NP-MRD: Showing NP-Card for (2s,2'r,5r,5's,6's,11'r)-5',6'-dihydroxy-11'-(hydroxymethyl)-4,4,5,10'-tetramethyl-1',10'-diazaspiro[oxolane-2,4'-tricyclo[6.4.0.0²,⁶]dodecan]-7'-ene-3,9',12'-trione (NP0214379)

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Record Information

Version

2.0

Created at

2022-09-05 13:39:36 UTC

Updated at

2022-09-05 13:39:36 UTC

NP-MRD ID

NP0214379

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s,2'r,5r,5's,6's,11'r)-5',6'-dihydroxy-11'-(hydroxymethyl)-4,4,5,10'-tetramethyl-1',10'-diazaspiro[oxolane-2,4'-tricyclo[6.4.0.0²,⁶]dodecan]-7'-ene-3,9',12'-trione

Description

(2S,2'R,5R,5'S,6'S,11'R)-5',6'-dihydroxy-11'-(hydroxymethyl)-4,4,5,10'-tetramethyl-1',10'-diazaspiro[oxolane-2,4'-tricyclo[6.4.0.0²,⁶]Dodecan]-7'-ene-3,9',12'-trione belongs to the class of organic compounds known as alpha amino acids and derivatives. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon), or a derivative thereof. (2s,2'r,5r,5's,6's,11'r)-5',6'-dihydroxy-11'-(hydroxymethyl)-4,4,5,10'-tetramethyl-1',10'-diazaspiro[oxolane-2,4'-tricyclo[6.4.0.0²,⁶]dodecan]-7'-ene-3,9',12'-trione is found in Leptosphaeria maculans. Based on a literature review very few articles have been published on (2S,2'R,5R,5'S,6'S,11'R)-5',6'-dihydroxy-11'-(hydroxymethyl)-4,4,5,10'-tetramethyl-1',10'-diazaspiro[oxolane-2,4'-tricyclo[6.4.0.0²,⁶]Dodecan]-7'-ene-3,9',12'-trione.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052215392D          

 27 30  0  0  1  0            999 V2000
    0.0666   -2.0903    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6197   -2.7024    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4400   -2.6147    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7769   -3.3678    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3890   -2.8147    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1042   -3.2260    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9245   -3.1383    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.4083   -2.4700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0714   -1.7169    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2289   -2.5548    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7127   -1.8866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3758   -1.1335    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5658   -3.3079    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.3864   -3.3927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0820   -3.9762    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4189   -4.7293    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2614   -3.8914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6493   -4.4445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9341   -4.0333    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7640   -4.8405    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1138   -4.1209    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7025   -4.8361    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1648   -3.9209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2524   -4.7413    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4496   -3.5097    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0412   -4.1729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3719   -3.4335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  4  3  1  1  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  1  0  0  0
 11 12  1  0  0  0  0
 10 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
  7 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
  6 19  1  0  0  0  0
 19 20  1  6  0  0  0
 19 21  1  0  0  0  0
  4 21  1  0  0  0  0
 21 22  1  6  0  0  0
  4 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
  2 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
M  END

