NP-MRD: Showing NP-Card for (1r,4r,5s,7r,10r,11s,13r,18s)-5,10,16-trimethyl-14,19-dioxahexacyclo[9.8.0.0¹,¹⁸.0⁴,¹⁰.0⁵,⁷.0¹³,¹⁷]nonadec-16-en-15-one (NP0257791)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-07 23:00:58 UTC

Updated at

2022-09-07 23:00:58 UTC

NP-MRD ID

NP0257791

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,4r,5s,7r,10r,11s,13r,18s)-5,10,16-trimethyl-14,19-dioxahexacyclo[9.8.0.0¹,¹⁸.0⁴,¹⁰.0⁵,⁷.0¹³,¹⁷]nonadec-16-en-15-one

Description

Suregadolide B belongs to the class of organic compounds known as naphthofurans. Naphthofurans are compounds containing a furan ring fused to a naphthalene moiety. Furan is a 5 membered- ring aromatic ring with four carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings. (1r,4r,5s,7r,10r,11s,13r,18s)-5,10,16-trimethyl-14,19-dioxahexacyclo[9.8.0.0¹,¹⁸.0⁴,¹⁰.0⁵,⁷.0¹³,¹⁷]nonadec-16-en-15-one is found in Suregada multiflora. Based on a literature review very few articles have been published on Suregadolide B.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 49 54  0  0  0  0  0  0  0  0999 V2000
    5.4867    0.3126   -1.0066 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4847   -0.5130   -0.2594 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3271   -0.1434    0.2323 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5895    1.1182    0.2563 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7090    1.2802    1.4673 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1674    0.9631    0.2548 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3862    2.0190   -0.5313 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0779    1.9905   -0.1593 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6061    0.6350   -0.5034 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0749    0.6100   -0.4140 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.7613    1.9644   -0.1935 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8582   -0.2819   -1.3613 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7377   -0.5418    0.1357 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9311   -1.7160    0.5296 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5264   -1.7263    0.0280 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8992   -0.3909    0.3476 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0840   -0.1011    1.8002 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5808   -0.3594   -0.0648 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3048   -1.5621    0.4276 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7146   -1.3085    0.8870 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5827   -2.3550    0.6954 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6970   -1.9278    0.0126 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7232   -2.6033   -0.3290 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6790   -0.2295   -1.9534 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4622    0.3518   -0.4539 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1405    1.3442   -1.1495 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0562    2.0712    0.0110 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5382    1.9009   -1.6122 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7902    3.0046   -0.2362 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5876    2.7296   -0.8015 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1783    2.2563    0.8993 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3050    0.4223   -1.5651 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7966    1.8018    0.1994 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8245    2.5431   -1.1348 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1959    2.4693    0.6043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3020   -0.9451   -2.0510 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8242    0.0487   -1.7536 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6831   -0.4042    0.6954 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4528   -2.6384    0.1388 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9739   -1.8247    1.6429 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0016   -2.5877    0.4292 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5572   -1.8171   -1.0783 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8570   -0.9425    2.4585 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1476    0.1675    1.9610 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4907    0.7648    2.1570 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5446   -0.4421   -1.1929 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3587   -2.3675   -0.3434 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7528   -2.0048    1.2820 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6587   -1.0345    1.9827 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  6  5  1  1
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  1
 10 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  1
 16 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  2  0
 22  2  1  0
 20  3  1  0
  6  4  1  0
 18  6  1  0
 16  9  1  0
 13 10  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  4 27  1  6
  7 28  1  0
  7 29  1  0
  8 30  1  0
  8 31  1  0
  9 32  1  6
 11 33  1  0
 11 34  1  0
 11 35  1  0
 12 36  1  0
 12 37  1  0
 13 38  1  1
 14 39  1  0
 14 40  1  0
 15 41  1  0
 15 42  1  0
 17 43  1  0
 17 44  1  0
 17 45  1  0
 18 46  1  6
 19 47  1  0
 19 48  1  0
 20 49  1  1
M  END


