NP-MRD: Showing NP-Card for methyl (1s,4ar,4bs,8ar,10as)-10a-hydroxy-7-(2-hydroxyethyl)-1,4a,8-trimethyl-6-oxo-2,3,4,4b,5,8a,9,10-octahydrophenanthrene-1-carboxylate (NP0318499)

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Record Information

Version

2.0

Created at

2022-09-11 19:02:15 UTC

Updated at

2022-09-11 19:02:15 UTC

NP-MRD ID

NP0318499

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (1s,4ar,4bs,8ar,10as)-10a-hydroxy-7-(2-hydroxyethyl)-1,4a,8-trimethyl-6-oxo-2,3,4,4b,5,8a,9,10-octahydrophenanthrene-1-carboxylate

Description

Caesaldekarin g belongs to the class of organic compounds known as isocopalane and spongiane diterpenoids. These are diterpenoids with a structure based on the isocopalane (Tetradecahydro-1,1,4a,7,8,8a-hexamethylphenanthrene) or the 15,16-epoxyisocopalane skeleton. methyl (1s,4ar,4bs,8ar,10as)-10a-hydroxy-7-(2-hydroxyethyl)-1,4a,8-trimethyl-6-oxo-2,3,4,4b,5,8a,9,10-octahydrophenanthrene-1-carboxylate is found in Guilandina bonduc. Based on a literature review very few articles have been published on Caesaldekarin g.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112221022D          

 26 28  0  0  1  0            999 V2000
   -0.9620   -1.7164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1053   -2.5288    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4733   -3.0591    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6165   -3.8716    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -2.7770    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4452   -3.5894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -2.0625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9520   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -2.0625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7770   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145   -0.6336    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2520   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395   -0.6336    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -2.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145   -3.4914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -2.7770    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3645   -3.4914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -3.4914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -2.7770    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145   -3.4914    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  5  3  1  1  0  0  0
  5  6  1  6  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  1  0  0  0
 10 12  1  0  0  0  0
 12 13  1  1  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 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
 16 20  2  0  0  0  0
 20 21  1  0  0  0  0
 22 20  1  6  0  0  0
 12 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
  5 25  1  0  0  0  0
 10 25  1  0  0  0  0
 25 26  1  6  0  0  0
M  END

     RDKit          3D

 58 60  0  0  0  0  0  0  0  0999 V2000
    5.4535    2.1288   -1.1707 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8304    1.0357   -0.5655 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4749    0.7849   -0.6742 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7706    1.5612   -1.3381 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8953   -0.4053    0.0036 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6294   -1.5572   -0.7416 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2736   -0.4660    1.4471 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2552   -0.5488    2.4789 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8202   -0.5189    2.0995 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5873    0.1759    0.7422 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0024    1.5999    0.9956 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8662    0.1452    0.4509 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5800    1.4784    0.7320 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0632    1.2163    0.5635 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8543    2.0419    1.0759 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5660    0.0600   -0.1572 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9883   -0.3703   -0.1002 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8970    0.5851   -0.7829 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9443    1.8623   -0.3047 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7099   -0.6665   -0.8819 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2326   -1.8402   -1.6085 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3078   -0.2267   -0.9074 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4041   -1.1835   -1.6329 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9765   -0.5026   -1.6362 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4427   -0.5981   -0.2062 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2012   -1.9653    0.1272 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3518    1.7462   -1.7148 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8360    2.6446   -1.9108 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8358    2.8753   -0.4488 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7168   -1.2996   -0.5435 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4829   -2.5181   -0.2685 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5175   -1.4793   -1.8175 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9621   -1.3597    1.5735 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0127    0.3773    1.6245 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4080    0.3132    3.2007 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3870   -1.4492    3.1535 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1644    0.0199    2.8158 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3773   -1.5293    1.9737 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0791    1.7128    1.2776 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6621    2.3147    0.2292 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5135    1.8742    1.9855 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3763   -0.5733    1.1597 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3547    2.2346   -0.0453 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4823    1.8100    1.7614 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3196   -0.4018    0.9835 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0783   -1.4067   -0.4442 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5925    0.5909   -1.8702 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9487    0.1795   -0.7142 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6304    1.9480    0.4148 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5029   -2.2981   -2.2788 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1265   -1.6044   -2.2316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5530   -2.6681   -0.9105 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2973    0.7139   -1.5376 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7800   -1.2945   -2.6644 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3916   -2.1226   -1.0924 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8363    0.5377   -1.9960 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5964   -1.1354   -2.2672 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4942   -2.5788   -0.5612 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  5  3  1  6
  5  6  1  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  1
 10 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 14 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 16 20  2  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  1
 25  5  1  0
 25 10  1  0
 22 12  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  6 30  1  0
  6 31  1  0
  6 32  1  0
  7 33  1  0
  7 34  1  0
  8 35  1  0
  8 36  1  0
  9 37  1  0
  9 38  1  0
 11 39  1  0
 11 40  1  0
 11 41  1  0
 12 42  1  1
 13 43  1  0
 13 44  1  0
 17 45  1  0
 17 46  1  0
 18 47  1  0
 18 48  1  0
 19 49  1  0
 21 50  1  0
 21 51  1  0
 21 52  1  0
 22 53  1  6
 23 54  1  0
 23 55  1  0
 24 56  1  0
 24 57  1  0
 26 58  1  0
M  END


