NP-MRD: Showing NP-Card for 10-(dimethylamino)-3,4,5,14-tetramethoxytricyclo[9.5.0.0²,⁷]hexadeca-1(16),2(7),3,5,11,14-hexaen-13-one (NP0319430)

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Record Information

Version

2.0

Created at

2022-09-11 20:27:02 UTC

Updated at

2022-09-11 20:27:02 UTC

NP-MRD ID

NP0319430

Secondary Accession Numbers

None

Natural Product Identification

Common Name

10-(dimethylamino)-3,4,5,14-tetramethoxytricyclo[9.5.0.0²,⁷]hexadeca-1(16),2(7),3,5,11,14-hexaen-13-one

Description

AC1MYPXZ belongs to the class of organic compounds known as tropones. Tropones are compounds containing a tropone ring, which is a cycloheptatrienone ring bearing a ketone group. 10-(dimethylamino)-3,4,5,14-tetramethoxytricyclo[9.5.0.0²,⁷]hexadeca-1(16),2(7),3,5,11,14-hexaen-13-one is found in Colchicum crocifolium. AC1MYPXZ is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004231520072D          

 28 30  0  0  0  0            999 V2000
    7.0240    0.4618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2669    0.7895    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6045    0.2976    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8740    0.6810    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1188    0.3489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9076   -0.4486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3994   -1.1110    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2239   -1.1394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7602   -0.5125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5578   -0.7237    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1882   -1.9085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4330   -2.2406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7025   -1.8572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5468   -1.0471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7357   -0.8960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4610   -0.1181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6499    0.0329    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1136   -0.5940    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9973    0.5088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7225    1.2867    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2588    1.9136    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8083    0.3577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3447    0.9846    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0699    1.7625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0831   -0.4202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8151   -2.4448    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.6641   -3.2559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5930   -2.1701    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
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  3  9  1  0  0  0  0
  9 10  2  0  0  0  0
  7 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  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 16 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 19 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 22 25  2  0  0  0  0
  6 25  1  0  0  0  0
 14 25  1  0  0  0  0
 11 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
M  END

     RDKit          3D

 55 57  0  0  0  0  0  0  0  0999 V2000
    4.9674   -2.8864    1.1893 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7412   -1.7040    0.4485 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4425   -1.1747    0.4768 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4349   -1.7835    1.1960 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1970   -1.2647    1.2164 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9314   -0.0709    0.4852 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8902    0.5560   -0.2395 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5852    1.6998   -0.9516 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1700    1.5787   -2.3268 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1462   -0.0128   -0.2289 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1398    0.6021   -0.9489 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4719    0.3451   -2.2805 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3153    0.6753    0.4685 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1430    1.9720    0.4675 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5837    3.0588    0.0718 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9629    3.2176   -0.1234 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5204    4.3860   -0.1202 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0255    5.5797   -0.1072 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8418    2.1333   -0.3360 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8956    2.3917   -0.9933 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7340    0.8175    0.0644 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6113    0.1484    0.4992 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0512   -1.1719    1.0038 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2445   -1.6460    0.3309 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0317   -1.9017   -1.0785 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6667   -2.8589    1.0017 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9807   -2.2054    0.9446 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1430   -2.0084    1.9753 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0125   -3.2296    1.1211 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2667   -3.6738    0.7896 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6402   -2.6792    2.2323 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6367   -2.6997    1.7593 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0522    1.7667   -2.9894 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7147    0.5917   -2.4603 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4168    2.3581   -2.5048 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6341   -0.0328   -2.8955 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8110    1.3169   -2.7306 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3570   -0.3269   -2.3588 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1324    2.0644    0.8491 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0191    3.9543   -0.1268 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9962    5.7631   -0.6583 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1735    5.9545    0.9673 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3762    6.4257   -0.5305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6177    0.1960    0.0528 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3648   -0.9971    2.0654 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0235   -1.7944   -1.5809 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6436   -2.9404   -1.2263 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3116   -1.2099   -1.5452 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7779   -2.8841    1.0935 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2805   -2.9216    2.0461 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3370   -3.7511    0.4338 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4572   -3.1984    1.0777 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5638   -2.2220   -0.0961 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2016   -1.3436    2.7703 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5316   -2.9591    2.3397 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3 10  2  0
 10 11  1  0
 11 12  1  0
 10  7  1  0
  7  8  1  0
  8  9  1  0
  7  6  2  0
  6  5  1  0
  5 28  1  0
 28 27  1  0
 27 23  1  0
 23 24  1  0
 24 25  1  0
 24 26  1  0
 23 22  1  0
 22 21  2  0
 21 19  1  0
 19 20  2  0
 19 16  1  0
 16 17  1  0
 17 18  1  0
 16 15  2  0
 15 14  1  0
 14 13  2  0
  5  4  2  0
  4  3  1  0
 13  6  1  0
 13 22  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
 12 36  1  0
 12 37  1  0
 12 38  1  0
  9 33  1  0
  9 34  1  0
  9 35  1  0
 28 54  1  0
 28 55  1  0
 27 52  1  0
 27 53  1  0
 23 45  1  1
 25 46  1  0
 25 47  1  0
 25 48  1  0
 26 49  1  0
 26 50  1  0
 26 51  1  0
 21 44  1  0
 18 41  1  0
 18 42  1  0
 18 43  1  0
 15 40  1  0
 14 39  1  0
  4 32  1  0
M  END