     RDKit          3D

 51 54  0  0  0  0  0  0  0  0999 V2000
   -4.5188   -1.5927   -1.4224 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2846   -1.1675   -0.6625 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6067   -0.2428   -1.4576 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7487    0.3578   -0.5703 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4875   -0.3927   -0.3159 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3280    0.6128    0.4685 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7355    0.4064    0.2651 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.6253   -0.6268    0.7317 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1775   -1.7435    1.0662 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0683   -0.3187    0.7986 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8864   -1.5308    1.1127 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7400   -2.4940    0.1176 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4555    0.2914   -0.4578 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.6076   -0.1066   -1.2206 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6425    1.3380   -0.9489 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1079    2.2285   -1.7085 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2081    1.4230   -0.5847 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2587    2.2943   -0.8624 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0169    1.9127   -0.1812 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3645    2.8915    0.7627 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1501    1.6525   -1.1350 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0481    2.7004   -1.0898 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5681    0.6024    0.6326 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4439    1.4490    1.4874 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6384   -0.4321    0.6146 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0111    0.1667    0.5661 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5313   -1.3207    1.8223 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8316   -0.7555   -2.0971 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3195   -1.9652   -0.7829 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1988   -2.4204   -2.1119 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6639   -2.0382   -0.3966 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6198   -1.3429    0.2249 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0291   -0.5242   -1.2890 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0544    0.5904    1.5530 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2286    0.4228    1.6083 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5243   -1.9258    2.0946 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9348   -1.2521    1.2605 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5431   -3.3924    0.4687 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9555    0.7462   -1.8364 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3353   -0.9896   -1.8366 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4412   -0.4618   -0.5529 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4419    3.1540   -1.5146 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0748    2.7134    1.6452 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7279    1.4613   -2.1197 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8924    3.3260   -0.3362 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0845    1.1277    1.1292 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7583   -0.5505    1.0167 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3689    0.3743   -0.4554 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6896   -1.0104    2.4992 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4453   -1.2421    2.4459 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4191   -2.4033    1.5543 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  4  3  1  6
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  1  1
 19 21  1  0
 21 22  1  0
 17 15  1  0
 15 16  2  0
 15 13  1  0
 13 14  1  0
 13 10  1  0
 10 11  1  0
 11 12  1  0
 10  8  1  0
  8  9  2  0
  4 23  1  0
 23 24  2  0
 23 25  1  0
 25 26  1  0
 25 27  1  0
 25  2  1  0
 21  4  1  0
 19  6  1  0
  8  7  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  2 31  1  1
  5 32  1  0
  5 33  1  0
  6 34  1  1
 18 42  1  0
 20 43  1  0
 21 44  1  6
 22 45  1  0
 14 39  1  0
 14 40  1  0
 14 41  1  0
 10 35  1  1
 11 36  1  0
 11 37  1  0
 12 38  1  0
 26 46  1  0
 26 47  1  0
 26 48  1  0
 27 49  1  0
 27 50  1  0
 27 51  1  0
M  END


  Mrv1652309052215392D          

 27 30  0  0  1  0            999 V2000
    0.0666   -2.0903    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6197   -2.7024    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4400   -2.6147    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7769   -3.3678    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3890   -2.8147    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1042   -3.2260    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9245   -3.1383    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.4083   -2.4700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0714   -1.7169    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2289   -2.5548    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7127   -1.8866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3758   -1.1335    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5658   -3.3079    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.3864   -3.3927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0820   -3.9762    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4189   -4.7293    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2614   -3.8914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6493   -4.4445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9341   -4.0333    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7640   -4.8405    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1138   -4.1209    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7025   -4.8361    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1648   -3.9209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2524   -4.7413    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4496   -3.5097    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0412   -4.1729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3719   -3.4335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  4  3  1  1  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  1  0  0  0
 11 12  1  0  0  0  0
 10 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
  7 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
  6 19  1  0  0  0  0
 19 20  1  6  0  0  0
 19 21  1  0  0  0  0
  4 21  1  0  0  0  0
 21 22  1  6  0  0  0
  4 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
  2 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0214379

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1O[C@]2(C[C@H]3N4C(=C[C@@]3(O)[C@@H]2O)C(=O)N(C)[C@H](CO)C4=O)C(=O)C1(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C18H24N2O7/c1-8-16(2,3)14(24)18(27-8)6-11-17(26,15(18)25)5-9-12(22)19(4)10(7-21)13(23)20(9)11/h5,8,10-11,15,21,25-26H,6-7H2,1-4H3/t8-,10-,11-,15+,17+,18-/m1/s1

> <INCHI_KEY>
NEEWDQXYMAKGIR-KMSXASFBSA-N

> <FORMULA>
C18H24N2O7

> <MOLECULAR_WEIGHT>
380.397

> <EXACT_MASS>
380.158351121

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
51

> <JCHEM_AVERAGE_POLARIZABILITY>
37.068275656971466

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,2'R,5R,5'S,6'S,11'R)-5',6'-dihydroxy-11'-(hydroxymethyl)-4,4,5,10'-tetramethyl-1',10'-diazaspiro[oxolane-2,4'-tricyclo[6.4.0.0^{2,6}]dodecan]-7'-ene-3,9',12'-trione