  Mrv1652309112221022D          

 26 28  0  0  1  0            999 V2000
   -0.9620   -1.7164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1053   -2.5288    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4733   -3.0591    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6165   -3.8716    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -2.7770    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4452   -3.5894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -2.0625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9520   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -2.0625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7770   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145   -0.6336    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2520   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395   -0.6336    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -2.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145   -3.4914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -2.7770    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3645   -3.4914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -3.4914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -2.7770    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145   -3.4914    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  5  3  1  1  0  0  0
  5  6  1  6  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  1  0  0  0
 10 12  1  0  0  0  0
 12 13  1  1  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 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
 16 20  2  0  0  0  0
 20 21  1  0  0  0  0
 22 20  1  6  0  0  0
 12 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
  5 25  1  0  0  0  0
 10 25  1  0  0  0  0
 25 26  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0318499

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)[C@@]1(C)CCC[C@]2(C)[C@H]3CC(=O)C(CCO)=C(C)[C@@H]3CC[C@@]12O

> <INCHI_IDENTIFIER>
InChI=1S/C21H32O5/c1-13-14-6-10-21(25)19(2,8-5-9-20(21,3)18(24)26-4)16(14)12-17(23)15(13)7-11-22/h14,16,22,25H,5-12H2,1-4H3/t14-,16-,19+,20+,21-/m0/s1

> <INCHI_KEY>
FMXLUDDVSRJLED-KXLDAGHISA-N

> <FORMULA>
C21H32O5

> <MOLECULAR_WEIGHT>
364.482

> <EXACT_MASS>
364.22497413

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
40.55293951485608

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (1S,4aR,4bS,8aR,10aS)-10a-hydroxy-7-(2-hydroxyethyl)-1,4a,8-trimethyl-6-oxo-1,2,3,4,4a,4b,5,6,8a,9,10,10a-dodecahydrophenanthrene-1-carboxylate

> <JCHEM_LOGP>
2.3530264900000004

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.91614694643527

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.777741572226272

> <JCHEM_PKA_STRONGEST_BASIC>
-2.399247301365353

> <JCHEM_POLAR_SURFACE_AREA>
83.83000000000001

> <JCHEM_REFRACTIVITY>
98.86269999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
methyl (1S,4aR,4bS,8aR,10aS)-10a-hydroxy-7-(2-hydroxyethyl)-1,4a,8-trimethyl-6-oxo-2,3,4,4b,5,8a,9,10-octahydrophenanthrene-1-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0      -1.796  -3.204   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -2.063  -4.720   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -0.883  -5.710   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -1.151  -7.227   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       0.564  -5.184   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.831  -6.700   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.206  -3.850   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.564  -2.516   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.104  -2.516   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.874  -3.850   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.644  -2.516   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.414  -3.850   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.184  -2.516   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.724  -2.516   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       7.494  -1.183   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       7.494  -3.850   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.034  -3.850   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.804  -2.516   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       9.034  -1.183   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       6.724  -5.184   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.494  -6.517   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.184  -5.184   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.414  -6.517   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.874  -6.517   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.104  -5.184   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       1.334  -6.517   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    7   25                                             
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12   25                                             
CONECT   11   10                                                            
CONECT   12   10   13   22                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   20                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18                                                            
CONECT   20   16   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   12   23                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24    5   10   26                                             
CONECT   26   25                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   56    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₃₂O₅

