NP-MRD: Showing NP-Card for (2s,4ar,5s,8ar)-1,1,4a,8a-tetramethyl-6-methylidene-5-{[(2-oxochromen-7-yl)oxy]methyl}-hexahydronaphthalen-2-yl (2z)-2-methylbut-2-enoate (NP0229168)

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Record Information

Version

2.0

Created at

2022-09-06 09:07:00 UTC

Updated at

2022-09-06 09:07:00 UTC

NP-MRD ID

NP0229168

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s,4ar,5s,8ar)-1,1,4a,8a-tetramethyl-6-methylidene-5-{[(2-oxochromen-7-yl)oxy]methyl}-hexahydronaphthalen-2-yl (2z)-2-methylbut-2-enoate

Description

3-Angeloxycoladin belongs to the class of organic compounds known as coumarins and derivatives. These are polycyclic aromatic compounds containing a 1-benzopyran moiety with a ketone group at the C2 carbon atom (1-benzopyran-2-one). (2s,4ar,5s,8ar)-1,1,4a,8a-tetramethyl-6-methylidene-5-{[(2-oxochromen-7-yl)oxy]methyl}-hexahydronaphthalen-2-yl (2z)-2-methylbut-2-enoate is found in Ferula vesceritensis. Based on a literature review very few articles have been published on 3-Angeloxycoladin.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062211072D          

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M  END

     RDKit          3D

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  Mrv1652309062211072D          

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 20 22  1  0  0  0  0
  2 22  1  0  0  0  0
 22 23  1  1  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 31 33  1  0  0  0  0
 33 34  1  0  0  0  0
 28 34  1  0  0  0  0
 34 35  2  0  0  0  0
 25 35  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0229168

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C=C(\C)C(=O)O[C@H]1CC[C@]2(C)[C@@H](COC3=CC=C4C=CC(=O)OC4=C3)C(=C)CC[C@@]2(C)C1(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C30H38O5/c1-8-19(2)27(32)35-25-14-15-29(6)23(20(3)13-16-30(29,7)28(25,4)5)18-33-22-11-9-21-10-12-26(31)34-24(21)17-22/h8-12,17,23,25H,3,13-16,18H2,1-2,4-7H3/b19-8-/t23-,25-,29+,30-/m0/s1

> <INCHI_KEY>
IOPRWFZXNNJKTN-VPRYEBPISA-N

> <FORMULA>
C30H38O5

> <MOLECULAR_WEIGHT>
478.629

> <EXACT_MASS>
478.271924324

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
73

> <JCHEM_AVERAGE_POLARIZABILITY>
54.333195741624536

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,4aR,5S,8aR)-1,1,4a,8a-tetramethyl-6-methylidene-5-{[(2-oxo-2H-chromen-7-yl)oxy]methyl}-decahydronaphthalen-2-yl (2Z)-2-methylbut-2-enoate

> <JCHEM_LOGP>
6.8480811473333345

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.844851988670244

> <JCHEM_POLAR_SURFACE_AREA>
61.83

> <JCHEM_REFRACTIVITY>
137.89909999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2S,4aR,5S,8aR)-1,1,4a,8a-tetramethyl-6-methylidene-5-{[(2-oxochromen-7-yl)oxy]methyl}-hexahydronaphthalen-2-yl (2Z)-2-methylbut-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.001  -5.390   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -5.335  -4.620   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -5.335  -3.080   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -6.668  -3.850   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -6.668  -2.310   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -7.195  -3.757   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -8.185  -2.043   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -8.002   0.000   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -8.002   1.540   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -6.668   2.310   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -9.336   2.310   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -9.336   3.850   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0     -10.669   1.540   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0     -10.669   0.000   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -5.335  -0.000   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -2.667  -1.540   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       0.000  -3.080   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       8.002  -3.080   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0       5.335  -3.080   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   22                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7   20                                             
CONECT    6    5                                                            
CONECT    7    5    8    9   10                                             
CONECT    8    7                                                            
CONECT    9    7                                                            
CONECT   10    7   11   18                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16                                                            
CONECT   18   10   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19    5   21   22                                             
CONECT   21   20                                                            
CONECT   22   20    2   23                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   35                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   34                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34                                                       
CONECT   34   33   28   35                                                  
CONECT   35   34   25                                                       
MASTER        0    0    0    0    0    0    0    0   35    0   76    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₀H₃₈O₅

Average Mass

478.6290 Da

Monoisotopic Mass

478.27192 Da

IUPAC Name

(2S,4aR,5S,8aR)-1,1,4a,8a-tetramethyl-6-methylidene-5-{[(2-oxo-2H-chromen-7-yl)oxy]methyl}-decahydronaphthalen-2-yl (2Z)-2-methylbut-2-enoate

