NP-MRD: Showing NP-Card for (1s,2s,3s,5r,7s,8s,10r,11r,14s)-14-(acetyloxy)-5,10-dihydroxy-3-isopropyl-10,14-dimethyl-6-methylidene-15-oxatricyclo[6.6.1.0²,⁷]pentadecan-11-yl butanoate (NP0321107)

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Record Information

Version

2.0

Created at

2022-09-11 23:08:05 UTC

Updated at

2022-09-11 23:08:05 UTC

NP-MRD ID

NP0321107

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2s,3s,5r,7s,8s,10r,11r,14s)-14-(acetyloxy)-5,10-dihydroxy-3-isopropyl-10,14-dimethyl-6-methylidene-15-oxatricyclo[6.6.1.0²,⁷]pentadecan-11-yl butanoate

Description

(1S,2S,3S,5R,7S,8S,10R,11R,14S)-14-(acetyloxy)-5,10-dihydroxy-10,14-dimethyl-6-methylidene-3-(propan-2-yl)-15-oxatricyclo[6.6.1.0²,⁷]Pentadecan-11-yl butanoate belongs to the class of organic compounds known as eunicellane and asbestinane diterpenoids. These are diterpenoids with a structure based on either the eunicellane (5,14-cyclocembrane) or the asbestinane skeleton. (1s,2s,3s,5r,7s,8s,10r,11r,14s)-14-(acetyloxy)-5,10-dihydroxy-3-isopropyl-10,14-dimethyl-6-methylidene-15-oxatricyclo[6.6.1.0²,⁷]pentadecan-11-yl butanoate is found in Cladiella australis. Based on a literature review very few articles have been published on (1S,2S,3S,5R,7S,8S,10R,11R,14S)-14-(acetyloxy)-5,10-dihydroxy-10,14-dimethyl-6-methylidene-3-(propan-2-yl)-15-oxatricyclo[6.6.1.0²,⁷]Pentadecan-11-yl butanoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122201082D          

 33 35  0  0  1  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1652309122201082D          

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  9 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  6  0  0  0
 18 20  1  1  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
 18 24  1  0  0  0  0
 24 25  1  6  0  0  0
  4 25  1  6  0  0  0
 26 24  1  6  0  0  0
  3 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  1  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 27 31  1  0  0  0  0
 31 32  1  0  0  0  0
  2 32  1  0  0  0  0
 32 33  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0321107

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCC(=O)O[C@@H]1CC[C@](C)(OC(C)=O)[C@H]2O[C@@H](C[C@@]1(C)O)[C@H]1[C@@H]2[C@@H](C[C@@H](O)C1=C)C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C26H42O7/c1-8-9-21(29)32-20-10-11-26(7,33-16(5)27)24-23-17(14(2)3)12-18(28)15(4)22(23)19(31-24)13-25(20,6)30/h14,17-20,22-24,28,30H,4,8-13H2,1-3,5-7H3/t17-,18+,19-,20+,22-,23-,24-,25+,26-/m0/s1

> <INCHI_KEY>
CDBMAXFWXOUPQK-BKOISJLFSA-N

> <FORMULA>
C26H42O7

> <MOLECULAR_WEIGHT>
466.615

> <EXACT_MASS>
466.293053692

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
75

> <JCHEM_AVERAGE_POLARIZABILITY>
51.74009826821148

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2S,3S,5R,7S,8S,10R,11R,14S)-14-(acetyloxy)-5,10-dihydroxy-10,14-dimethyl-6-methylidene-3-(propan-2-yl)-15-oxatricyclo[6.6.1.0^{2,7}]pentadecan-11-yl butanoate

