NP-MRD: Showing NP-Card for Delcarduchol (NP0067168)

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Record Information

Version

2.0

Created at

2022-04-28 11:24:35 UTC

Updated at

2022-04-28 11:24:36 UTC

NP-MRD ID

NP0067168

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Delcarduchol

Description

(1S,5R,8R,9S,11S,13S,14S,17R,18S)-13-hydroxy-5,7-dimethyl-12-methylidene-7-azahexacyclo[9.6.2.0¹,⁸.0⁵,¹⁷.0⁹,¹⁴.0¹⁴,¹⁸]Nonadecane-3,10-dione belongs to the class of organic compounds known as hetidine-type diterpenoid alkaloids. These are alkaloid diterpenoids with a structure based on the hetidine skeleton, which is a hexacyclic compound with an additional C-20-C-14 bond in the atisine-type. Delcarduchol is found in Delphinium carduchorum. Based on a literature review very few articles have been published on (1S,5R,8R,9S,11S,13S,14S,17R,18S)-13-hydroxy-5,7-dimethyl-12-methylidene-7-azahexacyclo[9.6.2.0¹,⁸.0⁵,¹⁷.0⁹,¹⁴.0¹⁴,¹⁸]Nonadecane-3,10-dione.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282213242D          

 25 30  0  0  1  0            999 V2000
    2.7486    3.4274    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2779    2.7639    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0645    2.4911    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2733    1.4837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7602    0.8595    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9714    0.0620    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0110    1.1457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8085    2.0895    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1108    1.6138    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6789    2.4475    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9301    3.2934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6396    1.7846    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6478    1.4935    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5795    1.4406    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.3682    1.9321    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0209    0.7436    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1588    0.8229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3148    0.0128    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6704    1.2572    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6269    0.9201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3298    1.9920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4874    2.1052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8540    2.6028    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5806    3.3812    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7808    3.2658    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  8  7  1  1  0  0  0
  2  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  6  0  0  0
  1 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
  8 13  1  0  0  0  0
 13 14  1  6  0  0  0
 14 15  1  0  0  0  0
  3 15  1  0  0  0  0
 14 16  1  0  0  0  0
 12 17  1  1  0  0  0
 17 18  2  0  0  0  0
 19 17  1  6  0  0  0
 19 20  1  0  0  0  0
  9 20  1  6  0  0  0
 19 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 10 23  1  0  0  0  0
 23 24  1  6  0  0  0
  3 25  1  1  0  0  0
M  END

     RDKit          3D

 52 57  0  0  0  0  0  0  0  0999 V2000
    4.9544    0.4176   -0.6098 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6707    0.2375   -0.4363 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0995   -0.2010    0.8949 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1730   -1.3759    0.5788 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0598   -1.0109   -0.3358 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2511    0.3911   -0.9171 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1962    0.7785   -1.8692 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0139   -0.0767   -1.9169 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3333   -0.8465   -0.7012 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2723   -0.7874    0.3792 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5684   -1.8628    1.3719 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9446   -2.3876    1.3077 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1380   -3.5140    1.7877 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1038   -1.7032    0.7305 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6383   -0.4730   -0.0410 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.6822   -0.0343   -1.0332 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4782    0.6340    0.9768 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2966    1.4246    0.6409 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2414    2.6122    1.4789 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1474    0.5791    0.9568 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1067    1.2223    0.3509 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2111    0.9155    1.2867 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3929    1.5167    2.2985 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6335    0.4331   -1.4887 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8756    1.5568   -2.2609 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3268    0.7318   -1.5767 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6117    0.2449    0.2288 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8506   -0.4818    1.6122 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8011   -2.1746    0.1298 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8421   -1.7581    1.5744 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9626   -1.7548   -1.1490 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6645    0.8540   -2.8954 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1098    1.8435   -1.6464 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9038    0.5773   -2.1576 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9290   -0.7393   -2.8287 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4103   -1.9386   -0.9815 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1087   -2.7318    1.1191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3228   -1.5544    2.4098 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5459   -2.3900   -0.0477 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8709   -1.4496    1.4746 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6444    1.0826   -1.1613 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6834   -0.2278   -0.5634 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6687   -0.5783   -1.9763 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3754    1.2718    1.0583 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2552    0.1849    1.9873 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2098    3.5396    0.8713 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3606    2.5684    2.1472 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1599    2.6796    2.1202 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0592    0.5893    2.0744 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9701    2.2849    0.1447 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7265   -0.4639   -2.1678 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8783    1.3448   -3.2302 H   0  0  0  0  0  0  0  0  0  0  0  0
 19 18  1  0
 18 17  1  0
 17 15  1  0
 15 16  1  6
 15 14  1  0
 14 12  1  0
 12 13  2  0
 12 11  1  0
 10 11  1  1
 10 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  2  0
 22  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  6
  7  8  1  0
  8  9  1  0
  6 24  1  0
 24 25  1  0
 24  2  1  0
  2  1  2  3
 20 18  1  0
  6 21  1  0
  9 15  1  0
  5 10  1  0
  9 10  1  0
  2  3  1  0
 19 46  1  0
 19 47  1  0
 19 48  1  0
 17 44  1  0
 17 45  1  0
 16 41  1  0
 16 42  1  0
 16 43  1  0
 14 39  1  0
 14 40  1  0
 11 37  1  0
 11 38  1  0
 20 49  1  1
 21 50  1  6
  3 28  1  1
  4 29  1  0
  4 30  1  0
  5 31  1  6
  7 32  1  0
  7 33  1  0
  8 34  1  0
  8 35  1  0
  9 36  1  6
 24 51  1  6
 25 52  1  0
  1 26  1  0
  1 27  1  0
M  END


