NP-MRD: Showing NP-Card for saldedine A (NP0034344)

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Record Information

Version

2.0

Created at

2021-06-20 18:06:03 UTC

Updated at

2021-06-30 00:04:40 UTC

NP-MRD ID

NP0034344

Secondary Accession Numbers

None

Natural Product Identification

Common Name

saldedine A

Provided By

JEOL Database JEOL Logo

Description

saldedine A is found in Meconopsis cambrica. saldedine A was first documented in 2009 (Sorek, H., et al.).

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306202120063D          

 41 44  0  0  0  0            999 V2000
   -3.3974    1.0937    3.5498 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0220    0.8997    3.2415 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7184    0.6164    1.9316 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6493    0.4636    0.8873 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2083    0.1911   -0.4124 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8430    0.0795   -0.6248 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0957    0.1558    0.4026 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3430    0.4529    1.6770 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5614    0.5842    2.6919 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4814   -0.1337   -0.1332 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2367   -1.1281    0.7093 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4466   -0.9149    1.2482 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2815   -2.2190    2.2967 Br  0  0  0  0  0  0  0  0  0  0  0  0
    4.1662    0.3774    1.0221 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2839    0.5849    1.4871 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4643    1.3980    0.1810 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3259    3.0293   -0.1291 Br  0  0  0  0  0  0  0  0  0  0  0  0
    2.2542    1.1456   -0.3412 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1096   -0.8008   -1.5060 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2022   -0.1325   -1.9635 C   0  0  1  0  0  0  0  0  0  0  0  0
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   -3.1276   -0.1153   -1.5645 C   0  0  2  0  0  0  0  0  0  0  0  0
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   -3.8131    1.9380    2.9900 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.0244    0.7817    3.4848 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.4486   -1.5984   -4.1322 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3124   -0.0815   -4.6593 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1618   -1.6321   -4.8279 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2551    0.8014   -3.3305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0547   -0.7412   -3.6273 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9098    0.6495   -1.6307 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6112   -1.0785   -1.3584 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

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   -2.0220    0.8997    3.2415 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7184    0.6164    1.9316 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6493    0.4636    0.8873 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2083    0.1911   -0.4124 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8430    0.0795   -0.6248 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0957    0.1558    0.4026 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3430    0.4529    1.6770 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5614    0.5842    2.6919 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4814   -0.1337   -0.1332 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2367   -1.1281    0.7093 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4466   -0.9149    1.2482 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2815   -2.2190    2.2967 Br  0  0  0  0  0  0  0  0  0  0  0  0
    4.1662    0.3774    1.0221 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2839    0.5849    1.4871 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4643    1.3980    0.1810 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3259    3.0293   -0.1291 Br  0  0  0  0  0  0  0  0  0  0  0  0
    2.2542    1.1456   -0.3412 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1652306202120063D          

 41 44  0  0  0  0            999 V2000
   -3.3974    1.0937    3.5498 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0220    0.8997    3.2415 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7184    0.6164    1.9316 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6493    0.4636    0.8873 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.4814   -0.1337   -0.1332 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2367   -1.1281    0.7093 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4466   -0.9149    1.2482 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2815   -2.2190    2.2967 Br  0  0  0  0  0  0  0  0  0  0  0  0
    4.1662    0.3774    1.0221 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2839    0.5849    1.4871 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4643    1.3980    0.1810 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3259    3.0293   -0.1291 Br  0  0  0  0  0  0  0  0  0  0  0  0
    2.2542    1.1456   -0.3412 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1096   -0.8008   -1.5060 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2022   -0.1325   -1.9635 C   0  0  1  0  0  0  0  0  0  0  0  0
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M  END
> <DATABASE_ID>
NP0034344

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C(OC([H])([H])[H])C([H])=C2C3=C1C1(C([H])=C(Br)C(=O)C(Br)=C1[H])C([H])([H])[C@@]3([H])N(C([H])([H])[H])C([H])([H])C2([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C18H17Br2NO3/c1-21-4-3-9-5-13(24-2)17(23)15-14(9)12(21)8-18(15)6-10(19)16(22)11(20)7-18/h5-7,12,23H,3-4,8H2,1-2H3/t12-/m1/s1

> <INCHI_KEY>
CHIIYNHRBKMNTF-GFCCVEGCSA-N

> <FORMULA>
C18H17Br2NO3

> <MOLECULAR_WEIGHT>
455.146

> <EXACT_MASS>
452.957519

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
41

> <JCHEM_AVERAGE_POLARIZABILITY>
39.69602559381295

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(4'R)-3,5-dibromo-11'-hydroxy-10'-methoxy-5'-methyl-5'-azaspiro[cyclohexane-1,2'-tricyclo[6.3.1.0^{4,12}]dodecane]-1'(12'),2,5,8',10'-pentaen-4-one

