ChemFOnt: Showing chemical card for [(2-{16,17-dimethoxy-12-oxo-2,7,20-trioxapentacyclo[11.8.0.0³,¹¹.0⁴,⁸.0¹⁴,¹⁹]henicosa-3(11),4(8),9,14,16,18-hexaen-6-yl}prop-2-en-1-yl)oxy]sulfonic acid (CFc000129678)

Record Information

Version

1.0

Creation Date

2022-08-28 10:25:12 UTC

Update Date

2022-09-13 21:58:46 UTC

Chemfont ID

CFc000129678

Molecule Identification

Common Name

[(2-{16,17-dimethoxy-12-oxo-2,7,20-trioxapentacyclo[11.8.0.0³,¹¹.0⁴,⁸.0¹⁴,¹⁹]henicosa-3(11),4(8),9,14,16,18-hexaen-6-yl}prop-2-en-1-yl)oxy]sulfonic acid

Definition

[(2-{16,17-dimethoxy-12-oxo-2,7,20-trioxapentacyclo[11.8.0.0³,¹¹.0⁴,⁸.0¹⁴,¹⁹]henicosa-3(11),4(8),9,14,16,18-hexaen-6-yl}prop-2-en-1-yl)oxy]sulfonic acid belongs to the class of organic compounds known as rotenones. These are rotenoids with a structure based on a 6a,12a-dihydrochromeno[3,4-b]chromen-12(6H)-one skeleton. Based on a literature review very few articles have been published on [(2-{16,17-dimethoxy-12-oxo-2,7,20-trioxapentacyclo[11.8.0.0³,¹¹.0⁴,⁸.0¹⁴,¹⁹]henicosa-3(11),4(8),9,14,16,18-hexaen-6-yl}prop-2-en-1-yl)oxy]sulfonic acid.

Structure

MOL SDF PDB SMILES InChI

Synonyms

Value	Source
[(2-{16,17-dimethoxy-12-oxo-2,7,20-trioxapentacyclo[11.8.0.0,.0,.0,]henicosa-3(11),4(8),9,14,16,18-hexaen-6-yl}prop-2-en-1-yl)oxy]sulfonate	Generator
[(2-{16,17-dimethoxy-12-oxo-2,7,20-trioxapentacyclo[11.8.0.0,.0,.0,]henicosa-3(11),4(8),9,14,16,18-hexaen-6-yl}prop-2-en-1-yl)oxy]sulphonate	Generator
[(2-{16,17-dimethoxy-12-oxo-2,7,20-trioxapentacyclo[11.8.0.0,.0,.0,]henicosa-3(11),4(8),9,14,16,18-hexaen-6-yl}prop-2-en-1-yl)oxy]sulphonic acid	Generator
[(2-{16,17-dimethoxy-12-oxo-2,7,20-trioxapentacyclo[11.8.0.0³,¹¹.0⁴,⁸.0¹⁴,¹⁹]henicosa-3(11),4(8),9,14,16,18-hexaen-6-yl}prop-2-en-1-yl)oxy]sulfonate	Generator
[(2-{16,17-dimethoxy-12-oxo-2,7,20-trioxapentacyclo[11.8.0.0³,¹¹.0⁴,⁸.0¹⁴,¹⁹]henicosa-3(11),4(8),9,14,16,18-hexaen-6-yl}prop-2-en-1-yl)oxy]sulphonate	Generator
[(2-{16,17-dimethoxy-12-oxo-2,7,20-trioxapentacyclo[11.8.0.0³,¹¹.0⁴,⁸.0¹⁴,¹⁹]henicosa-3(11),4(8),9,14,16,18-hexaen-6-yl}prop-2-en-1-yl)oxy]sulphonic acid	Generator

Chemical Formula

C₂₃H₂₂O₁₀S

Average Molecular Weight

490.48

Monoisotopic Molecular Weight

490.093368082

IUPAC Name

[(2-{16,17-dimethoxy-12-oxo-2,7,20-trioxapentacyclo[11.8.0.0^{3,11}.0^{4,8}.0^{14,19}]henicosa-3(11),4(8),9,14,16,18-hexaen-6-yl}prop-2-en-1-yl)oxy]sulfonic acid

Traditional Name

(2-{16,17-dimethoxy-12-oxo-2,7,20-trioxapentacyclo[11.8.0.0^{3,11}.0^{4,8}.0^{14,19}]henicosa-3(11),4(8),9,14,16,18-hexaen-6-yl}prop-2-en-1-yl)oxysulfonic acid

CAS Registry Number

Not Available

SMILES

COC1=C(OC)C=C2C3C(COC2=C1)OC1=C(C=CC2=C1CC(O2)C(=C)COS(O)(=O)=O)C3=O

InChI Identifier

InChI=1S/C23H22O10S/c1-11(9-31-34(25,26)27)16-7-14-15(32-16)5-4-12-22(24)21-13-6-18(28-2)19(29-3)8-17(13)30-10-20(21)33-23(12)14/h4-6,8,16,20-21H,1,7,9-10H2,2-3H3,(H,25,26,27)