Traditional Name

(2S,4aR,5S,8aR)-1,1,4a,8a-tetramethyl-6-methylidene-5-{[(2-oxochromen-7-yl)oxy]methyl}-hexahydronaphthalen-2-yl (2Z)-2-methylbut-2-enoate

CAS Registry Number

Not Available

SMILES

C\C=C(\C)C(=O)O[C@H]1CC[C@]2(C)[C@@H](COC3=CC=C4C=CC(=O)OC4=C3)C(=C)CC[C@@]2(C)C1(C)C

InChI Identifier

InChI=1S/C30H38O5/c1-8-19(2)27(32)35-25-14-15-29(6)23(20(3)13-16-30(29,7)28(25,4)5)18-33-22-11-9-21-10-12-26(31)34-24(21)17-22/h8-12,17,23,25H,3,13-16,18H2,1-2,4-7H3/b19-8-/t23-,25-,29+,30-/m0/s1

InChI Key

IOPRWFZXNNJKTN-VPRYEBPISA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Ferula vesceritensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as coumarins and derivatives. These are polycyclic aromatic compounds containing a 1-benzopyran moiety with a ketone group at the C2 carbon atom (1-benzopyran-2-one).

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Coumarins and derivatives

Sub Class

Not Available

Direct Parent

Coumarins and derivatives

Alternative Parents

Substituents

Coumarin
1-benzopyran
Benzopyran
Pyranone
Fatty acid ester
Alkyl aryl ether
Fatty acyl
Benzenoid
Pyran
Heteroaromatic compound
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Lactone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Ether
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	6.85	ChemAxon
pKa (Strongest Basic)	-4.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	61.83 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	137.9 m³·mol⁻¹	ChemAxon
Polarizability	54.33 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB 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

102469381

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2s,4ar,5s,8ar)-1,1,4a,8a-tetramethyl-6-methylidene-5-{[(2-oxochromen-7-yl)oxy]methyl}-hexahydronaphthalen-2-yl (2z)-2-methylbut-2-enoate (NP0229168)

MOL for NP0229168 ((2s,4ar,5s,8ar)-1,1,4a,8a-tetramethyl-6-methylidene-5-{[(2-oxochromen-7-yl)oxy]methyl}-hexahydronaphthalen-2-yl (2z)-2-methylbut-2-enoate)

3D MOL for NP0229168 ((2s,4ar,5s,8ar)-1,1,4a,8a-tetramethyl-6-methylidene-5-{[(2-oxochromen-7-yl)oxy]methyl}-hexahydronaphthalen-2-yl (2z)-2-methylbut-2-enoate)

3D SDF for NP0229168 ((2s,4ar,5s,8ar)-1,1,4a,8a-tetramethyl-6-methylidene-5-{[(2-oxochromen-7-yl)oxy]methyl}-hexahydronaphthalen-2-yl (2z)-2-methylbut-2-enoate)

3D-SDF for NP0229168 ((2s,4ar,5s,8ar)-1,1,4a,8a-tetramethyl-6-methylidene-5-{[(2-oxochromen-7-yl)oxy]methyl}-hexahydronaphthalen-2-yl (2z)-2-methylbut-2-enoate)

PDB for NP0229168 ((2s,4ar,5s,8ar)-1,1,4a,8a-tetramethyl-6-methylidene-5-{[(2-oxochromen-7-yl)oxy]methyl}-hexahydronaphthalen-2-yl (2z)-2-methylbut-2-enoate)

3D PDB for NP0229168 ((2s,4ar,5s,8ar)-1,1,4a,8a-tetramethyl-6-methylidene-5-{[(2-oxochromen-7-yl)oxy]methyl}-hexahydronaphthalen-2-yl (2z)-2-methylbut-2-enoate)

SMILES for NP0229168 ((2s,4ar,5s,8ar)-1,1,4a,8a-tetramethyl-6-methylidene-5-{[(2-oxochromen-7-yl)oxy]methyl}-hexahydronaphthalen-2-yl (2z)-2-methylbut-2-enoate)

INCHI for NP0229168 ((2s,4ar,5s,8ar)-1,1,4a,8a-tetramethyl-6-methylidene-5-{[(2-oxochromen-7-yl)oxy]methyl}-hexahydronaphthalen-2-yl (2z)-2-methylbut-2-enoate)

Structure for NP0229168 ((2s,4ar,5s,8ar)-1,1,4a,8a-tetramethyl-6-methylidene-5-{[(2-oxochromen-7-yl)oxy]methyl}-hexahydronaphthalen-2-yl (2z)-2-methylbut-2-enoate)

3D Structure for NP0229168 ((2s,4ar,5s,8ar)-1,1,4a,8a-tetramethyl-6-methylidene-5-{[(2-oxochromen-7-yl)oxy]methyl}-hexahydronaphthalen-2-yl (2z)-2-methylbut-2-enoate)