NP-MRD: Showing NP-Card for 8'-chloro-2',3',4-trimethoxy-10'-azaspiro[cyclopentane-1,7'-tricyclo[4.3.3.0¹,⁶]dodecane]-2',3-diene-4',5-dione (NP0315381)

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Record Information

Version

2.0

Created at

2022-09-11 13:59:09 UTC

Updated at

2022-09-11 13:59:09 UTC

NP-MRD ID

NP0315381

Secondary Accession Numbers

None

Natural Product Identification

Common Name

8'-chloro-2',3',4-trimethoxy-10'-azaspiro[cyclopentane-1,7'-tricyclo[4.3.3.0¹,⁶]dodecane]-2',3-diene-4',5-dione

Description

8'-Chloro-2',3,3'-trimethoxy-10'-azaspiro[cyclopentane-1,7'-tricyclo[4.3.3.0¹,⁶]Dodecane]-2',3-diene-2,4'-dione belongs to the class of organic compounds known as acutumine and related alkaloids. These are alkaloids with a structure based on the tricyclic acutumine skeleton, which contains an indoline moiety and two cyclopentene rings. 8'-Chloro-2',3,3'-trimethoxy-10'-azaspiro[cyclopentane-1,7'-tricyclo[4.3.3.0¹,⁶]Dodecane]-2',3-diene-2,4'-dione is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004161520462D          

 25 28  0  0  0  0            999 V2000
    4.0157    1.9592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1989    1.8438    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8903    1.0787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3280    0.3794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7982   -0.2530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9450   -0.0211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9760   -0.7675    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6084   -1.2974    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    1.2637   -0.8911    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7380   -0.2683    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0271    0.0402    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0298    0.8632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8302    1.0634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2679    0.3640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0804    0.2213    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3631   -0.5537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1757   -0.6964    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8333   -1.1861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0207   -1.0434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4909   -1.6757    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3217   -1.5330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1160   -1.9611    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5861   -2.5935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0900    0.8785    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4576    1.4084    0.0000 O   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  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
  6 14  1  0  0  0  0
 10 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 10 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 18 22  1  0  0  0  0
 22 23  1  0  0  0  0
  6 24  1  0  0  0  0
  3 24  1  0  0  0  0
 24 25  2  0  0  0  0
M  END

     RDKit          3D

 47 50  0  0  0  0  0  0  0  0999 V2000
    5.6667    0.3968    1.4936 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4084   -0.2387    1.4683 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4432    0.2295    0.5626 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2379    1.4884    0.2417 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1426    1.6204   -0.7425 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4234    0.3215   -0.7292 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4956   -0.5866   -0.1849 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6052   -1.8244   -0.3179 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0390   -0.0851   -2.1300 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9506   -1.5403   -2.5679 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -0.4358   -0.3937   -2.1189 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7014   -0.6935   -0.6601 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1478   -1.9690   -0.2576 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0193   -1.8030    1.1773 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3381   -0.3521    1.4161 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1610    0.2846    0.0596 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4661    1.6565    0.1537 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9106    1.5923    0.4507 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4719    2.5857    0.9449 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6949    0.4030    0.1826 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0515    0.3896    0.4748 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9336    1.4333    0.1893 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1320   -0.6524   -0.3313 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8739   -1.7921   -0.5914 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6912   -2.4531    0.3239 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2876   -0.1089    2.2659 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1751    0.3737    0.5015 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6048    1.4608    1.7894 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8286    2.3173    0.6730 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5427    2.4986   -0.4424 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6173    1.7438   -1.7357 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2149    0.7378   -2.8418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6836   -1.2842   -2.7327 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0696    0.4660   -2.3929 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8050   -2.7392   -0.4852 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7661   -2.4867    1.6063 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9488   -2.0922    1.7290 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3822    0.0463    2.1592 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3790   -0.3104    1.7853 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3980    2.0869   -0.8897 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0257    2.2787    0.9028 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9806    1.6577   -0.8959 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7925    2.3349    0.8178 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9665    1.0598    0.4495 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5152   -1.8679    0.7451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1454   -3.3123   -0.2175 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1360   -2.8782    1.1898 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  6  9  1  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 16 15  1  1
 16 17  1  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 20 23  2  0
 23 24  1  0
 24 25  1  0
  6  7  1  1
  7  8  2  0
  7  3  1  0
 16  6  1  0
 16 12  1  0
 12 23  1  6
  1 26  1  0
  1 27  1  0
  1 28  1  0
  4 29  1  0
  5 30  1  0
  5 31  1  0
  9 32  1  6
 11 33  1  0
 11 34  1  0
 13 35  1  0
 14 36  1  0
 14 37  1  0
 15 38  1  0
 15 39  1  0
 17 40  1  0
 17 41  1  0
 22 42  1  0
 22 43  1  0
 22 44  1  0
 25 45  1  0
 25 46  1  0
 25 47  1  0
M  END


