NP-MRD: Showing NP-Card for (+)-Caesalmin G (NP0078366)

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Record Information

Version

2.0

Created at

2022-04-28 23:27:44 UTC

Updated at

2022-04-28 23:27:44 UTC

NP-MRD ID

NP0078366

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(+)-Caesalmin G

Description

CAESALMIN G belongs to the class of organic compounds known as eudesmanolides, secoeudesmanolides, and derivatives. These are terpenoids with a structure based on the eudesmanolide (a 3,5a,9-trimethyl-naphtho[1,2-b]furan-2-one derivative) or secoeudesmanolide (a 3,6-dimethyl-5-(pentan-2-yl)-1-benzofuran-2-one derivative) skeleton. (+)-Caesalmin G is found in Caesalpinia minax and Caesalpinia crista . Based on a literature review very few articles have been published on CAESALMIN G.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292201272D          

 25 29  0  0  1  0            999 V2000
    0.3576   -1.5739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9550   -1.0049    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7610   -0.2030    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0304    0.0299    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6279   -0.5391    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4338   -1.3410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1365   -1.7733    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7648   -1.2386    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4504   -0.4758    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0535    0.8545    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7342    1.3206    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7237    1.1313    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2271    0.4777    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0496    0.4144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4061   -0.3296    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9401   -1.0103    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2966   -1.7543    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1191   -1.8176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5852   -1.1368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2287   -0.3928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9598   -0.0106    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3206    0.4270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8305   -2.4350    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4986   -1.7072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8722    0.3512    0.0000 O   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
  3  4  1  6  0  0  0
  4  5  1  1  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  5  9  1  0  0  0  0
  4 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 13 12  1  1  0  0  0
  3 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
  2 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 15 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 17 23  1  6  0  0  0
 16 24  1  1  0  0  0
 15 25  1  6  0  0  0
M  END

     RDKit          3D

 51 55  0  0  0  0  0  0  0  0999 V2000
   -3.3978   -1.6823    0.2579 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6542   -0.3653    0.5706 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9049   -0.1232    2.0483 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3194    0.6479   -0.3000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5118    1.8148   -0.7176 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0987    1.4667   -1.1219 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1051    0.6506   -2.2203 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4336    0.7103    0.0415 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4313    1.6419    1.1970 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9705    0.4444   -0.4072 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9313    1.5866   -0.1488 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3330    1.1111   -0.1839 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4078    1.8631   -0.1866 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4972    1.1775   -0.2203 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1381   -0.1543   -0.2425 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7599   -0.1867   -0.2192 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7990   -1.2694   -0.2292 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9495   -2.3300    0.7942 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0354   -2.8066    1.1719 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6646   -2.6814    1.2410 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7196   -1.9319    0.4565 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5387   -1.5640    1.1430 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2226   -0.5455    0.2195 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2083   -1.1761   -1.0538 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5204   -0.6592    0.3738 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3426   -1.9495   -0.7930 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4823   -1.4009    0.4307 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1935   -2.4639    0.9842 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9791   -0.1437    2.6589 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4990    0.8241    2.2119 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5577   -0.9086    2.5151 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2600    1.0494    0.1803 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7022    0.1567   -1.2433 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9869    2.2448   -1.6513 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5427    2.6818   -0.0023 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5400    2.4037   -1.2316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6583    0.9673   -2.9554 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0805    2.6445    0.8017 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4749    1.9084    1.5451 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2086    1.3509    2.0357 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9956    0.1597   -1.4891 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8062    2.4165   -0.8571 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7994    1.9238    0.9206 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5023    1.5701   -0.2295 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8636   -0.9551   -0.2723 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5809   -1.6866   -1.2350 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6326   -2.3646   -0.5399 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2747   -1.1120    2.1207 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1794   -2.4402    1.2171 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3315   -2.1348   -0.9992 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7962   -0.3808    1.4147 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  6  8  1  0
  8  9  1  1
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 16  2  0
 16 15  1  0
 15 14  2  0
 14 13  1  0
 16 17  1  0
 17 25  1  0
 25 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  6
 21 20  1  0
 20 18  1  0
 18 19  2  0
 23  2  1  0
 23  8  1  0
 25 10  1  0
 13 12  1  0
 18 17  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  3 29  1  0
  3 30  1  0
  3 31  1  0
  4 32  1  0
  4 33  1  0
  5 34  1  0
  5 35  1  0
  6 36  1  6
  7 37  1  0
  9 38  1  0
  9 39  1  0
  9 40  1  0
 10 41  1  6
 11 42  1  0
 11 43  1  0
 15 45  1  0
 14 44  1  0
 17 46  1  6
 25 51  1  1
 21 47  1  6
 22 48  1  0
 22 49  1  0
 24 50  1  0
M  END


