NP-MRD: Showing NP-Card for 4-ethylidene-7-hydroxy-7-(hydroxymethyl)-6,14-dimethyl-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-ene-3,8,17-trione (NP0237181)

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Record Information

Version

2.0

Created at

2022-09-06 20:14:51 UTC

Updated at

2022-09-06 20:14:51 UTC

NP-MRD ID

NP0237181

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4-ethylidene-7-hydroxy-7-(hydroxymethyl)-6,14-dimethyl-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-ene-3,8,17-trione

Description

4-Ethylidene-7-hydroxy-7-(hydroxymethyl)-6,14-dimethyl-2,9-dioxa-14-azabicyclo[9.5.1]Heptadec-11-ene-3,8,17-trione 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. 4-ethylidene-7-hydroxy-7-(hydroxymethyl)-6,14-dimethyl-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-ene-3,8,17-trione is found in Crotalaria laburnifolia and Tephroseris integrifolia. 4-Ethylidene-7-hydroxy-7-(hydroxymethyl)-6,14-dimethyl-2,9-dioxa-14-azabicyclo[9.5.1]Heptadec-11-ene-3,8,17-trione is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004261500392D          

 27 28  0  0  0  0            999 V2000
    6.7515    0.4339    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9266    0.4215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5249   -0.2991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3498   -0.2867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7730   -0.9949    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5979   -0.9825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3712   -1.7155    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2402   -2.5300    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1506   -1.9860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3061   -2.7962    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5463   -1.7278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1232   -1.0196    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1446   -2.4484    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3197   -2.4608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8965   -1.7526    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1392   -2.0797    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3723   -1.7755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0452   -1.0181    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2203   -1.0305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3494   -0.2512    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1068    0.0759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8751   -0.3238    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2768    0.3968    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1017    0.4091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5035    1.1297    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2983   -1.0320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9583   -0.5371    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  4  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
  7 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  4  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
  3 24  1  0  0  0  0
 24 25  2  0  0  0  0
 22 26  1  0  0  0  0
 15 26  1  0  0  0  0
 26 27  2  0  0  0  0
M  END

     RDKit          3D

 54 55  0  0  0  0  0  0  0  0999 V2000
   -3.2635    3.8152   -0.5526 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1109    2.3733   -0.8270 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9553    1.7042   -0.6895 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0425    0.2621   -1.0225 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7856   -0.5192    0.0374 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6320    0.1210    1.4134 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4285   -1.9805    0.0857 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1387   -2.3785    1.3974 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6554   -2.7862   -0.3657 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3652   -4.1553   -0.3191 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3339   -2.3730   -0.8342 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6080   -2.4043   -2.0644 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0434   -2.6981   -0.3598 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6677   -1.8899    0.5124 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7351   -1.0303   -0.0269 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8403   -1.5307    0.5812 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1440   -0.9474    1.0968 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3572    0.2346    0.3430 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.1697    0.1273   -0.8048 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8515    1.4555    0.7203 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4012    1.7332    0.7339 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6619    1.5941   -0.5512 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4571    2.1699   -0.7109 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7455    2.3962   -0.2383 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0283    3.2571    0.6842 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6470    0.0974   -0.9079 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5382    0.0263   -2.1801 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0686    4.2069   -1.2022 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3325    4.3368   -0.9198 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4566    4.0384    0.5130 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9775    1.8336   -1.1540 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6161    0.2233   -2.0020 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1193   -0.2510   -1.2101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8802   -0.3859   -0.2113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6206    0.5526    1.5573 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7557   -0.6973    2.1486 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4378    0.8561    1.6175 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4392   -3.3172    1.5032 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5489   -2.5300    0.2167 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8660   -2.5450   -1.4275 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3677   -4.3006   -0.2886 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1116   -1.2639    1.0640 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0345   -2.5629    1.3246 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8057   -2.5820    0.7524 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1934   -0.8717    2.1751 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9181   -1.7003    0.7792 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2510    0.0237   -0.6297 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8641   -0.7052   -1.4892 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0370    1.0571   -1.4191 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3550    2.2581    0.0956 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2264    1.7053    1.7614 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9428    1.1341    1.5593 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2690    2.8004    1.0699 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3671    2.0126   -1.3351 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
  5  6  1  0
  5  7  1  0
  7  8  1  1
  7  9  1  0
  9 10  1  0
  7 11  1  0
 11 12  2  0
 11 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  2  0
 22 26  1  0
 26 27  2  0
 24  3  1  0
 26 15  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  2 31  1  0
  4 32  1  0
  4 33  1  0
  5 34  1  6
  6 35  1  0
  6 36  1  0
  6 37  1  0
  8 38  1  0
  9 39  1  0
  9 40  1  0
 10 41  1  0
 14 42  1  0
 14 43  1  0
 16 44  1  0
 17 45  1  0
 17 46  1  0
 19 47  1  0
 19 48  1  0
 19 49  1  0
 20 50  1  0
 20 51  1  0
 21 52  1  0
 21 53  1  0
 22 54  1  6
M  END


