NP-MRD: Showing NP-Card for (3s,5ar,5br,7as,11as,11br,13as)-3,5b,8,8,11a,13a-hexamethyl-3h,4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h-chryseno[1,2-c]furan-1,13-dione (NP0240761)

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Record Information

Version

2.0

Created at

2022-09-07 00:39:54 UTC

Updated at

2022-09-07 00:39:54 UTC

NP-MRD ID

NP0240761

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3s,5ar,5br,7as,11as,11br,13as)-3,5b,8,8,11a,13a-hexamethyl-3h,4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h-chryseno[1,2-c]furan-1,13-dione

Description

(1R,2R,6S,10S,13R,14S,19S)-1,6,10,14,18,18-hexamethyl-7-oxapentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]Henicos-5(9)-ene-8,11-dione belongs to the class of organic compounds known as scalarane sesterterpenoids. These are sesterterpenoids with a structure based on the scalarane backbone. Scalarane is a tetracyclic compound, which is similar the homoandrostane with five methyl groups at the 4-, 4-, 8-, 17-, 17a-positions. (3s,5ar,5br,7as,11as,11br,13as)-3,5b,8,8,11a,13a-hexamethyl-3h,4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h-chryseno[1,2-c]furan-1,13-dione is found in Carteriospongia foliascens. Based on a literature review very few articles have been published on (1R,2R,6S,10S,13R,14S,19S)-1,6,10,14,18,18-hexamethyl-7-oxapentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]Henicos-5(9)-ene-8,11-dione.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072202392D          

 29 33  0  0  1  0            999 V2000
    6.6880    1.4167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0666    0.8741    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.1403    0.0524    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3816   -0.2717    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1979   -1.0759    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8390    0.3498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2623    1.0579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8607    1.7785    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0358    1.7911    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6125    1.0830    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0141    0.3623    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4157   -0.3583    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5908   -0.3458    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9924   -1.0665    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7659   -0.3333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3643    0.3874    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5394    0.4000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9410   -0.3207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1161   -0.3082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2912   -0.2956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1104    0.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3129    1.1332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4580    1.4271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4685    1.9434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1378    1.1206    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5611    1.8287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3860    1.8162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7876    1.0955    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2109    1.8036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  8  9  1  0  0  0  0
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 10 11  1  0  0  0  0
  6 11  1  0  0  0  0
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M  END

     RDKit          3D

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   -3.7441   -0.8727   -0.0242 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8862   -2.3308   -0.4956 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6073   -0.8161    1.2489 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3268   -0.5694    0.2722 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0245   -0.6849    1.7459 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5258   -0.8124    1.8823 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2062    0.3324    1.2194 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0550    1.4547    2.1990 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.7204    2.8254    0.2652 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5364   -0.2393   -2.2111 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1652309072202392D          

 29 33  0  0  1  0            999 V2000
    6.6880    1.4167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0666    0.8741    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.1403    0.0524    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    2.7876    1.0955    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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M  END
> <DATABASE_ID>
NP0240761

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1OC(=O)C2=C1CC[C@@H]1[C@]3(C)CC[C@H]4C(C)(C)CCC[C@]4(C)[C@H]3CC(=O)[C@]21C

> <INCHI_IDENTIFIER>
InChI=1S/C26H38O3/c1-15-16-8-9-18-25(5)13-10-17-23(2,3)11-7-12-24(17,4)19(25)14-20(27)26(18,6)21(16)22(28)29-15/h15,17-19H,7-14H2,1-6H3/t15-,17-,18+,19+,24-,25-,26+/m0/s1

> <INCHI_KEY>
VFRNXSMOWWJWSC-MIJWNDIOSA-N

> <FORMULA>
C26H38O3

> <MOLECULAR_WEIGHT>
398.587

> <EXACT_MASS>
398.282095084

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
67

> <JCHEM_AVERAGE_POLARIZABILITY>
45.929392243765825

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2R,6S,10S,13R,14S,19S)-1,6,10,14,18,18-hexamethyl-7-oxapentacyclo[11.8.0.0^{2,10}.0^{5,9}.0^{14,19}]henicos-5(9)-ene-8,11-dione

