NP-MRD: Showing NP-Card for Carduchoron (NP0067149)

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Record Information

Version

2.0

Created at

2022-04-28 11:21:28 UTC

Updated at

2022-04-28 11:21:28 UTC

NP-MRD ID

NP0067149

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Carduchoron

Description

Carduchoron belongs to the class of organic compounds known as atisane diterpenoids. These are diterpenoids with a structure based on the atisane skeleton, which is a tetracyclic compound containing the [2,2,2]bicyc1ic ring system with the C15-C16 bridge attached at C12. Carduchoron is found in Delphinium carduchorum. Based on a literature review very few articles have been published on Carduchoron.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282213212D          

 25 30  0  0  1  0            999 V2000
    1.3988    0.1337    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8734    0.8347    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4829    1.5615    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6977    0.8433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1524    0.1024    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7378   -0.7925    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9555   -0.4400    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9903   -1.4455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2638   -1.7704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5851   -1.1291    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6216   -0.1864    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2523   -0.8230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5394   -1.0550    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0781   -1.2477    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9545   -0.9634    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6824   -0.1724    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7431   -0.3674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0753   -1.1713    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3275   -1.4259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1261   -2.2259    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5186   -0.4646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3428   -0.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9977    0.2251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0116   -2.0700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8513    0.6060    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  1  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  1  7  1  0  0  0  0
  7  8  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  1 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 15 14  1  1  0  0  0
  7 15  1  0  0  0  0
 15 16  1  0  0  0  0
  5 16  1  0  0  0  0
 16 17  1  1  0  0  0
 18 17  1  1  0  0  0
 18 19  1  0  0  0  0
  6 19  1  1  0  0  0
 19 20  2  0  0  0  0
 18 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
  5 23  1  0  0  0  0
 14 24  1  0  0  0  0
 11 25  1  6  0  0  0
M  END

     RDKit          3D

 50 55  0  0  0  0  0  0  0  0999 V2000
    5.0159   -0.3643    0.3094 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6967   -0.3686    0.1631 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9967    0.2654   -0.9865 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5246    0.3265   -0.6504 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7522    1.0459   -1.7018 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6475    0.6489   -1.8326 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3351    1.2530   -2.6467 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3233   -0.4271   -1.0660 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4133   -0.6939    0.1422 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9752   -1.7309    1.0472 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2823   -2.2500    0.4796 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2213   -1.0689    0.3386 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6662    0.0064   -0.5345 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5902    0.2327   -1.7252 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4237    1.2910    0.1685 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4123    2.0408    0.3706 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1068    1.6219    0.5805 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7984    3.0297    0.6392 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2049    0.5698    0.9083 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2524    0.8654    0.7383 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0017    0.0896    1.7963 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8036   -1.0265    1.1673 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8125   -1.8345    0.3666 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8138   -3.0443    0.4768 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9122   -1.0689   -0.4969 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.6899    0.0991   -0.3927 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4334   -0.8505    1.1770 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3268    1.2805   -1.2036 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0929   -0.4156   -1.8615 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8822    2.1557   -1.6452 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2477    0.7829   -2.6863 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3837   -1.3454   -1.6706 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2514   -1.2819    2.0483 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2949   -2.5544    1.2936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7259   -2.8980    1.2809 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1158   -2.8000   -0.4453 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4623   -0.7287    1.3617 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1695   -1.4677   -0.1037 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2516   -0.4259   -2.5426 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5794    1.3078   -1.9950 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6197   -0.0199   -1.3640 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7188    3.4295   -0.4101 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1161    3.2962    1.1551 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6808    3.5379    1.0847 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3580    0.3789    2.0188 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5499    1.9038    0.8306 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3062   -0.4060    2.5270 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6538    0.7538    2.4246 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3303   -1.6418    1.8867 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8008   -1.4992   -1.5013 H   0  0  0  0  0  0  0  0  0  0  0  0
 18 17  1  0
 17 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22  2  1  0
  2  1  2  3
  2  3  1  0
  3  4  1  0
  4  5  1  6
  5  6  1  0
  6  7  2  0
  6  8  1  0
  8  9  1  0
  9 10  1  1
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  6
 13 15  1  0
 15 16  2  0
  9 25  1  0
 25 23  1  0
 23 24  2  0
 15 17  1  0
  9 19  1  0
  4 20  1  0
 25  4  1  0
 23 22  1  0
 13  8  1  0
 18 42  1  0
 18 43  1  0
 18 44  1  0
 19 45  1  1
 20 46  1  6
 21 47  1  0
 21 48  1  0
 22 49  1  1
  1 26  1  0
  1 27  1  0
  3 28  1  0
  3 29  1  0
  5 30  1  0
  5 31  1  0
  8 32  1  6
 10 33  1  0
 10 34  1  0
 11 35  1  0
 11 36  1  0
 12 37  1  0
 12 38  1  0
 14 39  1  0
 14 40  1  0
 14 41  1  0
 25 50  1  6
M  END