  Mrv1652304292201272D          

 25 29  0  0  1  0            999 V2000
    0.3576   -1.5739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9550   -1.0049    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7610   -0.2030    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0304    0.0299    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6279   -0.5391    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4338   -1.3410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1365   -1.7733    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7648   -1.2386    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4504   -0.4758    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0535    0.8545    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7342    1.3206    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7237    1.1313    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2271    0.4777    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0496    0.4144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4061   -0.3296    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9401   -1.0103    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2966   -1.7543    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1191   -1.8176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5852   -1.1368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2287   -0.3928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9598   -0.0106    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3206    0.4270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8305   -2.4350    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4986   -1.7072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8722    0.3512    0.0000 O   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
  3  4  1  6  0  0  0
  4  5  1  1  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  5  9  1  0  0  0  0
  4 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 13 12  1  1  0  0  0
  3 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
  2 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 15 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 17 23  1  6  0  0  0
 16 24  1  1  0  0  0
 15 25  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0078366

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(C)CC[C@H](O)[C@]2(C)[C@H]3CC4=C(C=CO4)[C@@H]4[C@@H]3[C@H](C[C@@]12O)OC4=O

> <INCHI_IDENTIFIER>
InChI=1S/C20H26O5/c1-18(2)6-4-14(21)19(3)11-8-12-10(5-7-24-12)15-16(11)13(25-17(15)22)9-20(18,19)23/h5,7,11,13-16,21,23H,4,6,8-9H2,1-3H3/t11-,13-,14-,15+,16-,19-,20+/m0/s1

> <INCHI_KEY>
NSXNSJSUAMXKCX-QQUVXZFBSA-N

> <FORMULA>
C20H26O5

> <MOLECULAR_WEIGHT>
346.423

> <EXACT_MASS>
346.178023937

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
51

> <JCHEM_AVERAGE_POLARIZABILITY>
37.09465345627733

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,8S,11S,13R,17S,18S,19R)-13,17-dihydroxy-14,14,18-trimethyl-4,10-dioxapentacyclo[9.7.1.0^{3,7}.0^{8,19}.0^{13,18}]nonadeca-3(7),5-dien-9-one

> <ALOGPS_LOGP>
2.01

> <JCHEM_LOGP>
1.4873052453333324

> <ALOGPS_LOGS>
-3.32

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.781787134866306

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.810872524214602

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8238500402552984

> <JCHEM_POLAR_SURFACE_AREA>
79.9

> <JCHEM_REFRACTIVITY>
89.7641

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.67e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,8S,11S,13R,17S,18S,19R)-13,17-dihydroxy-14,14,18-trimethyl-4,10-dioxapentacyclo[9.7.1.0^{3,7}.0^{8,19}.0^{13,18}]nonadeca-3(7),5-dien-9-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  C   UNK     0       0.668  -2.938   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.783  -1.876   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.421  -0.379   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.057   0.056   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.172  -1.006   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.810  -2.503   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -2.121  -3.310   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -3.294  -2.312   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.707  -0.888   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.100   1.595   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -1.371   2.465   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0       1.351   2.112   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       2.291   0.892   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.826   0.774   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.491  -0.615   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.621  -1.886   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.287  -3.275   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.822  -3.393   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.692  -2.122   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.027  -0.733   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.392  -0.020   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.199   0.797   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       3.417  -4.545   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       2.797  -3.187   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       5.361   0.656   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3   16                                                  
CONECT    3    2    4   13                                                  
CONECT    4    3    5   10                                                  
CONECT    5    4    6    9                                                  
CONECT    6    5    1    7                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8    5                                                       
CONECT   10    4   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12    3   14                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   20   25                                             
CONECT   16   15    2   17   24                                             
CONECT   17   16   18   23                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   15   21   22                                             
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   17                                                            
CONECT   24   16                                                            
CONECT   25   15                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   58    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₂₆O₅

