NP-MRD: Showing NP-Card for (3s,4s)-4-(hydroxymethyl)-3,8,9-trimethyl-3,4-dihydro-2h-1-oxatetraphene-5,12-dione (NP0222265)

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Record Information

Version

2.0

Created at

2022-09-06 00:03:35 UTC

Updated at

2022-09-06 00:03:35 UTC

NP-MRD ID

NP0222265

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3s,4s)-4-(hydroxymethyl)-3,8,9-trimethyl-3,4-dihydro-2h-1-oxatetraphene-5,12-dione

Description

(3S,4S)-4-(hydroxymethyl)-3,8,9-trimethyl-3,4,5,12-tetrahydro-2H-1-oxatetraphene-5,12-dione belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. (3s,4s)-4-(hydroxymethyl)-3,8,9-trimethyl-3,4-dihydro-2h-1-oxatetraphene-5,12-dione is found in Clerodendrum bungei. Based on a literature review very few articles have been published on (3S,4S)-4-(hydroxymethyl)-3,8,9-trimethyl-3,4,5,12-tetrahydro-2H-1-oxatetraphene-5,12-dione.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062202032D          

 25 28  0  0  1  0            999 V2000
    6.1154    0.1007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3052    0.2566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7651   -0.3671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9550   -0.2111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6850    0.5684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8748    0.7243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6048    1.5039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1449    2.1275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9550    1.9716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2251    1.1921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0352    1.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5753    1.6598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7946    1.6598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5246    2.4393    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2546    1.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5246    0.2566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9845   -0.3671    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1744   -0.2111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0957    0.5684    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9058    0.7243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4444    1.1921    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1744    1.9716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.5952    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3347    0.1007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6048   -0.6789    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
  5 10  1  0  0  0  0
 10 11  2  0  0  0  0
  2 11  1  0  0  0  0
 11 12  1  0  0  0  0
  7 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  2  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  1  0  0  0
 19 21  1  0  0  0  0
 15 21  1  0  0  0  0
 21 22  1  6  0  0  0
 22 23  1  0  0  0  0
 16 24  1  0  0  0  0
  6 24  1  0  0  0  0
 24 25  2  0  0  0  0
M  END

     RDKit          3D

 45 48  0  0  0  0  0  0  0  0999 V2000
    6.2893    0.2281    0.3604 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8047    0.2282    0.3230 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0256    0.3905    1.4322 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6353    0.3841    1.3523 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0409    0.2120    0.1399 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6654    0.2002    0.0206 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1141    0.0193   -1.2548 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8785   -0.1467   -2.3903 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2370   -0.1299   -2.2366 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8336    0.0436   -1.0116 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2020    0.0551   -0.8971 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0369   -0.1251   -2.1290 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3532    0.0134   -1.3421 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8474   -0.1520   -2.4916 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1957    0.1834   -0.1888 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6288    0.3497    1.0075 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5409    0.4991    2.0720 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6970   -0.3648    2.1742 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0803   -0.8970    0.7817 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.5687   -1.0362    0.7562 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6658    0.2086   -0.1715 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.3581    0.2214   -1.4686 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9225    1.2795   -2.2424 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1811    0.3698    1.1840 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2390    0.5355    2.3482 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7389    0.9440   -0.3329 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6954   -0.8108    0.2264 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5831    0.5449    1.3943 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5257    0.5248    2.3794 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1226    0.5156    2.2518 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3703   -0.2799   -3.3319 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8925   -0.2585   -3.1144 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1025   -0.3065   -1.8147 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9775    0.7492   -2.7885 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7303   -1.0405   -2.6844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5383    0.1488    2.6501 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3398   -1.2486    2.7424 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5252   -1.8035    0.5245 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9313   -1.7973    1.4637 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9276   -1.2893   -0.2693 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0000   -0.0481    1.0338 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9388    1.1767    0.3532 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4497    0.4298   -1.2625 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3624   -0.7421   -2.0146 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6885    2.0214   -1.6129 H   0  0  0  0  0  0  0  0  0  0  0  0
 20 19  1  0
 19 18  1  0
 18 17  1  0
 17 16  1  0
 16 15  2  0
 15 21  1  0
 21 22  1  0
 22 23  1  0
 15 13  1  0
 13 14  2  0
 13  7  1  0
  7  6  2  0
  6 24  1  0
 24 25  2  0
  6  5  1  0
  5  4  2  0
  4  3  1  0
  3  2  2  0
  2  1  1  0
  2 11  1  0
 11 12  1  0
 11 10  2  0
 10  9  1  0
  9  8  2  0
 21 19  1  0
  8  7  1  0
 24 16  1  0
 10  5  1  0
 20 39  1  0
 20 40  1  0
 20 41  1  0
 19 38  1  6
 18 36  1  0
 18 37  1  0
 21 42  1  1
 22 43  1  0
 22 44  1  0
 23 45  1  0
  4 30  1  0
  3 29  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
 12 33  1  0
 12 34  1  0
 12 35  1  0
  9 32  1  0
  8 31  1  0
M  END