> <ALOGPS_LOGP>
3.77

> <JCHEM_LOGP>
3.418314837333333

> <ALOGPS_LOGS>
-4.21

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.836360739485755

> <JCHEM_PKA_STRONGEST_BASIC>
5.6545574380126

> <JCHEM_POLAR_SURFACE_AREA>
49.77

> <JCHEM_REFRACTIVITY>
103.00629999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.78e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(4'R)-3,5-dibromo-11'-hydroxy-10'-methoxy-5'-methyl-5'-azaspiro[cyclohexane-1,2'-tricyclo[6.3.1.0^{4,12}]dodecane]-1'(12'),2,5,8',10'-pentaen-4-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 41 44  0  0  0  0  0  0  0  0999 V2000
   -3.3974    1.0937    3.5498 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0220    0.8997    3.2415 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7184    0.6164    1.9316 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6493    0.4636    0.8873 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2083    0.1911   -0.4124 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8430    0.0795   -0.6248 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0957    0.1558    0.4026 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3430    0.4529    1.6770 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5614    0.5842    2.6919 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4814   -0.1337   -0.1332 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2367   -1.1281    0.7093 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4466   -0.9149    1.2482 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2815   -2.2190    2.2967 Br  0  0  0  0  0  0  0  0  0  0  0  0
    4.1662    0.3774    1.0221 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2839    0.5849    1.4871 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4643    1.3980    0.1810 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3259    3.0293   -0.1291 Br  0  0  0  0  0  0  0  0  0  0  0  0
    2.2542    1.1456   -0.3412 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1096   -0.8008   -1.5060 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2022   -0.1325   -1.9635 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0826   -0.9053   -2.8478 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4978   -1.0494   -4.1797 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3937   -0.2125   -2.9292 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1276   -0.1153   -1.5645 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4699    1.3331    4.6151 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8131    1.9380    2.9900 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9728    0.1788    3.3745 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7171    0.5366    1.0647 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0244    0.7817    3.4848 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7314   -2.0718    0.9085 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7728    1.9179   -0.9376 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9025   -0.6936   -2.2564 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9416   -1.8812   -1.3760 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0173    0.8533   -2.3987 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4486   -1.5984   -4.1322 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3124   -0.0815   -4.6593 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1618   -1.6321   -4.8279 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2551    0.8014   -3.3305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0547   -0.7412   -3.6273 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9098    0.6495   -1.6307 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6112   -1.0785   -1.3584 H   0  0  0  0  0  0  0  0  0  0  0  0
 14 16  1  0
 16 18  2  0
 10 11  1  0
  3  8  2  0
  5 24  1  0
  6 20  1  0
 20 21  1  0
 21 23  1  0
 23 24  1  0
 10 18  1  0
  3  2  1  0
  8  7  1  0
  2  1  1  0
  7  6  2  0
  8  9  1  0
 11 12  2  0
 21 22  1  0
  5  4  2  0
 20 19  1  0
  7 10  1  0
 10 19  1  0
  4  3  1  0
 14 15  2  0
  5  6  1  0
 12 13  1  0
 12 14  1  0
 16 17  1  0
 11 30  1  0
 18 31  1  0
  4 28  1  0
 20 34  1  0
 23 38  1  0
 23 39  1  0
 24 40  1  0
 24 41  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  9 29  1  0
 22 35  1  0
 22 36  1  0
 22 37  1  0
 19 32  1  0
 19 33  1  0
M  END

