NP-MRD: Showing NP-Card for n-{6-hydroxy-5,13,14,15-tetramethoxytricyclo[9.4.0.0²,⁷]pentadeca-1(15),2,4,6,11,13-hexaen-8-yl}ethanimidic acid (NP0195271)

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Record Information

Version

2.0

Created at

2022-09-04 13:06:01 UTC

Updated at

2022-09-04 13:06:01 UTC

NP-MRD ID

NP0195271

Secondary Accession Numbers

None

Natural Product Identification

Common Name

n-{6-hydroxy-5,13,14,15-tetramethoxytricyclo[9.4.0.0²,⁷]pentadeca-1(15),2,4,6,11,13-hexaen-8-yl}ethanimidic acid

Description

N-{6-hydroxy-5,13,14,15-tetramethoxytricyclo[9.4.0.0²,⁷]Pentadeca-1(15),2(7),3,5,11,13-hexaen-8-yl}ethanimidic acid belongs to the class of organic compounds known as allocolchicine alkaloids. These are alkaloids with a structure based on the tricyclic allocolchicine skeleton, which consists of a dibenzocycloheptane where the cycloheptane moiety carries the N-acetamide group. n-{6-hydroxy-5,13,14,15-tetramethoxytricyclo[9.4.0.0²,⁷]pentadeca-1(15),2,4,6,11,13-hexaen-8-yl}ethanimidic acid is found in Colchicum szovitsii. N-{6-hydroxy-5,13,14,15-tetramethoxytricyclo[9.4.0.0²,⁷]Pentadeca-1(15),2(7),3,5,11,13-hexaen-8-yl}ethanimidic acid is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241512592D          

 28 30  0  0  0  0            999 V2000
    6.6616    0.7447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3602   -0.0232    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5444   -0.1462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0300    0.4988    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2142    0.3759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9128   -0.3921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4272   -1.0371    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2436   -1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5003   -2.1994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7570   -1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5734   -1.0371    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7576   -0.9142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4562   -0.1462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6404   -0.0232    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1261   -0.6682    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9706    0.4988    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6692    1.2668    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1836    1.9118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7864    0.3759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3008    1.0209    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9994    1.7888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0878   -0.3921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8886   -2.3558    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.7657   -3.1716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4107   -3.6860    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9977   -3.4730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2430   -0.9142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7573   -1.5592    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  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 13 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 16 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 19 22  2  0  0  0  0
  6 22  1  0  0  0  0
 11 22  1  0  0  0  0
  8 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
  7 27  2  0  0  0  0
  3 27  1  0  0  0  0
 27 28  1  0  0  0  0
M  END

     RDKit          3D

 53 55  0  0  0  0  0  0  0  0999 V2000
   -3.3348    4.4642   -1.6152 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4028    3.3585   -0.7704 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3430    2.4397   -0.6404 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1720    2.5708   -1.3363 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1319    1.6746   -1.2091 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3023    0.6249   -0.3455 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4923    0.4207    0.4016 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4910    1.3510    0.2326 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6821    1.2606    0.9160 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8879   -0.7323    1.2424 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9150   -1.4601    0.4914 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0408   -2.0888    1.0287 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0267   -2.8007    0.1878 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2284   -2.0520    2.2684 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7662   -1.7059    1.5450 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1921   -2.3679    0.2825 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0135   -1.5316   -0.0870 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1886   -2.1590   -0.0949 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3542   -1.4027   -0.2764 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5423   -2.0783   -0.2815 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7105   -3.4487   -0.1238 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2607   -0.0254   -0.4406 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4655    0.6426   -0.6116 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2434    1.1664    0.4293 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0329    0.6291   -0.4324 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9785    1.9755   -0.5783 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0254    2.9208    0.4762 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9284   -0.1534   -0.2593 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7059    4.2542   -2.6531 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0498    5.2335   -1.2078 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3407    4.9622   -1.6223 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0658    3.4100   -2.0082 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7354    1.7342   -1.8102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8788    0.5727    1.5755 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3020   -0.4477    2.2009 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7730   -1.5023   -0.5443 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0121   -2.2977    0.2208 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6856   -2.7824   -0.8831 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0781   -3.8625    0.5197 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0043   -1.2028    2.1312 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2104   -2.5199    2.1445 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8915   -2.2825   -0.5332 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1262   -3.3800    0.4872 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2563   -3.2510    0.0383 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4560   -3.8187    0.8985 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9714   -3.9600   -0.8081 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6995   -3.7843   -0.4593 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3425    2.2640    0.2882 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2753    0.7679    0.4644 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6884    0.9440    1.3831 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8444    2.6030    1.1876 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1628    3.9453    0.1259 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1055    2.9083    1.0986 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  2  0
  6  7  1  0
  7 10  1  0
 10 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 19 22  2  0
 22 23  1  0
 23 24  1  0
 22 25  1  0
 25 26  1  0
 26 27  1  0
 25 28  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  2  0
  7  8  2  0
  8  9  1  0
  8  3  1  0
 28  6  1  0
 28 17  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  4 32  1  0
  5 33  1  0
 10 35  1  1
 15 40  1  0
 15 41  1  0
 16 42  1  0
 16 43  1  0
 18 44  1  0
 21 45  1  0
 21 46  1  0
 21 47  1  0
 24 48  1  0
 24 49  1  0
 24 50  1  0
 27 51  1  0
 27 52  1  0
 27 53  1  0
 11 36  1  0
 13 37  1  0
 13 38  1  0
 13 39  1  0
  9 34  1  0
M  END


