NP-MRD: Showing NP-Card for [(1r,3r,5s,8e,10s,12e,14r,15r)-10,14-dihydroxy-9,13-dimethyl-18-methylidene-17-oxo-4,16-dioxatricyclo[13.3.0.0³,⁵]octadeca-8,12-dien-5-yl]methyl acetate (NP0294346)

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Record Information

Version

2.0

Created at

2022-09-10 02:50:42 UTC

Updated at

2022-09-10 02:50:42 UTC

NP-MRD ID

NP0294346

Secondary Accession Numbers

None

Natural Product Identification

Common Name

[(1r,3r,5s,8e,10s,12e,14r,15r)-10,14-dihydroxy-9,13-dimethyl-18-methylidene-17-oxo-4,16-dioxatricyclo[13.3.0.0³,⁵]octadeca-8,12-dien-5-yl]methyl acetate

Description

Zurumolide A belongs to the class of organic compounds known as macrolides and analogues. These are organic compounds containing a lactone ring of at least twelve members. Based on a literature review very few articles have been published on Zurumolide A.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102204502D          

 29 31  0  0  1  0            999 V2000
    2.5813    0.6647    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9697    1.3925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7868    1.5061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3590    0.9118    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9313    2.3184    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2035    2.7068    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6092    2.1346    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8254    1.8769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0075    1.9849    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2710    1.6133    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3174    2.4370    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4834    2.2386    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0556    2.8329    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8563    2.6345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4285    3.2289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0850    1.8418    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1082    3.1437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1850    3.9651    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4094    4.5373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6966    5.3107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1244    5.9050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4803    5.5684    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4035    6.3898    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2982    5.4605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7238    4.7537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4139    4.3016    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1207    4.7272    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4907    3.4802    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3086    3.3723    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  6  5  1  6  0  0  0
  6  7  1  0  0  0  0
  7  2  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  1  0  0  0
 10 11  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  2  0  0  0  0
 11 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  1  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
  6 28  1  0  0  0  0
 28 29  1  1  0  0  0
M  END

     RDKit          3D

 59 61  0  0  0  0  0  0  0  0999 V2000
    0.3387   -4.4482    1.5371 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5401   -3.7906    0.8023 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6949   -4.3644    0.1244 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9566   -5.6034    0.0636 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4586   -3.3285   -0.4425 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7587   -2.1042   -0.3370 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5443   -2.3570    0.5128 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6775   -1.9256   -0.2950 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8914   -0.4631    0.0058 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8305   -0.2746    1.0437 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0816    0.1655   -0.2503 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1818   -0.4514   -1.0677 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4050   -0.2530   -0.3810 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6086   -0.7086   -0.8794 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8804   -0.4714   -0.1096 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6186   -1.3150   -1.9709 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9670    1.6662   -0.3981 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0819    2.2602    0.6888 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0644    3.1107    0.0458 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2088    3.2113    0.3801 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1240    4.1396   -0.3905 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8452    2.4709    1.4823 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2503    3.3911    2.4821 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0941    1.7247    1.0925 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1046    1.2612   -0.3181 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8779    0.0074   -0.6860 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9085   -0.3756   -2.1442 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5916   -1.0354    0.3378 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.7788   -1.5831    0.8355 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2842   -5.5138    1.7127 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1644   -3.9234    1.9989 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4761   -1.8282   -1.3836 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5479   -1.7669    1.4536 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4866   -2.0743   -1.3901 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5453   -2.5577   -0.0447 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0815    0.0994    0.0729 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2252    0.1017   -2.0273 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0033   -1.5094   -1.3154 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3873    0.3704   -0.6071 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4707   -1.4001   -0.1270 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6035   -0.2186    0.9526 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9957    2.0787   -0.3819 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5587    1.9009   -1.4033 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7786    2.8694    1.3389 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6913    1.4786    1.3559 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3996    3.7311   -0.8071 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1424    4.1371   -0.0145 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7328    5.1820   -0.2227 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0130    3.9729   -1.4787 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1793    1.7713    2.0116 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0841    3.8216    2.1382 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2924    0.8963    1.7865 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9729    2.4252    1.1883 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3122    2.0012   -1.0827 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6642    0.2681   -2.6853 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2633   -1.3979   -2.2533 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9209   -0.2778   -2.6216 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0599   -0.6185    1.2127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7418   -2.5748    0.8594 H   0  0  0  0  0  0  0  0  0  0  0  0
 15 14  1  0
 14 16  2  0
 14 13  1  0
 13 12  1  0
 11 12  1  6
 11 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 22 24  1  0
 24 25  1  0
 25 26  2  0
 26 27  1  0
 26 28  1  0
 28 29  1  0
 28  6  1  0
  6  5  1  0
  5  3  1  0
  3  4  2  0
  3  2  1  0
  2  1  2  3
  2  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
  9 11  1  0
 10 11  1  0
  7  6  1  0
 15 39  1  0
 15 40  1  0
 15 41  1  0
 12 37  1  0
 12 38  1  0
 17 42  1  0
 17 43  1  0
 18 44  1  0
 18 45  1  0
 19 46  1  0
 21 47  1  0
 21 48  1  0
 21 49  1  0
 22 50  1  1
 23 51  1  0
 24 52  1  0
 24 53  1  0
 25 54  1  0
 27 55  1  0
 27 56  1  0
 27 57  1  0
 28 58  1  1
 29 59  1  0
  6 32  1  6
  1 30  1  0
  1 31  1  0
  7 33  1  1
  8 34  1  0
  8 35  1  0
  9 36  1  1
M  END


