NP-MRD: Showing NP-Card for n-[(9s)-5,13,19-trimethoxy-6-oxo-15,17-dioxatetracyclo[10.7.0.0²,⁸.0¹⁴,¹⁸]nonadeca-1(19),2,4,7,12,14(18)-hexaen-9-yl]ethanimidic acid (NP0288939)

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Record Information

Version

2.0

Created at

2022-09-09 18:53:08 UTC

Updated at

2022-09-09 18:53:09 UTC

NP-MRD ID

NP0288939

Secondary Accession Numbers

None

Natural Product Identification

Common Name

n-[(9s)-5,13,19-trimethoxy-6-oxo-15,17-dioxatetracyclo[10.7.0.0²,⁸.0¹⁴,¹⁸]nonadeca-1(19),2,4,7,12,14(18)-hexaen-9-yl]ethanimidic acid

Description

Gloriosamine A belongs to the class of organic compounds known as benzodioxoles. These are organic compounds containing a benzene ring fused to either isomers of dioxole. Dioxole is a five-membered unsaturated ring of two oxygen atoms and three carbon atoms. n-[(9s)-5,13,19-trimethoxy-6-oxo-15,17-dioxatetracyclo[10.7.0.0²,⁸.0¹⁴,¹⁸]nonadeca-1(19),2,4,7,12,14(18)-hexaen-9-yl]ethanimidic acid is found in Gloriosa superba. Based on a literature review very few articles have been published on Gloriosamine A.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092220532D          

 30 33  0  0  1  0            999 V2000
    4.9386    2.5056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1145    2.4669    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7360    1.7338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9119    1.6951    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5334    0.9621    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9790    0.2678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6005   -0.4653    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0460   -1.1596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8031    0.3065    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1816    1.0395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9957    0.9060    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1204    0.0905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3833   -0.2800    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7243    0.8010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7013   -0.0237    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0422   -0.5199    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2433   -0.3140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2888   -0.9444    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0089   -1.7205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0938    0.4390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9185    0.4620    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2847    1.1720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0939    1.3331    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1168    2.1578    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3838    2.5363    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3105    2.0908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0436    2.4693    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2718    1.2667    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7759    2.6540    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5748    2.4481    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  1  0  0  0  0
  6  9  1  0  0  0  0
  9 10  2  0  0  0  0
  3 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
  9 13  1  0  0  0  0
  5 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 17 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 22 23  2  0  0  0  0
 14 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  1  0  0  0
 25 26  2  0  0  0  0
 26 27  1  4  0  0  0
 26 28  1  0  0  0  0
 24 29  1  0  0  0  0
 29 30  1  0  0  0  0
  4 30  1  0  0  0  0
M  END

