NP-MRD: Showing NP-Card for (8s,11bs)-7,11-dihydroxy-3,4,8,11b-tetramethyl-1h,2h,8h,9h-phenanthro[3,2-b]furan-6-one (NP0144473)

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Record Information

Version

2.0

Created at

2022-09-01 23:27:23 UTC

Updated at

2022-09-01 23:27:23 UTC

NP-MRD ID

NP0144473

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(8s,11bs)-7,11-dihydroxy-3,4,8,11b-tetramethyl-1h,2h,8h,9h-phenanthro[3,2-b]furan-6-one

Description

(2S,13S)-11,17-dihydroxy-2,5,6,13-tetramethyl-15-oxatetracyclo[8.7.0.0²,⁷.0¹²,¹⁶]Heptadeca-1(17),5,7,10,12(16)-pentaen-9-one belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. (8s,11bs)-7,11-dihydroxy-3,4,8,11b-tetramethyl-1h,2h,8h,9h-phenanthro[3,2-b]furan-6-one is found in Clerodendrum indicum. Based on a literature review very few articles have been published on (2S,13S)-11,17-dihydroxy-2,5,6,13-tetramethyl-15-oxatetracyclo[8.7.0.0²,⁷.0¹²,¹⁶]Heptadeca-1(17),5,7,10,12(16)-pentaen-9-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 46 49  0  0  0  0  0  0  0  0999 V2000
   -5.3122    0.0588   -0.1330 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8317   -0.0053   -0.2342 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1690   -0.9903    0.3652 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8467   -2.0599    1.1365 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6937   -1.0647    0.2720 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0448   -2.1953    0.4133 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4236   -2.2791    0.3178 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0066   -3.3826    0.4614 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1326   -1.0350    0.0537 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5279   -1.0292   -0.0521 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2163   -2.1698    0.0898 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2350    0.1656   -0.3080 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5460    1.3325   -0.4541 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1816    1.3227   -0.3498 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5070    2.5196   -0.5005 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4389    0.1550   -0.0962 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0219    0.2315    0.0105 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4537    1.2374    1.0685 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6742    0.7183   -1.2875 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1240    1.0377   -1.0117 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4403    2.3916   -0.7010 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7441    1.9442   -0.3048 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6871    0.4353   -0.4629 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5163   -0.2686    0.5765 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7603   -0.9299   -0.4470 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6331    0.3116    0.9008 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7387    0.7952   -0.8419 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6245   -3.0763    0.7485 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5465   -1.9498    2.2024 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9493   -1.9449    1.1243 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5912   -3.0904    0.6045 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1470   -3.0964    0.2523 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9753    3.3880   -0.6819 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5699    2.2366    0.6232 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7094    1.2646    1.9144 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4164    0.9513    1.5327 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1979    1.5876   -1.7167 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6744   -0.1720   -1.9773 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6076    1.1305   -2.0273 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2341    2.0238   -0.5290 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5278    2.3580   -0.9640 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9801    2.2491    0.7310 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0403    0.1988   -1.4842 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4166    0.3552    0.7675 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8030   -1.2563    0.1481 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9320   -0.4046    1.4967 H   0  0  0  0  0  0  0  0  0  0  0  0
 24 23  1  0
 23 22  1  0
 22 21  1  0
 21 13  1  0
 13 12  2  0
 12 10  1  0
 10 11  1  0
 10  9  2  0
  9  7  1  0
  7  8  2  0
  7  6  1  0
  6  5  2  0
  5  3  1  0
  3  4  1  0
  3  2  2  0
  2  1  1  0
  2 20  1  0
 20 19  1  0
 19 17  1  0
 17 18  1  1
 17 16  1  0
 16 14  2  0
 14 15  1  0
 12 23  1  0
 16  9  1  0
 14 13  1  0
 17  5  1  0
 24 44  1  0
 24 45  1  0
 24 46  1  0
 23 43  1  6
 22 41  1  0
 22 42  1  0
 11 32  1  0
  6 31  1  0
  4 28  1  0
  4 29  1  0
  4 30  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
 20 39  1  0
 20 40  1  0
 19 37  1  0
 19 38  1  0
 18 34  1  0
 18 35  1  0
 18 36  1  0
 15 33  1  0
M  END