  Mrv1652309102204502D          

 29 31  0  0  1  0            999 V2000
    2.5813    0.6647    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9697    1.3925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7868    1.5061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3590    0.9118    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9313    2.3184    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2035    2.7068    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6092    2.1346    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8254    1.8769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0075    1.9849    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2710    1.6133    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3174    2.4370    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4834    2.2386    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0556    2.8329    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8563    2.6345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4285    3.2289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0850    1.8418    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1082    3.1437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1850    3.9651    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4094    4.5373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6966    5.3107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1244    5.9050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4803    5.5684    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4035    6.3898    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2982    5.4605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7238    4.7537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4139    4.3016    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1207    4.7272    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4907    3.4802    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3086    3.3723    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  6  5  1  6  0  0  0
  6  7  1  0  0  0  0
  7  2  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  1  0  0  0
 10 11  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  2  0  0  0  0
 11 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  1  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
  6 28  1  0  0  0  0
 28 29  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0294346

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OC[C@@]12CC\C=C(C)\[C@@H](O)C\C=C(C)\[C@@H](O)[C@@H]3OC(=O)C(=C)[C@H]3C[C@H]1O2

> <INCHI_IDENTIFIER>
InChI=1S/C22H30O7/c1-12-6-5-9-22(11-27-15(4)23)18(29-22)10-16-14(3)21(26)28-20(16)19(25)13(2)7-8-17(12)24/h6-7,16-20,24-25H,3,5,8-11H2,1-2,4H3/b12-6+,13-7+/t16-,17+,18-,19-,20-,22+/m1/s1

> <INCHI_KEY>
SBTZVNIBVMVSSU-FZQNJNHXSA-N

> <FORMULA>
C22H30O7

> <MOLECULAR_WEIGHT>
406.475

> <EXACT_MASS>
406.199153306

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
42.42536097223699

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
[(1R,3R,5S,8E,10S,12E,14R,15R)-10,14-dihydroxy-9,13-dimethyl-18-methylidene-17-oxo-4,16-dioxatricyclo[13.3.0.0^{3,5}]octadeca-8,12-dien-5-yl]methyl acetate

> <JCHEM_LOGP>
1.663600183000001

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
18.181760315278492

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.580462615686933

> <JCHEM_PKA_STRONGEST_BASIC>
-1.4064632552640393

> <JCHEM_POLAR_SURFACE_AREA>
105.59

> <JCHEM_REFRACTIVITY>
106.0817

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
[(1R,3R,5S,8E,10S,12E,14R,15R)-10,14-dihydroxy-9,13-dimethyl-18-methylidene-17-oxo-4,16-dioxatricyclo[13.3.0.0^{3,5}]octadeca-8,12-dien-5-yl]methyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0       4.818   1.241   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.543   2.599   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.069   2.811   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       8.137   1.702   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0       7.339   4.328   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       5.980   5.053   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.870   3.985   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.407   3.504   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.881   3.705   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       0.506   3.011   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       0.593   4.549   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.902   4.179   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -1.970   5.288   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -3.465   4.918   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -4.533   6.027   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -3.892   3.438   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -0.202   5.868   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -0.345   7.402   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.764   8.470   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.300   9.913   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.232  11.023   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.763  10.394   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       2.620  11.928   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       4.290  10.193   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.084   8.874   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.373   8.030   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       7.692   8.824   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       6.516   6.496   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       8.043   6.295   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    7                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7   28                                                  
CONECT    7    6    2    8                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9   11                                                       
CONECT   11   10    9   12   17                                             
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14                                                            
CONECT   17   11   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26    6   29                                                  
CONECT   29   28                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   62    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₃₀O₇

