NP-MRD: Showing NP-Card for phanginin F (NP0025341)

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Record Information

Version

2.0

Created at

2021-06-19 17:29:17 UTC

Updated at

2021-06-29 23:50:14 UTC

NP-MRD ID

NP0025341

Secondary Accession Numbers

None

Natural Product Identification

Common Name

phanginin F

Provided By

JEOL Database JEOL Logo

Description

phanginin F is found in Caesalpinia sappan Linn. phanginin F was first documented in 2008 (Yodsaoue, O., et al.).

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306192119293D          

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M  END

     RDKit          3D

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M  END


  Mrv1652306192119293D          

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    5.1235   -0.8492   -3.6864 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6514    0.0694   -3.9256 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0182   -0.7052   -1.9096 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4751   -1.8562    0.8457 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6062    1.0681   -0.0586 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9016    0.4485    1.5626 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9532    1.0156    0.3171 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9215   -0.6652    0.8049 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1039    0.4448   -1.9354 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4601   -0.7878    1.6421 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0029    0.6497    0.2452 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7721    0.6993   -1.0199 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4543    1.4047    0.5807 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1932   -1.9038    1.1168 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6879   -4.0130   -0.5991 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6643   -2.7890   -2.7766 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6496   -4.6649   -1.3674 H   0  0  0  0  0  0  0  0  0  0  0  0
 25 21  2  0  0  0  0
 17 16  1  0  0  0  0
 16 15  1  0  0  0  0
 14  9  1  0  0  0  0
 14 15  1  0  0  0  0
  6  5  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
  5 18  1  0  0  0  0
 19 20  1  0  0  0  0
  9 18  1  0  0  0  0
  5  3  1  6  0  0  0
 14 26  1  0  0  0  0
 10  9  1  0  0  0  0
 15 19  1  0  0  0  0
  5 13  1  0  0  0  0
 25 26  1  0  0  0  0
 13 12  1  0  0  0  0
 10 12  1  0  0  0  0
  9  8  1  1  0  0  0
 18 47  1  6  0  0  0
  7  6  1  0  0  0  0
  3  2  1  0  0  0  0
 21 19  1  0  0  0  0
  2  1  1  0  0  0  0
  3  4  2  0  0  0  0
  8  7  1  0  0  0  0
 15 42  1  1  0  0  0
 18 17  1  0  0  0  0
 26 27  1  0  0  0  0
 14 41  1  6  0  0  0
 10 11  1  0  0  0  0
  8 35  1  0  0  0  0
  8 36  1  0  0  0  0
  7 33  1  0  0  0  0
  7 34  1  0  0  0  0
 17 45  1  0  0  0  0
 17 46  1  0  0  0  0
 16 43  1  0  0  0  0
 16 44  1  0  0  0  0
 26 54  1  6  0  0  0
  6 31  1  0  0  0  0
  6 32  1  0  0  0  0
 19 48  1  1  0  0  0
 10 37  1  1  0  0  0
 22 52  1  0  0  0  0
 23 53  1  0  0  0  0
 20 49  1  0  0  0  0
 20 50  1  0  0  0  0
 20 51  1  0  0  0  0
 13 39  1  0  0  0  0
 13 40  1  0  0  0  0
  1 28  1  0  0  0  0
  1 29  1  0  0  0  0
  1 30  1  0  0  0  0
 27 55  1  0  0  0  0
 11 38  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0025341

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]O[C@@]1([H])OC([H])([H])[C@]2(C(=O)OC([H])([H])[H])C([H])([H])C([H])([H])C([H])([H])[C@]11[C@@]3([H])[C@@]([H])(O[H])C4=C(C([H])=C([H])O4)[C@]([H])(C([H])([H])[H])[C@]3([H])C([H])([H])C([H])([H])[C@@]21[H]

> <INCHI_IDENTIFIER>
InChI=1S/C21H28O6/c1-11-12-4-5-14-20(18(23)25-2)7-3-8-21(14,19(24)27-10-20)15(12)16(22)17-13(11)6-9-26-17/h6,9,11-12,14-16,19,22,24H,3-5,7-8,10H2,1-2H3/t11-,12+,14+,15-,16-,19+,20-,21+/m1/s1