  Mrv1533004231520072D          

 28 30  0  0  0  0            999 V2000
    7.0240    0.4618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2669    0.7895    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6045    0.2976    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8740    0.6810    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1188    0.3489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9076   -0.4486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3994   -1.1110    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2239   -1.1394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7602   -0.5125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5578   -0.7237    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1882   -1.9085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4330   -2.2406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7025   -1.8572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5468   -1.0471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7357   -0.8960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4610   -0.1181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6499    0.0329    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1136   -0.5940    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9973    0.5088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7225    1.2867    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2588    1.9136    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8083    0.3577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3447    0.9846    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0699    1.7625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0831   -0.4202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8151   -2.4448    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.6641   -3.2559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5930   -2.1701    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
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  3  9  1  0  0  0  0
  9 10  2  0  0  0  0
  7 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  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 16 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 19 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 22 25  2  0  0  0  0
  6 25  1  0  0  0  0
 14 25  1  0  0  0  0
 11 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0319430

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(OC)C(OC)=C2C(CCC(N(C)C)C3=CC(=O)C(OC)=CC=C23)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C22H27NO5/c1-23(2)16-9-7-13-11-19(26-4)21(27-5)22(28-6)20(13)14-8-10-18(25-3)17(24)12-15(14)16/h8,10-12,16H,7,9H2,1-6H3

> <INCHI_KEY>
NDKXARFZWSQXGE-UHFFFAOYSA-N

> <FORMULA>
C22H27NO5

> <MOLECULAR_WEIGHT>
385.46

> <EXACT_MASS>
385.188922973

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
41.946913290784344

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
10-(dimethylamino)-3,4,5,14-tetramethoxytricyclo[9.5.0.0²,⁷]hexadeca-1(16),2,4,6,11,14-hexaen-13-one

> <ALOGPS_LOGP>
2.59

> <JCHEM_LOGP>
2.4587702983333335

> <ALOGPS_LOGS>
-4.00

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.775861550503326

> <JCHEM_PKA_STRONGEST_BASIC>
8.828983908881268

> <JCHEM_POLAR_SURFACE_AREA>
57.23000000000001

> <JCHEM_REFRACTIVITY>
112.00109999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.86e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
10-(dimethylamino)-3,4,5,14-tetramethoxytricyclo[9.5.0.0²,⁷]hexadeca-1(16),2,4,6,11,14-hexaen-13-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 23-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-APR-15         0                                  
HETATM    1  C   UNK     0      13.111   0.862   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      11.698   1.474   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      10.462   0.556   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.098   1.271   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.688   0.651   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.294  -0.837   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.212  -2.074   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.751  -2.127   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      10.752  -0.957   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      12.241  -1.351   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       7.818  -3.563   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.408  -4.182   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.045  -3.467   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.754  -1.955   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.240  -1.673   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.727  -0.221   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       1.213   0.061   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       0.212  -1.109   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.728   0.950   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       3.215   2.402   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       4.217   3.572   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.242   0.668   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       6.243   1.838   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       5.730   3.290   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.755  -0.784   0.000  0.00  0.00           C+0
HETATM   26  N   UNK     0       8.988  -4.564   0.000  0.00  0.00           N+0
HETATM   27  C   UNK     0       8.706  -6.078   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      10.440  -4.051   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    9                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   25                                                  
CONECT    7    6    8   11                                                  
CONECT    8    7    9                                                       
CONECT    9    8    3   10                                                  
CONECT   10    9                                                            
CONECT   11    7   12   26                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   25                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   19                                                  
CONECT   17   16   18                                                       
CONECT   18   17                                                            
CONECT   19   16   20   22                                                  
CONECT   20   19   21                                                       
CONECT   21   20                                                            
CONECT   22   19   23   25                                                  
CONECT   23   22   24                                                       
CONECT   24   23                                                            
CONECT   25   22    6   14                                                  
CONECT   26   11   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   60    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₂₇NO₅

