NP-MRD: Showing NP-Card for (3br,9bs)-7-isopropyl-9b-methyl-3h,3bh,4h,5h,10h,11h-phenanthro[1,2-c]furan-1,6,9-trione (NP0209982)

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Record Information

Version

2.0

Created at

2022-09-05 07:36:35 UTC

Updated at

2022-09-05 07:36:35 UTC

NP-MRD ID

NP0209982

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3br,9bs)-7-isopropyl-9b-methyl-3h,3bh,4h,5h,10h,11h-phenanthro[1,2-c]furan-1,6,9-trione

Description

Triptoquinonide belongs to the class of organic compounds known as oxosteroids. These are steroid derivatives carrying a C=O group attached to steroid skeleton. (3br,9bs)-7-isopropyl-9b-methyl-3h,3bh,4h,5h,10h,11h-phenanthro[1,2-c]furan-1,6,9-trione is found in Tripterygium doianum and Tripterygium hypoglaucum. (3br,9bs)-7-isopropyl-9b-methyl-3h,3bh,4h,5h,10h,11h-phenanthro[1,2-c]furan-1,6,9-trione was first documented in 2000 (PMID: 10774048). Based on a literature review very few articles have been published on Triptoquinonide.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 46 49  0  0  0  0  0  0  0  0999 V2000
    5.1918   -0.2021   -0.8598 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3992    0.9887   -0.3646 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0718    1.4751    0.8922 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9973    0.6452   -0.0703 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4869    0.7740    1.1413 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1013    0.4352    1.4357 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7011    0.5849    2.5945 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2589   -0.0579    0.3664 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7330   -0.2002   -0.8634 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0758   -0.6895   -2.0136 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5391   -0.6153   -1.8253 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8948    0.1967   -0.6008 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.3320    0.3240   -0.3747 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9258   -0.1462    0.7134 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1843   -0.5732    1.9159 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7540   -0.0084    1.8647 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1666   -0.4360    0.5659 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3435   -1.9587    0.4592 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3495   -0.1388    0.4511 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3069   -0.5010    1.2044 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5708    0.3509   -0.8263 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3743    0.9522   -1.2260 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1060    0.1389   -1.1384 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6392    0.0335   -2.2784 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7951   -1.1640   -0.5209 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2605   -0.1302   -1.9845 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2382   -0.1255   -0.4983 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4831    1.8103   -1.1064 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1489    1.7354    0.7012 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0070    0.6776    1.6550 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5185    2.3537    1.2772 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0916    1.1456    1.9853 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2371   -1.7045   -2.3120 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2208   -0.0392   -2.8859 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0050   -0.0953   -2.6920 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0225   -1.6023   -1.7756 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4121    1.2053   -0.7776 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6188   -0.1760    2.8609 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1313   -1.6739    2.0324 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2444   -0.5468    2.7006 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8289    1.0727    1.9982 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1651   -2.3785    1.4869 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3424   -2.2377    0.1198 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5568   -2.3638   -0.1736 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3835    2.0408   -0.9472 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1591    0.8243   -2.3064 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  6  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  6
 14 19  1  0
 19 20  2  0
 19 21  1  0
 21 22  1  0
  9 23  1  0
 23 24  2  0
 23  4  1  0
 17  8  1  0
 17 12  1  0
 22 13  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  2 28  1  0
  3 29  1  0
  3 30  1  0
  3 31  1  0
  5 32  1  0
 10 33  1  0
 10 34  1  0
 11 35  1  0
 11 36  1  0
 12 37  1  6
 15 38  1  0
 15 39  1  0
 16 40  1  0
 16 41  1  0
 18 42  1  0
 18 43  1  0
 18 44  1  0
 22 45  1  0
 22 46  1  0
M  END


  Mrv1652309052209362D          

 24 27  0  0  1  0            999 V2000
    0.9533    0.2414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2336   -0.5346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7018   -1.1653    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0458   -0.6798    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3261   -1.4557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1382   -1.6009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4185   -2.3768    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6700   -0.9702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3897   -0.1943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9215    0.4364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7336    0.2912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0139   -0.4847    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.8261   -0.6299    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1064   -1.4059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5745   -2.0366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7624   -1.8914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4821   -1.1154    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9503   -1.7461    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9309   -1.3791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4373   -2.0304    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1602   -0.5866    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4774   -0.1236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5776   -0.0491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2973    0.7268    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
  2  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
  6  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  1  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
  8 17  1  0  0  0  0
 12 17  1  0  0  0  0
 17 18  1  1  0  0  0
 14 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 13 22  1  0  0  0  0
  9 23  1  0  0  0  0
  4 23  1  0  0  0  0
 23 24  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0209982

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)C1=CC(=O)C2=C(CC[C@H]3C4=C(CC[C@]23C)C(=O)OC4)C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C20H22O4/c1-10(2)13-8-16(21)17-12(18(13)22)4-5-15-14-9-24-19(23)11(14)6-7-20(15,17)3/h8,10,15H,4-7,9H2,1-3H3/t15-,20-/m0/s1

> <INCHI_KEY>
SZTABFBXCBBJRR-YWZLYKJASA-N

> <FORMULA>
C20H22O4

> <MOLECULAR_WEIGHT>
326.392

> <EXACT_MASS>
326.151809188

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
46

> <JCHEM_AVERAGE_POLARIZABILITY>
35.50060515780363

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,10R)-1-methyl-5-(propan-2-yl)-13-oxatetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-2(7),4,11(15)-triene-3,6,14-trione