  Mrv1533004241512592D          

 28 30  0  0  0  0            999 V2000
    6.6616    0.7447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3602   -0.0232    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5444   -0.1462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0300    0.4988    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2142    0.3759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9128   -0.3921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4272   -1.0371    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2436   -1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5003   -2.1994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7570   -1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5734   -1.0371    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7576   -0.9142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4562   -0.1462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6404   -0.0232    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1261   -0.6682    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9706    0.4988    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6692    1.2668    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1836    1.9118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7864    0.3759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3008    1.0209    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9994    1.7888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0878   -0.3921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8886   -2.3558    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.7657   -3.1716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4107   -3.6860    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9977   -3.4730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2430   -0.9142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7573   -1.5592    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  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 13 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 16 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 19 22  2  0  0  0  0
  6 22  1  0  0  0  0
 11 22  1  0  0  0  0
  8 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
  7 27  2  0  0  0  0
  3 27  1  0  0  0  0
 27 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0195271

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C2C(C(CCC3=CC(OC)=C(OC)C(OC)=C23)NC(C)=O)=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C21H25NO6/c1-11(23)22-14-8-6-12-10-16(26-3)20(27-4)21(28-5)17(12)13-7-9-15(25-2)19(24)18(13)14/h7,9-10,14,24H,6,8H2,1-5H3,(H,22,23)

> <INCHI_KEY>
DMFNBXZGZQLZMS-UHFFFAOYSA-N

> <FORMULA>
C21H25NO6

> <MOLECULAR_WEIGHT>
387.432

> <EXACT_MASS>
387.168187529

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
40.533182232184004

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
N-{6-hydroxy-5,13,14,15-tetramethoxytricyclo[9.4.0.0²,⁷]pentadeca-1(15),2,4,6,11,13-hexaen-8-yl}acetamide

> <ALOGPS_LOGP>
2.18

> <JCHEM_LOGP>
2.175060074

> <ALOGPS_LOGS>
-3.89

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.205746782410156

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.396874058828738

> <JCHEM_PKA_STRONGEST_BASIC>
-1.5332301487706026

> <JCHEM_POLAR_SURFACE_AREA>
86.25000000000001

> <JCHEM_REFRACTIVITY>
104.52589999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.05e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
N-{6-hydroxy-5,13,14,15-tetramethoxytricyclo[9.4.0.0²,⁷]pentadeca-1(15),2,4,6,11,13-hexaen-8-yl}acetamide

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0      12.435   1.390   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      11.872  -0.043   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      10.350  -0.273   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.389   0.931   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.867   0.702   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.304  -0.732   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.264  -1.936   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.921  -3.437   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.534  -4.106   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.146  -3.437   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.804  -1.936   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.281  -1.706   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.718  -0.273   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       1.196  -0.043   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       0.235  -1.247   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.678   0.931   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       3.116   2.365   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       4.076   3.569   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.201   0.702   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       6.161   1.906   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       5.599   3.339   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.764  -0.732   0.000  0.00  0.00           C+0
HETATM   23  N   UNK     0       9.125  -4.398   0.000  0.00  0.00           N+0
HETATM   24  C   UNK     0       8.896  -5.920   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      10.100  -6.880   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       7.462  -6.483   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       9.787  -1.706   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      10.747  -2.910   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   27                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   22                                                  
CONECT    7    6    8   27                                                  
CONECT    8    7    9   23                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   22                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   16                                                  
CONECT   14   13   15                                                       
CONECT   15   14                                                            
CONECT   16   13   17   19                                                  
CONECT   17   16   18                                                       
CONECT   18   17                                                            
CONECT   19   16   20   22                                                  
CONECT   20   19   21                                                       
CONECT   21   20                                                            
CONECT   22   19    6   11                                                  
CONECT   23    8   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24                                                            
CONECT   27    7    3   28                                                  
CONECT   28   27                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   60    0
END

View in JSmol

Synonyms

Value	Source
N-{6-hydroxy-5,13,14,15-tetramethoxytricyclo[9.4.0.0,]pentadeca-1(15),2(7),3,5,11,13-hexaen-8-yl}ethanimidate	Generator
N-{6-hydroxy-5,13,14,15-tetramethoxytricyclo[9.4.0.0²,⁷]pentadeca-1(15),2(7),3,5,11,13-hexaen-8-yl}ethanimidate	Generator