  Mrv1652309062202032D          

 25 28  0  0  1  0            999 V2000
    6.1154    0.1007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3052    0.2566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7651   -0.3671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9550   -0.2111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6850    0.5684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8748    0.7243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6048    1.5039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1449    2.1275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9550    1.9716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2251    1.1921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0352    1.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5753    1.6598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7946    1.6598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5246    2.4393    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2546    1.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5246    0.2566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9845   -0.3671    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1744   -0.2111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0957    0.5684    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9058    0.7243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4444    1.1921    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1744    1.9716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.5952    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3347    0.1007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6048   -0.6789    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
  5 10  1  0  0  0  0
 10 11  2  0  0  0  0
  2 11  1  0  0  0  0
 11 12  1  0  0  0  0
  7 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  2  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  1  0  0  0
 19 21  1  0  0  0  0
 15 21  1  0  0  0  0
 21 22  1  6  0  0  0
 22 23  1  0  0  0  0
 16 24  1  0  0  0  0
  6 24  1  0  0  0  0
 24 25  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0222265

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1COC2=C([C@H]1CO)C(=O)C1=C(C2=O)C2=CC=C(C)C(C)=C2C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C21H20O4/c1-10-4-5-14-13(12(10)3)6-7-15-17(14)20(24)21-18(19(15)23)16(8-22)11(2)9-25-21/h4-7,11,16,22H,8-9H2,1-3H3/t11-,16+/m1/s1

> <INCHI_KEY>
VTSFLCVRCKVBCB-BZNIZROVSA-N

> <FORMULA>
C21H20O4

> <MOLECULAR_WEIGHT>
336.387

> <EXACT_MASS>
336.136159124

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
37.23818957905637

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3S,4S)-4-(hydroxymethyl)-3,8,9-trimethyl-3,4,5,12-tetrahydro-2H-1-oxatetraphene-5,12-dione

> <JCHEM_LOGP>
2.764660501333333

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.389208373550552

> <JCHEM_PKA_STRONGEST_BASIC>
-2.6285602574089886

> <JCHEM_POLAR_SURFACE_AREA>
63.6

> <JCHEM_REFRACTIVITY>
97.5328

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(3S,4S)-4-(hydroxymethyl)-3,8,9-trimethyl-3,4-dihydro-2H-1-oxatetraphene-5,12-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0      11.415   0.188   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.903   0.479   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.895  -0.685   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.383  -0.394   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.879   1.061   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.366   1.352   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.862   2.807   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.870   3.971   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.383   3.680   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.887   2.225   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.399   1.934   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.407   3.098   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.350   3.098   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       2.846   4.553   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       2.342   1.934   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.846   0.479   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       1.838  -0.685   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       0.326  -0.394   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.179   1.061   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.691   1.352   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.830   2.225   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.326   3.680   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       1.334   4.844   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       4.358   0.188   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       4.862  -1.267   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   11                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   10                                                  
CONECT    6    5    7   24                                                  
CONECT    7    6    8   13                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9    5   11                                                  
CONECT   11   10    2   12                                                  
CONECT   12   11                                                            
CONECT   13    7   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   21                                                  
CONECT   16   15   17   24                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   15   22                                                  
CONECT   22   21   23                                                       
CONECT   23   22                                                            
CONECT   24   16    6   25                                                  
CONECT   25   24                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   56    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₂₀O₄