> <JCHEM_LOGP>
3.6007879949999997

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.200007996718394

> <JCHEM_PKA_STRONGEST_BASIC>
-6.8655901688873815

> <JCHEM_POLAR_SURFACE_AREA>
60.440000000000005

> <JCHEM_REFRACTIVITY>
91.30189999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,10R)-5-isopropyl-1-methyl-13-oxatetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-2(7),4,11(15)-triene-3,6,14-trione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0       1.780   0.451   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.303  -0.998   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.310  -2.175   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.819  -1.269   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.342  -2.717   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.858  -2.988   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       6.381  -4.437   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       6.851  -1.811   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.327  -0.363   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.320   0.815   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.836   0.544   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.359  -0.905   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.875  -1.176   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      11.399  -2.624   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      10.406  -3.802   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.890  -3.531   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.367  -2.082   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.374  -3.259   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      12.938  -2.574   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      13.883  -3.790   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      13.366  -1.095   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      12.091  -0.231   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.811  -0.092   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       4.288   1.357   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   23                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   17                                                  
CONECT    9    8   10   23                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   17                                                  
CONECT   13   12   14   22                                                  
CONECT   14   13   15   19                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16    8   12   18                                             
CONECT   18   17                                                            
CONECT   19   14   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   13                                                       
CONECT   23    9    4   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

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(C)C1=CC(=O)C2=C(CC[C@H]3C4=C(CC[C@]23C)C(=O)OC4)C1=O

InChI Identifier

InChI=1S/C20H22O4/c1-10(2)13-8-16(21)17-12(18(13)22)4-5-15-14-9-24-19(23)11(14)6-7-20(15,17)3/h8,10,15H,4-7,9H2,1-3H3/t15-,20-/m0/s1

InChI Key

SZTABFBXCBBJRR-YWZLYKJASA-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
Tripterygium doianum	LOTUS Database	35616633
Tripterygium hypoglaucum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oxosteroids. These are steroid derivatives carrying a C=O group attached to steroid skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Oxosteroids

Direct Parent

Oxosteroids

Alternative Parents

Substituents

1-oxosteroid
17-oxosteroid
Oxosteroid
4-oxosteroid
16-oxasteroid
2-furanone
Dihydrofuran
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Lactone
Ketone
Carboxylic acid ester
Oxacycle
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organoheterocyclic compound
Hydrocarbon derivative
Organic oxide
Organooxygen compound
Organic oxygen compound
Carbonyl group
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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

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

28424545

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

15762010

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Yang D, Ye XY, Xu M: Enantioselective total synthesis of (-)-triptolide, (-)-triptonide, (+)-triptophenolide, and (+)-triptoquinonide. J Org Chem. 2000 Apr 7;65(7):2208-17. doi: 10.1021/jo9919613. [PubMed:10774048 ]
LOTUS database [Link]

Showing NP-Card for (3br,9bs)-7-isopropyl-9b-methyl-3h,3bh,4h,5h,10h,11h-phenanthro[1,2-c]furan-1,6,9-trione (NP0209982)

MOL for NP0209982 ((3br,9bs)-7-isopropyl-9b-methyl-3h,3bh,4h,5h,10h,11h-phenanthro[1,2-c]furan-1,6,9-trione)

3D MOL for NP0209982 ((3br,9bs)-7-isopropyl-9b-methyl-3h,3bh,4h,5h,10h,11h-phenanthro[1,2-c]furan-1,6,9-trione)

3D SDF for NP0209982 ((3br,9bs)-7-isopropyl-9b-methyl-3h,3bh,4h,5h,10h,11h-phenanthro[1,2-c]furan-1,6,9-trione)

3D-SDF for NP0209982 ((3br,9bs)-7-isopropyl-9b-methyl-3h,3bh,4h,5h,10h,11h-phenanthro[1,2-c]furan-1,6,9-trione)

PDB for NP0209982 ((3br,9bs)-7-isopropyl-9b-methyl-3h,3bh,4h,5h,10h,11h-phenanthro[1,2-c]furan-1,6,9-trione)

3D PDB for NP0209982 ((3br,9bs)-7-isopropyl-9b-methyl-3h,3bh,4h,5h,10h,11h-phenanthro[1,2-c]furan-1,6,9-trione)

SMILES for NP0209982 ((3br,9bs)-7-isopropyl-9b-methyl-3h,3bh,4h,5h,10h,11h-phenanthro[1,2-c]furan-1,6,9-trione)

INCHI for NP0209982 ((3br,9bs)-7-isopropyl-9b-methyl-3h,3bh,4h,5h,10h,11h-phenanthro[1,2-c]furan-1,6,9-trione)

Structure for NP0209982 ((3br,9bs)-7-isopropyl-9b-methyl-3h,3bh,4h,5h,10h,11h-phenanthro[1,2-c]furan-1,6,9-trione)

3D Structure for NP0209982 ((3br,9bs)-7-isopropyl-9b-methyl-3h,3bh,4h,5h,10h,11h-phenanthro[1,2-c]furan-1,6,9-trione)