NP-MRD: Showing NP-Card for (1s,2s,3r,4r,5r,7s,8r,11s,12r,14z,17s)-12-(acetyloxy)-5,8,11,15-tetramethyl-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]octadec-14-en-4-yl butanoate (NP0231238)

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Record Information

Version

2.0

Created at

2022-09-06 12:00:10 UTC

Updated at

2022-09-06 12:00:11 UTC

NP-MRD ID

NP0231238

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2s,3r,4r,5r,7s,8r,11s,12r,14z,17s)-12-(acetyloxy)-5,8,11,15-tetramethyl-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]octadec-14-en-4-yl butanoate

Description

(1s,2s,3r,4r,5r,7s,8r,11s,12r,14z,17s)-12-(acetyloxy)-5,8,11,15-tetramethyl-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]octadec-14-en-4-yl butanoate is found in Briareum asbestinum.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062214002D          

 32 35  0  0  1  0            999 V2000
    3.5513    4.2655    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4216    3.4507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6512    3.1557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5215    2.3410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1622    1.8213    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7510    2.0459    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6213    1.2312    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2876    0.7227    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0473    1.0443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1889   -0.1102    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4300   -0.4731    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8134    0.0851    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0394   -0.1245    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1224    0.6387    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0165    1.3055    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8705    1.5913    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7097    1.3322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2145    1.9847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1583    0.6059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0074   -0.2246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3442   -0.7448    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6211   -1.5220    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4325   -1.6708    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7094   -2.4480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9671   -1.0425    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4870   -0.7613    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9402   -1.4507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1362   -1.5325    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6571   -1.7978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3524   -1.3253    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0632   -1.7440    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8354    0.9565    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  4  6  1  0  0  0  0
  7  6  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
  8 10  1  0  0  0  0
 11 10  1  1  0  0  0
 11 12  1  0  0  0  0
 12 13  1  6  0  0  0
 13 14  1  1  0  0  0
 15 14  1  6  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  6  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  2  0  0  0  0
 21 26  1  0  0  0  0
 13 26  1  0  0  0  0
 26 27  1  6  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 11 30  1  0  0  0  0
 30 31  1  1  0  0  0
 32 15  1  6  0  0  0
 12 32  1  0  0  0  0
  7 32  1  0  0  0  0
M  END

     RDKit          3D

 72 75  0  0  0  0  0  0  0  0999 V2000
    5.3065   -2.9304   -0.1014 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7509   -1.7752    0.7806 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5618   -0.9588    1.2468 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8076   -0.3852    0.1254 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0661   -0.5182   -1.0890 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7045    0.3794    0.3526 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8688    1.0022   -0.5662 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9008    2.4955   -0.5756 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3558    2.9110   -0.3205 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.9600    0.1187    1.2702 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3454   -1.0600    0.9936 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4152   -1.0107   -0.1103 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0385   -1.9412   -1.1670 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6651   -3.1960   -0.8256 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1309   -4.5030   -0.8394 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9456   -3.2077   -0.5075 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5084   -2.2392    0.3887 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7695   -0.8384   -0.0044 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.0551   -0.6343   -0.5590 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3455   -0.0490   -1.7538 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7118    0.1430   -2.2936 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3379    0.3296   -2.3876 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4956    0.0275    1.2071 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9529   -0.5533    2.4917 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8929    1.3471    0.9923 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3899    2.2337    1.8922 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3011    3.1256    1.3851 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7974    3.9640    0.2311 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4683    0.4400   -0.5924 C   0  0  2  0  0  0  0  0  0  0  0  0
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    5.7003   -3.9016    0.2647 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2011   -2.9841   -0.1756 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1924   -2.2282    1.6945 H   0  0  0  0  0  0  0  0  0  0  0  0
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    3.9428   -1.6365    1.8818 H   0  0  0  0  0  0  0  0  0  0  0  0
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    1.6854    2.8608   -1.6137 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7131    2.5114    0.6472 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4479    4.0191   -0.2520 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9929    2.6047   -1.1773 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3984    4.0192   -0.1685 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5809    3.7322    1.1064 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3678    2.0322    2.0018 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3905    1.4736   -0.3806 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6956    0.4027    2.3080 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4757   -1.2155    0.2434 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4691   -1.4244   -2.0853 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.7709   -4.4491   -1.7357 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5206   -5.3646   -0.9321 H   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0
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M  END