> <JCHEM_LOGP>
5.835786876666667

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
19.72230034461662

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.334525137565212

> <JCHEM_PKA_STRONGEST_BASIC>
-6.8399339550486085

> <JCHEM_POLAR_SURFACE_AREA>
43.370000000000005

> <JCHEM_REFRACTIVITY>
114.33829999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,6S,10S,13R,14S,19S)-1,6,10,14,18,18-hexamethyl-7-oxapentacyclo[11.8.0.0^{2,10}.0^{5,9}.0^{14,19}]henicos-5(9)-ene-8,11-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0      12.484   2.645   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      11.324   1.632   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      11.462   0.098   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      10.046  -0.507   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       9.703  -2.008   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       9.033   0.653   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.823   1.975   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.073   3.320   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.534   3.343   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.743   2.022   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.493   0.676   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.243  -0.669   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.703  -0.645   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       7.452  -1.991   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       5.163  -0.622   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.413   0.723   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.874   0.747   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.623  -0.599   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.083  -0.575   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.543  -0.552   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -0.206   0.793   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.584   2.115   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -0.855   2.664   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.875   3.628   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.124   2.092   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.914   3.414   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.454   3.390   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       5.204   2.045   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       5.994   3.367   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    7                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7   11                                                  
CONECT    7    6    2    8                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   28                                                  
CONECT   11   10    6   12   13                                             
CONECT   12   11                                                            
CONECT   13   11   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17   28                                                  
CONECT   17   16   18   19   25                                             
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24   25                                             
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25   22   17   26                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   10   16   29                                             
CONECT   29   28                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₆H₃₈O₃

Average Mass

398.5870 Da

Monoisotopic Mass

398.28210 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C[C@@H]1OC(=O)C2=C1CC[C@@H]1[C@]3(C)CC[C@H]4C(C)(C)CCC[C@]4(C)[C@H]3CC(=O)[C@]21C

InChI Identifier

InChI=1S/C26H38O3/c1-15-16-8-9-18-25(5)13-10-17-23(2,3)11-7-12-24(17,4)19(25)14-20(27)26(18,6)21(16)22(28)29-15/h15,17-19H,7-14H2,1-6H3/t15-,17-,18+,19+,24-,25-,26+/m0/s1

InChI Key

VFRNXSMOWWJWSC-MIJWNDIOSA-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
Phyllospongia foliascens	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as scalarane sesterterpenoids. These are sesterterpenoids with a structure based on the scalarane backbone. Scalarane is a tetracyclic compound, which is similar the homoandrostane with five methyl groups at the 4-, 4-, 8-, 17-, 17a-positions.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesterterpenoids

Direct Parent

Scalarane sesterterpenoids

Alternative Parents

Substituents

Scalarane sesterterpenoid
Steroid lactone
Oxosteroid
7-oxosteroid
16-oxasteroid
Steroid
2-furanone
Dihydrofuran
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Lactone
Ketone
Carboxylic acid ester
Oxacycle
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organoheterocyclic compound
Hydrocarbon derivative
Organic oxide
Organooxygen compound
Organic oxygen compound
Carbonyl group
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

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

163082752

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3s,5ar,5br,7as,11as,11br,13as)-3,5b,8,8,11a,13a-hexamethyl-3h,4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h-chryseno[1,2-c]furan-1,13-dione (NP0240761)

MOL for NP0240761 ((3s,5ar,5br,7as,11as,11br,13as)-3,5b,8,8,11a,13a-hexamethyl-3h,4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h-chryseno[1,2-c]furan-1,13-dione)

3D MOL for NP0240761 ((3s,5ar,5br,7as,11as,11br,13as)-3,5b,8,8,11a,13a-hexamethyl-3h,4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h-chryseno[1,2-c]furan-1,13-dione)

3D SDF for NP0240761 ((3s,5ar,5br,7as,11as,11br,13as)-3,5b,8,8,11a,13a-hexamethyl-3h,4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h-chryseno[1,2-c]furan-1,13-dione)

3D-SDF for NP0240761 ((3s,5ar,5br,7as,11as,11br,13as)-3,5b,8,8,11a,13a-hexamethyl-3h,4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h-chryseno[1,2-c]furan-1,13-dione)

PDB for NP0240761 ((3s,5ar,5br,7as,11as,11br,13as)-3,5b,8,8,11a,13a-hexamethyl-3h,4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h-chryseno[1,2-c]furan-1,13-dione)

3D PDB for NP0240761 ((3s,5ar,5br,7as,11as,11br,13as)-3,5b,8,8,11a,13a-hexamethyl-3h,4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h-chryseno[1,2-c]furan-1,13-dione)

SMILES for NP0240761 ((3s,5ar,5br,7as,11as,11br,13as)-3,5b,8,8,11a,13a-hexamethyl-3h,4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h-chryseno[1,2-c]furan-1,13-dione)

INCHI for NP0240761 ((3s,5ar,5br,7as,11as,11br,13as)-3,5b,8,8,11a,13a-hexamethyl-3h,4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h-chryseno[1,2-c]furan-1,13-dione)

Structure for NP0240761 ((3s,5ar,5br,7as,11as,11br,13as)-3,5b,8,8,11a,13a-hexamethyl-3h,4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h-chryseno[1,2-c]furan-1,13-dione)

3D Structure for NP0240761 ((3s,5ar,5br,7as,11as,11br,13as)-3,5b,8,8,11a,13a-hexamethyl-3h,4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h-chryseno[1,2-c]furan-1,13-dione)