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Methyl (2β,3β,4β,5α,12β,19α)-4-acetoxy-15-[(13S,15R,16S,17R)-17-ethyl-16-hydroxy-13-(methoxycarbonyl)-1,11-diazatetracyclo[13.3.1.0^4,12.0^5,10]nonadeca-4(12),5,7,9-tetraen-13-yl ]-3-hydroxy-16-methoxy-1-methyl-6,7-didehydroaspidospermidine-3-carboxylate

ChemSpider ID: 291131
Molecular Formula: C₄₆H₅₈N₄O₉
Monoisotopic mass: 810.420349 Da
Systematic name

Methyl (2β,3β,4β,5α,12β,19α)-4-acetoxy-15-[(13S,15R,16S,17R)-17-ethyl-16-hydroxy-13-(methoxycarbonyl)-1,11-diazatetracyclo[13.3.1.0^4,12.0^5,10]nonadeca-4(12),5,7,9-tetraen-13-yl ]-3-hydroxy-16-methoxy-1-methyl-6,7-didehydroaspidospermidine-3-carboxylate
SMILES and InChIs

SMILES:

O=C(OC)[C@]4(c2c(c1ccccc1n2)CCN3C[C@@H](CC)[C@H](O)[C@@H](C3)C4)c9cc5c(N([C@@H]6[C@]58CCN7C\C=C/[C@@](CC)([C@@H](OC(=O)C)[C@]6(O)C(=O)OC)[C@H]78)C)cc9OC Copied

Std. InChI:

InChI=1S/C46H58N4O9/c1-8-27-24-49-19-15-30-29-13-10-11-14-33(29)47-37(30)45(41(53)57-6,23-28(25-49)36(27)52)32-21-31-34(22-35(32)56-5)48(4)39-44(31)17-20-50-18-12-16-43(9-2,38(44)50)40(59-26(3)51)46(39,55)42(54)58-7/h10-14,16,21-22,27-28,36,38-40,47,52,55H,8-9,15,17-20,23-25H2,1-7H3/t27-,28-,36+,38+,39-,40-,43-,44-,45+,46+/m1/s1 Copied

Std. InChIKey:

WZESQBIPMBSRTJ-SWEJZCQFSA-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:	5.495	# of Rule of 5 Violations:	3
ACD/LogD (pH 5.5):	2.92	ACD/LogD (pH 7.4):	4.89
ACD/BCF (pH 5.5):	23.37	ACD/BCF (pH 7.4):	2206.11
ACD/KOC (pH 5.5):	61.49	ACD/KOC (pH 7.4):	5804.33
#H bond acceptors:	13	#H bond donors:	3
#Freely Rotating Bonds:	12	Polar Surface Area:	154.1 Å²
Index of Refraction:	1.67	Molar Refractivity:	220.688 cm³
Molar Volume:	590.864 cm³	Polarizability:	87.488 10^-24cm³
Surface Tension:	70.5289993286133 dyne/cm	Density:	1.373 g/cm³
Flash Point:	°C	Enthalpy of Vaporization:	kJ/mol
Boiling Point:	°C at 760 mmHg	Vapour Pressure:	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
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
Kinases	SRC, tyrosine kinase SRC	2src	0.01
Serine Proteases	Thrombin	1ba8	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
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
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
Other Enzymes	COX-2, cyclooxygenase-2	1cx2	0.00
Other Enzymes	InhA, enoyl ACP reductase	1p44	0.00
Metalloenzymes	COMT, catechol O-methyltransferase	1h1d	0.00
Other Enzymes	ALR2, aldose reductase	1ah3	0.00
Other Enzymes	NA, neuraminidase	1a4g	0.00
Kinases	CDK2, cyclindependent kinase 2	1ckp	0.00
Kinases	TK, thymidine kinase	1kim	0.00
Metalloenzymes	ADA, adenosine deaminase	1stw	0.00
Other Enzymes	COX-1, cyclooxygenase-1	1p4g	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
Nuclear Hormone Receptors	GR, glucocorticoid receptor	1m2z	0.00
Folate Enzymes	GART, glycinamide ribonucleotide transformylase	1c2t	0.00
Kinases	PDGFrb, platelet derived growth factor receptor kinase	N/A	0.00
Nuclear Hormone Receptors	ER, estrogen receptor; antagonist	3ert	0.00
Kinases	HSP90, human heat shock protein 90	1uy6	0.00
Other Enzymes	HIVRT, HIV reverse transcriptase	1rt1	0.00
Serine Proteases	FXa, factor Xa	1f0r	0.00
Kinases	EGFr, epidermal growth factor receptor	1m17	0.00

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Methyl (2β,3β,4β,5α,12β,19α)-4-acetoxy-15-[(13S,15R,16S,17R)-17-ethyl-16-hydroxy-13-(methoxycarbonyl)-1,11-diazatetracyclo[13.3.1.0^4,12.0^5,10]nonadeca-4(12),5,7,9-tetraen-13-yl ]-3-hydroxy-16-methoxy-1-methyl-6,7-didehydroaspidospermidine-3-carboxylate

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Methyl (2β,3β,4β,5α,12β,19α)-4-acetoxy-15-[(13S,15R,16S,17R)-17-ethyl-16-hydroxy-13-(methoxycarbonyl)-1,11-diazatetracyclo[13.3.1.04,12.05,10]nonadeca-4(12),5,7,9-tetraen-13-yl ]-3-hydroxy-16-methoxy-1-methyl-6,7-didehydroaspidospermidine-3-carboxylate

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Methyl (2β,3β,4β,5α,12β,19α)-4-acetoxy-15-[(13S,15R,16S,17R)-17-ethyl-16-hydroxy-13-(methoxycarbonyl)-1,11-diazatetracyclo[13.3.1.0^4,12.0^5,10]nonadeca-4(12),5,7,9-tetraen-13-yl ]-3-hydroxy-16-methoxy-1-methyl-6,7-didehydroaspidospermidine-3-carboxylate