Average Mass

346.4230 Da

Monoisotopic Mass

346.17802 Da

IUPAC Name

(1S,8S,11S,13R,17S,18S,19R)-13,17-dihydroxy-14,14,18-trimethyl-4,10-dioxapentacyclo[9.7.1.0^{3,7}.0^{8,19}.0^{13,18}]nonadeca-3(7),5-dien-9-one

Traditional Name

(1S,8S,11S,13R,17S,18S,19R)-13,17-dihydroxy-14,14,18-trimethyl-4,10-dioxapentacyclo[9.7.1.0^{3,7}.0^{8,19}.0^{13,18}]nonadeca-3(7),5-dien-9-one

CAS Registry Number

Not Available

SMILES

CC1(C)CC[C@H](O)[C@]2(C)[C@H]3CC4=C(C=CO4)[C@@H]4[C@@H]3[C@H](C[C@@]12O)OC4=O

InChI Identifier

InChI=1S/C20H26O5/c1-18(2)6-4-14(21)19(3)11-8-12-10(5-7-24-12)15-16(11)13(25-17(15)22)9-20(18,19)23/h5,7,11,13-16,21,23H,4,6,8-9H2,1-3H3/t11-,13-,14-,15+,16-,19-,20+/m0/s1

InChI Key

NSXNSJSUAMXKCX-QQUVXZFBSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Caesalpinia minax	Plant	KNApSAcK
Guilandina crista	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as eudesmanolides, secoeudesmanolides, and derivatives. These are terpenoids with a structure based on the eudesmanolide (a 3,5a,9-trimethyl-naphtho[1,2-b]furan-2-one derivative) or secoeudesmanolide (a 3,6-dimethyl-5-(pentan-2-yl)-1-benzofuran-2-one derivative) skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Eudesmanolides, secoeudesmanolides, and derivatives

Alternative Parents

Substituents

Eudesmanolide
Sesquiterpenoid
Naphthofuran
Benzofuran
Gamma butyrolactone
Cyclic alcohol
Furan
Heteroaromatic compound
Tertiary alcohol
Tetrahydrofuran
Lactone
Carboxylic acid ester
Secondary alcohol
Monocarboxylic acid or derivatives
Oxacycle
Carboxylic acid derivative
Organoheterocyclic compound
Organooxygen compound
Organic oxygen compound
Hydrocarbon derivative
Organic oxide
Alcohol
Carbonyl group
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	2.01	ALOGPS
logP	1.49	ChemAxon
logS	-3.3	ALOGPS
pKa (Strongest Acidic)	13.81	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	79.9 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	89.76 m³·mol⁻¹	ChemAxon
Polarizability	37.09 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

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00042324

Chemspider ID

9112151

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10936915

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (+)-Caesalmin G (NP0078366)

MOL for NP0078366 ((+)-Caesalmin G)

3D MOL for NP0078366 ((+)-Caesalmin G)

3D SDF for NP0078366 ((+)-Caesalmin G)

3D-SDF for NP0078366 ((+)-Caesalmin G)

PDB for NP0078366 ((+)-Caesalmin G)

3D PDB for NP0078366 ((+)-Caesalmin G)

SMILES for NP0078366 ((+)-Caesalmin G)

INCHI for NP0078366 ((+)-Caesalmin G)

Structure for NP0078366 ((+)-Caesalmin G)

3D Structure for NP0078366 ((+)-Caesalmin G)