  Mrv1533004261500392D          

 27 28  0  0  0  0            999 V2000
    6.7515    0.4339    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9266    0.4215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5249   -0.2991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3498   -0.2867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7730   -0.9949    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5979   -0.9825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3712   -1.7155    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2402   -2.5300    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1506   -1.9860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3061   -2.7962    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5463   -1.7278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1232   -1.0196    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1446   -2.4484    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3197   -2.4608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8965   -1.7526    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1392   -2.0797    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3723   -1.7755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0452   -1.0181    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2203   -1.0305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3494   -0.2512    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1068    0.0759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8751   -0.3238    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2768    0.3968    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1017    0.4091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5035    1.1297    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2983   -1.0320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9583   -0.5371    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  4  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
  7 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  4  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
  3 24  1  0  0  0  0
 24 25  2  0  0  0  0
 22 26  1  0  0  0  0
 15 26  1  0  0  0  0
 26 27  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0237181

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC=C1CC(C)C(O)(CO)C(=O)OCC2=CCN(C)CCC(OC1=O)C2=O

> <INCHI_IDENTIFIER>
InChI=1S/C19H27NO7/c1-4-13-9-12(2)19(25,11-21)18(24)26-10-14-5-7-20(3)8-6-15(16(14)22)27-17(13)23/h4-5,12,15,21,25H,6-11H2,1-3H3

> <INCHI_KEY>
FKDPVQYTQVJUGD-UHFFFAOYSA-N

> <FORMULA>
C19H27NO7

> <MOLECULAR_WEIGHT>
381.425

> <EXACT_MASS>
381.178752213

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
38.98617696637709

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-ethylidene-7-hydroxy-7-(hydroxymethyl)-6,14-dimethyl-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-ene-3,8,17-trione

> <ALOGPS_LOGP>
0.66

> <JCHEM_LOGP>
0.8457409719999994

> <ALOGPS_LOGS>
-1.76

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
14.957199841509116

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.442648707153094

> <JCHEM_PKA_STRONGEST_BASIC>
6.95928554013673

> <JCHEM_POLAR_SURFACE_AREA>
113.37

> <JCHEM_REFRACTIVITY>
98.51999999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.65e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-ethylidene-7-hydroxy-7-(hydroxymethyl)-6,14-dimethyl-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-ene-3,8,17-trione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 26-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   26-APR-15         0                                  
HETATM    1  C   UNK     0      12.603   0.810   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      11.063   0.787   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      10.313  -0.558   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.853  -0.535   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      12.643  -1.857   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      14.183  -1.834   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      11.893  -3.202   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      11.648  -4.723   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      13.348  -3.707   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      13.638  -5.220   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      10.353  -3.225   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       9.563  -1.903   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0       9.603  -4.570   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       8.063  -4.593   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.274  -3.272   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.860  -3.882   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.428  -3.314   0.000  0.00  0.00           C+0
HETATM   18  N   UNK     0       3.818  -1.900   0.000  0.00  0.00           N+0
HETATM   19  C   UNK     0       2.278  -1.924   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.386  -0.469   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.799   0.142   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.233  -0.604   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       7.983   0.741   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       9.523   0.764   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      10.273   2.109   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       8.023  -1.926   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       9.256  -1.003   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   24                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8    9   11                                             
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9                                                            
CONECT   11    7   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   26                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   26                                                  
CONECT   23   22   24                                                       
CONECT   24   23    3   25                                                  
CONECT   25   24                                                            
CONECT   26   22   15   27                                                  
CONECT   27   26                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   56    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₂₇NO₇

