(4β,5β,6α,17α,22R)-4,5,6,14,17,20-Hexahydroxy-22,26-epoxyergosta-2,24-diene-1,26-dione

ChemSpider ID: 295493
Molecular Formula: C₂₈H₄₀O₉
Average mass: 520.611816 Da
Monoisotopic mass: 520.267212 Da
Systematic name

(4β,5β,6α,17α,22R)-4,5,6,14,17,20-Hexahydroxy-22,26-epoxyergosta-2,24-diene-1,26-dione
SMILES and InChIs

SMILES:

O=C1\C=C/[C@H](O)[C@]4(O)[C@@]1(C)[C@H]5CC[C@@]3(C)[C@@](O)(CC[C@@]3(O)[C@](O)(C)[C@@H]2OC(=O)\C(=C(\C)C2)C)[C@@H]5C[C@@H]4O Copied

Std. InChI:

InChI=1S/C28H40O9/c1-14-12-21(37-22(32)15(14)2)25(5,33)27(35)11-10-26(34)17-13-20(31)28(36)19(30)7-6-18(29)24(28,4)16(17)8-9-23(26,27)3/h6-7,16-17,19-21,30-31,33-36H,8-13H2,1-5H3/t16-,17+,19-,20-,21+,23-,24-,25-,26+,27-,28+/m0/s1 Copied

Std. InChIKey:

XLUKITCTLVOOAW-VQDSAXESSA-N Copied
Cite this record
CSID:295493, http://www.chemspider.com/Chemical-Structure.295493.html (accessed 04:07, Jun 20, 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:	-0.868	# of Rule of 5 Violations:	2
ACD/LogD (pH 5.5):	-0.87	ACD/LogD (pH 7.4):	-0.87
ACD/BCF (pH 5.5):	1.00	ACD/BCF (pH 7.4):	1.00
ACD/KOC (pH 5.5):	8.04	ACD/KOC (pH 7.4):	8.04
#H bond acceptors:	9	#H bond donors:	6
#Freely Rotating Bonds:	8	Polar Surface Area:	164.75 Å²
Index of Refraction:	1.643	Molar Refractivity:	131.436 cm³
Molar Volume:	363.36 cm³	Polarizability:	52.105 10^-24cm³
Surface Tension:	75.8539962768555 dyne/cm	Density:	1.433 g/cm³
Flash Point:	237.112 °C	Enthalpy of Vaporization:	120.647 kJ/mol
Boiling Point:	723.22 °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
Other Enzymes	HMGR, hydroxymethylglutaryl-CoA reductase	1hw8	0.03
Metalloenzymes	ACE, angiotensin-converting enzyme	1o86	0.03
Nuclear Hormone Receptors	RXRa, retinoic X receptor R	1mvc	0.03
Nuclear Hormone Receptors	PPARg, peroxisome proliferator activated receptor	1fm9	0.03
Other Enzymes	GPB, glycogen phosphorylase	1a8i	0.02
Kinases	SRC, tyrosine kinase SRC	2src	0.01
Other Enzymes	HIVPR, HIV protease	1hpx	0.01
Nuclear Hormone Receptors	MR, mineralocorticoid receptor	2aa2	0.01
Kinases	HSP90, human heat shock protein 90	1uy6	0.01
Metalloenzymes	PDE5, phosphodiesterase 5	1xp0	0.01
Other Enzymes	PARP, poly(ADP-ribose) polymerase	1efy	0.01
Other Enzymes	NA, neuraminidase	1a4g	0.01
Nuclear Hormone Receptors	AR, androgen receptor	1xq2	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
Other Enzymes	SAHH, S-adenosyl-homocysteine hydrolase	1a7a	0.00
Kinases	VEGFr2, vascular endothelial growth factor receptor	1vr2	0.00
Serine Proteases	Trypsin	1bju	0.00
Kinases	FGFr1, fibroblast growth factor receptor kinase	1agw	0.00
Metalloenzymes	COMT, catechol O-methyltransferase	1h1d	0.00
Other Enzymes	COX-2, cyclooxygenase-2	1cx2	0.00
Serine Proteases	Thrombin	1ba8	0.00
Other Enzymes	ALR2, aldose reductase	1ah3	0.00
Kinases	TK, thymidine kinase	1kim	0.00
Other Enzymes	COX-1, cyclooxygenase-1	1p4g	0.00
Kinases	P38 MAP, P38 mitogen activated protein	1kv2	0.00
Other Enzymes	AChE, acetylcholinesterase	1eve	0.00
Nuclear Hormone Receptors	GR, glucocorticoid receptor	1m2z	0.00
Other Enzymes	InhA, enoyl ACP reductase	1p44	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
Kinases	EGFr, epidermal growth factor receptor	1m17	0.00
Serine Proteases	FXa, factor Xa	1f0r	0.00
Metalloenzymes	ADA, adenosine deaminase	1stw	0.00
Kinases	CDK2, cyclindependent kinase 2	1ckp	0.00
Other Enzymes	HIVRT, HIV reverse transcriptase	1rt1	0.00

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(4β,5β,6α,17α,22R)-4,5,6,14,17,20-Hexahydroxy-22,26-epoxyergosta-2,24-diene-1,26-dione

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(4β,5β,6α,17α,22R)-4,5,6,14,17,20-Hexahydroxy-22,26-epoxyergosta-2,24-diene-1,26-dione

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