Average Mass

364.4820 Da

Monoisotopic Mass

364.22497 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

COC(=O)[C@@]1(C)CCC[C@]2(C)[C@H]3CC(=O)C(CCO)=C(C)[C@@H]3CC[C@@]12O

InChI Identifier

InChI=1S/C21H32O5/c1-13-14-6-10-21(25)19(2,8-5-9-20(21,3)18(24)26-4)16(14)12-17(23)15(13)7-11-22/h14,16,22,25H,5-12H2,1-4H3/t14-,16-,19+,20+,21-/m0/s1

InChI Key

FMXLUDDVSRJLED-KXLDAGHISA-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
Guilandina bonduc	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as isocopalane and spongiane diterpenoids. These are diterpenoids with a structure based on the isocopalane (Tetradecahydro-1,1,4a,7,8,8a-hexamethylphenanthrene) or the 15,16-epoxyisocopalane skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Isocopalane and spongiane diterpenoids

Alternative Parents

Substituents

Isocopalane diterpenoid
Hydrophenanthrene
Phenanthrene
Cyclohexenone
Cyclic alcohol
Methyl ester
Tertiary alcohol
Carboxylic acid ester
Ketone
Cyclic ketone
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Alcohol
Organooxygen compound
Carbonyl group
Primary alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic 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

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

15381601

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl (1s,4ar,4bs,8ar,10as)-10a-hydroxy-7-(2-hydroxyethyl)-1,4a,8-trimethyl-6-oxo-2,3,4,4b,5,8a,9,10-octahydrophenanthrene-1-carboxylate (NP0318499)

MOL for NP0318499 (methyl (1s,4ar,4bs,8ar,10as)-10a-hydroxy-7-(2-hydroxyethyl)-1,4a,8-trimethyl-6-oxo-2,3,4,4b,5,8a,9,10-octahydrophenanthrene-1-carboxylate)

3D MOL for NP0318499 (methyl (1s,4ar,4bs,8ar,10as)-10a-hydroxy-7-(2-hydroxyethyl)-1,4a,8-trimethyl-6-oxo-2,3,4,4b,5,8a,9,10-octahydrophenanthrene-1-carboxylate)

3D SDF for NP0318499 (methyl (1s,4ar,4bs,8ar,10as)-10a-hydroxy-7-(2-hydroxyethyl)-1,4a,8-trimethyl-6-oxo-2,3,4,4b,5,8a,9,10-octahydrophenanthrene-1-carboxylate)

3D-SDF for NP0318499 (methyl (1s,4ar,4bs,8ar,10as)-10a-hydroxy-7-(2-hydroxyethyl)-1,4a,8-trimethyl-6-oxo-2,3,4,4b,5,8a,9,10-octahydrophenanthrene-1-carboxylate)

PDB for NP0318499 (methyl (1s,4ar,4bs,8ar,10as)-10a-hydroxy-7-(2-hydroxyethyl)-1,4a,8-trimethyl-6-oxo-2,3,4,4b,5,8a,9,10-octahydrophenanthrene-1-carboxylate)

3D PDB for NP0318499 (methyl (1s,4ar,4bs,8ar,10as)-10a-hydroxy-7-(2-hydroxyethyl)-1,4a,8-trimethyl-6-oxo-2,3,4,4b,5,8a,9,10-octahydrophenanthrene-1-carboxylate)

SMILES for NP0318499 (methyl (1s,4ar,4bs,8ar,10as)-10a-hydroxy-7-(2-hydroxyethyl)-1,4a,8-trimethyl-6-oxo-2,3,4,4b,5,8a,9,10-octahydrophenanthrene-1-carboxylate)

INCHI for NP0318499 (methyl (1s,4ar,4bs,8ar,10as)-10a-hydroxy-7-(2-hydroxyethyl)-1,4a,8-trimethyl-6-oxo-2,3,4,4b,5,8a,9,10-octahydrophenanthrene-1-carboxylate)

Structure for NP0318499 (methyl (1s,4ar,4bs,8ar,10as)-10a-hydroxy-7-(2-hydroxyethyl)-1,4a,8-trimethyl-6-oxo-2,3,4,4b,5,8a,9,10-octahydrophenanthrene-1-carboxylate)

3D Structure for NP0318499 (methyl (1s,4ar,4bs,8ar,10as)-10a-hydroxy-7-(2-hydroxyethyl)-1,4a,8-trimethyl-6-oxo-2,3,4,4b,5,8a,9,10-octahydrophenanthrene-1-carboxylate)