NP-MRD: Showing NP-Card for 1,4,13-trihydroxy-5b,8,8,11a,13a-pentamethyl-1h,4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h-chryseno[1,2-c]furan-3-one (NP0207988)

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Record Information

Version

2.0

Created at

2022-09-05 04:49:07 UTC

Updated at

2022-09-05 04:49:07 UTC

NP-MRD ID

NP0207988

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1,4,13-trihydroxy-5b,8,8,11a,13a-pentamethyl-1h,4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h-chryseno[1,2-c]furan-3-one

Description

4,8,11-Trihydroxy-1,10,14,18,18-pentamethyl-7-oxapentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]Henicos-5(9)-en-6-one 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. 1,4,13-trihydroxy-5b,8,8,11a,13a-pentamethyl-1h,4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h-chryseno[1,2-c]furan-3-one is found in Hyrtios erectus. 4,8,11-Trihydroxy-1,10,14,18,18-pentamethyl-7-oxapentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]Henicos-5(9)-en-6-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004201502462D          

 30 34  0  0  0  0            999 V2000
    7.9927   -0.6021    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2218   -0.3082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0662   -1.1184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6451    0.4000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2435    1.1206    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4186    1.1332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9953    0.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5937    1.1457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3969   -0.2956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9736   -1.0037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1487   -0.9912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7471   -0.2705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3238   -0.9786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1704    0.4376    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7688    1.1583    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9439    1.1708    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5423    1.8915    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5206    0.4627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1190    1.1833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9222   -0.2580    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4988   -0.9661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6739   -0.9535    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2506   -1.6617    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2724   -0.2329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.3368    1.9009    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3943    0.7726    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4681   -0.0491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
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  7  9  1  0  0  0  0
  2  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
  7 14  1  0  0  0  0
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 15 16  1  0  0  0  0
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 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
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 29 30  2  0  0  0  0
M  END

     RDKit          3D

 68 72  0  0  0  0  0  0  0  0999 V2000
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    4.5183    0.9771    2.2667 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0525    0.8266    3.3815 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6949   -0.2333   -0.6359 C   0  0  1  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1533004201502462D          

 30 34  0  0  0  0            999 V2000
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 29 30  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0207988

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(C)CCCC2(C)C1CCC1(C)C2CC(O)C2(C)C1CC(O)C1=C2C(O)OC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C25H38O5/c1-22(2)8-6-9-23(3)14(22)7-10-24(4)15(23)12-17(27)25(5)16(24)11-13(26)18-19(25)21(29)30-20(18)28/h13-17,21,26-27,29H,6-12H2,1-5H3

> <INCHI_KEY>
GAQSWPYYPSDAAV-UHFFFAOYSA-N

> <FORMULA>
C25H38O5

> <MOLECULAR_WEIGHT>
418.574

> <EXACT_MASS>
418.271924324

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
68

> <JCHEM_AVERAGE_POLARIZABILITY>
46.96820404047185

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4,8,11-trihydroxy-1,10,14,18,18-pentamethyl-7-oxapentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]henicos-5(9)-en-6-one

> <ALOGPS_LOGP>
2.84

> <JCHEM_LOGP>
3.2606491376666664

> <ALOGPS_LOGS>
-4.13

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.085301798655081

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.466668155563367

> <JCHEM_PKA_STRONGEST_BASIC>
-2.965568529428894

> <JCHEM_POLAR_SURFACE_AREA>
86.99000000000001

> <JCHEM_REFRACTIVITY>
113.28719999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.09e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4,8,11-trihydroxy-1,10,14,18,18-pentamethyl-7-oxapentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]henicos-5(9)-en-6-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 20-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-APR-15         0                                  
HETATM    1  C   UNK     0      14.920  -1.124   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      13.481  -0.575   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      13.190  -2.088   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      14.271   0.747   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      13.521   2.092   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      11.981   2.115   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      11.191   0.793   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      10.442   2.139   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      11.941  -0.552   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      11.151  -1.874   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.611  -1.850   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.861  -0.505   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.071  -1.827   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.651   0.817   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.902   2.162   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.362   2.185   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       6.612   3.531   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       6.572   0.864   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.822   2.209   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.321  -0.482   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.531  -1.803   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.991  -1.780   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       4.201  -3.102   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       4.242  -0.435   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.032   0.887   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.019   2.047   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       4.362   3.548   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       2.603   1.442   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       2.740  -0.092   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       1.580  -1.105   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4    9                                             
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9   14                                             
CONECT    8    7                                                            
CONECT    9    7    2   10                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14   20                                             
CONECT   13   12                                                            
CONECT   14   12    7   15                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   20   25                                             
CONECT   19   18                                                            
CONECT   20   18   12   21                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   29                                                  
CONECT   25   24   18   26                                                  
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   24   30                                                  
CONECT   30   29                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   68    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₅H₃₈O₅