> <INCHI_KEY>
IUERDUXXUQLZOY-OYXWAZNXSA-N

> <FORMULA>
C21H28O6

> <MOLECULAR_WEIGHT>
376.449

> <EXACT_MASS>
376.188588622

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
40.0967314342613

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (1S,2S,3R,9R,10S,13R,14S,17S)-3,17-dihydroxy-9-methyl-5,16-dioxapentacyclo[12.3.3.0^{1,13}.0^{2,10}.0^{4,8}]icosa-4(8),6-diene-14-carboxylate

> <ALOGPS_LOGP>
1.49

> <JCHEM_LOGP>
2.0794449740000007

> <ALOGPS_LOGS>
-3.33

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.224295901014592

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.91498192648343

> <JCHEM_PKA_STRONGEST_BASIC>
-2.837628061944891

> <JCHEM_POLAR_SURFACE_AREA>
89.13000000000001

> <JCHEM_REFRACTIVITY>
95.96650000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.75e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl (1S,2S,3R,9R,10S,13R,14S,17S)-3,17-dihydroxy-9-methyl-5,16-dioxapentacyclo[12.3.3.0^{1,13}.0^{2,10}.0^{4,8}]icosa-4(8),6-diene-14-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 55 59  0  0  0  0  0  0  0  0999 V2000
    4.6782    3.2434   -2.0618 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0583    1.9607   -2.1667 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8071    0.9338   -1.6736 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9262    1.0700   -1.1955 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0841   -0.4070   -1.8246 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8405   -1.4892   -1.0202 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1666   -2.8564   -1.0227 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6431   -2.8150   -0.8589 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9074   -1.6921   -1.6629 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0615   -1.9901   -3.1882 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3077   -1.0747   -3.9664 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4099   -1.9532   -3.6352 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0929   -0.7384   -3.3282 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3674   -1.5358   -1.2974 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1380   -1.0452    0.1850 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9858    0.2031    0.4971 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4546    0.0574    0.1292 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6114   -0.3379   -1.3516 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3797   -0.7822    0.5463 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9258    0.5679    0.0566 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2350   -1.8821    0.0130 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5400   -2.3111    0.3579 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8291   -3.3673   -0.4791 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7829   -3.6218   -1.3120 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8286   -2.7068   -1.0053 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5195   -2.7634   -1.6913 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0586   -3.9975   -1.2971 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9900    3.9863   -2.4743 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6052    3.2691   -2.6429 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8688    3.4923   -1.0132 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8628   -1.6025   -1.4053 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9644   -1.1612    0.0200 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5972   -3.4728   -0.2238 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4176   -3.3832   -1.9509 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2888   -3.8047   -1.1579 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4180   -2.7308    0.2091 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6830   -2.9944   -3.4073 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3457   -1.4353   -4.8689 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1235   -0.8492   -3.6864 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6514    0.0694   -3.9256 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0182   -0.7052   -1.9096 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4751   -1.8562    0.8457 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6062    1.0681   -0.0586 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9016    0.4485    1.5626 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9532    1.0156    0.3171 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9215   -0.6652    0.8049 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1039    0.4448   -1.9354 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4601   -0.7878    1.6421 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0029    0.6497    0.2452 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7721    0.6993   -1.0199 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4543    1.4047    0.5807 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1932   -1.9038    1.1168 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6879   -4.0130   -0.5991 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6643   -2.7890   -2.7766 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6496   -4.6649   -1.3674 H   0  0  0  0  0  0  0  0  0  0  0  0
 25 21  2  0
 17 16  1  0
 16 15  1  0
 14  9  1  0
 14 15  1  0
  6  5  1  0
 21 22  1  0
 22 23  2  0
 23 24  1  0
 24 25  1  0
  5 18  1  0
 19 20  1  0
  9 18  1  0
  5  3  1  6
 14 26  1  0
 10  9  1  0
 15 19  1  0
  5 13  1  0
 25 26  1  0
 13 12  1  0
 10 12  1  0
  9  8  1  1
 18 47  1  6
  7  6  1  0
  3  2  1  0
 21 19  1  0
  2  1  1  0
  3  4  2  0
  8  7  1  0
 15 42  1  1
 18 17  1  0
 26 27  1  0
 14 41  1  6
 10 11  1  0
  8 35  1  0
  8 36  1  0
  7 33  1  0
  7 34  1  0
 17 45  1  0
 17 46  1  0
 16 43  1  0
 16 44  1  0
 26 54  1  6
  6 31  1  0
  6 32  1  0
 19 48  1  1
 10 37  1  1
 22 52  1  0
 23 53  1  0
 20 49  1  0
 20 50  1  0
 20 51  1  0
 13 39  1  0
 13 40  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
 27 55  1  0
 11 38  1  0
M  END

