NP-MRD: Showing NP-Card for n-[(10s,12s,16r)-3,4,5,14-tetramethoxy-13-oxotetracyclo[9.5.0.0²,⁷.0¹²,¹⁶]hexadeca-1(11),2,4,6,14-pentaen-10-yl]ethanimidic acid (NP0280266)

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Record Information

Version

2.0

Created at

2022-09-09 05:57:16 UTC

Updated at

2022-09-09 05:57:16 UTC

NP-MRD ID

NP0280266

Secondary Accession Numbers

None

Natural Product Identification

Common Name

n-[(10s,12s,16r)-3,4,5,14-tetramethoxy-13-oxotetracyclo[9.5.0.0²,⁷.0¹²,¹⁶]hexadeca-1(11),2,4,6,14-pentaen-10-yl]ethanimidic acid

Description

Gamma-Lumicolchicine, also known as lumicolchicines, belongs to the class of organic compounds known as lumicolchicine alkaloids. These are alkaloids with a structure based on the tetracyclic lumicolchicine skeleton. They can derive from a colchicine precursor where the cycloheptatriene ring is replaced with a bicyclo[3.2.0]Hepta-2,6-diene ring system. n-[(10s,12s,16r)-3,4,5,14-tetramethoxy-13-oxotetracyclo[9.5.0.0²,⁷.0¹²,¹⁶]hexadeca-1(11),2,4,6,14-pentaen-10-yl]ethanimidic acid is found in Colchicum autumnale. n-[(10s,12s,16r)-3,4,5,14-tetramethoxy-13-oxotetracyclo[9.5.0.0²,⁷.0¹²,¹⁶]hexadeca-1(11),2,4,6,14-pentaen-10-yl]ethanimidic acid was first documented in 2007 (PMID: 26637043). Based on a literature review very few articles have been published on gamma-Lumicolchicine.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092207572D          

 29 32  0  0  1  0            999 V2000
   -2.5794   -1.7152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8612   -2.1213    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1505   -1.7024    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3938   -2.0312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1527   -1.4132    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8635   -0.9943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4446   -0.2836    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7391    0.4871    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1726    1.0868    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6301    0.8960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1966    1.4957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8662    0.1055    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5252    0.7373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2110    0.2787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2800   -0.5435    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0705   -0.7796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2613   -1.5822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0518   -1.8183    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6515   -1.2518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6616   -2.1487    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8523   -2.9514    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2526   -3.5179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8711   -1.9126    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2714   -2.4792    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4809   -2.2430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6803   -1.1100    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2662   -0.7024    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0716   -0.8812    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6896   -0.3347    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  6  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  9 10  2  0  0  0  0
 10 11  1  4  0  0  0
 10 12  1  0  0  0  0
  8 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 17 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 20 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 23 26  2  0  0  0  0
 15 26  1  0  0  0  0
  6 26  1  0  0  0  0
 27  7  1  6  0  0  0
  5 27  1  0  0  0  0
 27 28  1  0  0  0  0
  3 28  1  0  0  0  0
 28 29  2  0  0  0  0
M  END