  Mrv1652309082201002D          

 23 28  0  0  1  0            999 V2000
    0.5066    0.5710    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9654   -0.1147    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7897   -0.1466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3651    0.4447    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9404    1.0360    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1648    0.2421    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7402    0.8334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5399    0.6307    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7643   -0.1632    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.5640   -0.3658    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7666    0.4340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3637   -0.5684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7884   -1.1597    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2131   -1.7509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4133   -1.5483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1889   -0.7544    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6136   -1.3457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3892   -0.5518    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8139   -1.1431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0141   -0.9405    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3284   -1.3992    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6803   -0.8888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1136   -1.1132    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  6  0  0  0
  6  5  1  6  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  9  8  1  6  0  0  0
  9 10  1  0  0  0  0
 10 11  1  6  0  0  0
 10 12  1  0  0  0  0
 13 12  1  1  0  0  0
 10 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
  9 16  1  0  0  0  0
 16 17  1  6  0  0  0
 16 18  1  0  0  0  0
  6 18  1  0  0  0  0
 18 19  1  6  0  0  0
 19 20  1  0  0  0  0
  3 20  1  0  0  0  0
 20 21  1  1  0  0  0
 21 22  1  0  0  0  0
  2 22  1  0  0  0  0
 22 23  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0257791

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1=C2[C@@H]3O[C@@]33CC[C@@H]4[C@@]5(C)C[C@H]5CC[C@@]4(C)[C@@H]3C[C@H]2OC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C20H26O3/c1-10-15-12(22-17(10)21)8-14-18(2)6-4-11-9-19(11,3)13(18)5-7-20(14)16(15)23-20/h11-14,16H,4-9H2,1-3H3/t11-,12-,13+,14+,16+,18-,19+,20-/m1/s1

> <INCHI_KEY>
XLQPKIPZCCDQMM-GRLXCJONSA-N

> <FORMULA>
C20H26O3

> <MOLECULAR_WEIGHT>
314.425

> <EXACT_MASS>
314.188194697

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
49

> <JCHEM_AVERAGE_POLARIZABILITY>
35.58074548123242

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,4R,5S,7R,10R,11S,13R,18S)-5,10,16-trimethyl-14,19-dioxahexacyclo[9.8.0.0^{1,18}.0^{4,10}.0^{5,7}.0^{13,17}]nonadec-16-en-15-one

> <JCHEM_LOGP>
3.3656585669999997

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.097394422969654

> <JCHEM_PKA_STRONGEST_BASIC>
-4.2603642084068865

> <JCHEM_POLAR_SURFACE_AREA>
38.83

> <JCHEM_REFRACTIVITY>
85.56879999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,4R,5S,7R,10R,11S,13R,18S)-5,10,16-trimethyl-14,19-dioxahexacyclo[9.8.0.0^{1,18}.0^{4,10}.0^{5,7}.0^{13,17}]nonadec-16-en-15-one

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0       0.946   1.066   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.802  -0.214   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.341  -0.274   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.415   0.830   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       5.489   1.934   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       5.908   0.452   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.982   1.556   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.474   1.177   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.893  -0.305   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.386  -0.683   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.764   0.810   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      11.879  -1.061   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.805  -2.165   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.731  -3.268   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.238  -2.890   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.819  -1.408   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.745  -2.512   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.327  -1.030   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.253  -2.134   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.760  -1.756   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       2.480  -2.612   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       1.270  -1.659   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -0.212  -2.078   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   22                                                  
CONECT    3    2    4   20                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4    6                                                       
CONECT    6    5    4    7   18                                             
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   16                                                  
CONECT   10    9   11   12   13                                             
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   10   14                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15    9   17   18                                             
CONECT   17   16                                                            
CONECT   18   16    6   19                                                  
CONECT   19   18   20                                                       
CONECT   20   19    3   21                                                  
CONECT   21   20   22                                                       
CONECT   22   21    2   23                                                  
CONECT   23   22                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   56    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₂₆O₃

Average Mass

314.4250 Da

Monoisotopic Mass

314.18819 Da

IUPAC Name

(1R,4R,5S,7R,10R,11S,13R,18S)-5,10,16-trimethyl-14,19-dioxahexacyclo[9.8.0.0^{1,18}.0^{4,10}.0^{5,7}.0^{13,17}]nonadec-16-en-15-one

Traditional Name

(1R,4R,5S,7R,10R,11S,13R,18S)-5,10,16-trimethyl-14,19-dioxahexacyclo[9.8.0.0^{1,18}.0^{4,10}.0^{5,7}.0^{13,17}]nonadec-16-en-15-one

CAS Registry Number

Not Available

SMILES

CC1=C2[C@@H]3O[C@@]33CC[C@@H]4[C@@]5(C)C[C@H]5CC[C@@]4(C)[C@@H]3C[C@H]2OC1=O

InChI Identifier

InChI=1S/C20H26O3/c1-10-15-12(22-17(10)21)8-14-18(2)6-4-11-9-19(11,3)13(18)5-7-20(14)16(15)23-20/h11-14,16H,4-9H2,1-3H3/t11-,12-,13+,14+,16+,18-,19+,20-/m1/s1