HEADER    PROTEIN                                 19-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-JUN-21         0                                  
HETATM    1  C   UNK     0       4.678   3.243  -2.062  0.00  0.00           C+0
HETATM    2  O   UNK     0       4.058   1.961  -2.167  0.00  0.00           O+0
HETATM    3  C   UNK     0       4.807   0.934  -1.674  0.00  0.00           C+0
HETATM    4  O   UNK     0       5.926   1.070  -1.196  0.00  0.00           O+0
HETATM    5  C   UNK     0       4.084  -0.407  -1.825  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.840  -1.489  -1.020  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.167  -2.856  -1.023  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.643  -2.815  -0.859  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.907  -1.692  -1.663  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.062  -1.990  -3.188  0.00  0.00           C+0
HETATM   11  O   UNK     0       1.308  -1.075  -3.966  0.00  0.00           O+0
HETATM   12  O   UNK     0       3.410  -1.953  -3.635  0.00  0.00           O+0
HETATM   13  C   UNK     0       4.093  -0.738  -3.328  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.367  -1.536  -1.297  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.138  -1.045   0.185  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.986   0.203   0.497  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.455   0.057   0.129  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.611  -0.338  -1.352  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.380  -0.782   0.546  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.926   0.568   0.057  0.00  0.00           C+0
HETATM   21  C   UNK     0      -2.235  -1.882   0.013  0.00  0.00           C+0
HETATM   22  C   UNK     0      -3.540  -2.311   0.358  0.00  0.00           C+0
HETATM   23  C   UNK     0      -3.829  -3.367  -0.479  0.00  0.00           C+0
HETATM   24  O   UNK     0      -2.783  -3.622  -1.312  0.00  0.00           O+0
HETATM   25  C   UNK     0      -1.829  -2.707  -1.005  0.00  0.00           C+0
HETATM   26  C   UNK     0      -0.520  -2.763  -1.691  0.00  0.00           C+0
HETATM   27  O   UNK     0       0.059  -3.998  -1.297  0.00  0.00           O+0
HETATM   28  H   UNK     0       3.990   3.986  -2.474  0.00  0.00           H+0
HETATM   29  H   UNK     0       5.605   3.269  -2.643  0.00  0.00           H+0
HETATM   30  H   UNK     0       4.869   3.492  -1.013  0.00  0.00           H+0
HETATM   31  H   UNK     0       5.863  -1.603  -1.405  0.00  0.00           H+0
HETATM   32  H   UNK     0       4.964  -1.161   0.020  0.00  0.00           H+0
HETATM   33  H   UNK     0       4.597  -3.473  -0.224  0.00  0.00           H+0
HETATM   34  H   UNK     0       4.418  -3.383  -1.951  0.00  0.00           H+0
HETATM   35  H   UNK     0       2.289  -3.805  -1.158  0.00  0.00           H+0
HETATM   36  H   UNK     0       2.418  -2.731   0.209  0.00  0.00           H+0
HETATM   37  H   UNK     0       1.683  -2.994  -3.407  0.00  0.00           H+0
HETATM   38  H   UNK     0       1.346  -1.435  -4.869  0.00  0.00           H+0
HETATM   39  H   UNK     0       5.123  -0.849  -3.686  0.00  0.00           H+0
HETATM   40  H   UNK     0       3.651   0.069  -3.926  0.00  0.00           H+0
HETATM   41  H   UNK     0      -0.018  -0.705  -1.910  0.00  0.00           H+0
HETATM   42  H   UNK     0       0.475  -1.856   0.846  0.00  0.00           H+0
HETATM   43  H   UNK     0       0.606   1.068  -0.059  0.00  0.00           H+0
HETATM   44  H   UNK     0       0.902   0.449   1.563  0.00  0.00           H+0
HETATM   45  H   UNK     0       2.953   1.016   0.317  0.00  0.00           H+0
HETATM   46  H   UNK     0       2.922  -0.665   0.805  0.00  0.00           H+0
HETATM   47  H   UNK     0       2.104   0.445  -1.935  0.00  0.00           H+0
HETATM   48  H   UNK     0      -1.460  -0.788   1.642  0.00  0.00           H+0
HETATM   49  H   UNK     0      -3.003   0.650   0.245  0.00  0.00           H+0
HETATM   50  H   UNK     0      -1.772   0.699  -1.020  0.00  0.00           H+0
HETATM   51  H   UNK     0      -1.454   1.405   0.581  0.00  0.00           H+0
HETATM   52  H   UNK     0      -4.193  -1.904   1.117  0.00  0.00           H+0
HETATM   53  H   UNK     0      -4.688  -4.013  -0.599  0.00  0.00           H+0
HETATM   54  H   UNK     0      -0.664  -2.789  -2.777  0.00  0.00           H+0
HETATM   55  H   UNK     0      -0.650  -4.665  -1.367  0.00  0.00           H+0
CONECT    1    2   28   29   30                                             
CONECT    2    3    1                                                       
CONECT    3    5    2    4                                                  
CONECT    4    3                                                            
CONECT    5    6   18    3   13                                             
CONECT    6    5    7   31   32                                             
CONECT    7    6    8   33   34                                             
CONECT    8    9    7   35   36                                             
CONECT    9   14   18   10    8                                             
CONECT   10    9   12   11   37                                             
CONECT   11   10   38                                                       
CONECT   12   13   10                                                       
CONECT   13    5   12   39   40                                             
CONECT   14    9   15   26   41                                             
CONECT   15   16   14   19   42                                             
CONECT   16   17   15   43   44                                             
CONECT   17   16   18   45   46                                             
CONECT   18    5    9   47   17                                             
CONECT   19   20   15   21   48                                             
CONECT   20   19   49   50   51                                             
CONECT   21   25   22   19                                                  
CONECT   22   21   23   52                                                  
CONECT   23   22   24   53                                                  
CONECT   24   23   25                                                       
CONECT   25   21   24   26                                                  
CONECT   26   14   25   27   54                                             
CONECT   27   26   55                                                       
CONECT   28    1                                                            
CONECT   29    1                                                            
CONECT   30    1                                                            
CONECT   31    6                                                            
CONECT   32    6                                                            
CONECT   33    7                                                            
CONECT   34    7                                                            
CONECT   35    8                                                            
CONECT   36    8                                                            
CONECT   37   10                                                            
CONECT   38   11                                                            
CONECT   39   13                                                            
CONECT   40   13                                                            
CONECT   41   14                                                            
CONECT   42   15                                                            
CONECT   43   16                                                            
CONECT   44   16                                                            
CONECT   45   17                                                            
CONECT   46   17                                                            
CONECT   47   18                                                            
CONECT   48   19                                                            
CONECT   49   20                                                            
CONECT   50   20                                                            
CONECT   51   20                                                            
CONECT   52   22                                                            
CONECT   53   23                                                            
CONECT   54   26                                                            
CONECT   55   27                                                            
MASTER        0    0    0    0    0    0    0    0   55    0  118    0
END

