NP-MRD: Showing NP-Card for methyl (4r,4ar,6as,7r,11as,11br)-4-(hydroxymethyl)-7,11b-dimethyl-1h,2h,3h,4ah,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-4-carboxylate (NP0146659)

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Record Information

Version

2.0

Created at

2022-09-02 02:05:51 UTC

Updated at

2022-09-02 02:05:51 UTC

NP-MRD ID

NP0146659

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (4r,4ar,6as,7r,11as,11br)-4-(hydroxymethyl)-7,11b-dimethyl-1h,2h,3h,4ah,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-4-carboxylate

Description

Taepeenin I belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. Based on a literature review very few articles have been published on Taepeenin I.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022204052D          

 25 28  0  0  1  0            999 V2000
   -1.9717   -2.3426    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1589   -2.2012    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6302   -2.8345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9142   -3.6091    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1827   -2.6932    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1807   -3.5182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5348   -3.9290    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0976   -1.9173    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4342   -1.2866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2463   -1.4318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5266   -2.2077    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0584   -1.5770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3387   -2.3529    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8705   -1.7222    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6826   -1.8674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3340   -1.3611    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0168   -1.8241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7875   -2.6166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9629   -2.6434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4311   -3.2741    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7114   -4.0500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6190   -3.1289    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0872   -3.7596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2751   -3.6143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9948   -2.8384    0.0000 C   0  0  1  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  6  0  0  0
  5  6  1  1  0  0  0
  6  7  1  0  0  0  0
  5  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  1  0  0  0
 11 13  1  0  0  0  0
 13 14  1  1  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 15 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  6  0  0  0
 20 22  1  0  0  0  0
 13 22  1  0  0  0  0
 22 23  1  6  0  0  0
 23 24  1  0  0  0  0
 25 24  1  1  0  0  0
  5 25  1  0  0  0  0
 11 25  1  0  0  0  0
M  END

     RDKit          3D

 55 58  0  0  0  0  0  0  0  0999 V2000
   -4.2260    2.4333    1.9213 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5707    1.6401    0.9574 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0714    0.3838    1.1941 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2374   -0.0490    2.3826 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3757   -0.4373    0.1403 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.2873   -0.3580   -1.0586 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5639   -0.8856   -0.7415 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3960   -1.8470    0.7007 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4672   -2.7542   -0.0207 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0674   -2.2172   -0.0861 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0153   -0.8448   -0.7292 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3126   -1.0524   -2.1822 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3600   -0.3317   -0.5053 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3969   -0.8743   -1.4984 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7318   -0.5338   -0.8984 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8835   -1.1108   -1.0588 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8140   -0.5068   -0.3554 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2397    0.5346    0.3114 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8896    0.5203   -0.0382 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7802    1.4290    0.3924 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5025    1.1094    1.8407 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5822    1.1220   -0.4819 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4573    1.9696   -0.0266 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8789    1.4751   -0.5419 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0045    0.0395   -0.0149 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.9141    1.8505    2.5592 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8458    3.1714    1.3650 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4909    3.0183    2.5112 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4621    0.6565   -1.4102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9002   -1.0608   -1.8216 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7754   -0.5553    0.1859 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4251   -2.2405    0.5987 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1128   -1.8045    1.7752 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3982   -3.6954    0.5974 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8625   -3.0779   -0.9866 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3457   -2.1586    0.9464 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5413   -2.9220   -0.7050 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8186   -2.0484   -2.3798 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8242   -0.2325   -2.6827 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6539   -1.1948   -2.7106 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7371   -0.7411    0.4843 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3551   -1.9447   -1.6385 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3732   -0.2583   -2.4358 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8618   -0.8085   -0.3275 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7082    1.2585    0.9924 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0851    2.4866    0.2491 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5131    0.6954    2.0292 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5678    2.0642    2.4251 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2593    0.4259    2.2829 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8521    1.4745   -1.5181 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6296    3.0103   -0.4091 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3544    2.0728    1.0694 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9385    1.5130   -1.6475 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6376    2.0782   -0.0434 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5948    0.1140    1.0423 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  1
  5  6  1  0
  6  7  1  0
  5  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  6
 11 13  1  0
 13 14  1  0
 14 15  1  0
 15 19  2  0
 19 18  1  0
 18 17  2  0
 17 16  1  0
 19 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25  5  1  0
 25 11  1  0
 22 13  1  0
 16 15  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  6 29  1  0
  6 30  1  0
  7 31  1  0
  8 32  1  0
  8 33  1  0
  9 34  1  0
  9 35  1  0
 10 36  1  0
 10 37  1  0
 12 38  1  0
 12 39  1  0
 12 40  1  0
 13 41  1  1
 14 42  1  0
 14 43  1  0
 18 45  1  0
 17 44  1  0
 20 46  1  1
 21 47  1  0
 21 48  1  0
 21 49  1  0
 22 50  1  6
 23 51  1  0
 23 52  1  0
 24 53  1  0
 24 54  1  0
 25 55  1  1
M  END