  Mrv1652309022201272D          

 24 27  0  0  1  0            999 V2000
    1.2336   -1.1154    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0458   -0.9702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3261   -0.1943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7942    0.4364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1382   -0.0491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4185    0.7268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2306    0.8721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5109    1.6480    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7624    0.2414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5745    0.3866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8548    1.1625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1064   -0.2441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8261   -1.0201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0139   -1.1653    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7336   -1.9412    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4821   -0.5346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6700   -0.6798    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2018   -1.3105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3897   -1.4557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5776   -1.6009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4774   -1.5264    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1602   -1.0634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9309   -0.2709    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.4373    0.3804    0.0000 C   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
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  2  0  0  0  0
  9 16  1  0  0  0  0
 16 17  1  0  0  0  0
  5 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
  2 20  1  0  0  0  0
 13 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 12 23  1  0  0  0  0
 23 24  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0144473

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1COC2=C1C(O)=C1C(=O)C=C3C(C)=C(C)CC[C@]3(C)C1=C2O

> <INCHI_IDENTIFIER>
InChI=1S/C20H22O4/c1-9-5-6-20(4)12(11(9)3)7-13(21)15-16(20)18(23)19-14(17(15)22)10(2)8-24-19/h7,10,22-23H,5-6,8H2,1-4H3/t10-,20+/m1/s1

> <INCHI_KEY>
YOJNWDYXALZJGT-SBKAZYGRSA-N

> <FORMULA>
C20H22O4

> <MOLECULAR_WEIGHT>
326.392

> <EXACT_MASS>
326.151809188

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
46

> <JCHEM_AVERAGE_POLARIZABILITY>
35.93729191703781

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S,13S)-11,17-dihydroxy-2,5,6,13-tetramethyl-15-oxatetracyclo[8.7.0.0^{2,7}.0^{12,16}]heptadeca-1(17),5,7,10,12(16)-pentaen-9-one

> <ALOGPS_LOGP>
3.26

> <JCHEM_LOGP>
3.949647383666667

> <ALOGPS_LOGS>
-3.91

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.13267432311162

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.329390482890444

> <JCHEM_PKA_STRONGEST_BASIC>
-4.937133462290774

> <JCHEM_POLAR_SURFACE_AREA>
66.76

> <JCHEM_REFRACTIVITY>
94.01230000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.00e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,13S)-11,17-dihydroxy-2,5,6,13-tetramethyl-15-oxatetracyclo[8.7.0.0^{2,7}.0^{12,16}]heptadeca-1(17),5,7,10,12(16)-pentaen-9-one

> <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       2.303  -2.082   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.819  -1.811   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.342  -0.363   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.349   0.815   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.858  -0.092   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.381   1.357   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.897   1.628   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       8.420   3.076   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       8.890   0.451   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.406   0.722   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      10.929   2.170   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      11.399  -0.456   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.875  -1.904   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.359  -2.175   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       8.836  -3.624   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       8.367  -0.998   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.851  -1.269   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.843  -2.446   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.327  -2.717   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.811  -2.988   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      12.091  -2.849   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      13.366  -1.985   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      12.938  -0.506   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      13.883   0.710   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   20                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   17                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   16                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   23                                                  
CONECT   13   12   14   21                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14    9   17                                                  
CONECT   17   16    5   18   19                                             
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19    2                                                       
CONECT   21   13   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   12   24                                                  
CONECT   24   23                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   54    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₂₂O₄