> <JCHEM_LOGP>
2.6956682466666644

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.696709764864114

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.86265171811587

> <JCHEM_PKA_STRONGEST_BASIC>
-2.968774051242889

> <JCHEM_POLAR_SURFACE_AREA>
102.29000000000002

> <JCHEM_REFRACTIVITY>
122.8779

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,3S,5R,7S,8S,10R,11R,14S)-14-(acetyloxy)-5,10-dihydroxy-3-isopropyl-10,14-dimethyl-6-methylidene-15-oxatricyclo[6.6.1.0^{2,7}]pentadecan-11-yl butanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0      -1.740  -0.442   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.419   1.064   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.045   1.540   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.672   0.133   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.005  -0.637   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.537  -0.476   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.217  -1.982   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       4.871  -1.246   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       4.681   0.555   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       6.015  -0.215   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       7.349   0.555   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       7.349   2.095   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       8.682  -0.215   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      10.016   0.555   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      11.350  -0.215   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.002   2.061   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.375   3.468   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.041   4.238   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.186   5.268   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       2.415   5.645   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       3.320   6.891   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.694   8.297   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       4.852   6.730   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       1.510   4.077   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       0.598   2.210   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       0.365   3.046   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -0.779   4.077   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -0.459   5.583   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -1.603   6.614   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       1.006   6.059   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -2.244   3.601   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -2.564   2.095   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      -4.028   1.619   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   32                                                  
CONECT    3    2    4   26                                                  
CONECT    4    3    5   25                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8    9                                             
CONECT    7    6                                                            
CONECT    8    6                                                            
CONECT    9    6   10   16                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14                                                            
CONECT   16    9   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20   24                                             
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24   18   25   26                                                  
CONECT   25   24    4                                                       
CONECT   26   24    3   27                                                  
CONECT   27   26   28   31                                                  
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28                                                            
CONECT   31   27   32                                                       
CONECT   32   31    2   33                                                  
CONECT   33   32                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   70    0
END

View in JSmol

Synonyms

Value	Source
(1S,2S,3S,5R,7S,8S,10R,11R,14S)-14-(Acetyloxy)-5,10-dihydroxy-10,14-dimethyl-6-methylidene-3-(propan-2-yl)-15-oxatricyclo[6.6.1.0,]pentadecan-11-yl butanoic acid	Generator

Chemical Formula

C₂₆H₄₂O₇

Average Mass

466.6150 Da

Monoisotopic Mass

466.29305 Da

IUPAC Name

(1S,2S,3S,5R,7S,8S,10R,11R,14S)-14-(acetyloxy)-5,10-dihydroxy-10,14-dimethyl-6-methylidene-3-(propan-2-yl)-15-oxatricyclo[6.6.1.0^{2,7}]pentadecan-11-yl butanoate

Traditional Name

(1S,2S,3S,5R,7S,8S,10R,11R,14S)-14-(acetyloxy)-5,10-dihydroxy-3-isopropyl-10,14-dimethyl-6-methylidene-15-oxatricyclo[6.6.1.0^{2,7}]pentadecan-11-yl butanoate

CAS Registry Number

Not Available

SMILES

CCCC(=O)O[C@@H]1CC[C@](C)(OC(C)=O)[C@H]2O[C@@H](C[C@@]1(C)O)[C@H]1[C@@H]2[C@@H](C[C@@H](O)C1=C)C(C)C

InChI Identifier

InChI=1S/C26H42O7/c1-8-9-21(29)32-20-10-11-26(7,33-16(5)27)24-23-17(14(2)3)12-18(28)15(4)22(23)19(31-24)13-25(20,6)30/h14,17-20,22-24,28,30H,4,8-13H2,1-3,5-7H3/t17-,18+,19-,20+,22-,23-,24-,25+,26-/m0/s1

InChI Key

CDBMAXFWXOUPQK-BKOISJLFSA-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
Cladiella australis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as eunicellane and asbestinane diterpenoids. These are diterpenoids with a structure based on either the eunicellane (5,14-cyclocembrane) or the asbestinane skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Eunicellane and asbestinane diterpenoids