  Mrv1652309022204052D          

 25 28  0  0  1  0            999 V2000
   -1.9717   -2.3426    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1589   -2.2012    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6302   -2.8345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9142   -3.6091    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1827   -2.6932    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1807   -3.5182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5348   -3.9290    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0976   -1.9173    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4342   -1.2866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2463   -1.4318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5266   -2.2077    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0584   -1.5770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3387   -2.3529    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8705   -1.7222    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6826   -1.8674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3340   -1.3611    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0168   -1.8241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7875   -2.6166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9629   -2.6434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4311   -3.2741    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7114   -4.0500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6190   -3.1289    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0872   -3.7596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2751   -3.6143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9948   -2.8384    0.0000 C   0  0  1  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  6  0  0  0
  5  6  1  1  0  0  0
  6  7  1  0  0  0  0
  5  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  1  0  0  0
 11 13  1  0  0  0  0
 13 14  1  1  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 15 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  6  0  0  0
 20 22  1  0  0  0  0
 13 22  1  0  0  0  0
 22 23  1  6  0  0  0
 23 24  1  0  0  0  0
 25 24  1  1  0  0  0
  5 25  1  0  0  0  0
 11 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0146659

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)[C@]1(CO)CCC[C@]2(C)[C@H]3CC4=C(C=CO4)[C@H](C)[C@@H]3CC[C@@H]12

> <INCHI_IDENTIFIER>
InChI=1S/C21H30O4/c1-13-14-5-6-18-20(2,16(14)11-17-15(13)7-10-25-17)8-4-9-21(18,12-22)19(23)24-3/h7,10,13-14,16,18,22H,4-6,8-9,11-12H2,1-3H3/t13-,14+,16+,18-,20-,21+/m1/s1

> <INCHI_KEY>
BJNVOKJLYMPWOF-WVDARTDPSA-N

> <FORMULA>
C21H30O4

> <MOLECULAR_WEIGHT>
346.467

> <EXACT_MASS>
346.214409446

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
39.534826944404344

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (1S,2R,6R,7R,10S,11R)-6-(hydroxymethyl)-2,11-dimethyl-15-oxatetracyclo[8.7.0.0^{2,7}.0^{12,16}]heptadeca-12(16),13-diene-6-carboxylate

> <ALOGPS_LOGP>
3.75

> <JCHEM_LOGP>
3.5596863769999993

> <ALOGPS_LOGS>
-4.39

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.866478147580555

> <JCHEM_PKA_STRONGEST_BASIC>
-2.74305871586439

> <JCHEM_POLAR_SURFACE_AREA>
59.67

> <JCHEM_REFRACTIVITY>
95.38749999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.42e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl (1S,2R,6R,7R,10S,11R)-6-(hydroxymethyl)-2,11-dimethyl-15-oxatetracyclo[8.7.0.0^{2,7}.0^{12,16}]heptadeca-12(16),13-diene-6-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0      -3.681  -4.373   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -2.163  -4.109   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -1.176  -5.291   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -1.706  -6.737   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       0.341  -5.027   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.337  -6.567   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -0.998  -7.334   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -0.182  -3.579   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.810  -2.402   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.326  -2.673   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.850  -4.121   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.842  -2.944   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.366  -4.392   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.358  -3.215   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.874  -3.486   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       8.090  -2.541   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       9.365  -3.405   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.937  -4.884   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.398  -4.934   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.405  -6.112   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.928  -7.560   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.889  -5.841   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.896  -7.018   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.380  -6.747   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.857  -5.298   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    8   25                                             
CONECT    6    5    7                                                       
CONECT    7    6                                                            
CONECT    8    5    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13   25                                             
CONECT   12   11                                                            
CONECT   13   11   14   22                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   19                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   15   20                                                  
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   13   23                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24    5   11                                                  
MASTER        0    0    0    0    0    0    0    0   25    0   56    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₃₀O₄