     RDKit          3D

 54 57  0  0  0  0  0  0  0  0999 V2000
   -4.2415    3.7389    2.1521 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6891    2.4444    1.9444 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7385    2.2318    0.9272 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4285    2.3083    1.0442 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7530    2.0271   -0.2169 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1309    0.6891   -0.3845 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3295    0.0802   -0.4897 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8099   -1.2447   -0.1345 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6952   -1.6977   -1.1818 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6998   -2.4636   -0.9103 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6261   -2.9446   -1.9658 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9188   -2.8481    0.4115 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7571   -2.2291    0.2210 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3122   -2.3903   -0.8072 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3702   -1.3665   -0.6614 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6448   -1.8509   -0.7354 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6911   -0.9605   -0.6113 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.4098   -0.6808 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2285   -2.7870   -0.8795 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4820    0.3729   -0.4190 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5860    1.2057   -0.3034 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2141    1.4752    0.9344 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1838    0.8846   -0.3406 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9617    2.2157   -0.1463 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8850    2.7237    1.1676 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1425    0.0055   -0.4637 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8274    1.3485   -1.0852 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0443    1.8836   -0.4548 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1526    2.0207   -0.9984 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9626    3.7403    2.9759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7419    4.0486    1.1947 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4580    4.4854    2.3836 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9321    2.5516    1.9717 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2808    2.8640   -0.7426 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4659   -1.1247    0.7784 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1346   -3.7476   -2.5610 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9132   -2.0675   -2.5810 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5323   -3.3452   -1.5061 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1992   -2.2109    1.1316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2524   -3.2080    0.4226 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2781   -1.9081    1.1728 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8107   -3.3808   -0.6229 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0705   -2.4437   -1.8442 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7791   -2.9072   -0.8874 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6277   -3.3519   -0.1455 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2916   -3.0626   -0.7045 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9093   -3.1350   -1.8843 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2147    1.0364    1.0249 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6009    1.0101    1.7607 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2187    2.5688    1.1708 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8865    3.0424    1.5705 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1791    3.5979    1.2374 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5098    1.9760    1.8977 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6675    1.5086   -2.1458 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 27  1  0
 27  7  1  0
  7  6  2  0
  6 26  1  0
 26 23  2  0
 23 24  1  0
 24 25  1  0
 23 20  1  0
 20 21  1  0
 21 22  1  0
 20 17  2  0
 17 18  1  0
 18 19  1  0
 17 16  1  0
 16 15  2  0
 15 14  1  0
 14 13  1  0
 13  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 10 12  1  0
 27 28  1  0
 28 29  2  0
 28  3  1  0
  6  5  1  0
 15 26  1  0
  8  7  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  4 33  1  0
  5 34  1  6
 27 54  1  6
 25 51  1  0
 25 52  1  0
 25 53  1  0
 22 48  1  0
 22 49  1  0
 22 50  1  0
 19 45  1  0
 19 46  1  0
 19 47  1  0
 16 44  1  0
 14 42  1  0
 14 43  1  0
 13 40  1  0
 13 41  1  0
  8 35  1  1
 11 36  1  0
 11 37  1  0
 11 38  1  0
 12 39  1  0
M  END


  Mrv1652309092207572D          

 29 32  0  0  1  0            999 V2000
   -2.5794   -1.7152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8612   -2.1213    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1505   -1.7024    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3938   -2.0312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1527   -1.4132    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8635   -0.9943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4446   -0.2836    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7391    0.4871    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1726    1.0868    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6301    0.8960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1966    1.4957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8662    0.1055    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5252    0.7373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2110    0.2787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2800   -0.5435    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0705   -0.7796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2613   -1.5822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0518   -1.8183    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6515   -1.2518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6616   -2.1487    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8523   -2.9514    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2526   -3.5179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8711   -1.9126    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2714   -2.4792    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4809   -2.2430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6803   -1.1100    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2662   -0.7024    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0716   -0.8812    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6896   -0.3347    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  6  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  9 10  2  0  0  0  0
 10 11  1  4  0  0  0
 10 12  1  0  0  0  0
  8 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 17 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 20 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 23 26  2  0  0  0  0
 15 26  1  0  0  0  0
  6 26  1  0  0  0  0
 27  7  1  6  0  0  0
  5 27  1  0  0  0  0
 27 28  1  0  0  0  0
  3 28  1  0  0  0  0
 28 29  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0280266

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C[C@@H]2[C@@H](C3=C2C2=C(OC)C(OC)=C(OC)C=C2CC[C@@H]3N=C(C)O)C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C22H25NO6/c1-10(24)23-13-7-6-11-8-15(27-3)21(28-4)22(29-5)16(11)17-12-9-14(26-2)20(25)18(12)19(13)17/h8-9,12-13,18H,6-7H2,1-5H3,(H,23,24)/t12-,13-,18-/m0/s1

> <INCHI_KEY>
VKPVZFOUXUQJMW-LXIYXOSZSA-N

> <FORMULA>
C22H25NO6

> <MOLECULAR_WEIGHT>
399.443

> <EXACT_MASS>
399.168187529

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
42.89385715206778

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
N-[(10S,12S,16R)-3,4,5,14-tetramethoxy-13-oxotetracyclo[9.5.0.0^{2,7}.0^{12,16}]hexadeca-1(11),2,4,6,14-pentaen-10-yl]ethanimidic acid

