NP-MRD: Showing NP-Card for Bemadienolide (NP0063477)

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Record Information

Version

2.0

Created at

2022-04-28 07:53:08 UTC

Updated at

2022-04-28 07:53:08 UTC

NP-MRD ID

NP0063477

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Bemadienolide

Description

Bemadienolide belongs to the class of organic compounds known as naphthofurans. Naphthofurans are compounds containing a furan ring fused to a naphthalene moiety. Furan is a 5 membered- ring aromatic ring with four carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings. Bemadienolide is found in Cinnamosma fragrans and Cinnamosma macrocarpa. Bemadienolide is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 37 39  0  0  0  0  0  0  0  0999 V2000
    2.7510   -1.0147    0.6607 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7605   -0.1118   -0.0948 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0079   -0.3716   -1.5667 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0514    1.2959    0.3140 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9302    2.1920    0.6112 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3761    1.5868    1.0199 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6780    0.4275    0.0892 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6426    0.9931   -1.3108 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9874   -0.1734    0.2819 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2252   -1.4376   -0.0495 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1154   -2.3858   -0.2083 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1153   -1.9523   -0.0104 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3976   -0.5795    0.3587 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6555   -1.6446   -0.1812 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2636   -2.7089   -0.4838 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2693   -0.4100    0.0967 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2680    0.3471    0.8013 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1440   -1.8109    0.0146 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6346   -0.4016    0.9999 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3129   -1.4461    1.5578 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7781   -1.1812   -1.7374 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4529    0.5188   -2.0815 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1041   -0.7544   -2.0913 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6322    1.7495   -0.5475 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8071    1.3310    1.1547 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2256    2.8913    1.4504 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7230    2.9062   -0.2407 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3385    1.2290    2.0821 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1640    2.3570    0.8893 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3988    1.8362   -1.3064 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3002    1.4486   -1.5980 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0588    0.2759   -2.0639 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3402   -3.4138   -0.4833 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9208   -2.6457   -0.1295 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4952   -0.5953    1.4952 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3844    0.2609    1.8817 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3789    1.3927    0.4258 H   0  0  0  0  0  0  0  0  0  0  0  0
 13 12  1  0
 12 11  2  0
 11 10  1  0
 10  9  2  0
  9 17  1  0
 17 16  1  0
 16 14  1  0
 14 15  2  0
  9  7  1  0
  7  8  1  6
  7  6  1  0
  6  5  1  0
  5  4  1  0
  4  2  1  0
  2  1  1  1
  2  3  1  0
  7 13  1  0
  2 13  1  0
 14 10  1  0
 13 35  1  1
 12 34  1  0
 11 33  1  0
 17 36  1  0
 17 37  1  0
  8 30  1  0
  8 31  1  0
  8 32  1  0
  6 28  1  0
  6 29  1  0
  5 26  1  0
  5 27  1  0
  4 24  1  0
  4 25  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  3 21  1  0
  3 22  1  0
  3 23  1  0
M  END


  Mrv1652309272007342D          

 18 20  0  0  1  0            999 V2000
    1.6368   -0.0304    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8633   -1.4875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3443   -0.4455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9067    0.3842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6256   -0.8605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9067   -0.4455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1213    0.6372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1213   -0.6986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3509    1.2143    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3577    2.0602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6421    1.6496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6464    0.8282    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3594    0.4146    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0702    1.6458    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3681    0.0598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8782    0.9632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0701    0.8249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6526    0.0032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  7  1  0  0  0  0
  1  8  1  0  0  0  0
  2  8  2  0  0  0  0
  3  5  2  0  0  0  0
  4  6  2  0  0  0  0
  4  7  1  0  0  0  0
  5  6  1  0  0  0  0
  6  8  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 17 15  1  0  0  0  0
 17 16  1  0  0  0  0
 13 17  1  0  0  0  0
 17 14  1  0  0  0  0
 14 10  1  0  0  0  0
 13 12  1  0  0  0  0
 13  3  1  0  0  0  0
 13  9  1  1  0  0  0
 12  4  1  0  0  0  0
 12 18  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0063477

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H][C@@]12C=CC3=C(COC3=O)[C@@]1(C)CCCC2(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C15H20O2/c1-14(2)7-4-8-15(3)11-9-17-13(16)10(11)5-6-12(14)15/h5-6,12H,4,7-9H2,1-3H3/t12-,15+/m0/s1

> <INCHI_KEY>
IQJQVMRLNOWNDT-SWLSCSKDSA-N

> <FORMULA>
C15H20O2

> <MOLECULAR_WEIGHT>
232.323

> <EXACT_MASS>
232.146329884

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
37

> <JCHEM_AVERAGE_POLARIZABILITY>
26.127063834805714

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(5aS,9aS)-6,6,9a-trimethyl-1H,3H,5aH,6H,7H,8H,9H,9aH-naphtho[1,2-c]furan-3-one