> <JCHEM_LOGP>
-1.9785693073333328

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.703651873231536

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.340589864794598

> <JCHEM_PKA_STRONGEST_BASIC>
-0.46438826988261017

> <JCHEM_POLAR_SURFACE_AREA>
127.61000000000001

> <JCHEM_REFRACTIVITY>
91.94279999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2S,2'R,5R,5'S,6'S,11'R)-5',6'-dihydroxy-11'-(hydroxymethyl)-4,4,5,10'-tetramethyl-1',10'-diazaspiro[oxolane-2,4'-tricyclo[6.4.0.0^{2,6}]dodecan]-7'-ene-3,9',12'-trione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0       0.124  -3.902   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.157  -5.045   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       2.688  -4.881   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       3.317  -6.287   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.459  -5.254   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.795  -6.022   0.000  0.00  0.00           C+0
HETATM    7  N   UNK     0       7.326  -5.858   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0       8.229  -4.611   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       7.600  -3.205   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       9.761  -4.769   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.664  -3.522   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      10.035  -2.116   0.000  0.00  0.00           O+0
HETATM   13  N   UNK     0      10.389  -6.175   0.000  0.00  0.00           N+0
HETATM   14  C   UNK     0      11.921  -6.333   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.486  -7.422   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      10.115  -8.828   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       7.955  -7.264   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.812  -8.296   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.477  -7.529   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       5.159  -9.036   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       3.946  -7.692   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       3.178  -9.027   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       2.174  -7.319   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       2.338  -8.850   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       0.839  -6.551   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -0.077  -7.789   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -0.694  -6.409   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   25                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   21   23                                             
CONECT    5    4    6                                                       
CONECT    6    5    7   19                                                  
CONECT    7    6    8   17                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   13                                                  
CONECT   11   10   12                                                       
CONECT   12   11                                                            
CONECT   13   10   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15    7   18                                                  
CONECT   18   17   19                                                       
CONECT   19   18    6   20   21                                             
CONECT   20   19                                                            
CONECT   21   19    4   22                                                  
CONECT   22   21                                                            
CONECT   23    4   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23    2   26   27                                             
CONECT   26   25                                                            
CONECT   27   25                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   60    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₂₄N₂O₇

Average Mass

380.3970 Da

Monoisotopic Mass

380.15835 Da

IUPAC Name

(2S,2'R,5R,5'S,6'S,11'R)-5',6'-dihydroxy-11'-(hydroxymethyl)-4,4,5,10'-tetramethyl-1',10'-diazaspiro[oxolane-2,4'-tricyclo[6.4.0.0^{2,6}]dodecan]-7'-ene-3,9',12'-trione

Traditional Name

(2S,2'R,5R,5'S,6'S,11'R)-5',6'-dihydroxy-11'-(hydroxymethyl)-4,4,5,10'-tetramethyl-1',10'-diazaspiro[oxolane-2,4'-tricyclo[6.4.0.0^{2,6}]dodecan]-7'-ene-3,9',12'-trione

CAS Registry Number

Not Available

SMILES

C[C@H]1O[C@]2(C[C@H]3N4C(=C[C@@]3(O)[C@@H]2O)C(=O)N(C)[C@H](CO)C4=O)C(=O)C1(C)C

InChI Identifier

InChI=1S/C18H24N2O7/c1-8-16(2,3)14(24)18(27-8)6-11-17(26,15(18)25)5-9-12(22)19(4)10(7-21)13(23)20(9)11/h5,8,10-11,15,21,25-26H,6-7H2,1-4H3/t8-,10-,11-,15+,17+,18-/m1/s1

InChI Key

NEEWDQXYMAKGIR-KMSXASFBSA-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
Leptosphaeria maculans	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as alpha amino acids and derivatives. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon), or a derivative thereof.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Alpha amino acids and derivatives

Alternative Parents

Substituents

Alpha-amino acid or derivatives
Dioxopiperazine
2,5-dioxopiperazine
N-methylpiperazine
N-alkylpiperazine
1,4-diazinane
3-furanone
Piperazine
Cyclic alcohol
Pyrroline
Tertiary alcohol
Tetrahydrofuran
Tertiary carboxylic acid amide
Carboxamide group
Ketone
Lactam
Secondary alcohol
Organoheterocyclic compound
Azacycle
Ether
Dialkyl ether
Oxacycle
Organic nitrogen compound
Organooxygen compound
Organonitrogen compound
Organopnictogen compound
Alcohol
Organic oxygen compound
Primary alcohol
Hydrocarbon derivative
Carbonyl group
Organic oxide
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	-2	ChemAxon
pKa (Strongest Acidic)	12.34	ChemAxon
pKa (Strongest Basic)	-0.46	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	127.61 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	91.94 m³·mol⁻¹	ChemAxon
Polarizability	37.07 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	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

