NP-MRD: Showing NP-Card for (1r,5s,8r,9s,11s,13r,14s,16s,17r,18s)-10,13-dihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.0¹,⁸.0⁵,¹⁷.0⁷,¹⁶.0⁹,¹⁴.0¹⁴,¹⁸]nonadecan-3-one (NP0148617)

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Record Information

Version

2.0

Created at

2022-09-02 04:23:22 UTC

Updated at

2022-09-02 04:23:22 UTC

NP-MRD ID

NP0148617

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,5s,8r,9s,11s,13r,14s,16s,17r,18s)-10,13-dihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.0¹,⁸.0⁵,¹⁷.0⁷,¹⁶.0⁹,¹⁴.0¹⁴,¹⁸]nonadecan-3-one

Description

Venuluson belongs to the class of organic compounds known as hetisine-type diterpenoid alkaloids. These are alkaloid diterpenoids with a structure based on the hetisine skeleton, which is a heptacyclic compound with an additional N-C-6 bond as compared with the hetidine-type, and thus, is one of most complex entries in the atisane-class. (1r,5s,8r,9s,11s,13r,14s,16s,17r,18s)-10,13-dihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.0¹,⁸.0⁵,¹⁷.0⁷,¹⁶.0⁹,¹⁴.0¹⁴,¹⁸]nonadecan-3-one is found in Delphinium venulosum. Based on a literature review very few articles have been published on Venuluson.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022206232D          

 24 30  0  0  1  0            999 V2000
   -1.0137   -0.7847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2512   -0.4698    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0506    0.3584    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7603    0.1256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6923    0.1443    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1918   -0.4206    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0038   -0.7475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6913   -0.1849    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4049    0.3006    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1557    0.7011    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8024    1.2133    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6038   -0.0240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0695   -0.6761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3091   -1.4656    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2476   -0.4261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5488    0.2779    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0153    0.9479    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2150    0.5743    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4727    1.0248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3251    1.8365    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8479    0.7974    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5547    1.3010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4727   -0.9138    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4938   -1.7385    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  3  2  1  1  0  0  0
  3  4  1  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  1  0  0  0
  8  7  1  6  0  0  0
  9  8  1  1  0  0  0
  9 10  1  0  0  0  0
 10 11  1  6  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 16 15  1  6  0  0  0
  5 16  1  0  0  0  0
  9 16  1  0  0  0  0
 16 17  1  0  0  0  0
 18 17  1  6  0  0  0
  6 18  1  0  0  0  0
 18 19  1  0  0  0  0
  3 19  1  0  0  0  0
 19 20  1  0  0  0  0
 17 21  1  1  0  0  0
  8 21  1  0  0  0  0
 21 22  1  0  0  0  0
 10 22  1  0  0  0  0
  6 23  1  0  0  0  0
  2 23  1  0  0  0  0
 23 24  1  6  0  0  0
M  END