Average Mass

385.4600 Da

Monoisotopic Mass

385.18892 Da

IUPAC Name

10-(dimethylamino)-3,4,5,14-tetramethoxytricyclo[9.5.0.0²,⁷]hexadeca-1(16),2,4,6,11,14-hexaen-13-one

Traditional Name

10-(dimethylamino)-3,4,5,14-tetramethoxytricyclo[9.5.0.0²,⁷]hexadeca-1(16),2,4,6,11,14-hexaen-13-one

CAS Registry Number

Not Available

SMILES

COC1=C(OC)C(OC)=C2C(CCC(N(C)C)C3=CC(=O)C(OC)=CC=C23)=C1

InChI Identifier

InChI=1S/C22H27NO5/c1-23(2)16-9-7-13-11-19(26-4)21(27-5)22(28-6)20(13)14-8-10-18(25-3)17(24)12-15(14)16/h8,10-12,16H,7,9H2,1-6H3

InChI Key

NDKXARFZWSQXGE-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Colchicum crocifolium	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tropones. Tropones are compounds containing a tropone ring, which is a cycloheptatrienone ring bearing a ketone group.

Kingdom

Organic compounds

Super Class

Hydrocarbon derivatives

Class

Tropones

Sub Class

Not Available

Direct Parent

Tropones

Alternative Parents

Substituents

Anisole
Phenol ether
Tropone
Alkyl aryl ether
Aralkylamine
Benzenoid
Tertiary amine
Tertiary aliphatic amine
Cyclic ketone
Ether
Organic oxide
Organooxygen compound
Organonitrogen compound
Organic nitrogen compound
Amine
Organic oxygen compound
Aromatic homopolycyclic compound

Molecular Framework

Aromatic homopolycyclic 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	2.59	ALOGPS
logP	2.46	ChemAxon
logS	-4	ALOGPS
pKa (Strongest Acidic)	18.78	ChemAxon
pKa (Strongest Basic)	8.83	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	57.23 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	112 m³·mol⁻¹	ChemAxon
Polarizability	41.95 Å³	ChemAxon
Number of Rings	3	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

3885665

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 10-(dimethylamino)-3,4,5,14-tetramethoxytricyclo[9.5.0.0²,⁷]hexadeca-1(16),2(7),3,5,11,14-hexaen-13-one (NP0319430)

MOL for NP0319430 (10-(dimethylamino)-3,4,5,14-tetramethoxytricyclo[9.5.0.0²,⁷]hexadeca-1(16),2(7),3,5,11,14-hexaen-13-one)

3D MOL for NP0319430 (10-(dimethylamino)-3,4,5,14-tetramethoxytricyclo[9.5.0.0²,⁷]hexadeca-1(16),2(7),3,5,11,14-hexaen-13-one)

3D SDF for NP0319430 (10-(dimethylamino)-3,4,5,14-tetramethoxytricyclo[9.5.0.0²,⁷]hexadeca-1(16),2(7),3,5,11,14-hexaen-13-one)

3D-SDF for NP0319430 (10-(dimethylamino)-3,4,5,14-tetramethoxytricyclo[9.5.0.0²,⁷]hexadeca-1(16),2(7),3,5,11,14-hexaen-13-one)

PDB for NP0319430 (10-(dimethylamino)-3,4,5,14-tetramethoxytricyclo[9.5.0.0²,⁷]hexadeca-1(16),2(7),3,5,11,14-hexaen-13-one)

3D PDB for NP0319430 (10-(dimethylamino)-3,4,5,14-tetramethoxytricyclo[9.5.0.0²,⁷]hexadeca-1(16),2(7),3,5,11,14-hexaen-13-one)

SMILES for NP0319430 (10-(dimethylamino)-3,4,5,14-tetramethoxytricyclo[9.5.0.0²,⁷]hexadeca-1(16),2(7),3,5,11,14-hexaen-13-one)

INCHI for NP0319430 (10-(dimethylamino)-3,4,5,14-tetramethoxytricyclo[9.5.0.0²,⁷]hexadeca-1(16),2(7),3,5,11,14-hexaen-13-one)

Structure for NP0319430 (10-(dimethylamino)-3,4,5,14-tetramethoxytricyclo[9.5.0.0²,⁷]hexadeca-1(16),2(7),3,5,11,14-hexaen-13-one)

3D Structure for NP0319430 (10-(dimethylamino)-3,4,5,14-tetramethoxytricyclo[9.5.0.0²,⁷]hexadeca-1(16),2(7),3,5,11,14-hexaen-13-one)