NP-MRD: Showing NP-Card for 9'',10''-Didehydroacidissiminin epoxide (NP0084791)

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Record Information

Version

2.0

Created at

2022-04-29 05:26:26 UTC

Updated at

2022-04-29 05:26:26 UTC

NP-MRD ID

NP0084791

Secondary Accession Numbers

None

Natural Product Identification

Common Name

9'',10''-Didehydroacidissiminin epoxide

Description

9'',10''-Didehydroacidissiminin epoxide is found in Limonia acidissima. Based on a literature review very few articles have been published on N-[2-(4-{[(2E,4R)-5-[(2R)-3,3-dimethyloxiran-2-yl]-3-methyl-4-(octadec-9-enoyloxy)pent-2-en-1-yl]oxy}phenyl)ethyl]benzenecarboximidic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292207262D          

 49 51  0  0  1  0            999 V2000
    4.2720   -7.1152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7516   -7.7554    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0308   -7.3540    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2917   -8.3790    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4815   -8.5349    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8579   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0138   -9.8851    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7933  -10.1552    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4170   -9.6151    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1965   -9.8851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8202   -9.3450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5997   -9.6151    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2234   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0029   -9.3450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6266   -8.8050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4061   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0298   -8.5349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8093   -8.8050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4330   -8.2649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2125   -8.5349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8361   -7.9948    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6157   -8.2649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2393   -7.7248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0189   -7.9948    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6425   -7.4547    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4221   -7.7248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2611   -8.8050    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3902  -10.4252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5461  -11.2354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6106  -10.1552    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9870  -10.6953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1429  -11.5054    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5192  -12.0455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6751  -12.8556    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0515  -13.3957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7281  -13.1257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3517  -13.6658    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1958  -14.4759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8194  -15.0160    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6635  -15.8261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2872  -16.3662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1312  -17.1763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7549  -17.7164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5344  -17.4464    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6904  -16.6362    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0667  -16.0962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8840  -16.0962    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8840  -12.3155    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2603  -11.7754    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  2  5  1  0  0  0  0
  5  6  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  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  0  0  0  0
 12 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
 17 16  1  4  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 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
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
  9 27  2  0  0  0  0
  7 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  2  0  0  0  0
 42 43  1  0  0  0  0
 43 44  2  0  0  0  0
 44 45  1  0  0  0  0
 45 46  2  0  0  0  0
 41 46  1  0  0  0  0
 40 47  2  0  0  0  0
 36 48  1  0  0  0  0
 48 49  2  0  0  0  0
 33 49  1  0  0  0  0
M  END

     RDKit          3D

112114  0  0  0  0  0  0  0  0999 V2000
   12.5971    3.1020   -4.5197 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1814    3.2626   -4.0250 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8871    2.1136   -3.0781 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8678    2.2168   -1.9408 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7044    1.1291   -0.9155 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3266    1.1115   -0.2700 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3363   -0.0203    0.7054 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0526   -0.2202    1.4222 C   0  0  0  0  0  0  0  0  0  0  0  0
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 21 83  1  1
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 22 85  1  0
 23 86  1  6
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 27 91  1  0
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 29 93  1  0
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 35100  1  0
 37101  1  0
 37102  1  0
 38103  1  0
 38104  1  0
 39105  1  0
 43106  1  0
 44107  1  0
 45108  1  0
 46109  1  0
 47110  1  0
 48111  1  0
 49112  1  0
M  END