HEADER    PROTEIN                                 20-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-JUN-21         0                                  
HETATM    1  C   UNK     0      -3.397   1.094   3.550  0.00  0.00           C+0
HETATM    2  O   UNK     0      -2.022   0.900   3.241  0.00  0.00           O+0
HETATM    3  C   UNK     0      -1.718   0.616   1.932  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.649   0.464   0.887  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.208   0.191  -0.412  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.843   0.080  -0.625  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.096   0.156   0.403  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.343   0.453   1.677  0.00  0.00           C+0
HETATM    9  O   UNK     0       0.561   0.584   2.692  0.00  0.00           O+0
HETATM   10  C   UNK     0       1.481  -0.134  -0.133  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.237  -1.128   0.709  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.447  -0.915   1.248  0.00  0.00           C+0
HETATM   13 Br   UNK     0       4.282  -2.219   2.297  0.00  0.00          Br+0
HETATM   14  C   UNK     0       4.166   0.377   1.022  0.00  0.00           C+0
HETATM   15  O   UNK     0       5.284   0.585   1.487  0.00  0.00           O+0
HETATM   16  C   UNK     0       3.464   1.398   0.181  0.00  0.00           C+0
HETATM   17 Br   UNK     0       4.326   3.029  -0.129  0.00  0.00          Br+0
HETATM   18  C   UNK     0       2.254   1.146  -0.341  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.110  -0.801  -1.506  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.202  -0.133  -1.964  0.00  0.00           C+0
HETATM   21  N   UNK     0      -1.083  -0.905  -2.848  0.00  0.00           N+0
HETATM   22  C   UNK     0      -0.498  -1.049  -4.180  0.00  0.00           C+0
HETATM   23  C   UNK     0      -2.394  -0.213  -2.929  0.00  0.00           C+0
HETATM   24  C   UNK     0      -3.128  -0.115  -1.565  0.00  0.00           C+0
HETATM   25  H   UNK     0      -3.470   1.333   4.615  0.00  0.00           H+0
HETATM   26  H   UNK     0      -3.813   1.938   2.990  0.00  0.00           H+0
HETATM   27  H   UNK     0      -3.973   0.179   3.374  0.00  0.00           H+0
HETATM   28  H   UNK     0      -3.717   0.537   1.065  0.00  0.00           H+0
HETATM   29  H   UNK     0       0.024   0.782   3.485  0.00  0.00           H+0
HETATM   30  H   UNK     0       1.731  -2.072   0.909  0.00  0.00           H+0
HETATM   31  H   UNK     0       1.773   1.918  -0.938  0.00  0.00           H+0
HETATM   32  H   UNK     0       1.903  -0.694  -2.256  0.00  0.00           H+0
HETATM   33  H   UNK     0       0.942  -1.881  -1.376  0.00  0.00           H+0
HETATM   34  H   UNK     0       0.017   0.853  -2.399  0.00  0.00           H+0
HETATM   35  H   UNK     0       0.449  -1.598  -4.132  0.00  0.00           H+0
HETATM   36  H   UNK     0      -0.312  -0.082  -4.659  0.00  0.00           H+0
HETATM   37  H   UNK     0      -1.162  -1.632  -4.828  0.00  0.00           H+0
HETATM   38  H   UNK     0      -2.255   0.801  -3.330  0.00  0.00           H+0
HETATM   39  H   UNK     0      -3.055  -0.741  -3.627  0.00  0.00           H+0
HETATM   40  H   UNK     0      -3.910   0.650  -1.631  0.00  0.00           H+0
HETATM   41  H   UNK     0      -3.611  -1.079  -1.358  0.00  0.00           H+0
CONECT    1    2   25   26   27                                             
CONECT    2    3    1                                                       
CONECT    3    8    2    4                                                  
CONECT    4    5    3   28                                                  
CONECT    5   24    4    6                                                  
CONECT    6   20    7    5                                                  
CONECT    7    8    6   10                                                  
CONECT    8    3    7    9                                                  
CONECT    9    8   29                                                       
CONECT   10   11   18    7   19                                             
CONECT   11   10   12   30                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   16   15   12                                                  
CONECT   15   14                                                            
CONECT   16   14   18   17                                                  
CONECT   17   16                                                            
CONECT   18   16   10   31                                                  
CONECT   19   20   10   32   33                                             
CONECT   20    6   21   19   34                                             
CONECT   21   20   23   22                                                  
CONECT   22   21   35   36   37                                             
CONECT   23   21   24   38   39                                             
CONECT   24    5   23   40   41                                             
CONECT   25    1                                                            
CONECT   26    1                                                            
CONECT   27    1                                                            
CONECT   28    4                                                            
CONECT   29    9                                                            
CONECT   30   11                                                            
CONECT   31   18                                                            
CONECT   32   19                                                            
CONECT   33   19                                                            
CONECT   34   20                                                            
CONECT   35   22                                                            
CONECT   36   22                                                            
CONECT   37   22                                                            
CONECT   38   23                                                            
CONECT   39   23                                                            
CONECT   40   24                                                            
CONECT   41   24                                                            
MASTER        0    0    0    0    0    0    0    0   41    0   88    0
END