     RDKit          3D

 53 56  0  0  0  0  0  0  0  0999 V2000
    2.2295   -4.2020   -0.0751 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3379   -3.1750    0.8741 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2307   -1.8246    0.5557 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9707   -1.2669    0.6055 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8645    0.0920    0.2867 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9189    0.8756   -0.0709 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7317    2.2043   -0.3969 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5127    2.5039   -1.7980 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1736    0.2851   -0.1099 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3181   -1.0681    0.2063 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6723   -1.3305    0.0717 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3825   -0.1399   -0.2130 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3913    0.8391   -0.4289 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3496    0.8883    0.3646 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1278    2.0964    0.8216 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5396    3.2859    0.6585 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8532    3.5150    0.2420 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3030    4.8090    0.3141 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4386    5.8158    0.7927 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7742    2.6108   -0.2382 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8469    3.0395   -0.7448 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7190    1.2066   -0.2612 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6402    0.4414    0.0732 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1272   -0.9711    0.0919 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9740   -1.6302   -1.1555 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5315   -2.7606   -1.3881 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3668   -3.4523   -0.3814 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3651   -3.3865   -2.6215 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4018   -1.6382    1.2412 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0913   -2.2315    0.9454 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8390   -3.8503   -1.0510 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4827   -4.9359    0.3230 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1898   -4.7276   -0.1640 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4915    2.7665   -2.2239 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1313    1.6189   -2.3171 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8572    3.3978   -1.8882 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9609    0.1243    0.7076 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0187   -0.2259   -1.1077 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0500    2.0073    1.3468 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0730    4.1481    0.8975 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0017    6.7784    0.8927 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5938    5.8997    0.0942 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0391    5.5925    1.8110 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6015    0.6783   -0.5665 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1951   -0.8989    0.3897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7398   -4.1643    0.1998 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1304   -4.0915   -0.8974 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9555   -2.7739    0.2608 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1093   -3.6501   -3.2266 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0595   -2.4141    1.6844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2848   -0.8616    2.0415 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2586   -2.9305    1.7488 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1824   -2.9185    0.0415 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 30  1  0
 30 29  1  0
 29 24  1  0
 24 25  1  0
 25 26  2  0
 26 27  1  0
 26 28  1  0
 24 23  1  0
 23 22  2  0
 22 20  1  0
 20 21  2  0
 20 17  1  0
 17 18  1  0
 18 19  1  0
 17 16  2  0
 16 15  1  0
 15 14  2  0
 14  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  6  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 10  3  1  0
  5  4  1  0
 13  9  1  0
 14 23  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
 30 52  1  0
 30 53  1  0
 29 50  1  0
 29 51  1  0
 24 45  1  1
 27 46  1  0
 27 47  1  0
 27 48  1  0
 28 49  1  0
 22 44  1  0
 19 41  1  0
 19 42  1  0
 19 43  1  0
 16 40  1  0
 15 39  1  0
  8 34  1  0
  8 35  1  0
  8 36  1  0
 12 37  1  0
 12 38  1  0
M  END


  Mrv1652309092220532D          

 30 33  0  0  1  0            999 V2000
    4.9386    2.5056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1145    2.4669    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7360    1.7338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9119    1.6951    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5334    0.9621    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9790    0.2678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6005   -0.4653    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0460   -1.1596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8031    0.3065    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1816    1.0395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9957    0.9060    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1204    0.0905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3833   -0.2800    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7243    0.8010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7013   -0.0237    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0422   -0.5199    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2433   -0.3140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2888   -0.9444    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0089   -1.7205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0938    0.4390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9185    0.4620    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2847    1.1720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0939    1.3331    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1168    2.1578    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3838    2.5363    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3105    2.0908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0436    2.4693    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2718    1.2667    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7759    2.6540    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5748    2.4481    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  1  0  0  0  0
  6  9  1  0  0  0  0
  9 10  2  0  0  0  0
  3 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
  9 13  1  0  0  0  0
  5 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 17 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 22 23  2  0  0  0  0
 14 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  1  0  0  0
 25 26  2  0  0  0  0
 26 27  1  4  0  0  0
 26 28  1  0  0  0  0
 24 29  1  0  0  0  0
 29 30  1  0  0  0  0
  4 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0288939

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C2CC[C@H](N=C(C)O)C3=CC(=O)C(OC)=CC=C3C2=C(OC)C2=C1OCO2

> <INCHI_IDENTIFIER>
InChI=1S/C22H23NO7/c1-11(24)23-15-7-5-13-18(12-6-8-17(26-2)16(25)9-14(12)15)20(28-4)22-21(19(13)27-3)29-10-30-22/h6,8-9,15H,5,7,10H2,1-4H3,(H,23,24)/t15-/m0/s1

> <INCHI_KEY>
QNZWJVKAXMQWLU-HNNXBMFYSA-N

> <FORMULA>
C22H23NO7

> <MOLECULAR_WEIGHT>
413.426

> <EXACT_MASS>
413.147452085

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
42.64265092050096

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
N-[(9S)-5,13,19-trimethoxy-6-oxo-15,17-dioxatetracyclo[10.7.0.0^{2,8}.0^{14,18}]nonadeca-1(19),2,4,7,12,14(18)-hexaen-9-yl]ethanimidic acid