  Mrv1652304282213242D          

 25 30  0  0  1  0            999 V2000
    2.7486    3.4274    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2779    2.7639    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0645    2.4911    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2733    1.4837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7602    0.8595    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9714    0.0620    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0110    1.1457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8085    2.0895    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1108    1.6138    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6789    2.4475    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9301    3.2934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6396    1.7846    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6478    1.4935    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5795    1.4406    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.3682    1.9321    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0209    0.7436    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1588    0.8229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3148    0.0128    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6704    1.2572    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6269    0.9201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3298    1.9920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4874    2.1052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8540    2.6028    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5806    3.3812    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7808    3.2658    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  8  7  1  1  0  0  0
  2  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  6  0  0  0
  1 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
  8 13  1  0  0  0  0
 13 14  1  6  0  0  0
 14 15  1  0  0  0  0
  3 15  1  0  0  0  0
 14 16  1  0  0  0  0
 12 17  1  1  0  0  0
 17 18  2  0  0  0  0
 19 17  1  6  0  0  0
 19 20  1  0  0  0  0
  9 20  1  6  0  0  0
 19 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 10 23  1  0  0  0  0
 23 24  1  6  0  0  0
  3 25  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0067168

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CN1C[C@]2(C)CC(=O)C[C@@]34[C@H]1[C@H]1C(=O)[C@H]5C[C@@H]3[C@]1(CC[C@H]24)[C@@H](O)C5=C

> <INCHI_IDENTIFIER>
InChI=1S/C21H27NO3/c1-10-12-6-14-20(18(10)25)5-4-13-19(2)7-11(23)8-21(13,14)17(22(3)9-19)15(20)16(12)24/h12-15,17-18,25H,1,4-9H2,2-3H3/t12-,13+,14+,15+,17+,18-,19-,20-,21-/m0/s1

> <INCHI_KEY>
SZIAAQYFFVRAJG-JJCUJZPCSA-N

> <FORMULA>
C21H27NO3

> <MOLECULAR_WEIGHT>
341.451

> <EXACT_MASS>
341.199093733

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
37.20272382855629

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,5R,8R,9S,11S,13S,14S,17R,18S)-13-hydroxy-5,7-dimethyl-12-methylidene-7-azahexacyclo[9.6.2.0^{1,8}.0^{5,17}.0^{9,14}.0^{14,18}]nonadecane-3,10-dione

> <ALOGPS_LOGP>
1.22

> <JCHEM_LOGP>
0.9451068396666666

> <ALOGPS_LOGS>
-2.18

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
15.074448912161014

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.532499968224634

> <JCHEM_PKA_STRONGEST_BASIC>
8.603433446114307

> <JCHEM_POLAR_SURFACE_AREA>
57.61

> <JCHEM_REFRACTIVITY>
93.08959999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.25e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,5R,8R,9S,11S,13S,14S,17R,18S)-13-hydroxy-5,7-dimethyl-12-methylidene-7-azahexacyclo[9.6.2.0^{1,8}.0^{5,17}.0^{9,14}.0^{14,18}]nonadecane-3,10-dione