Average Mass

326.3920 Da

Monoisotopic Mass

326.15181 Da

IUPAC Name

(2S,13S)-11,17-dihydroxy-2,5,6,13-tetramethyl-15-oxatetracyclo[8.7.0.0^{2,7}.0^{12,16}]heptadeca-1(17),5,7,10,12(16)-pentaen-9-one

Traditional Name

(2S,13S)-11,17-dihydroxy-2,5,6,13-tetramethyl-15-oxatetracyclo[8.7.0.0^{2,7}.0^{12,16}]heptadeca-1(17),5,7,10,12(16)-pentaen-9-one

CAS Registry Number

Not Available

SMILES

C[C@@H]1COC2=C1C(O)=C1C(=O)C=C3C(C)=C(C)CC[C@]3(C)C1=C2O

InChI Identifier

InChI=1S/C20H22O4/c1-9-5-6-20(4)12(11(9)3)7-13(21)15-16(20)18(23)19-14(17(15)22)10(2)8-24-19/h7,10,22-23H,5-6,8H2,1-4H3/t10-,20+/m1/s1

InChI Key

YOJNWDYXALZJGT-SBKAZYGRSA-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 indicum	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
Phenanthrene
Naphthofuran
Naphthalene
Coumaran
Aryl ketone
Alkyl aryl ether
Benzenoid
Vinylogous acid
Ketone
Ether
Oxacycle
Organoheterocyclic compound
Aldehyde
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
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	3.26	ALOGPS
logP	3.95	ChemAxon
logS	-3.9	ALOGPS
pKa (Strongest Acidic)	9.33	ChemAxon
pKa (Strongest Basic)	-4.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	66.76 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	94.01 m³·mol⁻¹	ChemAxon
Polarizability	35.94 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

9349872

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11174780

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (8s,11bs)-7,11-dihydroxy-3,4,8,11b-tetramethyl-1h,2h,8h,9h-phenanthro[3,2-b]furan-6-one (NP0144473)

MOL for NP0144473 ((8s,11bs)-7,11-dihydroxy-3,4,8,11b-tetramethyl-1h,2h,8h,9h-phenanthro[3,2-b]furan-6-one)

3D MOL for NP0144473 ((8s,11bs)-7,11-dihydroxy-3,4,8,11b-tetramethyl-1h,2h,8h,9h-phenanthro[3,2-b]furan-6-one)

3D SDF for NP0144473 ((8s,11bs)-7,11-dihydroxy-3,4,8,11b-tetramethyl-1h,2h,8h,9h-phenanthro[3,2-b]furan-6-one)

3D-SDF for NP0144473 ((8s,11bs)-7,11-dihydroxy-3,4,8,11b-tetramethyl-1h,2h,8h,9h-phenanthro[3,2-b]furan-6-one)

PDB for NP0144473 ((8s,11bs)-7,11-dihydroxy-3,4,8,11b-tetramethyl-1h,2h,8h,9h-phenanthro[3,2-b]furan-6-one)

3D PDB for NP0144473 ((8s,11bs)-7,11-dihydroxy-3,4,8,11b-tetramethyl-1h,2h,8h,9h-phenanthro[3,2-b]furan-6-one)

SMILES for NP0144473 ((8s,11bs)-7,11-dihydroxy-3,4,8,11b-tetramethyl-1h,2h,8h,9h-phenanthro[3,2-b]furan-6-one)

INCHI for NP0144473 ((8s,11bs)-7,11-dihydroxy-3,4,8,11b-tetramethyl-1h,2h,8h,9h-phenanthro[3,2-b]furan-6-one)

Structure for NP0144473 ((8s,11bs)-7,11-dihydroxy-3,4,8,11b-tetramethyl-1h,2h,8h,9h-phenanthro[3,2-b]furan-6-one)

3D Structure for NP0144473 ((8s,11bs)-7,11-dihydroxy-3,4,8,11b-tetramethyl-1h,2h,8h,9h-phenanthro[3,2-b]furan-6-one)