> <ALOGPS_LOGP>
3.75

> <JCHEM_LOGP>
3.125580076666667

> <ALOGPS_LOGS>
-3.59

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.340735353761286

> <JCHEM_PKA_STRONGEST_BASIC>
-6.952443927072153

> <JCHEM_POLAR_SURFACE_AREA>
26.3

> <JCHEM_REFRACTIVITY>
68.39869999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.02e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(5aS,9aS)-6,6,9a-trimethyl-1H,5aH,7H,8H,9H-naphtho[1,2-c]furan-3-one

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 27-SEP-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   27-SEP-20         0                                  
HETATM    1  O   UNK     0       3.055  -0.057   0.000  0.00  0.00           O+0
HETATM    2  O   UNK     0       3.478  -2.777   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       8.109  -0.832   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.426   0.717   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.768  -1.606   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.426  -0.832   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.960   1.189   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.960  -1.304   0.000  0.00  0.00           C+0
HETATM    9  H   UNK     0       8.122   2.267   0.000  0.00  0.00           H+0
HETATM   10  C   UNK     0       8.134   3.846   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.799   3.079   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.807   1.546   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.138   0.774   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.464   3.072   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      10.020   0.112   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      10.973   1.798   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.464   1.540   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.818   0.006   0.000  0.00  0.00           C+0
CONECT    1    7    8                                                       
CONECT    2    8                                                            
CONECT    3    5   13                                                       
CONECT    4    6    7   12                                                  
CONECT    5    3    6                                                       
CONECT    6    4    5    8                                                  
CONECT    7    1    4                                                       
CONECT    8    1    2    6                                                  
CONECT    9   13                                                            
CONECT   10   11   14                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13    4   18                                             
CONECT   13   17   12    3    9                                             
CONECT   14   17   10                                                       
CONECT   15   17                                                            
CONECT   16   17                                                            
CONECT   17   15   16   13   14                                             
CONECT   18   12                                                            
MASTER        0    0    0    0    0    0    0    0   18    0   40    0
END

View in JSmol

Synonyms

Value	Source
(+)-Bemadienolide	PhytoBank

Chemical Formula

C₁₅H₂₀O₂

Average Mass

232.3230 Da

Monoisotopic Mass

232.14633 Da

IUPAC Name

(5aS,9aS)-6,6,9a-trimethyl-1H,3H,5aH,6H,7H,8H,9H,9aH-naphtho[1,2-c]furan-3-one

Traditional Name

(5aS,9aS)-6,6,9a-trimethyl-1H,5aH,7H,8H,9H-naphtho[1,2-c]furan-3-one

CAS Registry Number

Not Available

SMILES

[H][C@@]12C=CC3=C(COC3=O)[C@@]1(C)CCCC2(C)C

InChI Identifier

InChI=1S/C15H20O2/c1-14(2)7-4-8-15(3)11-9-17-13(16)10(11)5-6-12(14)15/h5-6,12H,4,7-9H2,1-3H3/t12-,15+/m0/s1

InChI Key

IQJQVMRLNOWNDT-SWLSCSKDSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Cinnamosma fragrans	Plant	KNApSAcK
Cinnamosma macrocarpa	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as naphthofurans. Naphthofurans are compounds containing a furan ring fused to a naphthalene moiety. Furan is a 5 membered- ring aromatic ring with four carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Naphthofurans

Sub Class

Not Available

Direct Parent

Naphthofurans

Alternative Parents

Substituents

Naphthofuran
2-furanone
Dihydrofuran
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Carboxylic acid ester
Lactone
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Oxacycle
Hydrocarbon derivative
Organic oxygen compound
Organic oxide
Carbonyl group
Organooxygen compound
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	3.75	ALOGPS
logP	3.13	ChemAxon
logS	-3.6	ALOGPS
pKa (Strongest Acidic)	13.34	ChemAxon
pKa (Strongest Basic)	-7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	26.3 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	68.4 m³·mol⁻¹	ChemAxon
Polarizability	26.13 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	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

12300028

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Bemadienolide (NP0063477)

MOL for NP0063477 (Bemadienolide)

3D MOL for NP0063477 (Bemadienolide)

3D SDF for NP0063477 (Bemadienolide)

3D-SDF for NP0063477 (Bemadienolide)

PDB for NP0063477 (Bemadienolide)

3D PDB for NP0063477 (Bemadienolide)

SMILES for NP0063477 (Bemadienolide)

INCHI for NP0063477 (Bemadienolide)

Structure for NP0063477 (Bemadienolide)

3D Structure for NP0063477 (Bemadienolide)