Average Mass

346.4670 Da

Monoisotopic Mass

346.21441 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

COC(=O)[C@]1(CO)CCC[C@]2(C)[C@H]3CC4=C(C=CO4)[C@H](C)[C@@H]3CC[C@@H]12

InChI Identifier

InChI=1S/C21H30O4/c1-13-14-5-6-18-20(2,16(14)11-17-15(13)7-10-25-17)8-4-9-21(18,12-22)19(23)24-3/h7,10,13-14,16,18,22H,4-6,8-9,11-12H2,1-3H3/t13-,14+,16+,18-,20-,21+/m1/s1

InChI Key

BJNVOKJLYMPWOF-WVDARTDPSA-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

Not Available

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

Diterpenoid
Naphthofuran
Benzofuran
Beta-hydroxy acid
Hydroxy acid
Heteroaromatic compound
Furan
Methyl ester
Carboxylic acid ester
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Hydrocarbon derivative
Alcohol
Carbonyl group
Organic oxygen compound
Primary alcohol
Organic oxide
Organooxygen 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	3.75	ALOGPS
logP	3.56	ChemAxon
logS	-4.4	ALOGPS
pKa (Strongest Acidic)	14.87	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Hydrogen Acceptor Count	2	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

9777426

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11602670

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl (4r,4ar,6as,7r,11as,11br)-4-(hydroxymethyl)-7,11b-dimethyl-1h,2h,3h,4ah,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-4-carboxylate (NP0146659)

MOL for NP0146659 (methyl (4r,4ar,6as,7r,11as,11br)-4-(hydroxymethyl)-7,11b-dimethyl-1h,2h,3h,4ah,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-4-carboxylate)

3D MOL for NP0146659 (methyl (4r,4ar,6as,7r,11as,11br)-4-(hydroxymethyl)-7,11b-dimethyl-1h,2h,3h,4ah,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-4-carboxylate)

3D SDF for NP0146659 (methyl (4r,4ar,6as,7r,11as,11br)-4-(hydroxymethyl)-7,11b-dimethyl-1h,2h,3h,4ah,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-4-carboxylate)

3D-SDF for NP0146659 (methyl (4r,4ar,6as,7r,11as,11br)-4-(hydroxymethyl)-7,11b-dimethyl-1h,2h,3h,4ah,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-4-carboxylate)

PDB for NP0146659 (methyl (4r,4ar,6as,7r,11as,11br)-4-(hydroxymethyl)-7,11b-dimethyl-1h,2h,3h,4ah,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-4-carboxylate)

3D PDB for NP0146659 (methyl (4r,4ar,6as,7r,11as,11br)-4-(hydroxymethyl)-7,11b-dimethyl-1h,2h,3h,4ah,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-4-carboxylate)

SMILES for NP0146659 (methyl (4r,4ar,6as,7r,11as,11br)-4-(hydroxymethyl)-7,11b-dimethyl-1h,2h,3h,4ah,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-4-carboxylate)

INCHI for NP0146659 (methyl (4r,4ar,6as,7r,11as,11br)-4-(hydroxymethyl)-7,11b-dimethyl-1h,2h,3h,4ah,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-4-carboxylate)

Structure for NP0146659 (methyl (4r,4ar,6as,7r,11as,11br)-4-(hydroxymethyl)-7,11b-dimethyl-1h,2h,3h,4ah,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-4-carboxylate)

3D Structure for NP0146659 (methyl (4r,4ar,6as,7r,11as,11br)-4-(hydroxymethyl)-7,11b-dimethyl-1h,2h,3h,4ah,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-4-carboxylate)