  Mrv1652304292207262D          

 49 51  0  0  1  0            999 V2000
    4.2720   -7.1152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7516   -7.7554    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0308   -7.3540    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2917   -8.3790    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4815   -8.5349    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8579   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0138   -9.8851    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7933  -10.1552    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4170   -9.6151    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1965   -9.8851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8202   -9.3450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5997   -9.6151    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2234   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0029   -9.3450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6266   -8.8050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4061   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0298   -8.5349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8093   -8.8050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4330   -8.2649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2125   -8.5349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8361   -7.9948    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6157   -8.2649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2393   -7.7248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0189   -7.9948    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6425   -7.4547    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4221   -7.7248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2611   -8.8050    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3902  -10.4252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5461  -11.2354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6106  -10.1552    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9870  -10.6953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1429  -11.5054    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5192  -12.0455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6751  -12.8556    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0515  -13.3957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7281  -13.1257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3517  -13.6658    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1958  -14.4759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8194  -15.0160    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6635  -15.8261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2872  -16.3662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1312  -17.1763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7549  -17.7164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5344  -17.4464    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6904  -16.6362    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0667  -16.0962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8840  -16.0962    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8840  -12.3155    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2603  -11.7754    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  2  5  1  0  0  0  0
  5  6  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  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  0  0  0  0
 12 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
 17 16  1  4  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 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
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
  9 27  2  0  0  0  0
  7 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  2  0  0  0  0
 42 43  1  0  0  0  0
 43 44  2  0  0  0  0
 44 45  1  0  0  0  0
 45 46  2  0  0  0  0
 41 46  1  0  0  0  0
 40 47  2  0  0  0  0
 36 48  1  0  0  0  0
 48 49  2  0  0  0  0
 33 49  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0084791

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCC=CCCCCCCCC(=O)O[C@H](C[C@H]1OC1(C)C)C(\C)=C\COC1=CC=C(CCNC(=O)C2=CC=CC=C2)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C43H63NO5/c1-5-6-7-8-9-10-11-12-13-14-15-16-17-18-22-25-41(45)48-39(34-40-43(3,4)49-40)35(2)31-33-47-38-28-26-36(27-29-38)30-32-44-42(46)37-23-20-19-21-24-37/h12-13,19-21,23-24,26-29,31,39-40H,5-11,14-18,22,25,30,32-34H2,1-4H3,(H,44,46)/b13-12?,35-31+/t39-,40-/m1/s1

> <INCHI_KEY>
DSMUBNDRNPGPEI-QUUVHDGOSA-N

> <FORMULA>
C43H63NO5

> <MOLECULAR_WEIGHT>
673.979

> <EXACT_MASS>
673.470624133

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
112

> <JCHEM_AVERAGE_POLARIZABILITY>
84.38483024270224

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,3E)-1-[(2R)-3,3-dimethyloxiran-2-yl]-3-methyl-5-{4-[2-(phenylformamido)ethyl]phenoxy}pent-3-en-2-yl octadec-9-enoate

> <ALOGPS_LOGP>
9.91

> <JCHEM_LOGP>
11.089914861666667

> <ALOGPS_LOGS>
-7.56

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.004492845936461

> <JCHEM_PKA_STRONGEST_BASIC>
-0.8393011622400078

> <JCHEM_POLAR_SURFACE_AREA>
77.16

> <JCHEM_REFRACTIVITY>
203.0040999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
27

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.87e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3E)-1-[(2R)-3,3-dimethyloxiran-2-yl]-3-methyl-5-{4-[2-(phenylformamido)ethyl]phenoxy}pent-3-en-2-yl octadec-9-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  C   UNK     0       7.974 -13.282   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.003 -14.477   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.657 -13.728   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       8.011 -15.641   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       6.499 -15.932   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.335 -16.940   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.626 -18.452   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       7.081 -18.956   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       8.245 -17.948   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.700 -18.452   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.864 -17.444   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      12.319 -17.948   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      13.484 -16.940   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      14.939 -17.444   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      16.103 -16.436   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      17.558 -16.940   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      18.722 -15.932   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      20.177 -16.436   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      21.342 -15.428   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      22.797 -15.932   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      23.961 -14.924   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      25.416 -15.428   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      26.580 -14.420   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      28.035 -14.924   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      29.199 -13.916   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      30.655 -14.420   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       7.954 -16.436   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       4.462 -19.460   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       4.753 -20.973   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       3.006 -18.956   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       1.842 -19.964   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       2.133 -21.477   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       0.969 -22.485   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       1.260 -23.997   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       0.096 -25.005   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -1.359 -24.501   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      -2.523 -25.509   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      -2.232 -27.022   0.000  0.00  0.00           C+0
HETATM   39  N   UNK     0      -3.396 -28.030   0.000  0.00  0.00           N+0
HETATM   40  C   UNK     0      -3.105 -29.542   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      -4.269 -30.550   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -3.978 -32.062   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      -5.142 -33.071   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      -6.598 -32.567   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      -6.889 -31.054   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      -5.725 -30.046   0.000  0.00  0.00           C+0
HETATM   47  O   UNK     0      -1.650 -30.046   0.000  0.00  0.00           O+0
HETATM   48  C   UNK     0      -1.650 -22.989   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      -0.486 -21.981   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4    5                                             
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    2    6                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   28                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   27                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25                                                            
CONECT   27    9                                                            
CONECT   28    7   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34   49                                                  
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   37   48                                                  
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   41   47                                                  
CONECT   41   40   42   46                                                  
CONECT   42   41   43                                                       
CONECT   43   42   44                                                       
CONECT   44   43   45                                                       
CONECT   45   44   46                                                       
CONECT   46   45   41                                                       
CONECT   47   40                                                            
CONECT   48   36   49                                                       
CONECT   49   48   33                                                       
MASTER        0    0    0    0    0    0    0    0   49    0  102    0
END