162878086

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2s,2'r,5r,5's,6's,11'r)-5',6'-dihydroxy-11'-(hydroxymethyl)-4,4,5,10'-tetramethyl-1',10'-diazaspiro[oxolane-2,4'-tricyclo[6.4.0.0²,⁶]dodecan]-7'-ene-3,9',12'-trione (NP0214379)

MOL for NP0214379 ((2s,2'r,5r,5's,6's,11'r)-5',6'-dihydroxy-11'-(hydroxymethyl)-4,4,5,10'-tetramethyl-1',10'-diazaspiro[oxolane-2,4'-tricyclo[6.4.0.0²,⁶]dodecan]-7'-ene-3,9',12'-trione)

3D MOL for NP0214379 ((2s,2'r,5r,5's,6's,11'r)-5',6'-dihydroxy-11'-(hydroxymethyl)-4,4,5,10'-tetramethyl-1',10'-diazaspiro[oxolane-2,4'-tricyclo[6.4.0.0²,⁶]dodecan]-7'-ene-3,9',12'-trione)

3D SDF for NP0214379 ((2s,2'r,5r,5's,6's,11'r)-5',6'-dihydroxy-11'-(hydroxymethyl)-4,4,5,10'-tetramethyl-1',10'-diazaspiro[oxolane-2,4'-tricyclo[6.4.0.0²,⁶]dodecan]-7'-ene-3,9',12'-trione)

3D-SDF for NP0214379 ((2s,2'r,5r,5's,6's,11'r)-5',6'-dihydroxy-11'-(hydroxymethyl)-4,4,5,10'-tetramethyl-1',10'-diazaspiro[oxolane-2,4'-tricyclo[6.4.0.0²,⁶]dodecan]-7'-ene-3,9',12'-trione)

PDB for NP0214379 ((2s,2'r,5r,5's,6's,11'r)-5',6'-dihydroxy-11'-(hydroxymethyl)-4,4,5,10'-tetramethyl-1',10'-diazaspiro[oxolane-2,4'-tricyclo[6.4.0.0²,⁶]dodecan]-7'-ene-3,9',12'-trione)

3D PDB for NP0214379 ((2s,2'r,5r,5's,6's,11'r)-5',6'-dihydroxy-11'-(hydroxymethyl)-4,4,5,10'-tetramethyl-1',10'-diazaspiro[oxolane-2,4'-tricyclo[6.4.0.0²,⁶]dodecan]-7'-ene-3,9',12'-trione)

SMILES for NP0214379 ((2s,2'r,5r,5's,6's,11'r)-5',6'-dihydroxy-11'-(hydroxymethyl)-4,4,5,10'-tetramethyl-1',10'-diazaspiro[oxolane-2,4'-tricyclo[6.4.0.0²,⁶]dodecan]-7'-ene-3,9',12'-trione)

INCHI for NP0214379 ((2s,2'r,5r,5's,6's,11'r)-5',6'-dihydroxy-11'-(hydroxymethyl)-4,4,5,10'-tetramethyl-1',10'-diazaspiro[oxolane-2,4'-tricyclo[6.4.0.0²,⁶]dodecan]-7'-ene-3,9',12'-trione)

Structure for NP0214379 ((2s,2'r,5r,5's,6's,11'r)-5',6'-dihydroxy-11'-(hydroxymethyl)-4,4,5,10'-tetramethyl-1',10'-diazaspiro[oxolane-2,4'-tricyclo[6.4.0.0²,⁶]dodecan]-7'-ene-3,9',12'-trione)

3D Structure for NP0214379 ((2s,2'r,5r,5's,6's,11'r)-5',6'-dihydroxy-11'-(hydroxymethyl)-4,4,5,10'-tetramethyl-1',10'-diazaspiro[oxolane-2,4'-tricyclo[6.4.0.0²,⁶]dodecan]-7'-ene-3,9',12'-trione)