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1,6-Di(4-morpholinyl)-1,6-dioxo-2,3,4,5-hexanetetrayl tetraacetate (non-preferred name)

ChemSpider ID: 4048502
Molecular Formula: C₂₂H₃₂N₂O₁₂
Monoisotopic mass: 516.195496 Da
Systematic name

1,6-Di(4-morpholinyl)-1,6-dioxo-2,3,4,5-hexanetetrayl tetraacetate (non-preferred name)
SMILES and InChIs

SMILES:

O=C(N1CCOCC1)C(OC(=O)C)C(OC(=O)C)C(OC(=O)C)C(OC(=O)C)C(=O)N2CCOCC2 Copied

Std. InChI:

InChI=1S/C22H32N2O12/c1-13(25)33-17(19(35-15(3)27)21(29)23-5-9-31-10-6-23)18(34-14(2)26)20(36-16(4)28)22(30)24-7-11-32-12-8-24/h17-20H,5-12H2,1-4H3 Copied

Std. InChIKey:

GPMNWAXIRMNNKT-UHFFFAOYSA-N Copied

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

ACD/LogP:	-0.065	# of Rule of 5 Violations:	2
ACD/LogD (pH 5.5):	-0.07	ACD/LogD (pH 7.4):	-0.07
ACD/BCF (pH 5.5):	1.00	ACD/BCF (pH 7.4):	1.00
ACD/KOC (pH 5.5):	21.96	ACD/KOC (pH 7.4):	21.96
#H bond acceptors:	14	#H bond donors:	0
#Freely Rotating Bonds:	13	Polar Surface Area:	164.28 Å²
Index of Refraction:	1.509	Molar Refractivity:	116.862 cm³
Molar Volume:	391.588 cm³	Polarizability:	46.328 10^-24cm³
Surface Tension:	51.6809997558594 dyne/cm	Density:	1.319 g/cm³
Flash Point:	372.044 °C	Enthalpy of Vaporization:	101.338 kJ/mol
Boiling Point:	691.562 °C at 760 mmHg	Vapour Pressure:	0 mmHg at 25°C

Patents	Personal Collections
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
NIH Substance Repository	Physical Properties (including SAR/QSAR databases)
Protein 3D Structures	Spectroscopy Databases
Substance Vendors	Theoretical Properties
Toxicology/Environmental Databases	Virtual Library

Category	Target	PDB Code	LASSO Score
Metalloenzymes	ACE, angiotensin-converting enzyme	1o86	0.05
Other Enzymes	AChE, acetylcholinesterase	1eve	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
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
Other Enzymes	ALR2, aldose reductase	1ah3	0.00
Nuclear Hormone Receptors	ER, estrogen receptor; agonist	1l2i	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
Kinases	FGFr1, fibroblast growth factor receptor kinase	1agw	0.00
Nuclear Hormone Receptors	RXRa, retinoic X receptor R	1mvc	0.00
Other Enzymes	NA, neuraminidase	1a4g	0.00
Other Enzymes	InhA, enoyl ACP reductase	1p44	0.00
Kinases	TK, thymidine kinase	1kim	0.00
Kinases	CDK2, cyclindependent kinase 2	1ckp	0.00
Other Enzymes	COX-1, cyclooxygenase-1	1p4g	0.00
Serine Proteases	Trypsin	1bju	0.00
Nuclear Hormone Receptors	AR, androgen receptor	1xq2	0.00
Nuclear Hormone Receptors	GR, glucocorticoid receptor	1m2z	0.00
Kinases	PDGFrb, platelet derived growth factor receptor kinase	N/A	0.00
Folate Enzymes	GART, glycinamide ribonucleotide transformylase	1c2t	0.00
Nuclear Hormone Receptors	ER, estrogen receptor; antagonist	3ert	0.00
Other Enzymes	HIVRT, HIV reverse transcriptase	1rt1	0.00
Kinases	HSP90, human heat shock protein 90	1uy6	0.00
Kinases	P38 MAP, P38 mitogen activated protein	1kv2	0.00
Other Enzymes	SAHH, S-adenosyl-homocysteine hydrolase	1a7a	0.00
Serine Proteases	Thrombin	1ba8	0.00
Kinases	EGFr, epidermal growth factor receptor	1m17	0.00
Serine Proteases	FXa, factor Xa	1f0r	0.00
Metalloenzymes	ADA, adenosine deaminase	1stw	0.00
Other Enzymes	COX-2, cyclooxygenase-2	1cx2	0.00
Metalloenzymes	COMT, catechol O-methyltransferase	1h1d	0.00

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1,6-Di(4-morpholinyl)-1,6-dioxo-2,3,4,5-hexanetetrayl tetraacetate (non-preferred name)

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Std. InChI:

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1,6-Di(4-morpholinyl)-1,6-dioxo-2,3,4,5-hexanetetrayl tetraacetate (non-preferred name)

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Std. InChI:

Std. InChIKey:

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