> <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       5.131   6.398   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.119   5.159   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.587   4.650   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.977   2.770   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.019   1.604   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       7.413   0.116   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       5.620   2.139   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.242   3.900   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.940   3.012   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.134   4.569   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.603   6.148   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.061   3.331   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.943   2.788   0.000  0.00  0.00           C+0
HETATM   14  N   UNK     0       6.682   2.689   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0       8.154   3.607   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.506   1.388   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.163   1.536   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       2.454   0.024   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       1.251   2.347   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.037   1.717   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.616   3.718   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -0.910   3.930   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.594   4.859   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       1.084   6.312   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       7.058   6.096   0.000  0.00  0.00           C+0
CONECT    1    2   11                                                       
CONECT    2    1    3    8                                                  
CONECT    3    2    4   15   25                                             
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    2    9   13                                             
CONECT    9    8   10   20                                                  
CONECT   10    9   11   12   23                                             
CONECT   11   10    1                                                       
CONECT   12   10   13   17                                                  
CONECT   13   12    8   14                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14    3                                                       
CONECT   16   14                                                            
CONECT   17   12   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   21                                                  
CONECT   20   19    9                                                       
CONECT   21   19   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   10   24                                                  
CONECT   24   23                                                            
CONECT   25    3                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   60    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₂₇NO₃

Average Mass

341.4510 Da

Monoisotopic Mass

341.19909 Da

IUPAC Name

(1S,5R,8R,9S,11S,13S,14S,17R,18S)-13-hydroxy-5,7-dimethyl-12-methylidene-7-azahexacyclo[9.6.2.0^{1,8}.0^{5,17}.0^{9,14}.0^{14,18}]nonadecane-3,10-dione

Traditional Name

(1S,5R,8R,9S,11S,13S,14S,17R,18S)-13-hydroxy-5,7-dimethyl-12-methylidene-7-azahexacyclo[9.6.2.0^{1,8}.0^{5,17}.0^{9,14}.0^{14,18}]nonadecane-3,10-dione

CAS Registry Number

Not Available

SMILES

CN1C[C@]2(C)CC(=O)C[C@@]34[C@H]1[C@H]1C(=O)[C@H]5C[C@@H]3[C@]1(CC[C@H]24)[C@@H](O)C5=C

InChI Identifier

InChI=1S/C21H27NO3/c1-10-12-6-14-20(18(10)25)5-4-13-19(2)7-11(23)8-21(13,14)17(22(3)9-19)15(20)16(12)24/h12-15,17-18,25H,1,4-9H2,2-3H3/t12-,13+,14+,15+,17+,18-,19-,20-,21-/m0/s1

InChI Key

SZIAAQYFFVRAJG-JJCUJZPCSA-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 hetidine-type diterpenoid alkaloids. These are alkaloid diterpenoids with a structure based on the hetidine skeleton, which is a hexacyclic compound with an additional C-20-C-14 bond in the atisine-type.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Hetidine-type diterpenoid alkaloids

Alternative Parents

Substituents

Hetidine-type diterpenoid alkaloid
Alkaloid or derivatives
Piperidine
Cyclic alcohol
Cyclic ketone
Tertiary aliphatic amine
Tertiary amine
Secondary alcohol
Ketone
Azacycle
Organoheterocyclic compound
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Amine
Alcohol
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	1.22	ALOGPS
logP	0.95	ChemAxon
logS	-2.2	ALOGPS
pKa (Strongest Acidic)	13.53	ChemAxon
pKa (Strongest Basic)	8.6	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	57.61 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	93.09 m³·mol⁻¹	ChemAxon
Polarizability	37.2 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

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

162946178

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Delcarduchol (NP0067168)

MOL for NP0067168 (Delcarduchol)

3D MOL for NP0067168 (Delcarduchol)

3D SDF for NP0067168 (Delcarduchol)

3D-SDF for NP0067168 (Delcarduchol)

PDB for NP0067168 (Delcarduchol)

3D PDB for NP0067168 (Delcarduchol)

SMILES for NP0067168 (Delcarduchol)

INCHI for NP0067168 (Delcarduchol)

Structure for NP0067168 (Delcarduchol)

3D Structure for NP0067168 (Delcarduchol)