Average Mass

406.4750 Da

Monoisotopic Mass

406.19915 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(=O)OC[C@@]12CC\C=C(C)\[C@@H](O)C\C=C(C)\[C@@H](O)[C@@H]3OC(=O)C(=C)[C@H]3C[C@H]1O2

InChI Identifier

InChI=1S/C22H30O7/c1-12-6-5-9-22(11-27-15(4)23)18(29-22)10-16-14(3)21(26)28-20(16)19(25)13(2)7-8-17(12)24/h6-7,16-20,24-25H,3,5,8-11H2,1-2,4H3/b12-6+,13-7+/t16-,17+,18-,19-,20-,22+/m1/s1

InChI Key

SBTZVNIBVMVSSU-FZQNJNHXSA-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 macrolides and analogues. These are organic compounds containing a lactone ring of at least twelve members.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Macrolides and analogues

Sub Class

Not Available

Direct Parent

Macrolides and analogues

Alternative Parents

Substituents

Macrolide
Dicarboxylic acid or derivatives
Gamma butyrolactone
Tetrahydrofuran
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Secondary alcohol
Lactone
Carboxylic acid ester
Ether
Oxirane
Dialkyl ether
Carboxylic acid derivative
Organoheterocyclic compound
Oxacycle
Alcohol
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen 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

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

27023372

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

25112768

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for [(1r,3r,5s,8e,10s,12e,14r,15r)-10,14-dihydroxy-9,13-dimethyl-18-methylidene-17-oxo-4,16-dioxatricyclo[13.3.0.0³,⁵]octadeca-8,12-dien-5-yl]methyl acetate (NP0294346)

MOL for NP0294346 ([(1r,3r,5s,8e,10s,12e,14r,15r)-10,14-dihydroxy-9,13-dimethyl-18-methylidene-17-oxo-4,16-dioxatricyclo[13.3.0.0³,⁵]octadeca-8,12-dien-5-yl]methyl acetate)

3D MOL for NP0294346 ([(1r,3r,5s,8e,10s,12e,14r,15r)-10,14-dihydroxy-9,13-dimethyl-18-methylidene-17-oxo-4,16-dioxatricyclo[13.3.0.0³,⁵]octadeca-8,12-dien-5-yl]methyl acetate)

3D SDF for NP0294346 ([(1r,3r,5s,8e,10s,12e,14r,15r)-10,14-dihydroxy-9,13-dimethyl-18-methylidene-17-oxo-4,16-dioxatricyclo[13.3.0.0³,⁵]octadeca-8,12-dien-5-yl]methyl acetate)

3D-SDF for NP0294346 ([(1r,3r,5s,8e,10s,12e,14r,15r)-10,14-dihydroxy-9,13-dimethyl-18-methylidene-17-oxo-4,16-dioxatricyclo[13.3.0.0³,⁵]octadeca-8,12-dien-5-yl]methyl acetate)

PDB for NP0294346 ([(1r,3r,5s,8e,10s,12e,14r,15r)-10,14-dihydroxy-9,13-dimethyl-18-methylidene-17-oxo-4,16-dioxatricyclo[13.3.0.0³,⁵]octadeca-8,12-dien-5-yl]methyl acetate)

3D PDB for NP0294346 ([(1r,3r,5s,8e,10s,12e,14r,15r)-10,14-dihydroxy-9,13-dimethyl-18-methylidene-17-oxo-4,16-dioxatricyclo[13.3.0.0³,⁵]octadeca-8,12-dien-5-yl]methyl acetate)

SMILES for NP0294346 ([(1r,3r,5s,8e,10s,12e,14r,15r)-10,14-dihydroxy-9,13-dimethyl-18-methylidene-17-oxo-4,16-dioxatricyclo[13.3.0.0³,⁵]octadeca-8,12-dien-5-yl]methyl acetate)

INCHI for NP0294346 ([(1r,3r,5s,8e,10s,12e,14r,15r)-10,14-dihydroxy-9,13-dimethyl-18-methylidene-17-oxo-4,16-dioxatricyclo[13.3.0.0³,⁵]octadeca-8,12-dien-5-yl]methyl acetate)

Structure for NP0294346 ([(1r,3r,5s,8e,10s,12e,14r,15r)-10,14-dihydroxy-9,13-dimethyl-18-methylidene-17-oxo-4,16-dioxatricyclo[13.3.0.0³,⁵]octadeca-8,12-dien-5-yl]methyl acetate)

3D Structure for NP0294346 ([(1r,3r,5s,8e,10s,12e,14r,15r)-10,14-dihydroxy-9,13-dimethyl-18-methylidene-17-oxo-4,16-dioxatricyclo[13.3.0.0³,⁵]octadeca-8,12-dien-5-yl]methyl acetate)