Average Mass

381.4250 Da

Monoisotopic Mass

381.17875 Da

IUPAC Name

4-ethylidene-7-hydroxy-7-(hydroxymethyl)-6,14-dimethyl-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-ene-3,8,17-trione

Traditional Name

4-ethylidene-7-hydroxy-7-(hydroxymethyl)-6,14-dimethyl-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-ene-3,8,17-trione

CAS Registry Number

Not Available

SMILES

CC=C1CC(C)C(O)(CO)C(=O)OCC2=CCN(C)CCC(OC1=O)C2=O

InChI Identifier

InChI=1S/C19H27NO7/c1-4-13-9-12(2)19(25,11-21)18(24)26-10-14-5-7-20(3)8-6-15(16(14)22)27-17(13)23/h4-5,12,15,21,25H,6-11H2,1-3H3

InChI Key

FKDPVQYTQVJUGD-UHFFFAOYSA-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
Crotalaria laburnifolia	LOTUS Database	35616633
Tephroseris integrifolia	LOTUS Database	35616633

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
Alpha-acyloxy ketone
Dicarboxylic acid or derivatives
Tertiary alcohol
Alpha,beta-unsaturated carboxylic ester
Enoate ester
1,2-diol
Amino acid or derivatives
Carboxylic acid ester
Ketone
Lactone
Tertiary aliphatic amine
Tertiary amine
Carboxylic acid derivative
Oxacycle
Azacycle
Organoheterocyclic compound
Alcohol
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Organic nitrogen compound
Carbonyl group
Organic oxygen compound
Organonitrogen compound
Organooxygen compound
Primary alcohol
Amine
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	0.66	ALOGPS
logP	0.85	ChemAxon
logS	-1.8	ALOGPS
pKa (Strongest Acidic)	11.44	ChemAxon
pKa (Strongest Basic)	6.96	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	113.37 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	98.52 m³·mol⁻¹	ChemAxon
Polarizability	38.99 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

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

85433052

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4-ethylidene-7-hydroxy-7-(hydroxymethyl)-6,14-dimethyl-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-ene-3,8,17-trione (NP0237181)

MOL for NP0237181 (4-ethylidene-7-hydroxy-7-(hydroxymethyl)-6,14-dimethyl-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-ene-3,8,17-trione)

3D MOL for NP0237181 (4-ethylidene-7-hydroxy-7-(hydroxymethyl)-6,14-dimethyl-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-ene-3,8,17-trione)

3D SDF for NP0237181 (4-ethylidene-7-hydroxy-7-(hydroxymethyl)-6,14-dimethyl-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-ene-3,8,17-trione)

3D-SDF for NP0237181 (4-ethylidene-7-hydroxy-7-(hydroxymethyl)-6,14-dimethyl-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-ene-3,8,17-trione)

PDB for NP0237181 (4-ethylidene-7-hydroxy-7-(hydroxymethyl)-6,14-dimethyl-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-ene-3,8,17-trione)

3D PDB for NP0237181 (4-ethylidene-7-hydroxy-7-(hydroxymethyl)-6,14-dimethyl-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-ene-3,8,17-trione)

SMILES for NP0237181 (4-ethylidene-7-hydroxy-7-(hydroxymethyl)-6,14-dimethyl-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-ene-3,8,17-trione)

INCHI for NP0237181 (4-ethylidene-7-hydroxy-7-(hydroxymethyl)-6,14-dimethyl-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-ene-3,8,17-trione)

Structure for NP0237181 (4-ethylidene-7-hydroxy-7-(hydroxymethyl)-6,14-dimethyl-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-ene-3,8,17-trione)

3D Structure for NP0237181 (4-ethylidene-7-hydroxy-7-(hydroxymethyl)-6,14-dimethyl-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-ene-3,8,17-trione)