InChI Key

MMDRCQLJEWTLDF-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as rotenones. These are rotenoids with a structure based on a 6a,12a-dihydrochromeno[3,4-b]chromen-12(6H)-one skeleton.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Isoflavonoids

Sub Class

Rotenoids

Direct Parent

Rotenones

Alternative Parents

Substituents

Rotenone or derivatives
8-prenylated isoflavanone
Isoflavanone
Isoflavan
Chromone
Chromane
Benzopyran
1-benzopyran
Coumaran
Anisole
Aryl alkyl ketone
Aryl ketone
Alkyl aryl ether
Sulfate-ester
Sulfuric acid monoester
Alkyl sulfate
Sulfuric acid ester
Benzenoid
Organic sulfuric acid or derivatives
Ketone
Organoheterocyclic compound
Oxacycle
Ether
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Exogenous (HMDB: HMDB0149269)

Process

Not Available

Role

Not Available

Physical Properties

Predicted Properties

Property	Value	Source
Water Solubility	0.12 g/L	ALOGPS
logP	1.07	ALOGPS
logP	2.09	ChemAxon
logS	-3.6	ALOGPS
pKa (Strongest Acidic)	-2.1	ChemAxon
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	126.82 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	117.48 m³·mol⁻¹	ChemAxon
Polarizability	49.28 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

HMDB0149269

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

Showing chemical card for [(2-{16,17-dimethoxy-12-oxo-2,7,20-trioxapentacyclo[11.8.0.0³,¹¹.0⁴,⁸.0¹⁴,¹⁹]henicosa-3(11),4(8),9,14,16,18-hexaen-6-yl}prop-2-en-1-yl)oxy]sulfonic acid (CFc000129678)

MOL for CFc000129678 ([(2-{16,17-dimethoxy-12-oxo-2,7,20-trioxapentacyclo[11.8.0.0³,¹¹.0⁴,⁸.0¹⁴,¹⁹]henicosa-3(11),4(8),9,14,16,18-hexaen-6-yl}prop-2-en-1-yl)oxy]sulfonic acid)

3D MOL for CFc000129678 ([(2-{16,17-dimethoxy-12-oxo-2,7,20-trioxapentacyclo[11.8.0.0³,¹¹.0⁴,⁸.0¹⁴,¹⁹]henicosa-3(11),4(8),9,14,16,18-hexaen-6-yl}prop-2-en-1-yl)oxy]sulfonic acid)

3D SDF for CFc000129678 ([(2-{16,17-dimethoxy-12-oxo-2,7,20-trioxapentacyclo[11.8.0.0³,¹¹.0⁴,⁸.0¹⁴,¹⁹]henicosa-3(11),4(8),9,14,16,18-hexaen-6-yl}prop-2-en-1-yl)oxy]sulfonic acid)

3D-SDF for CFc000129678 ([(2-{16,17-dimethoxy-12-oxo-2,7,20-trioxapentacyclo[11.8.0.0³,¹¹.0⁴,⁸.0¹⁴,¹⁹]henicosa-3(11),4(8),9,14,16,18-hexaen-6-yl}prop-2-en-1-yl)oxy]sulfonic acid)

PDB for CFc000129678 ([(2-{16,17-dimethoxy-12-oxo-2,7,20-trioxapentacyclo[11.8.0.0³,¹¹.0⁴,⁸.0¹⁴,¹⁹]henicosa-3(11),4(8),9,14,16,18-hexaen-6-yl}prop-2-en-1-yl)oxy]sulfonic acid)

3D PDB for CFc000129678 ([(2-{16,17-dimethoxy-12-oxo-2,7,20-trioxapentacyclo[11.8.0.0³,¹¹.0⁴,⁸.0¹⁴,¹⁹]henicosa-3(11),4(8),9,14,16,18-hexaen-6-yl}prop-2-en-1-yl)oxy]sulfonic acid)

SMILES for CFc000129678 ([(2-{16,17-dimethoxy-12-oxo-2,7,20-trioxapentacyclo[11.8.0.0³,¹¹.0⁴,⁸.0¹⁴,¹⁹]henicosa-3(11),4(8),9,14,16,18-hexaen-6-yl}prop-2-en-1-yl)oxy]sulfonic acid)

INCHI for CFc000129678 ([(2-{16,17-dimethoxy-12-oxo-2,7,20-trioxapentacyclo[11.8.0.0³,¹¹.0⁴,⁸.0¹⁴,¹⁹]henicosa-3(11),4(8),9,14,16,18-hexaen-6-yl}prop-2-en-1-yl)oxy]sulfonic acid)

Structure for CFc000129678 ([(2-{16,17-dimethoxy-12-oxo-2,7,20-trioxapentacyclo[11.8.0.0³,¹¹.0⁴,⁸.0¹⁴,¹⁹]henicosa-3(11),4(8),9,14,16,18-hexaen-6-yl}prop-2-en-1-yl)oxy]sulfonic acid)

3D Structure for CFc000129678 ([(2-{16,17-dimethoxy-12-oxo-2,7,20-trioxapentacyclo[11.8.0.0³,¹¹.0⁴,⁸.0¹⁴,¹⁹]henicosa-3(11),4(8),9,14,16,18-hexaen-6-yl}prop-2-en-1-yl)oxy]sulfonic acid)