RDKit          3D

55 59  0  0  0  0  0  0  0  0999 V2000
    4.6782    3.2434   -2.0618 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0583    1.9607   -2.1667 O   0  0  0  0  0  0  0  0  0  0  0  0
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    5.9262    1.0700   -1.1955 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0841   -0.4070   -1.8246 C   0  0  2  0  0  0  0  0  0  0  0  0
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    1.3077   -1.0747   -3.9664 O   0  0  0  0  0  0  0  0  0  0  0  0
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    0.3674   -1.5358   -1.2974 C   0  0  2  0  0  0  0  0  0  0  0  0
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    2.6114   -0.3379   -1.3516 C   0  0  1  0  0  0  0  0  0  0  0  0
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   -3.5400   -2.3111    0.3579 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8291   -3.3673   -0.4791 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7829   -3.6218   -1.3120 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8286   -2.7068   -1.0053 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5195   -2.7634   -1.6913 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0586   -3.9975   -1.2971 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9900    3.9863   -2.4743 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6052    3.2691   -2.6429 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8688    3.4923   -1.0132 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8628   -1.6025   -1.4053 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9644   -1.1612    0.0200 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5972   -3.4728   -0.2238 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4176   -3.3832   -1.9509 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2888   -3.8047   -1.1579 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4180   -2.7308    0.2091 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6830   -2.9944   -3.4073 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3457   -1.4353   -4.8689 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1235   -0.8492   -3.6864 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6514    0.0694   -3.9256 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0182   -0.7052   -1.9096 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4751   -1.8562    0.8457 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6062    1.0681   -0.0586 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9016    0.4485    1.5626 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9532    1.0156    0.3171 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9215   -0.6652    0.8049 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1039    0.4448   -1.9354 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4601   -0.7878    1.6421 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0029    0.6497    0.2452 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7721    0.6993   -1.0199 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4543    1.4047    0.5807 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1932   -1.9038    1.1168 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6879   -4.0130   -0.5991 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6643   -2.7890   -2.7766 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6496   -4.6649   -1.3674 H   0  0  0  0  0  0  0  0  0  0  0  0
 25 21  2  0
 17 16  1  0
 16 15  1  0
 14  9  1  0
 14 15  1  0
  6  5  1  0
 21 22  1  0
 22 23  2  0
 23 24  1  0
 24 25  1  0
  5 18  1  0
 19 20  1  0
  9 18  1  0
  5  3  1  6
 14 26  1  0
 10  9  1  0
 15 19  1  0
  5 13  1  0
 25 26  1  0
 13 12  1  0
 10 12  1  0
  9  8  1  1
 18 47  1  6
  7  6  1  0
  3  2  1  0
 21 19  1  0
  2  1  1  0
  3  4  2  0
  8  7  1  0
 15 42  1  1
 18 17  1  0
 26 27  1  0
 14 41  1  6
 10 11  1  0
  8 35  1  0
  8 36  1  0
  7 33  1  0
  7 34  1  0
 17 45  1  0
 17 46  1  0
 16 43  1  0
 16 44  1  0
 26 54  1  6
  6 31  1  0
  6 32  1  0
 19 48  1  1
 10 37  1  1
 22 52  1  0
 23 53  1  0
 20 49  1  0
 20 50  1  0
 20 51  1  0
 13 39  1  0
 13 40  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
 27 55  1  0
 11 38  1  0
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₂₈O₆