InChI Key

XLQPKIPZCCDQMM-GRLXCJONSA-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
Suregada multiflora	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as naphthofurans. Naphthofurans are compounds containing a furan ring fused to a naphthalene moiety. Furan is a 5 membered- ring aromatic ring with four carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Naphthofurans

Sub Class

Not Available

Direct Parent

Naphthofurans

Alternative Parents

Substituents

Naphthofuran
Oxepane
2-furanone
Dihydrofuran
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Carboxylic acid ester
Lactone
Carboxylic acid derivative
Dialkyl ether
Oxirane
Ether
Oxacycle
Monocarboxylic acid or derivatives
Hydrocarbon derivative
Carbonyl group
Organic oxide
Organic oxygen compound
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	3.37	ChemAxon
pKa (Strongest Acidic)	12.1	ChemAxon
pKa (Strongest Basic)	-4.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	38.83 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	85.57 m³·mol⁻¹	ChemAxon
Polarizability	35.58 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	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

C00046442

Chemspider ID

9078389

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10903129

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,4r,5s,7r,10r,11s,13r,18s)-5,10,16-trimethyl-14,19-dioxahexacyclo[9.8.0.0¹,¹⁸.0⁴,¹⁰.0⁵,⁷.0¹³,¹⁷]nonadec-16-en-15-one (NP0257791)

MOL for NP0257791 ((1r,4r,5s,7r,10r,11s,13r,18s)-5,10,16-trimethyl-14,19-dioxahexacyclo[9.8.0.0¹,¹⁸.0⁴,¹⁰.0⁵,⁷.0¹³,¹⁷]nonadec-16-en-15-one)

3D MOL for NP0257791 ((1r,4r,5s,7r,10r,11s,13r,18s)-5,10,16-trimethyl-14,19-dioxahexacyclo[9.8.0.0¹,¹⁸.0⁴,¹⁰.0⁵,⁷.0¹³,¹⁷]nonadec-16-en-15-one)

3D SDF for NP0257791 ((1r,4r,5s,7r,10r,11s,13r,18s)-5,10,16-trimethyl-14,19-dioxahexacyclo[9.8.0.0¹,¹⁸.0⁴,¹⁰.0⁵,⁷.0¹³,¹⁷]nonadec-16-en-15-one)

3D-SDF for NP0257791 ((1r,4r,5s,7r,10r,11s,13r,18s)-5,10,16-trimethyl-14,19-dioxahexacyclo[9.8.0.0¹,¹⁸.0⁴,¹⁰.0⁵,⁷.0¹³,¹⁷]nonadec-16-en-15-one)

PDB for NP0257791 ((1r,4r,5s,7r,10r,11s,13r,18s)-5,10,16-trimethyl-14,19-dioxahexacyclo[9.8.0.0¹,¹⁸.0⁴,¹⁰.0⁵,⁷.0¹³,¹⁷]nonadec-16-en-15-one)

3D PDB for NP0257791 ((1r,4r,5s,7r,10r,11s,13r,18s)-5,10,16-trimethyl-14,19-dioxahexacyclo[9.8.0.0¹,¹⁸.0⁴,¹⁰.0⁵,⁷.0¹³,¹⁷]nonadec-16-en-15-one)

SMILES for NP0257791 ((1r,4r,5s,7r,10r,11s,13r,18s)-5,10,16-trimethyl-14,19-dioxahexacyclo[9.8.0.0¹,¹⁸.0⁴,¹⁰.0⁵,⁷.0¹³,¹⁷]nonadec-16-en-15-one)

INCHI for NP0257791 ((1r,4r,5s,7r,10r,11s,13r,18s)-5,10,16-trimethyl-14,19-dioxahexacyclo[9.8.0.0¹,¹⁸.0⁴,¹⁰.0⁵,⁷.0¹³,¹⁷]nonadec-16-en-15-one)

Structure for NP0257791 ((1r,4r,5s,7r,10r,11s,13r,18s)-5,10,16-trimethyl-14,19-dioxahexacyclo[9.8.0.0¹,¹⁸.0⁴,¹⁰.0⁵,⁷.0¹³,¹⁷]nonadec-16-en-15-one)

3D Structure for NP0257791 ((1r,4r,5s,7r,10r,11s,13r,18s)-5,10,16-trimethyl-14,19-dioxahexacyclo[9.8.0.0¹,¹⁸.0⁴,¹⁰.0⁵,⁷.0¹³,¹⁷]nonadec-16-en-15-one)