     RDKit          3D

 49 55  0  0  0  0  0  0  0  0999 V2000
    4.7030   -0.5821    0.3631 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4303   -0.2973    0.2550 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5168   -0.1107    1.4119 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4575   -1.2074    1.2883 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7289   -1.0365   -0.0176 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3487    0.0340   -0.8804 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5799    0.0798   -2.1618 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8072    0.3876   -1.9103 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5558   -0.4540   -0.9133 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7283    0.3360   -0.3911 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9251    1.0127    0.8690 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6241   -0.8159   -0.2515 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8569   -1.4828    0.8979 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4372   -2.2353    1.6289 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3909   -1.2492    1.1743 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6335   -0.3816    0.2848 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5264    1.0427    0.1875 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0048    1.2420   -0.0807 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7562    1.2072    1.2110 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9517    1.4608    2.3179 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0523    1.5894   -1.0765 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5213    1.4096   -1.2823 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8220   -0.1425   -1.0909 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0630   -1.2013   -1.9306 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1935   -0.7051    1.3211 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3074   -0.7039   -0.5234 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0068   -0.0952    2.3798 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8328   -1.1303    2.1762 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9622   -2.2149    1.3401 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5969   -1.9740   -0.5562 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0302    0.8862   -2.7838 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6744   -0.8452   -2.7244 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3564    0.4824   -2.8917 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6734   -1.4216   -1.3070 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0715    1.0406    1.0273 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5997    0.7112    1.8312 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8570    2.1560    0.8923 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7279   -1.4949   -1.0968 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6423   -0.5852    0.1215 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2019   -1.1537    2.2722 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9992   -2.3056    0.9940 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5807    1.6998    1.0478 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1960    2.1847   -0.5883 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5408    1.9926    1.2050 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1246    2.3546    2.7091 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7692    1.2225   -2.3207 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9278    2.4385   -1.0611 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2110    0.8038   -1.5225 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4264   -1.9487   -1.8444 H   0  0  0  0  0  0  0  0  0  0  0  0
 10 11  1  1
 10 22  1  0
 22 21  1  0
 21  8  1  0
  8  7  1  0
  6  7  1  6
  6 18  1  0
 18 17  1  0
 17 16  1  0
 16 15  1  1
 15 13  1  0
 13 14  2  0
 13 12  1  0
 16  5  1  0
  5  4  1  0
  4  3  1  0
  3 19  1  0
 19 20  1  0
  3  2  1  0
  2  1  2  3
  2 23  1  0
 23 24  1  0
 16  9  1  0
 12 10  1  0
  9 10  1  0
 17 21  1  0
  9  8  1  0
  5  6  1  0
 23  6  1  0
 19 18  1  0
 11 35  1  0
 11 36  1  0
 11 37  1  0
 22 46  1  0
 22 47  1  0
  8 33  1  6
  7 31  1  0
  7 32  1  0
 18 43  1  6
 17 42  1  1
 15 40  1  0
 15 41  1  0
 12 38  1  0
 12 39  1  0
  5 30  1  6
  4 28  1  0
  4 29  1  0
  3 27  1  1
 19 44  1  6
 20 45  1  0
  1 25  1  0
  1 26  1  0
 23 48  1  6
 24 49  1  0
  9 34  1  6
M  END


  Mrv1652309022206232D          

 24 30  0  0  1  0            999 V2000
   -1.0137   -0.7847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2512   -0.4698    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0506    0.3584    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7603    0.1256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6923    0.1443    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1918   -0.4206    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0038   -0.7475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6913   -0.1849    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4049    0.3006    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1557    0.7011    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8024    1.2133    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6038   -0.0240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0695   -0.6761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3091   -1.4656    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2476   -0.4261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5488    0.2779    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0153    0.9479    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2150    0.5743    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4727    1.0248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3251    1.8365    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8479    0.7974    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5547    1.3010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4727   -0.9138    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4938   -1.7385    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  3  2  1  1  0  0  0
  3  4  1  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  1  0  0  0
  8  7  1  6  0  0  0
  9  8  1  1  0  0  0
  9 10  1  0  0  0  0
 10 11  1  6  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 16 15  1  6  0  0  0
  5 16  1  0  0  0  0
  9 16  1  0  0  0  0
 16 17  1  0  0  0  0
 18 17  1  6  0  0  0
  6 18  1  0  0  0  0
 18 19  1  0  0  0  0
  3 19  1  0  0  0  0
 19 20  1  0  0  0  0
 17 21  1  1  0  0  0
  8 21  1  0  0  0  0
 21 22  1  0  0  0  0
 10 22  1  0  0  0  0
  6 23  1  0  0  0  0
  2 23  1  0  0  0  0
 23 24  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0148617

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@]12CN3[C@H]4C[C@@]56[C@H]7[C@@H]3[C@](CC(=O)C1)([C@@H]5C[C@H](C7O)C(=C)[C@H]6O)[C@@H]24