> <JCHEM_LOGP>
1.7212446830000006

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
6.708497755706616

> <JCHEM_PKA_STRONGEST_ACIDIC>
5.502287457454657

> <JCHEM_PKA_STRONGEST_BASIC>
3.2035856021309637

> <JCHEM_POLAR_SURFACE_AREA>
86.58000000000001

> <JCHEM_REFRACTIVITY>
108.92289999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
N-[(10S,12S,16R)-3,4,5,14-tetramethoxy-13-oxotetracyclo[9.5.0.0^{2,7}.0^{12,16}]hexadeca-1(11),2,4,6,14-pentaen-10-yl]ethanimidic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0      -4.815  -3.202   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -3.474  -3.960   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -2.148  -3.178   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.735  -3.792   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.285  -2.638   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.612  -1.856   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.830  -0.529   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.380   0.909   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0       0.322   2.029   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0      -1.176   1.673   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -2.234   2.792   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -1.617   0.197   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       2.847   1.376   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.127   0.520   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.256  -1.014   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.732  -1.455   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.088  -2.953   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       7.563  -3.394   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       8.683  -2.337   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.968  -4.011   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       5.324  -5.509   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       4.205  -6.567   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.493  -3.570   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       2.373  -4.628   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       0.898  -4.187   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       3.137  -2.072   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -0.497  -1.311   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -2.000  -1.645   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -3.154  -0.625   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   28                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   27                                                  
CONECT    6    5    7   26                                                  
CONECT    7    6    8   27                                                  
CONECT    8    7    9   13                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10                                                            
CONECT   13    8   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   26                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   20                                                  
CONECT   18   17   19                                                       
CONECT   19   18                                                            
CONECT   20   17   21   23                                                  
CONECT   21   20   22                                                       
CONECT   22   21                                                            
CONECT   23   20   24   26                                                  
CONECT   24   23   25                                                       
CONECT   25   24                                                            
CONECT   26   23   15    6                                                  
CONECT   27    7    5   28                                                  
CONECT   28   27    3   29                                                  
CONECT   29   28                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   64    0
END

View in JSmol

Synonyms

Value	Source
g-Lumicolchicine	Generator
Γ-lumicolchicine	Generator
Lumicolchicines	MeSH
beta Lumicolchicine	MeSH
beta-Lumicolchicine	MeSH
gamma Lumicolchicine	MeSH

Chemical Formula

C₂₂H₂₅NO₆

Average Mass

399.4430 Da

Monoisotopic Mass

399.16819 Da

IUPAC Name

N-[(10S,12S,16R)-3,4,5,14-tetramethoxy-13-oxotetracyclo[9.5.0.0^{2,7}.0^{12,16}]hexadeca-1(11),2,4,6,14-pentaen-10-yl]ethanimidic acid

Traditional Name

N-[(10S,12S,16R)-3,4,5,14-tetramethoxy-13-oxotetracyclo[9.5.0.0^{2,7}.0^{12,16}]hexadeca-1(11),2,4,6,14-pentaen-10-yl]ethanimidic acid

CAS Registry Number

Not Available

SMILES

COC1=C[C@@H]2[C@@H](C3=C2C2=C(OC)C(OC)=C(OC)C=C2CC[C@@H]3N=C(C)O)C1=O

InChI Identifier

InChI=1S/C22H25NO6/c1-10(24)23-13-7-6-11-8-15(27-3)21(28-4)22(29-5)16(11)17-12-9-14(26-2)20(25)18(12)19(13)17/h8-9,12-13,18H,6-7H2,1-5H3,(H,23,24)/t12-,13-,18-/m0/s1

InChI Key

VKPVZFOUXUQJMW-LXIYXOSZSA-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 autumnale	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as lumicolchicine alkaloids. These are alkaloids with a structure based on the tetracyclic lumicolchicine skeleton. They can derive from a colchicine precursor where the cycloheptatriene ring is replaced with a bicyclo[3.2.0]Hepta-2,6-diene ring system.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Lumicolchicine alkaloids