Average Mass

376.4490 Da

Monoisotopic Mass

376.18859 Da

IUPAC Name

methyl (1S,2S,3R,9R,10S,13R,14S,17S)-3,17-dihydroxy-9-methyl-5,16-dioxapentacyclo[12.3.3.0^{1,13}.0^{2,10}.0^{4,8}]icosa-4(8),6-diene-14-carboxylate

Traditional Name

methyl (1S,2S,3R,9R,10S,13R,14S,17S)-3,17-dihydroxy-9-methyl-5,16-dioxapentacyclo[12.3.3.0^{1,13}.0^{2,10}.0^{4,8}]icosa-4(8),6-diene-14-carboxylate

CAS Registry Number

Not Available

SMILES

[H]O[C@@]1([H])OC([H])([H])[C@]2(C(=O)OC([H])([H])[H])C([H])([H])C([H])([H])C([H])([H])[C@]11[C@@]3([H])[C@@]([H])(O[H])C4=C(C([H])=C([H])O4)[C@]([H])(C([H])([H])[H])[C@]3([H])C([H])([H])C([H])([H])[C@@]21[H]

InChI Identifier

InChI=1S/C21H28O6/c1-11-12-4-5-14-20(18(23)25-2)7-3-8-21(14,19(24)27-10-20)15(12)16(22)17-13(11)6-9-26-17/h6,9,11-12,14-16,19,22,24H,3-5,7-8,10H2,1-2H3/t11-,12+,14+,15-,16-,19+,20-,21+/m1/s1

InChI Key

IUERDUXXUQLZOY-OYXWAZNXSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
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, 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, 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, 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, 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
Caesalpinia sappan Linn.	JEOL database	Yodsaoue, O., et al, Phytochem. 69, 1242 (2008)

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	1.49	ALOGPS
logP	2.08	ChemAxon
logS	-3.3	ALOGPS
pKa (Strongest Acidic)	11.91	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	89.13 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	95.97 m³·mol⁻¹	ChemAxon
Polarizability	40.1 Å³	ChemAxon
Number of Rings	5	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

Yodsaoue, O., et al. (2008). Yodsaoue, O., et al, Phytochem. 69, 1242 (2008). Phytochem..

Showing NP-Card for phanginin F (NP0025341)

MOL for NP0025341 (phanginin F)

3D MOL for NP0025341 (phanginin F)

3D SDF for NP0025341 (phanginin F)

3D-SDF for NP0025341 (phanginin F)

PDB for NP0025341 (phanginin F)

3D PDB for NP0025341 (phanginin F)

SMILES for NP0025341 (phanginin F)

INCHI for NP0025341 (phanginin F)

Structure for NP0025341 (phanginin F)

3D Structure for NP0025341 (phanginin F)