  Mrv1652304282213212D          

 25 30  0  0  1  0            999 V2000
    1.3988    0.1337    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8734    0.8347    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4829    1.5615    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6977    0.8433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1524    0.1024    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7378   -0.7925    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9555   -0.4400    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9903   -1.4455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2638   -1.7704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5851   -1.1291    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6216   -0.1864    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2523   -0.8230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5394   -1.0550    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0781   -1.2477    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9545   -0.9634    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6824   -0.1724    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7431   -0.3674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0753   -1.1713    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3275   -1.4259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1261   -2.2259    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5186   -0.4646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3428   -0.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9977    0.2251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0116   -2.0700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8513    0.6060    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  1  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  1  7  1  0  0  0  0
  7  8  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  1 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 15 14  1  1  0  0  0
  7 15  1  0  0  0  0
 15 16  1  0  0  0  0
  5 16  1  0  0  0  0
 16 17  1  1  0  0  0
 18 17  1  1  0  0  0
 18 19  1  0  0  0  0
  6 19  1  1  0  0  0
 19 20  2  0  0  0  0
 18 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
  5 23  1  0  0  0  0
 14 24  1  0  0  0  0
 11 25  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0067149

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CN1[C@@H]2[C@H]3C[C@@H]4C(=C)C[C@]33CC(=O)[C@H]5[C@@]2(CCC[C@@]5(C)C1=O)[C@@H]3C4=O

> <INCHI_IDENTIFIER>
InChI=1S/C21H25NO3/c1-10-8-20-9-13(23)15-19(2)5-4-6-21(15)16(20)14(24)11(10)7-12(20)17(21)22(3)18(19)25/h11-12,15-17H,1,4-9H2,2-3H3/t11-,12-,15-,16-,17-,19-,20+,21+/m1/s1

> <INCHI_KEY>
YLHNZWYZUIPWIF-FWJCKRHVSA-N

> <FORMULA>
C21H25NO3

> <MOLECULAR_WEIGHT>
339.435

> <EXACT_MASS>
339.183443669

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
50

> <JCHEM_AVERAGE_POLARIZABILITY>
36.43112207710578

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,5R,8R,9S,11R,14S,17S,18R)-5,7-dimethyl-12-methylidene-7-azahexacyclo[9.6.2.0^{1,8}.0^{5,17}.0^{9,14}.0^{14,18}]nonadecane-6,16,19-trione