> <INCHI_IDENTIFIER>
InChI=1S/C20H25NO3/c1-8-10-3-12-19(17(8)24)6-11-15-18(2)4-9(22)5-20(12,15)16(21(11)7-18)13(19)14(10)23/h10-17,23-24H,1,3-7H2,2H3/t10-,11-,12+,13+,14?,15+,16+,17+,18+,19-,20+/m0/s1

> <INCHI_KEY>
RTPBIHZJNATNAO-XYGFAXLSSA-N

> <FORMULA>
C20H25NO3

> <MOLECULAR_WEIGHT>
327.424

> <EXACT_MASS>
327.183443669

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
49

> <JCHEM_AVERAGE_POLARIZABILITY>
0.0

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,5S,8R,9S,11S,13R,14S,16S,17R,18S)-10,13-dihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.0^{1,8}.0^{5,17}.0^{7,16}.0^{9,14}.0^{14,18}]nonadecan-3-one

> <ALOGPS_LOGP>
0.23

> <JCHEM_LOGP>
-0.5229593273333333

> <ALOGPS_LOGS>
-1.55

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
14.700285043396647

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.984310473370158

> <JCHEM_PKA_STRONGEST_BASIC>
8.37438703927632

> <JCHEM_POLAR_SURFACE_AREA>
60.769999999999996

> <JCHEM_REFRACTIVITY>
87.2983

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
9.16e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,5S,8R,9S,11S,13R,14S,16S,17R,18S)-10,13-dihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.0^{1,8}.0^{5,17}.0^{7,16}.0^{9,14}.0^{14,18}]nonadecan-3-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0      -1.892  -1.465   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.469  -0.877   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.094   0.669   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.419   0.234   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.159   0.269   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.225  -0.785   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.740  -1.395   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.024  -0.345   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.356   0.561   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.757   1.309   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.965   2.265   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.594  -0.045   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.596  -1.262   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       8.044  -2.736   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       6.062  -0.795   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.758   0.519   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.762   1.769   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.268   1.072   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.882   1.913   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       0.607   3.428   0.000  0.00  0.00           O+0
HETATM   21  N   UNK     0       5.316   1.488   0.000  0.00  0.00           N+0
HETATM   22  C   UNK     0       6.635   2.429   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.882  -1.706   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       0.922  -3.245   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   23                                                  
CONECT    3    2    4   19                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   16                                                  
CONECT    6    5    7   18   23                                             
CONECT    7    6    8                                                       
CONECT    8    7    9   21                                                  
CONECT    9    8   10   16                                                  
CONECT   10    9   11   12   22                                             
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15    5    9   17                                             
CONECT   17   16   18   21                                                  
CONECT   18   17    6   19                                                  
CONECT   19   18    3   20                                                  
CONECT   20   19                                                            
CONECT   21   17    8   22                                                  
CONECT   22   21   10                                                       
CONECT   23    6    2   24                                                  
CONECT   24   23                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   60    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₂₅NO₃

Average Mass

327.4240 Da

Monoisotopic Mass

327.18344 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C[C@]12CN3[C@H]4C[C@@]56[C@H]7[C@@H]3[C@](CC(=O)C1)([C@@H]5C[C@H](C7O)C(=C)[C@H]6O)[C@@H]24

InChI Identifier

InChI=1S/C20H25NO3/c1-8-10-3-12-19(17(8)24)6-11-15-18(2)4-9(22)5-20(12,15)16(21(11)7-18)13(19)14(10)23/h10-17,23-24H,1,3-7H2,2H3/t10-,11-,12+,13+,14?,15+,16+,17+,18+,19-,20+/m0/s1