Average Mass

418.5740 Da

Monoisotopic Mass

418.27192 Da

IUPAC Name

4,8,11-trihydroxy-1,10,14,18,18-pentamethyl-7-oxapentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]henicos-5(9)-en-6-one

Traditional Name

4,8,11-trihydroxy-1,10,14,18,18-pentamethyl-7-oxapentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]henicos-5(9)-en-6-one

CAS Registry Number

Not Available

SMILES

CC1(C)CCCC2(C)C1CCC1(C)C2CC(O)C2(C)C1CC(O)C1=C2C(O)OC1=O

InChI Identifier

InChI=1S/C25H38O5/c1-22(2)8-6-9-23(3)14(22)7-10-24(4)15(23)12-17(27)25(5)16(24)11-13(26)18-19(25)21(29)30-20(18)28/h13-17,21,26-27,29H,6-12H2,1-5H3

InChI Key

GAQSWPYYPSDAAV-UHFFFAOYSA-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
Hyrtios erectus	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
12-hydroxysteroid
15-hydroxysteroid
Hydroxysteroid
17-oxosteroid
Oxosteroid
7-hydroxysteroid
16-oxasteroid
Steroid
2-furanone
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Cyclic alcohol
Dihydrofuran
Secondary alcohol
Lactone
Carboxylic acid ester
Hemiacetal
Polyol
Organoheterocyclic compound
Oxacycle
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Alcohol
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
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	2.84	ALOGPS
logP	3.26	ChemAxon
logS	-4.1	ALOGPS
pKa (Strongest Acidic)	11.47	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	86.99 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	113.29 m³·mol⁻¹	ChemAxon
Polarizability	46.97 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	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

72994344

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 1,4,13-trihydroxy-5b,8,8,11a,13a-pentamethyl-1h,4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h-chryseno[1,2-c]furan-3-one (NP0207988)

MOL for NP0207988 (1,4,13-trihydroxy-5b,8,8,11a,13a-pentamethyl-1h,4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h-chryseno[1,2-c]furan-3-one)

3D MOL for NP0207988 (1,4,13-trihydroxy-5b,8,8,11a,13a-pentamethyl-1h,4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h-chryseno[1,2-c]furan-3-one)

3D SDF for NP0207988 (1,4,13-trihydroxy-5b,8,8,11a,13a-pentamethyl-1h,4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h-chryseno[1,2-c]furan-3-one)

3D-SDF for NP0207988 (1,4,13-trihydroxy-5b,8,8,11a,13a-pentamethyl-1h,4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h-chryseno[1,2-c]furan-3-one)

PDB for NP0207988 (1,4,13-trihydroxy-5b,8,8,11a,13a-pentamethyl-1h,4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h-chryseno[1,2-c]furan-3-one)

3D PDB for NP0207988 (1,4,13-trihydroxy-5b,8,8,11a,13a-pentamethyl-1h,4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h-chryseno[1,2-c]furan-3-one)

SMILES for NP0207988 (1,4,13-trihydroxy-5b,8,8,11a,13a-pentamethyl-1h,4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h-chryseno[1,2-c]furan-3-one)

INCHI for NP0207988 (1,4,13-trihydroxy-5b,8,8,11a,13a-pentamethyl-1h,4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h-chryseno[1,2-c]furan-3-one)

Structure for NP0207988 (1,4,13-trihydroxy-5b,8,8,11a,13a-pentamethyl-1h,4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h-chryseno[1,2-c]furan-3-one)

3D Structure for NP0207988 (1,4,13-trihydroxy-5b,8,8,11a,13a-pentamethyl-1h,4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h-chryseno[1,2-c]furan-3-one)