Alternative Parents

Substituents

Eunicellane-type diterpenoid
Cladiellane diterpenoid
Fatty acid ester
Dicarboxylic acid or derivatives
Fatty acyl
Cyclic alcohol
Tertiary alcohol
Tetrahydrofuran
Secondary alcohol
Carboxylic acid ester
Ether
Dialkyl ether
Carboxylic acid derivative
Organoheterocyclic compound
Oxacycle
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Alcohol
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
logP	2.7	ChemAxon
pKa (Strongest Acidic)	13.86	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	102.29 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	122.88 m³·mol⁻¹	ChemAxon
Polarizability	51.74 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	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

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

163021638

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,2s,3s,5r,7s,8s,10r,11r,14s)-14-(acetyloxy)-5,10-dihydroxy-3-isopropyl-10,14-dimethyl-6-methylidene-15-oxatricyclo[6.6.1.0²,⁷]pentadecan-11-yl butanoate (NP0321107)

MOL for NP0321107 ((1s,2s,3s,5r,7s,8s,10r,11r,14s)-14-(acetyloxy)-5,10-dihydroxy-3-isopropyl-10,14-dimethyl-6-methylidene-15-oxatricyclo[6.6.1.0²,⁷]pentadecan-11-yl butanoate)

3D MOL for NP0321107 ((1s,2s,3s,5r,7s,8s,10r,11r,14s)-14-(acetyloxy)-5,10-dihydroxy-3-isopropyl-10,14-dimethyl-6-methylidene-15-oxatricyclo[6.6.1.0²,⁷]pentadecan-11-yl butanoate)

3D SDF for NP0321107 ((1s,2s,3s,5r,7s,8s,10r,11r,14s)-14-(acetyloxy)-5,10-dihydroxy-3-isopropyl-10,14-dimethyl-6-methylidene-15-oxatricyclo[6.6.1.0²,⁷]pentadecan-11-yl butanoate)

3D-SDF for NP0321107 ((1s,2s,3s,5r,7s,8s,10r,11r,14s)-14-(acetyloxy)-5,10-dihydroxy-3-isopropyl-10,14-dimethyl-6-methylidene-15-oxatricyclo[6.6.1.0²,⁷]pentadecan-11-yl butanoate)

PDB for NP0321107 ((1s,2s,3s,5r,7s,8s,10r,11r,14s)-14-(acetyloxy)-5,10-dihydroxy-3-isopropyl-10,14-dimethyl-6-methylidene-15-oxatricyclo[6.6.1.0²,⁷]pentadecan-11-yl butanoate)

3D PDB for NP0321107 ((1s,2s,3s,5r,7s,8s,10r,11r,14s)-14-(acetyloxy)-5,10-dihydroxy-3-isopropyl-10,14-dimethyl-6-methylidene-15-oxatricyclo[6.6.1.0²,⁷]pentadecan-11-yl butanoate)

SMILES for NP0321107 ((1s,2s,3s,5r,7s,8s,10r,11r,14s)-14-(acetyloxy)-5,10-dihydroxy-3-isopropyl-10,14-dimethyl-6-methylidene-15-oxatricyclo[6.6.1.0²,⁷]pentadecan-11-yl butanoate)

INCHI for NP0321107 ((1s,2s,3s,5r,7s,8s,10r,11r,14s)-14-(acetyloxy)-5,10-dihydroxy-3-isopropyl-10,14-dimethyl-6-methylidene-15-oxatricyclo[6.6.1.0²,⁷]pentadecan-11-yl butanoate)

Structure for NP0321107 ((1s,2s,3s,5r,7s,8s,10r,11r,14s)-14-(acetyloxy)-5,10-dihydroxy-3-isopropyl-10,14-dimethyl-6-methylidene-15-oxatricyclo[6.6.1.0²,⁷]pentadecan-11-yl butanoate)

3D Structure for NP0321107 ((1s,2s,3s,5r,7s,8s,10r,11r,14s)-14-(acetyloxy)-5,10-dihydroxy-3-isopropyl-10,14-dimethyl-6-methylidene-15-oxatricyclo[6.6.1.0²,⁷]pentadecan-11-yl butanoate)