Average Mass

336.3870 Da

Monoisotopic Mass

336.13616 Da

IUPAC Name

(3S,4S)-4-(hydroxymethyl)-3,8,9-trimethyl-3,4,5,12-tetrahydro-2H-1-oxatetraphene-5,12-dione

Traditional Name

(3S,4S)-4-(hydroxymethyl)-3,8,9-trimethyl-3,4-dihydro-2H-1-oxatetraphene-5,12-dione

CAS Registry Number

Not Available

SMILES

C[C@@H]1COC2=C([C@H]1CO)C(=O)C1=C(C2=O)C2=CC=C(C)C(C)=C2C=C1

InChI Identifier

InChI=1S/C21H20O4/c1-10-4-5-14-13(12(10)3)6-7-15-17(14)20(24)21-18(19(15)23)16(8-22)11(2)9-25-21/h4-7,11,16,22H,8-9H2,1-3H3/t11-,16+/m1/s1

InChI Key

VTSFLCVRCKVBCB-BZNIZROVSA-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
Clerodendrum bungei	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Diterpenoids

Alternative Parents

Substituents

Abietane diterpenoid
Diterpenoid
Naphthopyranone
Naphthopyran
Phenanthrene
Naphthoquinone
Naphthalene
Aryl ketone
Quinone
Pyranone
Pyran
Benzenoid
Vinylogous ester
Ketone
Organoheterocyclic compound
Oxacycle
Primary alcohol
Alcohol
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
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	2.76	ChemAxon
pKa (Strongest Acidic)	15.39	ChemAxon
pKa (Strongest Basic)	-2.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	63.6 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	97.53 m³·mol⁻¹	ChemAxon
Polarizability	37.24 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

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

162983607

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3s,4s)-4-(hydroxymethyl)-3,8,9-trimethyl-3,4-dihydro-2h-1-oxatetraphene-5,12-dione (NP0222265)

MOL for NP0222265 ((3s,4s)-4-(hydroxymethyl)-3,8,9-trimethyl-3,4-dihydro-2h-1-oxatetraphene-5,12-dione)

3D MOL for NP0222265 ((3s,4s)-4-(hydroxymethyl)-3,8,9-trimethyl-3,4-dihydro-2h-1-oxatetraphene-5,12-dione)

3D SDF for NP0222265 ((3s,4s)-4-(hydroxymethyl)-3,8,9-trimethyl-3,4-dihydro-2h-1-oxatetraphene-5,12-dione)

3D-SDF for NP0222265 ((3s,4s)-4-(hydroxymethyl)-3,8,9-trimethyl-3,4-dihydro-2h-1-oxatetraphene-5,12-dione)

PDB for NP0222265 ((3s,4s)-4-(hydroxymethyl)-3,8,9-trimethyl-3,4-dihydro-2h-1-oxatetraphene-5,12-dione)

3D PDB for NP0222265 ((3s,4s)-4-(hydroxymethyl)-3,8,9-trimethyl-3,4-dihydro-2h-1-oxatetraphene-5,12-dione)

SMILES for NP0222265 ((3s,4s)-4-(hydroxymethyl)-3,8,9-trimethyl-3,4-dihydro-2h-1-oxatetraphene-5,12-dione)

INCHI for NP0222265 ((3s,4s)-4-(hydroxymethyl)-3,8,9-trimethyl-3,4-dihydro-2h-1-oxatetraphene-5,12-dione)

Structure for NP0222265 ((3s,4s)-4-(hydroxymethyl)-3,8,9-trimethyl-3,4-dihydro-2h-1-oxatetraphene-5,12-dione)

3D Structure for NP0222265 ((3s,4s)-4-(hydroxymethyl)-3,8,9-trimethyl-3,4-dihydro-2h-1-oxatetraphene-5,12-dione)