> <ALOGPS_LOGP>
1.44

> <JCHEM_LOGP>
1.6021506376666668

> <ALOGPS_LOGS>
-2.48

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
18.867519769665083

> <JCHEM_PKA_STRONGEST_ACIDIC>
16.7967129222083

> <JCHEM_PKA_STRONGEST_BASIC>
1.2101595655547674

> <JCHEM_POLAR_SURFACE_AREA>
54.45

> <JCHEM_REFRACTIVITY>
91.6623

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.12e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,5R,8R,9S,11R,14S,17S,18R)-5,7-dimethyl-12-methylidene-7-azahexacyclo[9.6.2.0^{1,8}.0^{5,17}.0^{9,14}.0^{14,18}]nonadecane-6,16,19-trione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       2.611   0.250   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.497   1.558   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       2.768   2.915   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       5.036   1.574   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.884   0.191   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.111  -1.479   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.650  -0.821   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.715  -2.698   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.359  -3.305   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.092  -2.108   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.160  -0.348   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.471  -1.536   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -1.007  -1.969   0.000  0.00  0.00           O+0
HETATM   14  N   UNK     0       2.012  -2.329   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0       3.648  -1.798   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.007  -0.322   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.987  -0.686   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.607  -2.186   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.211  -2.662   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       5.835  -4.155   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       8.435  -0.867   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       9.973  -0.801   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.462   0.420   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.888  -3.864   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.589   1.131   0.000  0.00  0.00           C+0
CONECT    1    2    7   11                                                  
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   16   23                                             
CONECT    6    5    7   19                                                  
CONECT    7    6    1    8   15                                             
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10    1   12   25                                             
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   24                                                  
CONECT   15   14    7   16                                                  
CONECT   16   15    5   17                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   21                                                  
CONECT   19   18    6   20                                                  
CONECT   20   19                                                            
CONECT   21   18   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21    5                                                       
CONECT   24   14                                                            
CONECT   25   11                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   60    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₂₅NO₃

Average Mass

339.4350 Da

Monoisotopic Mass

339.18344 Da

IUPAC Name

(1S,5R,8R,9S,11R,14S,17S,18R)-5,7-dimethyl-12-methylidene-7-azahexacyclo[9.6.2.0^{1,8}.0^{5,17}.0^{9,14}.0^{14,18}]nonadecane-6,16,19-trione

Traditional Name

(1S,5R,8R,9S,11R,14S,17S,18R)-5,7-dimethyl-12-methylidene-7-azahexacyclo[9.6.2.0^{1,8}.0^{5,17}.0^{9,14}.0^{14,18}]nonadecane-6,16,19-trione

CAS Registry Number

Not Available

SMILES

CN1[C@@H]2[C@H]3C[C@@H]4C(=C)C[C@]33CC(=O)[C@H]5[C@@]2(CCC[C@@]5(C)C1=O)[C@@H]3C4=O

InChI Identifier

InChI=1S/C21H25NO3/c1-10-8-20-9-13(23)15-19(2)5-4-6-21(15)16(20)14(24)11(10)7-12(20)17(21)22(3)18(19)25/h11-12,15-17H,1,4-9H2,2-3H3/t11-,12-,15-,16-,17-,19-,20+,21+/m1/s1

InChI Key

YLHNZWYZUIPWIF-FWJCKRHVSA-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
Delphinium carduchorum	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as atisane diterpenoids. These are diterpenoids with a structure based on the atisane skeleton, which is a tetracyclic compound containing the [2,2,2]bicyc1ic ring system with the C15-C16 bridge attached at C12.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Atisane diterpenoids

Alternative Parents

Substituents

Atisane diterpenoid
Isoquinolone
Alkaloid or derivatives
Delta-lactam
Piperidinone
Piperidine
Tertiary carboxylic acid amide
Lactam
Ketone
Carboxamide group
Organoheterocyclic compound
Carboxylic acid derivative
Azacycle
Hydrocarbon derivative
Organic oxide
Organooxygen compound
Organonitrogen compound
Organopnictogen compound
Organic oxygen compound
Carbonyl group
Organic nitrogen compound
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	1.44	ALOGPS
logP	1.6	ChemAxon
logS	-2.5	ALOGPS
pKa (Strongest Acidic)	16.8	ChemAxon
pKa (Strongest Basic)	1.21	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	54.45 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	91.66 m³·mol⁻¹	ChemAxon
Polarizability	36.43 Å³	ChemAxon
Number of Rings	6	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

C00024851

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

100978528

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Carduchoron (NP0067149)

MOL for NP0067149 (Carduchoron)

3D MOL for NP0067149 (Carduchoron)

3D SDF for NP0067149 (Carduchoron)

3D-SDF for NP0067149 (Carduchoron)

PDB for NP0067149 (Carduchoron)

3D PDB for NP0067149 (Carduchoron)

SMILES for NP0067149 (Carduchoron)

INCHI for NP0067149 (Carduchoron)

Structure for NP0067149 (Carduchoron)

3D Structure for NP0067149 (Carduchoron)