View in JSmol

Synonyms

Value	Source
N-[2-(4-{[(2E,4R)-5-[(2R)-3,3-dimethyloxiran-2-yl]-3-methyl-4-(octadec-9-enoyloxy)pent-2-en-1-yl]oxy}phenyl)ethyl]benzenecarboximidate	Generator

Chemical Formula

C₄₃H₆₃NO₅

Average Mass

673.9790 Da

Monoisotopic Mass

673.47062 Da

IUPAC Name

(2R,3E)-1-[(2R)-3,3-dimethyloxiran-2-yl]-3-methyl-5-{4-[2-(phenylformamido)ethyl]phenoxy}pent-3-en-2-yl octadec-9-enoate

Traditional Name

(2R,3E)-1-[(2R)-3,3-dimethyloxiran-2-yl]-3-methyl-5-{4-[2-(phenylformamido)ethyl]phenoxy}pent-3-en-2-yl octadec-9-enoate

CAS Registry Number

Not Available

SMILES

CCCCCCCCC=CCCCCCCCC(=O)O[C@H](C[C@H]1OC1(C)C)C(\C)=C\COC1=CC=C(CCNC(=O)C2=CC=CC=C2)C=C1

InChI Identifier

InChI=1S/C43H63NO5/c1-5-6-7-8-9-10-11-12-13-14-15-16-17-18-22-25-41(45)48-39(34-40-43(3,4)49-40)35(2)31-33-47-38-28-26-36(27-29-38)30-32-44-42(46)37-23-20-19-21-24-37/h12-13,19-21,23-24,26-29,31,39-40H,5-11,14-18,22,25,30,32-34H2,1-4H3,(H,44,46)/b13-12?,35-31+/t39-,40-/m1/s1

InChI Key

DSMUBNDRNPGPEI-QUUVHDGOSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Limonia acidissima	Plant	KNApSAcK

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	9.91	ALOGPS
logP	11.09	ChemAxon
logS	-7.6	ALOGPS
pKa (Strongest Acidic)	15	ChemAxon
pKa (Strongest Basic)	-0.84	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	77.16 Å²	ChemAxon
Rotatable Bond Count	27	ChemAxon
Refractivity	203 m³·mol⁻¹	ChemAxon
Polarizability	84.38 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

163184165

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 9'',10''-Didehydroacidissiminin epoxide (NP0084791)

MOL for NP0084791 (9'',10''-Didehydroacidissiminin epoxide)

3D MOL for NP0084791 (9'',10''-Didehydroacidissiminin epoxide)

3D SDF for NP0084791 (9'',10''-Didehydroacidissiminin epoxide)

3D-SDF for NP0084791 (9'',10''-Didehydroacidissiminin epoxide)

PDB for NP0084791 (9'',10''-Didehydroacidissiminin epoxide)

3D PDB for NP0084791 (9'',10''-Didehydroacidissiminin epoxide)

SMILES for NP0084791 (9'',10''-Didehydroacidissiminin epoxide)

INCHI for NP0084791 (9'',10''-Didehydroacidissiminin epoxide)

Structure for NP0084791 (9'',10''-Didehydroacidissiminin epoxide)

3D Structure for NP0084791 (9'',10''-Didehydroacidissiminin epoxide)