  Mrv1652309062214002D          

 32 35  0  0  1  0            999 V2000
    3.5513    4.2655    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.2876    0.7227    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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   -0.1224    0.6387    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.8705    1.5913    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  4  6  1  0  0  0  0
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 32 15  1  6  0  0  0
 12 32  1  0  0  0  0
  7 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0231238

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCC(=O)O[C@H]1[C@H]2[C@@H]3C\C(C)=C/C[C@@H](OC(C)=O)[C@]4(C)OC[C@H](C)[C@H](C[C@H]1C)[C@@H]2[C@@H]4O3

> <INCHI_IDENTIFIER>
InChI=1S/C26H40O6/c1-7-8-21(28)32-24-15(3)12-18-16(4)13-29-26(6)20(30-17(5)27)10-9-14(2)11-19-23(24)22(18)25(26)31-19/h9,15-16,18-20,22-25H,7-8,10-13H2,1-6H3/b14-9-/t15-,16+,18+,19?,20-,22+,23+,24-,25+,26+/m1/s1

> <INCHI_KEY>
GYTDPYQYARBTNQ-OTKHQYTRSA-N

> <FORMULA>
C26H40O6

> <MOLECULAR_WEIGHT>
448.6

> <EXACT_MASS>
448.282489008

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
72

> <JCHEM_AVERAGE_POLARIZABILITY>
50.11626896375817

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2S,3R,4R,5R,7S,8R,11S,12R,14Z,17S)-12-(acetyloxy)-5,8,11,15-tetramethyl-10,18-dioxatetracyclo[9.7.0.0^{2,7}.0^{3,17}]octadec-14-en-4-yl butanoate

> <JCHEM_LOGP>
3.8702712200000002

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-3.8969025085706197

> <JCHEM_POLAR_SURFACE_AREA>
71.06

> <JCHEM_REFRACTIVITY>
120.5547

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,3R,4R,5R,7S,8R,11S,12R,14Z,17S)-12-(acetyloxy)-5,8,11,15-tetramethyl-10,18-dioxatetracyclo[9.7.0.0^{2,7}.0^{3,17}]octadec-14-en-4-yl butanoate

> <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       6.629   7.962   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.387   6.441   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.949   5.891   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.707   4.370   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       5.903   3.400   0.000  0.00  0.00           O+0
HETATM    6  O   UNK     0       3.269   3.819   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       3.026   2.298   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.270   1.349   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.688   1.949   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.086  -0.206   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.669  -0.883   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.518   0.159   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.073  -0.232   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -0.228   1.192   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      -0.031   2.437   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.625   2.970   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -3.191   2.487   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -4.134   3.705   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -4.029   1.131   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -3.747  -0.419   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -2.509  -1.390   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -3.026  -2.841   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -4.541  -3.119   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -5.058  -4.570   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -5.539  -1.946   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      -0.909  -1.421   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -1.755  -2.708   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -0.254  -2.861   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       1.227  -3.356   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       2.524  -2.474   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       3.851  -3.256   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       1.559   1.786   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8   32                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   30                                                  
CONECT   12   11   13   32                                                  
CONECT   13   12   14   26                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   32                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   26                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23                                                            
CONECT   26   21   13   27   28                                             
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   11   31                                                  
CONECT   31   30                                                            
CONECT   32   15   12    7                                                  
MASTER        0    0    0    0    0    0    0    0   32    0   70    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₆H₄₀O₆

Average Mass

448.6000 Da

Monoisotopic Mass

448.28249 Da

IUPAC Name

(1S,2S,3R,4R,5R,7S,8R,11S,12R,14Z,17S)-12-(acetyloxy)-5,8,11,15-tetramethyl-10,18-dioxatetracyclo[9.7.0.0^{2,7}.0^{3,17}]octadec-14-en-4-yl butanoate

