NP-MRD: Showing NP-Card for (1r,2s,3r,4r,4as,5r,8ar)-1-(acetyloxy)-3,5-dihydroxy-3,4,8a-trimethyl-8-methylidene-4-[(1e)-2-(5-oxo-2h-furan-3-yl)ethenyl]-hexahydronaphthalen-2-yl butanoate (NP0148052)

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Record Information

Version

2.0

Created at

2022-09-02 03:45:33 UTC

Updated at

2022-09-02 03:45:33 UTC

NP-MRD ID

NP0148052

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2s,3r,4r,4as,5r,8ar)-1-(acetyloxy)-3,5-dihydroxy-3,4,8a-trimethyl-8-methylidene-4-[(1e)-2-(5-oxo-2h-furan-3-yl)ethenyl]-hexahydronaphthalen-2-yl butanoate

Description

Scuterulein D belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety. (1r,2s,3r,4r,4as,5r,8ar)-1-(acetyloxy)-3,5-dihydroxy-3,4,8a-trimethyl-8-methylidene-4-[(1e)-2-(5-oxo-2h-furan-3-yl)ethenyl]-hexahydronaphthalen-2-yl butanoate was first documented in 2001 (PMID: 11421742). Based on a literature review very few articles have been published on Scuterulein D.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022205452D          

 34 36  0  0  1  0            999 V2000
   -1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.7145    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    2.8188   -2.1354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
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  2  8  1  0  0  0  0
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 22 23  1  1  0  0  0
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  7 25  1  0  0  0  0
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 31 32  2  0  0  0  0
 31 33  1  0  0  0  0
 33 34  1  0  0  0  0
 29 34  1  0  0  0  0
M  END

     RDKit          3D

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    5.8559    1.1025   -0.6452 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1652309022205452D          

 34 36  0  0  1  0            999 V2000
   -1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END
> <DATABASE_ID>
NP0148052

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCC(=O)O[C@H]1[C@H](OC(C)=O)[C@]2(C)[C@H]([C@H](O)CCC2=C)[C@@](C)(\C=C\C2=CC(=O)OC2)[C@@]1(C)O

> <INCHI_IDENTIFIER>
InChI=1S/C26H36O8/c1-7-8-19(29)34-23-22(33-16(3)27)25(5)15(2)9-10-18(28)21(25)24(4,26(23,6)31)12-11-17-13-20(30)32-14-17/h11-13,18,21-23,28,31H,2,7-10,14H2,1,3-6H3/b12-11+/t18-,21-,22+,23+,24-,25+,26+/m1/s1

> <INCHI_KEY>
CZVDOSTXFXGDEB-BTVLSMNRSA-N

> <FORMULA>
C26H36O8

> <MOLECULAR_WEIGHT>
476.566

> <EXACT_MASS>
476.241018119

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
70

> <JCHEM_AVERAGE_POLARIZABILITY>
50.892974133251904

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,2S,3R,4R,4aS,5R,8aR)-1-(acetyloxy)-3,5-dihydroxy-3,4,8a-trimethyl-8-methylidene-4-[(E)-2-(5-oxo-2,5-dihydrofuran-3-yl)ethenyl]-decahydronaphthalen-2-yl butanoate

> <ALOGPS_LOGP>
2.39

> <JCHEM_LOGP>
2.2221339156666646

> <ALOGPS_LOGS>
-3.90

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.454188456339772

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.59564948098423

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8533208144404885

> <JCHEM_POLAR_SURFACE_AREA>
119.36000000000003

> <JCHEM_REFRACTIVITY>
124.61779999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.04e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2S,3R,4R,4aS,5R,8aR)-1-(acetyloxy)-3,5-dihydroxy-3,4,8a-trimethyl-8-methylidene-4-[(E)-2-(5-oxo-2H-furan-3-yl)ethenyl]-hexahydronaphthalen-2-yl butanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0      -2.667  -0.000   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       2.667  -3.080   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.334   0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -1.334   2.310   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -1.334   3.850   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.667   4.620   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -0.000   4.620   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       1.334   3.850   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       2.667   6.160   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.335   4.620   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.668   3.850   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.194   2.987   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       4.184   1.273   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.206  -0.054   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       3.483  -1.306   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       5.022  -1.252   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       5.839  -2.558   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       7.375  -2.666   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       7.747  -4.160   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       9.175  -4.737   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0       6.441  -4.976   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       5.262  -3.986   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    8                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   25                                                  
CONECT    8    7    2    9   10                                             
CONECT    9    8                                                            
CONECT   10    8   11   15                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15   10   16   22                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20                                                            
CONECT   22   15   23   24   25                                             
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25   22    7   26   27                                             
CONECT   26   25                                                            
CONECT   27   25   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30   34                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34                                                       
CONECT   34   33   29                                                       
MASTER        0    0    0    0    0    0    0    0   34    0   72    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₆H₃₆O₈

Average Mass

476.5660 Da

Monoisotopic Mass

476.24102 Da

IUPAC Name

(1R,2S,3R,4R,4aS,5R,8aR)-1-(acetyloxy)-3,5-dihydroxy-3,4,8a-trimethyl-8-methylidene-4-[(E)-2-(5-oxo-2,5-dihydrofuran-3-yl)ethenyl]-decahydronaphthalen-2-yl butanoate

Traditional Name

(1R,2S,3R,4R,4aS,5R,8aR)-1-(acetyloxy)-3,5-dihydroxy-3,4,8a-trimethyl-8-methylidene-4-[(E)-2-(5-oxo-2H-furan-3-yl)ethenyl]-hexahydronaphthalen-2-yl butanoate