Chemical Formula

C₂₁H₂₅NO₆

Average Mass

387.4320 Da

Monoisotopic Mass

387.16819 Da

IUPAC Name

N-{6-hydroxy-5,13,14,15-tetramethoxytricyclo[9.4.0.0²,⁷]pentadeca-1(15),2,4,6,11,13-hexaen-8-yl}acetamide

Traditional Name

N-{6-hydroxy-5,13,14,15-tetramethoxytricyclo[9.4.0.0²,⁷]pentadeca-1(15),2,4,6,11,13-hexaen-8-yl}acetamide

CAS Registry Number

Not Available

SMILES

COC1=CC=C2C(C(CCC3=CC(OC)=C(OC)C(OC)=C23)NC(C)=O)=C1O

InChI Identifier

InChI=1S/C21H25NO6/c1-11(23)22-14-8-6-12-10-16(26-3)20(27-4)21(28-5)17(12)13-7-9-15(25-2)19(24)18(13)14/h7,9-10,14,24H,6,8H2,1-5H3,(H,22,23)

InChI Key

DMFNBXZGZQLZMS-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 szovitsii	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as allocolchicine alkaloids. These are alkaloids with a structure based on the tricyclic allocolchicine skeleton, which consists of a dibenzocycloheptane where the cycloheptane moiety carries the N-acetamide group.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Allocolchicine alkaloids

Sub Class

Not Available

Direct Parent

Allocolchicine alkaloids

Alternative Parents

Substituents

Allocolchicine alkaloid skeleton
Anisole
Phenol ether
Alkyl aryl ether
1-hydroxy-4-unsubstituted benzenoid
Phenol
Benzenoid
Acetamide
Carboxamide group
Secondary carboxylic acid amide
Carboxylic acid derivative
Ether
Organonitrogen compound
Organic oxygen compound
Organic nitrogen compound
Organic oxide
Carbonyl group
Organooxygen compound
Hydrocarbon derivative
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	2.18	ALOGPS
logP	2.18	ChemAxon
logS	-3.9	ALOGPS
pKa (Strongest Acidic)	9.4	ChemAxon
pKa (Strongest Basic)	-1.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	86.25 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	104.53 m³·mol⁻¹	ChemAxon
Polarizability	40.53 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

11188363

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for n-{6-hydroxy-5,13,14,15-tetramethoxytricyclo[9.4.0.0²,⁷]pentadeca-1(15),2,4,6,11,13-hexaen-8-yl}ethanimidic acid (NP0195271)

MOL for NP0195271 (n-{6-hydroxy-5,13,14,15-tetramethoxytricyclo[9.4.0.0²,⁷]pentadeca-1(15),2,4,6,11,13-hexaen-8-yl}ethanimidic acid)

3D MOL for NP0195271 (n-{6-hydroxy-5,13,14,15-tetramethoxytricyclo[9.4.0.0²,⁷]pentadeca-1(15),2,4,6,11,13-hexaen-8-yl}ethanimidic acid)

3D SDF for NP0195271 (n-{6-hydroxy-5,13,14,15-tetramethoxytricyclo[9.4.0.0²,⁷]pentadeca-1(15),2,4,6,11,13-hexaen-8-yl}ethanimidic acid)

3D-SDF for NP0195271 (n-{6-hydroxy-5,13,14,15-tetramethoxytricyclo[9.4.0.0²,⁷]pentadeca-1(15),2,4,6,11,13-hexaen-8-yl}ethanimidic acid)

PDB for NP0195271 (n-{6-hydroxy-5,13,14,15-tetramethoxytricyclo[9.4.0.0²,⁷]pentadeca-1(15),2,4,6,11,13-hexaen-8-yl}ethanimidic acid)

3D PDB for NP0195271 (n-{6-hydroxy-5,13,14,15-tetramethoxytricyclo[9.4.0.0²,⁷]pentadeca-1(15),2,4,6,11,13-hexaen-8-yl}ethanimidic acid)

SMILES for NP0195271 (n-{6-hydroxy-5,13,14,15-tetramethoxytricyclo[9.4.0.0²,⁷]pentadeca-1(15),2,4,6,11,13-hexaen-8-yl}ethanimidic acid)

INCHI for NP0195271 (n-{6-hydroxy-5,13,14,15-tetramethoxytricyclo[9.4.0.0²,⁷]pentadeca-1(15),2,4,6,11,13-hexaen-8-yl}ethanimidic acid)

Structure for NP0195271 (n-{6-hydroxy-5,13,14,15-tetramethoxytricyclo[9.4.0.0²,⁷]pentadeca-1(15),2,4,6,11,13-hexaen-8-yl}ethanimidic acid)

3D Structure for NP0195271 (n-{6-hydroxy-5,13,14,15-tetramethoxytricyclo[9.4.0.0²,⁷]pentadeca-1(15),2,4,6,11,13-hexaen-8-yl}ethanimidic acid)