  Mrv1533004161520462D          

 25 28  0  0  0  0            999 V2000
    4.0157    1.9592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1989    1.8438    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8903    1.0787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3280    0.3794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7982   -0.2530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9450   -0.0211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9760   -0.7675    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6084   -1.2974    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    1.2637   -0.8911    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7380   -0.2683    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0271    0.0402    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0298    0.8632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8302    1.0634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2679    0.3640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0804    0.2213    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3631   -0.5537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1757   -0.6964    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8333   -1.1861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0207   -1.0434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4909   -1.6757    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3217   -1.5330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1160   -1.9611    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5861   -2.5935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0900    0.8785    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4576    1.4084    0.0000 O   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  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
  6 14  1  0  0  0  0
 10 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 10 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 18 22  1  0  0  0  0
 22 23  1  0  0  0  0
  6 24  1  0  0  0  0
  3 24  1  0  0  0  0
 24 25  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0315381

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CCC2(C(Cl)CC34NCCC23CC(=O)C(OC)=C4OC)C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C18H22ClNO5/c1-23-11-4-5-17(14(11)22)12(19)9-18-15(25-3)13(24-2)10(21)8-16(17,18)6-7-20-18/h4,12,20H,5-9H2,1-3H3

> <INCHI_KEY>
AWBBVBCVNQKGBX-UHFFFAOYSA-N

> <FORMULA>
C18H22ClNO5

> <MOLECULAR_WEIGHT>
367.83

> <EXACT_MASS>
367.1186505

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
36.32340526185157

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
8'-chloro-2',3',4-trimethoxy-10'-azaspiro[cyclopentane-1,7'-tricyclo[4.3.3.0¹,⁶]dodecane]-2',3-diene-4',5-dione

> <ALOGPS_LOGP>
1.47

> <JCHEM_LOGP>
0.21404369966666614

> <ALOGPS_LOGS>
-2.81

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
17.378403066615515

> <JCHEM_PKA_STRONGEST_BASIC>
8.911029756390796

> <JCHEM_POLAR_SURFACE_AREA>
73.86000000000001

> <JCHEM_REFRACTIVITY>
94.59999999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.74e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
8'-chloro-2',3',4-trimethoxy-10'-azaspiro[cyclopentane-1,7'-tricyclo[4.3.3.0¹,⁶]dodecane]-2',3-diene-4',5-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0       7.496   3.657   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       5.971   3.442   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       5.395   2.014   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.212   0.708   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.223  -0.472   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.631  -0.039   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.689  -1.433   0.000  0.00  0.00           C+0
HETATM    8 Cl   UNK     0       4.869  -2.422   0.000  0.00  0.00          Cl+0
HETATM    9  C   UNK     0       2.359  -1.663   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.378  -0.501   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0      -0.051   0.075   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0       0.056   1.611   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.550   1.985   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.367   0.680   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.883   0.413   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.411  -1.034   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       5.928  -1.300   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       3.422  -2.214   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.905  -1.948   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       0.916  -3.128   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -0.601  -2.862   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       3.950  -3.661   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       2.961  -4.841   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.901   1.640   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       2.721   2.629   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   24                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   14   24                                             
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11   14   19                                             
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13    6   10   15                                             
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   22                                                  
CONECT   19   18   10   20                                                  
CONECT   20   19   21                                                       
CONECT   21   20                                                            
CONECT   22   18   23                                                       
CONECT   23   22                                                            
CONECT   24    6    3   25                                                  
CONECT   25   24                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   56    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₂₂ClNO₅

Average Mass

367.8300 Da

Monoisotopic Mass

367.11865 Da

IUPAC Name

8'-chloro-2',3',4-trimethoxy-10'-azaspiro[cyclopentane-1,7'-tricyclo[4.3.3.0¹,⁶]dodecane]-2',3-diene-4',5-dione