Traditional Name

(1S,2S,3R,4R,5R,7S,8R,11S,12R,14Z,17S)-12-(acetyloxy)-5,8,11,15-tetramethyl-10,18-dioxatetracyclo[9.7.0.0^{2,7}.0^{3,17}]octadec-14-en-4-yl butanoate

CAS Registry Number

Not Available

SMILES

CCCC(=O)O[C@H]1[C@H]2[C@@H]3C\C(C)=C/C[C@@H](OC(C)=O)[C@]4(C)OC[C@H](C)[C@H](C[C@H]1C)[C@@H]2[C@@H]4O3

InChI Identifier

InChI=1S/C26H40O6/c1-7-8-21(28)32-24-15(3)12-18-16(4)13-29-26(6)20(30-17(5)27)10-9-14(2)11-19-23(24)22(18)25(26)31-19/h9,15-16,18-20,22-25H,7-8,10-13H2,1-6H3/b14-9-/t15-,16+,18+,19?,20-,22+,23+,24-,25+,26+/m1/s1

InChI Key

GYTDPYQYARBTNQ-OTKHQYTRSA-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
Briareum asbestinum	LOTUS Database	35616633

Chemical Taxonomy

Classification

Not classified

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	3.87	ChemAxon
pKa (Strongest Basic)	-3.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	71.06 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	120.55 m³·mol⁻¹	ChemAxon
Polarizability	50.12 Å³	ChemAxon
Number of Rings	4	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

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,2s,3r,4r,5r,7s,8r,11s,12r,14z,17s)-12-(acetyloxy)-5,8,11,15-tetramethyl-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]octadec-14-en-4-yl butanoate (NP0231238)

MOL for NP0231238 ((1s,2s,3r,4r,5r,7s,8r,11s,12r,14z,17s)-12-(acetyloxy)-5,8,11,15-tetramethyl-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]octadec-14-en-4-yl butanoate)

3D MOL for NP0231238 ((1s,2s,3r,4r,5r,7s,8r,11s,12r,14z,17s)-12-(acetyloxy)-5,8,11,15-tetramethyl-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]octadec-14-en-4-yl butanoate)

3D SDF for NP0231238 ((1s,2s,3r,4r,5r,7s,8r,11s,12r,14z,17s)-12-(acetyloxy)-5,8,11,15-tetramethyl-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]octadec-14-en-4-yl butanoate)

3D-SDF for NP0231238 ((1s,2s,3r,4r,5r,7s,8r,11s,12r,14z,17s)-12-(acetyloxy)-5,8,11,15-tetramethyl-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]octadec-14-en-4-yl butanoate)

PDB for NP0231238 ((1s,2s,3r,4r,5r,7s,8r,11s,12r,14z,17s)-12-(acetyloxy)-5,8,11,15-tetramethyl-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]octadec-14-en-4-yl butanoate)

3D PDB for NP0231238 ((1s,2s,3r,4r,5r,7s,8r,11s,12r,14z,17s)-12-(acetyloxy)-5,8,11,15-tetramethyl-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]octadec-14-en-4-yl butanoate)

SMILES for NP0231238 ((1s,2s,3r,4r,5r,7s,8r,11s,12r,14z,17s)-12-(acetyloxy)-5,8,11,15-tetramethyl-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]octadec-14-en-4-yl butanoate)

INCHI for NP0231238 ((1s,2s,3r,4r,5r,7s,8r,11s,12r,14z,17s)-12-(acetyloxy)-5,8,11,15-tetramethyl-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]octadec-14-en-4-yl butanoate)

Structure for NP0231238 ((1s,2s,3r,4r,5r,7s,8r,11s,12r,14z,17s)-12-(acetyloxy)-5,8,11,15-tetramethyl-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]octadec-14-en-4-yl butanoate)

3D Structure for NP0231238 ((1s,2s,3r,4r,5r,7s,8r,11s,12r,14z,17s)-12-(acetyloxy)-5,8,11,15-tetramethyl-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]octadec-14-en-4-yl butanoate)