CAS Registry Number

Not Available

SMILES

CCCC(=O)O[C@H]1[C@H](OC(C)=O)[C@]2(C)[C@H]([C@H](O)CCC2=C)[C@@](C)(\C=C\C2=CC(=O)OC2)[C@@]1(C)O

InChI Identifier

InChI=1S/C26H36O8/c1-7-8-19(29)34-23-22(33-16(3)27)25(5)15(2)9-10-18(28)21(25)24(4,26(23,6)31)12-11-17-13-20(30)32-14-17/h11-13,18,21-23,28,31H,2,7-10,14H2,1,3-6H3/b12-11+/t18-,21-,22+,23+,24-,25+,26+/m1/s1

InChI Key

CZVDOSTXFXGDEB-BTVLSMNRSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Diterpene lactones

Alternative Parents

Substituents

Clerodane diterpenoid
Diterpenoid
Diterpene lactone
Tricarboxylic acid or derivatives
Fatty acid ester
Fatty acyl
2-furanone
Cyclitol or derivatives
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tertiary alcohol
Dihydrofuran
Cyclic alcohol
Secondary alcohol
Lactone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
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	2.39	ALOGPS
logP	2.22	ChemAxon
logS	-3.9	ALOGPS
pKa (Strongest Acidic)	7.6	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	119.36 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	124.62 m³·mol⁻¹	ChemAxon
Polarizability	50.89 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

C00046395

Chemspider ID

9158829

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10983628

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Esquivel B, Dominguez RM, Toscano RA: Neoclerodane diterpenoids from Scutellaria caerulea. J Nat Prod. 2001 Jun;64(6):778-82. doi: 10.1021/np000588n. [PubMed:11421742 ]
LOTUS database [Link]

Showing NP-Card for (1r,2s,3r,4r,4as,5r,8ar)-1-(acetyloxy)-3,5-dihydroxy-3,4,8a-trimethyl-8-methylidene-4-[(1e)-2-(5-oxo-2h-furan-3-yl)ethenyl]-hexahydronaphthalen-2-yl butanoate (NP0148052)

MOL for NP0148052 ((1r,2s,3r,4r,4as,5r,8ar)-1-(acetyloxy)-3,5-dihydroxy-3,4,8a-trimethyl-8-methylidene-4-[(1e)-2-(5-oxo-2h-furan-3-yl)ethenyl]-hexahydronaphthalen-2-yl butanoate)

3D MOL for NP0148052 ((1r,2s,3r,4r,4as,5r,8ar)-1-(acetyloxy)-3,5-dihydroxy-3,4,8a-trimethyl-8-methylidene-4-[(1e)-2-(5-oxo-2h-furan-3-yl)ethenyl]-hexahydronaphthalen-2-yl butanoate)

3D SDF for NP0148052 ((1r,2s,3r,4r,4as,5r,8ar)-1-(acetyloxy)-3,5-dihydroxy-3,4,8a-trimethyl-8-methylidene-4-[(1e)-2-(5-oxo-2h-furan-3-yl)ethenyl]-hexahydronaphthalen-2-yl butanoate)

3D-SDF for NP0148052 ((1r,2s,3r,4r,4as,5r,8ar)-1-(acetyloxy)-3,5-dihydroxy-3,4,8a-trimethyl-8-methylidene-4-[(1e)-2-(5-oxo-2h-furan-3-yl)ethenyl]-hexahydronaphthalen-2-yl butanoate)

PDB for NP0148052 ((1r,2s,3r,4r,4as,5r,8ar)-1-(acetyloxy)-3,5-dihydroxy-3,4,8a-trimethyl-8-methylidene-4-[(1e)-2-(5-oxo-2h-furan-3-yl)ethenyl]-hexahydronaphthalen-2-yl butanoate)

3D PDB for NP0148052 ((1r,2s,3r,4r,4as,5r,8ar)-1-(acetyloxy)-3,5-dihydroxy-3,4,8a-trimethyl-8-methylidene-4-[(1e)-2-(5-oxo-2h-furan-3-yl)ethenyl]-hexahydronaphthalen-2-yl butanoate)

SMILES for NP0148052 ((1r,2s,3r,4r,4as,5r,8ar)-1-(acetyloxy)-3,5-dihydroxy-3,4,8a-trimethyl-8-methylidene-4-[(1e)-2-(5-oxo-2h-furan-3-yl)ethenyl]-hexahydronaphthalen-2-yl butanoate)

INCHI for NP0148052 ((1r,2s,3r,4r,4as,5r,8ar)-1-(acetyloxy)-3,5-dihydroxy-3,4,8a-trimethyl-8-methylidene-4-[(1e)-2-(5-oxo-2h-furan-3-yl)ethenyl]-hexahydronaphthalen-2-yl butanoate)

Structure for NP0148052 ((1r,2s,3r,4r,4as,5r,8ar)-1-(acetyloxy)-3,5-dihydroxy-3,4,8a-trimethyl-8-methylidene-4-[(1e)-2-(5-oxo-2h-furan-3-yl)ethenyl]-hexahydronaphthalen-2-yl butanoate)

3D Structure for NP0148052 ((1r,2s,3r,4r,4as,5r,8ar)-1-(acetyloxy)-3,5-dihydroxy-3,4,8a-trimethyl-8-methylidene-4-[(1e)-2-(5-oxo-2h-furan-3-yl)ethenyl]-hexahydronaphthalen-2-yl butanoate)