Sub Class

Not Available

Direct Parent

Lumicolchicine alkaloids

Alternative Parents

Substituents

Lumicolchicine alkaloid skeleton
Anisole
Phenol ether
Alkyl aryl ether
Benzenoid
Acetamide
Carboxamide group
Ketone
Secondary carboxylic acid amide
Ether
Carboxylic acid derivative
Organooxygen compound
Organonitrogen compound
Organic oxygen compound
Organic nitrogen compound
Carbonyl group
Organic oxide
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	1.72	ChemAxon
pKa (Strongest Acidic)	5.5	ChemAxon
pKa (Strongest Basic)	3.2	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	86.58 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	108.92 m³·mol⁻¹	ChemAxon
Polarizability	42.89 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

C00028292

Chemspider ID

5145931

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

6713941

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Cacelli I, D'Auria M, Villani V: Theoretical Study of the Photochemical Isomerization of Colchicine. J Chem Theory Comput. 2007 Mar;3(2):649-56. doi: 10.1021/ct600306t. [PubMed:26637043 ]
LOTUS database [Link]

Showing NP-Card for n-[(10s,12s,16r)-3,4,5,14-tetramethoxy-13-oxotetracyclo[9.5.0.0²,⁷.0¹²,¹⁶]hexadeca-1(11),2,4,6,14-pentaen-10-yl]ethanimidic acid (NP0280266)

MOL for NP0280266 (n-[(10s,12s,16r)-3,4,5,14-tetramethoxy-13-oxotetracyclo[9.5.0.0²,⁷.0¹²,¹⁶]hexadeca-1(11),2,4,6,14-pentaen-10-yl]ethanimidic acid)

3D MOL for NP0280266 (n-[(10s,12s,16r)-3,4,5,14-tetramethoxy-13-oxotetracyclo[9.5.0.0²,⁷.0¹²,¹⁶]hexadeca-1(11),2,4,6,14-pentaen-10-yl]ethanimidic acid)

3D SDF for NP0280266 (n-[(10s,12s,16r)-3,4,5,14-tetramethoxy-13-oxotetracyclo[9.5.0.0²,⁷.0¹²,¹⁶]hexadeca-1(11),2,4,6,14-pentaen-10-yl]ethanimidic acid)

3D-SDF for NP0280266 (n-[(10s,12s,16r)-3,4,5,14-tetramethoxy-13-oxotetracyclo[9.5.0.0²,⁷.0¹²,¹⁶]hexadeca-1(11),2,4,6,14-pentaen-10-yl]ethanimidic acid)

PDB for NP0280266 (n-[(10s,12s,16r)-3,4,5,14-tetramethoxy-13-oxotetracyclo[9.5.0.0²,⁷.0¹²,¹⁶]hexadeca-1(11),2,4,6,14-pentaen-10-yl]ethanimidic acid)

3D PDB for NP0280266 (n-[(10s,12s,16r)-3,4,5,14-tetramethoxy-13-oxotetracyclo[9.5.0.0²,⁷.0¹²,¹⁶]hexadeca-1(11),2,4,6,14-pentaen-10-yl]ethanimidic acid)

SMILES for NP0280266 (n-[(10s,12s,16r)-3,4,5,14-tetramethoxy-13-oxotetracyclo[9.5.0.0²,⁷.0¹²,¹⁶]hexadeca-1(11),2,4,6,14-pentaen-10-yl]ethanimidic acid)

INCHI for NP0280266 (n-[(10s,12s,16r)-3,4,5,14-tetramethoxy-13-oxotetracyclo[9.5.0.0²,⁷.0¹²,¹⁶]hexadeca-1(11),2,4,6,14-pentaen-10-yl]ethanimidic acid)

Structure for NP0280266 (n-[(10s,12s,16r)-3,4,5,14-tetramethoxy-13-oxotetracyclo[9.5.0.0²,⁷.0¹²,¹⁶]hexadeca-1(11),2,4,6,14-pentaen-10-yl]ethanimidic acid)

3D Structure for NP0280266 (n-[(10s,12s,16r)-3,4,5,14-tetramethoxy-13-oxotetracyclo[9.5.0.0²,⁷.0¹²,¹⁶]hexadeca-1(11),2,4,6,14-pentaen-10-yl]ethanimidic acid)