InChI Key

RTPBIHZJNATNAO-XYGFAXLSSA-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
Delphinium venulosum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hetisine-type diterpenoid alkaloids. These are alkaloid diterpenoids with a structure based on the hetisine skeleton, which is a heptacyclic compound with an additional N-C-6 bond as compared with the hetidine-type, and thus, is one of most complex entries in the atisane-class.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Hetisine-type diterpenoid alkaloids

Alternative Parents

Substituents

Hetisine-type diterpenoid alkaloid
Quinolizidine
Isoindolone
Azaspirodecane
Alkaloid or derivatives
Isoindole or derivatives
Isoindoline
Indolizidine
Indole or derivatives
Azepane
N-alkylpyrrolidine
Piperidine
Pyrrolidine
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	0.23	ALOGPS
logS	-1.6	ALOGPS

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00025033

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

101631695

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,5s,8r,9s,11s,13r,14s,16s,17r,18s)-10,13-dihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.0¹,⁸.0⁵,¹⁷.0⁷,¹⁶.0⁹,¹⁴.0¹⁴,¹⁸]nonadecan-3-one (NP0148617)

MOL for NP0148617 ((1r,5s,8r,9s,11s,13r,14s,16s,17r,18s)-10,13-dihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.0¹,⁸.0⁵,¹⁷.0⁷,¹⁶.0⁹,¹⁴.0¹⁴,¹⁸]nonadecan-3-one)

3D MOL for NP0148617 ((1r,5s,8r,9s,11s,13r,14s,16s,17r,18s)-10,13-dihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.0¹,⁸.0⁵,¹⁷.0⁷,¹⁶.0⁹,¹⁴.0¹⁴,¹⁸]nonadecan-3-one)

3D SDF for NP0148617 ((1r,5s,8r,9s,11s,13r,14s,16s,17r,18s)-10,13-dihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.0¹,⁸.0⁵,¹⁷.0⁷,¹⁶.0⁹,¹⁴.0¹⁴,¹⁸]nonadecan-3-one)

3D-SDF for NP0148617 ((1r,5s,8r,9s,11s,13r,14s,16s,17r,18s)-10,13-dihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.0¹,⁸.0⁵,¹⁷.0⁷,¹⁶.0⁹,¹⁴.0¹⁴,¹⁸]nonadecan-3-one)

PDB for NP0148617 ((1r,5s,8r,9s,11s,13r,14s,16s,17r,18s)-10,13-dihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.0¹,⁸.0⁵,¹⁷.0⁷,¹⁶.0⁹,¹⁴.0¹⁴,¹⁸]nonadecan-3-one)

3D PDB for NP0148617 ((1r,5s,8r,9s,11s,13r,14s,16s,17r,18s)-10,13-dihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.0¹,⁸.0⁵,¹⁷.0⁷,¹⁶.0⁹,¹⁴.0¹⁴,¹⁸]nonadecan-3-one)

SMILES for NP0148617 ((1r,5s,8r,9s,11s,13r,14s,16s,17r,18s)-10,13-dihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.0¹,⁸.0⁵,¹⁷.0⁷,¹⁶.0⁹,¹⁴.0¹⁴,¹⁸]nonadecan-3-one)

INCHI for NP0148617 ((1r,5s,8r,9s,11s,13r,14s,16s,17r,18s)-10,13-dihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.0¹,⁸.0⁵,¹⁷.0⁷,¹⁶.0⁹,¹⁴.0¹⁴,¹⁸]nonadecan-3-one)

Structure for NP0148617 ((1r,5s,8r,9s,11s,13r,14s,16s,17r,18s)-10,13-dihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.0¹,⁸.0⁵,¹⁷.0⁷,¹⁶.0⁹,¹⁴.0¹⁴,¹⁸]nonadecan-3-one)

3D Structure for NP0148617 ((1r,5s,8r,9s,11s,13r,14s,16s,17r,18s)-10,13-dihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.0¹,⁸.0⁵,¹⁷.0⁷,¹⁶.0⁹,¹⁴.0¹⁴,¹⁸]nonadecan-3-one)