NP-MRD: Showing NP-Card for (1r,4r,5as,7s,9as)-1,4-dihydroxy-7,9a-dimethyl-6-methylidene-1h,4h,5h,5ah,7h,8h,9h-naphtho[1,2-c]furan-3-one (NP0233051)

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Record Information

Version

1.0

Created at

2022-09-06 14:30:19 UTC

Updated at

2022-09-06 14:30:20 UTC

NP-MRD ID

NP0233051

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,4r,5as,7s,9as)-1,4-dihydroxy-7,9a-dimethyl-6-methylidene-1h,4h,5h,5ah,7h,8h,9h-naphtho[1,2-c]furan-3-one

Description

7Alpha,11alpha-dihydroxy-4(13),8-coloratadien-12,11-olide belongs to the class of organic compounds known as terpene lactones. These are prenol lipids containing a lactone ring. Thus, 7alpha,11alpha-dihydroxy-4(13),8-coloratadien-12,11-olide is considered to be an isoprenoid. (1r,4r,5as,7s,9as)-1,4-dihydroxy-7,9a-dimethyl-6-methylidene-1h,4h,5h,5ah,7h,8h,9h-naphtho[1,2-c]furan-3-one is found in Discopodium penninervium. It was first documented in 2008 (PMID: 18086481). Based on a literature review very few articles have been published on 7alpha,11alpha-dihydroxy-4(13),8-coloratadien-12,11-olide.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 39 41  0  0  0  0  0  0  0  0999 V2000
    2.0847    1.3390   -1.9255 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5868    0.4162   -1.1239 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4962   -0.6224   -0.5673 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3762   -0.0069    0.5041 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8153   -1.8508   -0.0852 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3378   -1.8253   -0.0815 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2148   -0.4719    0.3153 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3273    0.0004    1.6384 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6835   -0.5023    0.4113 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3419    0.6343    0.3135 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7878    0.3713    0.4497 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7168    1.2171    0.4081 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9353   -0.9887    0.6332 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6483   -1.5903    0.6053 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6239   -2.5302   -0.4248 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6753    1.9436    0.1002 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5499    2.8034   -0.6046 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3862    1.8523   -0.6421 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1379    0.4647   -0.8193 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4321    2.0940   -2.3321 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1315    1.3585   -2.1860 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2030   -0.9244   -1.3964 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0779    1.0669    0.6785 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2415   -0.5162    1.4735 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4371    0.0206    0.2352 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1386   -2.7688   -0.6601 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1568   -2.0735    0.9684 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0281   -2.0254   -1.1113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0406   -2.6456    0.5557 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9367   -0.8482    2.0529 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8649    0.9444    1.5985 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4928    0.1383    2.4019 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4611   -2.1373    1.5685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9960   -3.3652   -0.0462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4778    2.4670    1.0585 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2711    3.7364   -0.4266 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4237    2.4664   -0.1511 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4940    2.3200   -1.6581 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3806    0.0385   -1.7286 H   0  0  0  0  0  0  0  0  0  0  0  0
  4  3  1  0
  3  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  1
  7 19  1  0
 19 18  1  0
 18 16  1  0
 16 17  1  0
 16 10  1  0
 10  9  2  0
  9 14  1  0
 14 15  1  0
 14 13  1  0
 13 11  1  0
 11 12  2  0
 19  2  1  0
  2  1  2  3
  2  3  1  0
  9  7  1  0
 11 10  1  0
  4 23  1  0
  4 24  1  0
  4 25  1  0
  3 22  1  6
  5 26  1  0
  5 27  1  0
  6 28  1  0
  6 29  1  0
  8 30  1  0
  8 31  1  0
  8 32  1  0
 19 39  1  6
 18 37  1  0
 18 38  1  0
 16 35  1  1
 17 36  1  0
 14 33  1  1
 15 34  1  0
  1 20  1  0
  1 21  1  0
M  END


