(E)-(4-Bromophenyl){2-(3-bromophenyl)-1-[3-(morpholin-4-ium-4-yl)propyl]-4,5-dioxo-3-pyrrolidinylidene}methanolate

ChemSpider ID: 4726525
Molecular Formula: C₂₄H₂₄Br₂N₂O₄
Average mass: 564.266418 Da
Monoisotopic mass: 562.010254 Da
Systematic name

(E)-(4-Bromophenyl){2-(3-bromophenyl)-1-[3-(morpholin-4-ium-4-yl)propyl]-4,5-dioxo-3-pyrrolidinylidene}methanolate
SMILES and InChIs

SMILES:

Brc1cccc(c1)C4C(=C(/[O-])c2ccc(Br)cc2)\C(=O)C(=O)N4CCC[NH+]3CCOCC3 Copied

Std. InChI:

InChI=1S/C24H24Br2N2O4/c25-18-7-5-16(6-8-18)22(29)20-21(17-3-1-4-19(26)15-17)28(24(31)23(20)30)10-2-9-27-11-13-32-14-12-27/h1,3-8,15,21,29H,2,9-14H2/b22-20+ Copied

Std. InChIKey:

KSEJRNFGWCXTMX-LSDHQDQOSA-N Copied
Cite this record
CSID:4726525, http://www.chemspider.com/Chemical-Structure.4726525.html (accessed 17:29, May 23, 2013) Copied

Names and Identifiers

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Data supplied by datasources and users.

Experimental Physico-chemical Properties
- Experimental LogP:
  
  4.697 Vitas-M

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

ACD/LogP:	4.656	# of Rule of 5 Violations:	1
ACD/LogD (pH 5.5):	2.37	ACD/LogD (pH 7.4):	1.98
ACD/BCF (pH 5.5):	10.55	ACD/BCF (pH 7.4):	4.26
ACD/KOC (pH 5.5):	42.12	ACD/KOC (pH 7.4):	17.00
#H bond acceptors:	6	#H bond donors:	1
#Freely Rotating Bonds:	7	Polar Surface Area:	74.11 Å²
Index of Refraction:	1.64	Molar Refractivity:	128.5 cm³
Molar Volume:	356.6 cm³	Polarizability:	50.94 10^-24cm³
Surface Tension:	56.9 dyne/cm	Density:	1.582 g/cm³
Flash Point:	357.85 °C	Enthalpy of Vaporization:	103.166 kJ/mol
Boiling Point:	668.093 °C at 760 mmHg	Vapour Pressure:	0 mmHg at 25°C

Click to predict properties on the Chemicalize site

Spectra

CIFs

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Patents

Pharmacological Links

SimBioSys LASSO

Category	Target	PDB Code	LASSO Score
Nuclear Hormone Receptors	PPARg, peroxisome proliferator activated receptor	1fm9	0.03
Other Enzymes	HIVRT, HIV reverse transcriptase	1rt1	0.02
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
Other Enzymes	InhA, enoyl ACP reductase	1p44	0.01
Nuclear Hormone Receptors	PR, progesterone receptor	1sr7	0.01
Other Enzymes	PARP, poly(ADP-ribose) polymerase	1efy	0.01
Nuclear Hormone Receptors	ER, estrogen receptor; antagonist	3ert	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
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
Kinases	VEGFr2, vascular endothelial growth factor receptor	1vr2	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
Serine Proteases	Thrombin	1ba8	0.00
Kinases	TK, thymidine kinase	1kim	0.00
Other Enzymes	ALR2, aldose reductase	1ah3	0.00
Other Enzymes	NA, neuraminidase	1a4g	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
Nuclear Hormone Receptors	AR, androgen receptor	1xq2	0.00
Nuclear Hormone Receptors	RXRa, retinoic X receptor R	1mvc	0.00
Kinases	P38 MAP, P38 mitogen activated protein	1kv2	0.00
Kinases	HSP90, human heat shock protein 90	1uy6	0.00
Serine Proteases	Trypsin	1bju	0.00
Kinases	CDK2, cyclindependent kinase 2	1ckp	0.00
Metalloenzymes	COMT, catechol O-methyltransferase	1h1d	0.00
Other Enzymes	COX-1, cyclooxygenase-1	1p4g	0.00
Other Enzymes	COX-2, cyclooxygenase-2	1cx2	0.00
Kinases	EGFr, epidermal growth factor receptor	1m17	0.00
Serine Proteases	FXa, factor Xa	1f0r	0.00

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(E)-(4-Bromophenyl){2-(3-bromophenyl)-1-[3-(morpholin-4-ium-4-yl)propyl]-4,5-dioxo-3-pyrrolidinylidene}methanolate

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Std. InChI:

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(E)-(4-Bromophenyl){2-(3-bromophenyl)-1-[3-(morpholin-4-ium-4-yl)propyl]-4,5-dioxo-3-pyrrolidinylidene}methanolate

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