RDKit          3D

41 44  0  0  0  0  0  0  0  0999 V2000
   -3.3974    1.0937    3.5498 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0220    0.8997    3.2415 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7184    0.6164    1.9316 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6493    0.4636    0.8873 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2083    0.1911   -0.4124 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8430    0.0795   -0.6248 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0957    0.1558    0.4026 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3430    0.4529    1.6770 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5614    0.5842    2.6919 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4814   -0.1337   -0.1332 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2367   -1.1281    0.7093 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4466   -0.9149    1.2482 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2815   -2.2190    2.2967 Br  0  0  0  0  0  0  0  0  0  0  0  0
    4.1662    0.3774    1.0221 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2839    0.5849    1.4871 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4643    1.3980    0.1810 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3259    3.0293   -0.1291 Br  0  0  0  0  0  0  0  0  0  0  0  0
    2.2542    1.1456   -0.3412 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1096   -0.8008   -1.5060 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2022   -0.1325   -1.9635 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0826   -0.9053   -2.8478 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4978   -1.0494   -4.1797 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3937   -0.2125   -2.9292 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1276   -0.1153   -1.5645 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4699    1.3331    4.6151 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8131    1.9380    2.9900 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9728    0.1788    3.3745 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7171    0.5366    1.0647 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0244    0.7817    3.4848 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7314   -2.0718    0.9085 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7728    1.9179   -0.9376 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9025   -0.6936   -2.2564 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9416   -1.8812   -1.3760 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0173    0.8533   -2.3987 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4486   -1.5984   -4.1322 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3124   -0.0815   -4.6593 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1618   -1.6321   -4.8279 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2551    0.8014   -3.3305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0547   -0.7412   -3.6273 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9098    0.6495   -1.6307 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6112   -1.0785   -1.3584 H   0  0  0  0  0  0  0  0  0  0  0  0
 14 16  1  0
 16 18  2  0
 10 11  1  0
  3  8  2  0
  5 24  1  0
  6 20  1  0
 20 21  1  0
 21 23  1  0
 23 24  1  0
 10 18  1  0
  3  2  1  0
  8  7  1  0
  2  1  1  0
  7  6  2  0
  8  9  1  0
 11 12  2  0
 21 22  1  0
  5  4  2  0
 20 19  1  0
  7 10  1  0
 10 19  1  0
  4  3  1  0
 14 15  2  0
  5  6  1  0
 12 13  1  0
 12 14  1  0
 16 17  1  0
 11 30  1  0
 18 31  1  0
  4 28  1  0
 20 34  1  0
 23 38  1  0
 23 39  1  0
 24 40  1  0
 24 41  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  9 29  1  0
 22 35  1  0
 22 36  1  0
 22 37  1  0
 19 32  1  0
 19 33  1  0
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₁₇Br₂NO₃

Average Mass

455.1460 Da

Monoisotopic Mass

452.95752 Da

IUPAC Name

(4'R)-3,5-dibromo-11'-hydroxy-10'-methoxy-5'-methyl-5'-azaspiro[cyclohexane-1,2'-tricyclo[6.3.1.0^{4,12}]dodecane]-1'(12'),2,5,8',10'-pentaen-4-one

Traditional Name

(4'R)-3,5-dibromo-11'-hydroxy-10'-methoxy-5'-methyl-5'-azaspiro[cyclohexane-1,2'-tricyclo[6.3.1.0^{4,12}]dodecane]-1'(12'),2,5,8',10'-pentaen-4-one

CAS Registry Number

Not Available

SMILES

[H]OC1=C(OC([H])([H])[H])C([H])=C2C3=C1C1(C([H])=C(Br)C(=O)C(Br)=C1[H])C([H])([H])[C@@]3([H])N(C([H])([H])[H])C([H])([H])C2([H])[H]

InChI Identifier

InChI=1S/C18H17Br2NO3/c1-21-4-3-9-5-13(24-2)17(23)15-14(9)12(21)8-18(15)6-10(19)16(22)11(20)7-18/h5-7,12,23H,3-4,8H2,1-2H3/t12-/m1/s1

InChI Key

CHIIYNHRBKMNTF-GFCCVEGCSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Meconopsis cambrica	JEOL database	Sorek, H., et al, J. Nat. Prod. 72, 784 (2009)

Chemical Taxonomy

Classification

Not classified

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	3.77	ALOGPS
logP	3.42	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Acidic)	9.84	ChemAxon
pKa (Strongest Basic)	5.65	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	49.77 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	103.01 m³·mol⁻¹	ChemAxon
Polarizability	39.7 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

Not Available

References

General References

Sorek, H., et al. (2009). Sorek, H., et al, J. Nat. Prod. 72, 784 (2009). J. Nat. Prod..

Showing NP-Card for saldedine A (NP0034344)

MOL for NP0034344 (saldedine A)

3D MOL for NP0034344 (saldedine A)

3D SDF for NP0034344 (saldedine A)

3D-SDF for NP0034344 (saldedine A)

PDB for NP0034344 (saldedine A)

3D PDB for NP0034344 (saldedine A)

SMILES for NP0034344 (saldedine A)

INCHI for NP0034344 (saldedine A)

Structure for NP0034344 (saldedine A)

3D Structure for NP0034344 (saldedine A)