  Mrv1652309062216302D          

 19 21  0  0  1  0            999 V2000
    0.6490   -2.2790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0390   -1.5520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6043   -0.8508    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2203   -0.8765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9943   -0.1238    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8189   -0.0980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2535   -0.7992    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6435   -0.0722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0781   -0.7735    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5127   -1.4747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3140   -1.2781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9440   -1.8107    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3745   -0.4553    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6108   -0.1434    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4141    0.6578    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1228   -2.2017    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5574   -2.9030    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2982   -2.2275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8636   -1.5262    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  1  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
  9 14  1  0  0  0  0
 14 15  1  6  0  0  0
 10 16  1  0  0  0  0
 16 17  1  6  0  0  0
 16 18  1  0  0  0  0
 19 18  1  1  0  0  0
  2 19  1  0  0  0  0
  7 19  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0233051

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1CC[C@@]2(C)[C@@H](C[C@@H](O)C3=C2[C@H](O)OC3=O)C1=C

> <INCHI_IDENTIFIER>
InChI=1S/C15H20O4/c1-7-4-5-15(3)9(8(7)2)6-10(16)11-12(15)14(18)19-13(11)17/h7,9-10,14,16,18H,2,4-6H2,1,3H3/t7-,9-,10+,14+,15-/m0/s1

> <INCHI_KEY>
RKXFCMNFPWEQDW-AKHPIHOKSA-N

> <FORMULA>
C15H20O4

> <MOLECULAR_WEIGHT>
264.321

> <EXACT_MASS>
264.136159124

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
28.157115525575605

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,4R,5aS,7S,9aS)-1,4-dihydroxy-7,9a-dimethyl-6-methylidene-1H,3H,4H,5H,5aH,6H,7H,8H,9H,9aH-naphtho[1,2-c]furan-3-one

> <JCHEM_LOGP>
1.5317928900000002

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.23707524455816

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.50423328035289

> <JCHEM_PKA_STRONGEST_BASIC>
-3.118449395488322

> <JCHEM_POLAR_SURFACE_AREA>
66.76

> <JCHEM_REFRACTIVITY>
69.6785

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,4R,5aS,7S,9aS)-1,4-dihydroxy-7,9a-dimethyl-6-methylidene-1H,4H,5H,5aH,7H,8H,9H-naphtho[1,2-c]furan-3-one

> <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       1.211  -4.254   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.939  -2.897   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.128  -1.588   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.411  -1.636   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.856  -0.231   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.395  -0.183   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.207  -1.492   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.935  -0.135   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.746  -1.444   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.557  -2.753   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.053  -2.386   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       9.229  -3.380   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0       8.166  -0.850   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       6.740  -0.268   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       6.373   1.228   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       5.829  -4.110   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       6.640  -5.419   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       4.290  -4.158   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.479  -2.849   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   19                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9   19                                             
CONECT    8    7                                                            
CONECT    9    7   10   14                                                  
CONECT   10    9   11   16                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13    9   15                                                  
CONECT   15   14                                                            
CONECT   16   10   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18    2    7                                                  
MASTER        0    0    0    0    0    0    0    0   19    0   42    0
END

View in JSmol

Synonyms

Value	Source
7a,11a-Dihydroxy-4(13),8-coloratadien-12,11-olide	Generator
7Α,11α-dihydroxy-4(13),8-coloratadien-12,11-olide	Generator

Chemical Formula

C₁₅H₂₀O₄

Average Mass

264.3210 Da

Monoisotopic Mass

264.13616 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C[C@H]1CC[C@@]2(C)[C@@H](C[C@@H](O)C3=C2[C@H](O)OC3=O)C1=C

InChI Identifier

InChI=1S/C15H20O4/c1-7-4-5-15(3)9(8(7)2)6-10(16)11-12(15)14(18)19-13(11)17/h7,9-10,14,16,18H,2,4-6H2,1,3H3/t7-,9-,10+,14+,15-/m0/s1