> <JCHEM_LOGP>
2.0624974306666672

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
5.500394414911442

> <JCHEM_PKA_STRONGEST_BASIC>
2.926799080205267

> <JCHEM_POLAR_SURFACE_AREA>
95.81000000000002

> <JCHEM_REFRACTIVITY>
111.201

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
N-[(9S)-5,13,19-trimethoxy-6-oxo-15,17-dioxatetracyclo[10.7.0.0^{2,8}.0^{14,18}]nonadeca-1(19),2,4,7,12,14(18)-hexaen-9-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       9.219   4.677   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       7.680   4.605   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       6.974   3.237   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.436   3.164   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.729   1.796   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.561   0.500   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       4.854  -0.869   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       5.686  -2.165   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.099   0.572   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.806   1.940   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       9.325   1.691   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       9.558   0.169   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       8.182  -0.523   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       3.219   1.495   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.176  -0.044   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.945  -0.971   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.454  -0.586   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -0.539  -1.763   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -0.017  -3.212   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.175   0.819   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -1.714   0.862   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       0.532   2.188   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.042   2.489   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.085   4.028   0.000  0.00  0.00           C+0
HETATM   25  N   UNK     0       0.716   4.734   0.000  0.00  0.00           N+0
HETATM   26  C   UNK     0      -0.580   3.903   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -1.948   4.609   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -0.507   2.364   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       3.315   4.954   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       4.806   4.570   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   10                                                  
CONECT    4    3    5   30                                                  
CONECT    5    4    6   14                                                  
CONECT    6    5    7    9                                                  
CONECT    7    6    8                                                       
CONECT    8    7                                                            
CONECT    9    6   10   13                                                  
CONECT   10    9    3   11                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12    9                                                       
CONECT   14    5   15   23                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   20                                                  
CONECT   18   17   19                                                       
CONECT   19   18                                                            
CONECT   20   17   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   14   24                                                  
CONECT   24   23   25   29                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26                                                            
CONECT   29   24   30                                                       
CONECT   30   29    4                                                       
MASTER        0    0    0    0    0    0    0    0   30    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₂₃NO₇

Average Mass

413.4260 Da

Monoisotopic Mass

413.14745 Da

IUPAC Name

N-[(9S)-5,13,19-trimethoxy-6-oxo-15,17-dioxatetracyclo[10.7.0.0^{2,8}.0^{14,18}]nonadeca-1(19),2,4,7,12,14(18)-hexaen-9-yl]ethanimidic acid

Traditional Name

N-[(9S)-5,13,19-trimethoxy-6-oxo-15,17-dioxatetracyclo[10.7.0.0^{2,8}.0^{14,18}]nonadeca-1(19),2,4,7,12,14(18)-hexaen-9-yl]ethanimidic acid

CAS Registry Number

Not Available

SMILES

COC1=C2CC[C@H](N=C(C)O)C3=CC(=O)C(OC)=CC=C3C2=C(OC)C2=C1OCO2

InChI Identifier

InChI=1S/C22H23NO7/c1-11(24)23-15-7-5-13-18(12-6-8-17(26-2)16(25)9-14(12)15)20(28-4)22-21(19(13)27-3)29-10-30-22/h6,8-9,15H,5,7,10H2,1-4H3,(H,23,24)/t15-/m0/s1

InChI Key

QNZWJVKAXMQWLU-HNNXBMFYSA-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
Gloriosa superba	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as benzodioxoles. These are organic compounds containing a benzene ring fused to either isomers of dioxole. Dioxole is a five-membered unsaturated ring of two oxygen atoms and three carbon atoms.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzodioxoles

Sub Class

Not Available

Direct Parent

Benzodioxoles

Alternative Parents

Substituents

Benzodioxole
Anisole
Tropone
Alkyl aryl ether
Benzenoid
Acetamide
Carboxamide group
Secondary carboxylic acid amide
Cyclic ketone
Acetal
Carboxylic acid derivative
Ether
Oxacycle
Organic oxygen compound
Organic nitrogen compound
Organic oxide
Carbonyl group
Organopnictogen compound
Organonitrogen compound
Organooxygen compound
Hydrocarbon derivative
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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	2.06	ChemAxon
pKa (Strongest Acidic)	5.5	ChemAxon
pKa (Strongest Basic)	2.93	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	95.81 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	111.2 m³·mol⁻¹	ChemAxon
Polarizability	42.64 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

28284896

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

24796075

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for n-[(9s)-5,13,19-trimethoxy-6-oxo-15,17-dioxatetracyclo[10.7.0.0²,⁸.0¹⁴,¹⁸]nonadeca-1(19),2,4,7,12,14(18)-hexaen-9-yl]ethanimidic acid (NP0288939)

MOL for NP0288939 (n-[(9s)-5,13,19-trimethoxy-6-oxo-15,17-dioxatetracyclo[10.7.0.0²,⁸.0¹⁴,¹⁸]nonadeca-1(19),2,4,7,12,14(18)-hexaen-9-yl]ethanimidic acid)

3D MOL for NP0288939 (n-[(9s)-5,13,19-trimethoxy-6-oxo-15,17-dioxatetracyclo[10.7.0.0²,⁸.0¹⁴,¹⁸]nonadeca-1(19),2,4,7,12,14(18)-hexaen-9-yl]ethanimidic acid)

3D SDF for NP0288939 (n-[(9s)-5,13,19-trimethoxy-6-oxo-15,17-dioxatetracyclo[10.7.0.0²,⁸.0¹⁴,¹⁸]nonadeca-1(19),2,4,7,12,14(18)-hexaen-9-yl]ethanimidic acid)

3D-SDF for NP0288939 (n-[(9s)-5,13,19-trimethoxy-6-oxo-15,17-dioxatetracyclo[10.7.0.0²,⁸.0¹⁴,¹⁸]nonadeca-1(19),2,4,7,12,14(18)-hexaen-9-yl]ethanimidic acid)

PDB for NP0288939 (n-[(9s)-5,13,19-trimethoxy-6-oxo-15,17-dioxatetracyclo[10.7.0.0²,⁸.0¹⁴,¹⁸]nonadeca-1(19),2,4,7,12,14(18)-hexaen-9-yl]ethanimidic acid)

3D PDB for NP0288939 (n-[(9s)-5,13,19-trimethoxy-6-oxo-15,17-dioxatetracyclo[10.7.0.0²,⁸.0¹⁴,¹⁸]nonadeca-1(19),2,4,7,12,14(18)-hexaen-9-yl]ethanimidic acid)

SMILES for NP0288939 (n-[(9s)-5,13,19-trimethoxy-6-oxo-15,17-dioxatetracyclo[10.7.0.0²,⁸.0¹⁴,¹⁸]nonadeca-1(19),2,4,7,12,14(18)-hexaen-9-yl]ethanimidic acid)

INCHI for NP0288939 (n-[(9s)-5,13,19-trimethoxy-6-oxo-15,17-dioxatetracyclo[10.7.0.0²,⁸.0¹⁴,¹⁸]nonadeca-1(19),2,4,7,12,14(18)-hexaen-9-yl]ethanimidic acid)

Structure for NP0288939 (n-[(9s)-5,13,19-trimethoxy-6-oxo-15,17-dioxatetracyclo[10.7.0.0²,⁸.0¹⁴,¹⁸]nonadeca-1(19),2,4,7,12,14(18)-hexaen-9-yl]ethanimidic acid)

3D Structure for NP0288939 (n-[(9s)-5,13,19-trimethoxy-6-oxo-15,17-dioxatetracyclo[10.7.0.0²,⁸.0¹⁴,¹⁸]nonadeca-1(19),2,4,7,12,14(18)-hexaen-9-yl]ethanimidic acid)