NP-MRD: Showing NP-Card for [(1r,5as,5br,7ar,8r,11ar,11bs,13as,13br)-1-(acetyloxy)-5b,8,11a,13a-tetramethyl-3-oxo-1h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h,13bh-chryseno[1,2-c]furan-8-yl]methyl acetate (NP0329163)

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Record Information

Version

2.0

Created at

2022-09-12 13:17:43 UTC

Updated at

2022-09-12 13:17:44 UTC

NP-MRD ID

NP0329163

Secondary Accession Numbers

None

Natural Product Identification

Common Name

[(1r,5as,5br,7ar,8r,11ar,11bs,13as,13br)-1-(acetyloxy)-5b,8,11a,13a-tetramethyl-3-oxo-1h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h,13bh-chryseno[1,2-c]furan-8-yl]methyl acetate

Description

Hyrtiosin C 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. [(1r,5as,5br,7ar,8r,11ar,11bs,13as,13br)-1-(acetyloxy)-5b,8,11a,13a-tetramethyl-3-oxo-1h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h,13bh-chryseno[1,2-c]furan-8-yl]methyl acetate is found in Hyrtios erectus. Based on a literature review very few articles have been published on Hyrtiosin C.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122215172D          

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M  END

     RDKit          3D

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M  END


  Mrv1652309122215172D          

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    0.3530   -0.6714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4719   -0.6588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2968   -0.6463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7201   -1.3544    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  6  5  1  1  0  0  0
  6  7  1  6  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  6  0  0  0
 11 13  1  0  0  0  0
 13 14  1  6  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  6  0  0  0
 16 18  1  0  0  0  0
 18 19  1  6  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  1  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  2  0  0  0  0
 25 30  1  0  0  0  0
 30 21  1  6  0  0  0
 16 30  1  0  0  0  0
 18 31  1  0  0  0  0
 13 31  1  0  0  0  0
 31 32  1  6  0  0  0
 31 33  1  0  0  0  0
 33 34  1  0  0  0  0
 35 34  1  6  0  0  0
  6 35  1  0  0  0  0
 11 35  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0329163

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OC[C@]1(C)CCC[C@@]2(C)[C@H]1CC[C@]1(C)[C@@H]2CC[C@]2(C)[C@H]3[C@H](OC(C)=O)OC(=O)C3=CC[C@@H]12

> <INCHI_IDENTIFIER>
InChI=1S/C29H42O6/c1-17(30)33-16-26(3)12-7-13-27(4)20(26)10-14-28(5)21-9-8-19-23(29(21,6)15-11-22(27)28)25(34-18(2)31)35-24(19)32/h8,20-23,25H,7,9-16H2,1-6H3/t20-,21-,22+,23+,25+,26-,27-,28-,29-/m0/s1

> <INCHI_KEY>
MTKXOJFNAFCQEE-DTKPNDIQSA-N

> <FORMULA>
C29H42O6

> <MOLECULAR_WEIGHT>
486.649

> <EXACT_MASS>
486.298139072

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
77

> <JCHEM_AVERAGE_POLARIZABILITY>
55.668633608352664

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[(1R,2S,8R,9R,10S,13S,14R,18R,19R)-8-(acetyloxy)-1,10,14,18-tetramethyl-6-oxo-7-oxapentacyclo[11.8.0.0^{2,10}.0^{5,9}.0^{14,19}]henicos-4-en-18-yl]methyl acetate

> <JCHEM_LOGP>
5.175104297333332

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-6.525616450854214

> <JCHEM_POLAR_SURFACE_AREA>
78.9

> <JCHEM_REFRACTIVITY>
130.73269999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
[(1R,2S,8R,9R,10S,13S,14R,18R,19R)-8-(acetyloxy)-1,10,14,18-tetramethyl-6-oxo-7-oxapentacyclo[11.8.0.0^{2,10}.0^{5,9}.0^{14,19}]henicos-4-en-18-yl]methyl acetate

> <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      -8.117   1.634   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -7.873   0.113   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -9.068  -0.859   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      -6.434  -0.436   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -6.190  -1.956   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -4.751  -2.505   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -4.460  -0.992   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -5.541  -3.827   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -4.791  -5.172   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -3.251  -5.195   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -2.461  -3.873   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.712  -5.219   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.921  -3.897   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.172  -5.242   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.368  -5.265   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.158  -3.944   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.908  -5.289   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.409  -2.598   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.199  -1.277   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.739  -1.300   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.488  -2.645   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.990  -2.988   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       7.150  -1.975   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       6.127  -4.522   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       4.711  -5.127   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       4.368  -6.628   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       5.497  -7.676   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       6.968  -7.223   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       5.154  -9.177   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       3.698  -3.967   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -0.131  -2.575   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       0.659  -1.253   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -0.881  -1.230   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -2.421  -1.206   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -3.211  -2.528   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8   35                                             
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13   35                                             
CONECT   12   11                                                            
CONECT   13   11   14   31                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18   30                                             
CONECT   17   16                                                            
CONECT   18   16   19   31                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   30                                                  
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26   30                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27                                                            
CONECT   30   25   21   16                                                  
CONECT   31   18   13   32   33                                             
CONECT   32   31                                                            
CONECT   33   31   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34    6   11                                                  
MASTER        0    0    0    0    0    0    0    0   35    0   78    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₉H₄₂O₆

