrolase	1a7a	0.00
Kinases	FGFr1, fibroblast growth factor receptor kinase	1agw	0.00
Metalloenzymes	COMT, catechol O-methyltransferase	1h1d	0.00
Other Enzymes	NA, neuraminidase	1a4g	0.00
Kinases	CDK2, cyclindependent kinase 2	1ckp	0.00
Kinases	TK, thymidine kinase	1kim	0.00
Kinases	P38 MAP, P38 mitogen activated protein	1kv2	0.00
Nuclear Hormone Receptors	AR, androgen receptor	1xq2	0.00
Other Enzymes	AChE, acetylcholinesterase	1eve	0.00
Metalloenzymes	ADA, adenosine deaminase	1stw	0.00
Folate Enzymes	GART, glycinamide ribonucleotide transformylase	1c2t	0.00
Kinases	PDGFrb, platelet derived growth factor receptor kinase	N/A	0.00
Serine Proteases	FXa, factor Xa	1f0r	0.00
Other Enzymes	HIVRT, HIV reverse transcriptase	1rt1	0.00
Other Enzymes	COX-2, cyclooxygenase-2	1cx2	0.00
Kinases	EGFr, epidermal growth factor receptor	1m17	0.00

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3-Benzyl-5,6,12-trihydroxy-4,5,10,12-tetramethyl-1,11-dioxo-2,3,3a,4,5,6,6a,9,10,11,12,15-dodecahydro-1H-cycloundeca[d]isoindol-15-yl acetate

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3-Benzyl-5,6,12-trihydroxy-4,5,10,12-tetramethyl-1,11-dioxo-2,3,3a,4,5,6,6a,9,10,11,12,15-dodecahydro-1H-cycloundeca[d]isoindol-15-yl acetate

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