InChI Key

RKXFCMNFPWEQDW-AKHPIHOKSA-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
Discopodium penninervium	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as terpene lactones. These are prenol lipids containing a lactone ring.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Terpene lactones

Alternative Parents

Substituents

Terpene lactone
Sesquiterpenoid
Naphthofuran
2-furanone
Dihydrofuran
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Carboxylic acid ester
Hemiacetal
Lactone
Secondary alcohol
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Hydrocarbon derivative
Organic oxygen compound
Organic oxide
Alcohol
Organooxygen compound
Carbonyl group
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Coloratane sesquiterpenoids (LMPR0103380001 )

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

24846705

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

42608152

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Wube AA, Wenzig EM, Gibbons S, Asres K, Bauer R, Bucar F: Constituents of the stem bark of Discopodium penninervium and their LTB4 and COX-1 and -2 inhibitory activities. Phytochemistry. 2008 Feb;69(4):982-7. doi: 10.1016/j.phytochem.2007.11.001. Epub 2007 Dec 20. [PubMed:18086481 ]
LOTUS database [Link]

Showing NP-Card for (1r,4r,5as,7s,9as)-1,4-dihydroxy-7,9a-dimethyl-6-methylidene-1h,4h,5h,5ah,7h,8h,9h-naphtho[1,2-c]furan-3-one (NP0233051)

MOL for NP0233051 ((1r,4r,5as,7s,9as)-1,4-dihydroxy-7,9a-dimethyl-6-methylidene-1h,4h,5h,5ah,7h,8h,9h-naphtho[1,2-c]furan-3-one)

3D MOL for NP0233051 ((1r,4r,5as,7s,9as)-1,4-dihydroxy-7,9a-dimethyl-6-methylidene-1h,4h,5h,5ah,7h,8h,9h-naphtho[1,2-c]furan-3-one)

3D SDF for NP0233051 ((1r,4r,5as,7s,9as)-1,4-dihydroxy-7,9a-dimethyl-6-methylidene-1h,4h,5h,5ah,7h,8h,9h-naphtho[1,2-c]furan-3-one)

3D-SDF for NP0233051 ((1r,4r,5as,7s,9as)-1,4-dihydroxy-7,9a-dimethyl-6-methylidene-1h,4h,5h,5ah,7h,8h,9h-naphtho[1,2-c]furan-3-one)

PDB for NP0233051 ((1r,4r,5as,7s,9as)-1,4-dihydroxy-7,9a-dimethyl-6-methylidene-1h,4h,5h,5ah,7h,8h,9h-naphtho[1,2-c]furan-3-one)

3D PDB for NP0233051 ((1r,4r,5as,7s,9as)-1,4-dihydroxy-7,9a-dimethyl-6-methylidene-1h,4h,5h,5ah,7h,8h,9h-naphtho[1,2-c]furan-3-one)

SMILES for NP0233051 ((1r,4r,5as,7s,9as)-1,4-dihydroxy-7,9a-dimethyl-6-methylidene-1h,4h,5h,5ah,7h,8h,9h-naphtho[1,2-c]furan-3-one)

INCHI for NP0233051 ((1r,4r,5as,7s,9as)-1,4-dihydroxy-7,9a-dimethyl-6-methylidene-1h,4h,5h,5ah,7h,8h,9h-naphtho[1,2-c]furan-3-one)

Structure for NP0233051 ((1r,4r,5as,7s,9as)-1,4-dihydroxy-7,9a-dimethyl-6-methylidene-1h,4h,5h,5ah,7h,8h,9h-naphtho[1,2-c]furan-3-one)

3D Structure for NP0233051 ((1r,4r,5as,7s,9as)-1,4-dihydroxy-7,9a-dimethyl-6-methylidene-1h,4h,5h,5ah,7h,8h,9h-naphtho[1,2-c]furan-3-one)