Average Mass

486.6490 Da

Monoisotopic Mass

486.29814 Da

IUPAC Name

[(1R,2S,8R,9R,10S,13S,14R,18R,19R)-8-(acetyloxy)-1,10,14,18-tetramethyl-6-oxo-7-oxapentacyclo[11.8.0.0^{2,10}.0^{5,9}.0^{14,19}]henicos-4-en-18-yl]methyl acetate

Traditional Name

[(1R,2S,8R,9R,10S,13S,14R,18R,19R)-8-(acetyloxy)-1,10,14,18-tetramethyl-6-oxo-7-oxapentacyclo[11.8.0.0^{2,10}.0^{5,9}.0^{14,19}]henicos-4-en-18-yl]methyl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)OC[C@]1(C)CCC[C@@]2(C)[C@H]1CC[C@]1(C)[C@@H]2CC[C@]2(C)[C@H]3[C@H](OC(C)=O)OC(=O)C3=CC[C@@H]12

InChI Identifier

InChI=1S/C29H42O6/c1-17(30)33-16-26(3)12-7-13-27(4)20(26)10-14-28(5)21-9-8-19-23(29(21,6)15-11-22(27)28)25(34-18(2)31)35-24(19)32/h8,20-23,25H,7,9-16H2,1-6H3/t20-,21-,22+,23+,25+,26-,27-,28-,29-/m0/s1

InChI Key

MTKXOJFNAFCQEE-DTKPNDIQSA-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
17-oxosteroid
Oxosteroid
16-oxasteroid
Steroid
Tricarboxylic acid or derivatives
Acylal
Gamma butyrolactone
Alpha,beta-unsaturated carboxylic ester
Tetrahydrofuran
Enoate ester
Lactone
Carboxylic acid ester
Organoheterocyclic compound
Oxacycle
Acetal
Carboxylic acid derivative
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Organooxygen 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
logP	5.18	ChemAxon
pKa (Strongest Basic)	-6.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	78.9 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	130.73 m³·mol⁻¹	ChemAxon
Polarizability	55.67 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

10480824

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

21778224

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for [(1r,5as,5br,7ar,8r,11ar,11bs,13as,13br)-1-(acetyloxy)-5b,8,11a,13a-tetramethyl-3-oxo-1h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h,13bh-chryseno[1,2-c]furan-8-yl]methyl acetate (NP0329163)

MOL for NP0329163 ([(1r,5as,5br,7ar,8r,11ar,11bs,13as,13br)-1-(acetyloxy)-5b,8,11a,13a-tetramethyl-3-oxo-1h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h,13bh-chryseno[1,2-c]furan-8-yl]methyl acetate)

3D MOL for NP0329163 ([(1r,5as,5br,7ar,8r,11ar,11bs,13as,13br)-1-(acetyloxy)-5b,8,11a,13a-tetramethyl-3-oxo-1h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h,13bh-chryseno[1,2-c]furan-8-yl]methyl acetate)

3D SDF for NP0329163 ([(1r,5as,5br,7ar,8r,11ar,11bs,13as,13br)-1-(acetyloxy)-5b,8,11a,13a-tetramethyl-3-oxo-1h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h,13bh-chryseno[1,2-c]furan-8-yl]methyl acetate)

3D-SDF for NP0329163 ([(1r,5as,5br,7ar,8r,11ar,11bs,13as,13br)-1-(acetyloxy)-5b,8,11a,13a-tetramethyl-3-oxo-1h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h,13bh-chryseno[1,2-c]furan-8-yl]methyl acetate)

PDB for NP0329163 ([(1r,5as,5br,7ar,8r,11ar,11bs,13as,13br)-1-(acetyloxy)-5b,8,11a,13a-tetramethyl-3-oxo-1h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h,13bh-chryseno[1,2-c]furan-8-yl]methyl acetate)

3D PDB for NP0329163 ([(1r,5as,5br,7ar,8r,11ar,11bs,13as,13br)-1-(acetyloxy)-5b,8,11a,13a-tetramethyl-3-oxo-1h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h,13bh-chryseno[1,2-c]furan-8-yl]methyl acetate)

SMILES for NP0329163 ([(1r,5as,5br,7ar,8r,11ar,11bs,13as,13br)-1-(acetyloxy)-5b,8,11a,13a-tetramethyl-3-oxo-1h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h,13bh-chryseno[1,2-c]furan-8-yl]methyl acetate)

INCHI for NP0329163 ([(1r,5as,5br,7ar,8r,11ar,11bs,13as,13br)-1-(acetyloxy)-5b,8,11a,13a-tetramethyl-3-oxo-1h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h,13bh-chryseno[1,2-c]furan-8-yl]methyl acetate)

Structure for NP0329163 ([(1r,5as,5br,7ar,8r,11ar,11bs,13as,13br)-1-(acetyloxy)-5b,8,11a,13a-tetramethyl-3-oxo-1h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h,13bh-chryseno[1,2-c]furan-8-yl]methyl acetate)

3D Structure for NP0329163 ([(1r,5as,5br,7ar,8r,11ar,11bs,13as,13br)-1-(acetyloxy)-5b,8,11a,13a-tetramethyl-3-oxo-1h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h,13bh-chryseno[1,2-c]furan-8-yl]methyl acetate)