Traditional Name

8'-chloro-2',3',4-trimethoxy-10'-azaspiro[cyclopentane-1,7'-tricyclo[4.3.3.0¹,⁶]dodecane]-2',3-diene-4',5-dione

CAS Registry Number

Not Available

SMILES

COC1=CCC2(C(Cl)CC34NCCC23CC(=O)C(OC)=C4OC)C1=O

InChI Identifier

InChI=1S/C18H22ClNO5/c1-23-11-4-5-17(14(11)22)12(19)9-18-15(25-3)13(24-2)10(21)8-16(17,18)6-7-20-18/h4,12,20H,5-9H2,1-3H3

InChI Key

AWBBVBCVNQKGBX-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as acutumine and related alkaloids. These are alkaloids with a structure based on the tricyclic acutumine skeleton, which contains an indoline moiety and two cyclopentene rings.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Acutumine and related alkaloids

Sub Class

Not Available

Direct Parent

Acutumine and related alkaloids

Alternative Parents

Substituents

Acutumine skeketon
Indole or derivatives
Dihydroindole
Cyclohexenone
Pyrrolidine
Vinylogous ester
Ketone
Cyclic ketone
Secondary aliphatic amine
Azacycle
Secondary amine
Organoheterocyclic compound
Organonitrogen compound
Organochloride
Organohalogen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Organic nitrogen compound
Carbonyl group
Amine
Organooxygen compound
Alkyl chloride
Alkyl halide
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	1.47	ALOGPS
logP	0.21	ChemAxon
logS	-2.8	ALOGPS
pKa (Strongest Acidic)	17.38	ChemAxon
pKa (Strongest Basic)	8.91	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	73.86 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	94.6 m³·mol⁻¹	ChemAxon
Polarizability	36.32 Å³	ChemAxon
Number of Rings	4	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

14380734

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 8'-chloro-2',3',4-trimethoxy-10'-azaspiro[cyclopentane-1,7'-tricyclo[4.3.3.0¹,⁶]dodecane]-2',3-diene-4',5-dione (NP0315381)

MOL for NP0315381 (8'-chloro-2',3',4-trimethoxy-10'-azaspiro[cyclopentane-1,7'-tricyclo[4.3.3.0¹,⁶]dodecane]-2',3-diene-4',5-dione)

3D MOL for NP0315381 (8'-chloro-2',3',4-trimethoxy-10'-azaspiro[cyclopentane-1,7'-tricyclo[4.3.3.0¹,⁶]dodecane]-2',3-diene-4',5-dione)

3D SDF for NP0315381 (8'-chloro-2',3',4-trimethoxy-10'-azaspiro[cyclopentane-1,7'-tricyclo[4.3.3.0¹,⁶]dodecane]-2',3-diene-4',5-dione)

3D-SDF for NP0315381 (8'-chloro-2',3',4-trimethoxy-10'-azaspiro[cyclopentane-1,7'-tricyclo[4.3.3.0¹,⁶]dodecane]-2',3-diene-4',5-dione)

PDB for NP0315381 (8'-chloro-2',3',4-trimethoxy-10'-azaspiro[cyclopentane-1,7'-tricyclo[4.3.3.0¹,⁶]dodecane]-2',3-diene-4',5-dione)

3D PDB for NP0315381 (8'-chloro-2',3',4-trimethoxy-10'-azaspiro[cyclopentane-1,7'-tricyclo[4.3.3.0¹,⁶]dodecane]-2',3-diene-4',5-dione)

SMILES for NP0315381 (8'-chloro-2',3',4-trimethoxy-10'-azaspiro[cyclopentane-1,7'-tricyclo[4.3.3.0¹,⁶]dodecane]-2',3-diene-4',5-dione)

INCHI for NP0315381 (8'-chloro-2',3',4-trimethoxy-10'-azaspiro[cyclopentane-1,7'-tricyclo[4.3.3.0¹,⁶]dodecane]-2',3-diene-4',5-dione)

Structure for NP0315381 (8'-chloro-2',3',4-trimethoxy-10'-azaspiro[cyclopentane-1,7'-tricyclo[4.3.3.0¹,⁶]dodecane]-2',3-diene-4',5-dione)

3D Structure for NP0315381 (8'-chloro-2',3',4-trimethoxy-10'-azaspiro[cyclopentane-1,7'-tricyclo[4.3.3.0¹,⁶]dodecane]-2',3-diene-4',5-dione)