NP-MRD: Showing NP-Card for Triptobenzene A (NP0082813)

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Record Information

Version

2.0

Created at

2022-04-29 03:53:51 UTC

Updated at

2022-04-29 03:53:51 UTC

NP-MRD ID

NP0082813

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Triptobenzene A

Description

Triptobenzene A belongs to the class of organic compounds known as hydroxysteroids. Hydroxysteroids are compounds containing an steroid backbone, with at least one hydrogen substituted by a hydroxyl group. Triptobenzene A is found in Tripterygium hypoglaucum and Tripterygium wilfordii . Based on a literature review very few articles have been published on triptobenzene A.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 51 53  0  0  0  0  0  0  0  0999 V2000
    5.1544    1.8314   -0.2978 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5971    0.5247    0.1107 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1355   -0.7563   -0.4510 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1258    0.4360    0.3100 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5517    0.4891    1.5800 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1954    0.1991    1.7337 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4113   -0.1318    0.6850 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9515   -0.1877   -0.6193 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2767    0.0923   -0.7441 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8833    0.0556   -2.0165 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1629   -0.4430   -1.8184 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3260   -0.3629   -1.6685 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7132    0.1998   -0.3366 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.1997    0.3194   -0.1134 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4978    1.4283    0.9146 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0171    0.6354   -1.3058 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5791    1.8064   -1.8641 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6143   -0.9458    0.5742 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3983   -1.6856    0.0193 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0083   -1.1970    1.9308 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6508   -0.4974    2.0815 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0089   -0.5507    0.7329 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8979   -2.0758    0.4353 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3861    2.5785   -0.6288 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7017    2.3265    0.5204 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8777    1.6483   -1.1616 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9572    0.4356    1.2701 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1170   -0.6258   -0.9768 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4224   -1.2991   -1.0916 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3026   -1.5044    0.4091 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1374    0.7489    2.4262 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7957    0.2389    2.7573 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3655   -0.1768   -2.8488 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5077   -1.3635   -2.3250 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4581    0.3656   -2.5494 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8515   -1.3468   -1.8367 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7641    0.2823   -2.4677 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3321    1.2635   -0.2836 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3456    2.0864    0.5717 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6433    2.0567    1.1337 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9030    1.0065    1.8716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0988   -0.1445   -2.0612 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0584    0.8699   -0.9140 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7533    2.6089   -1.3174 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6760   -0.8317    2.7210 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9093   -2.2844    2.0760 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0613   -1.2112    2.7326 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7025    0.4512    2.5902 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5332   -2.4992    1.4385 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0900   -2.3116   -0.2451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8406   -2.5520    0.2666 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  9  2  0
  9 10  1  0
  9  8  1  0
  8  7  2  0
  7  6  1  0
  6  5  2  0
  7 22  1  0
 22 23  1  6
 22 21  1  0
 21 20  1  0
 20 18  1  0
 18 19  2  0
 18 14  1  0
 14 15  1  1
 14 16  1  0
 16 17  1  0
 14 13  1  0
 13 12  1  0
 12 11  1  0
  5  4  1  0
 13 22  1  0
 11  8  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  2 27  1  1
  3 28  1  0
  3 29  1  0
  3 30  1  0
 10 33  1  0
  6 32  1  0
  5 31  1  0
 23 49  1  0
 23 50  1  0
 23 51  1  0
 21 47  1  0
 21 48  1  0
 20 45  1  0
 20 46  1  0
 15 39  1  0
 15 40  1  0
 15 41  1  0
 16 42  1  0
 16 43  1  0
 17 44  1  0
 13 38  1  6
 12 36  1  0
 12 37  1  0
 11 34  1  0
 11 35  1  0
M  END


  Mrv1652304292205532D          

 23 25  0  0  1  0            999 V2000
    2.3645    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7770    1.1270    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3645    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020    1.1270    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6308    1.9515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3592    2.3388    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3016    1.5642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9520   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  1  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  5 10  1  0  0  0  0
 10 11  1  0  0  0  0
  9 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
  2 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
  1 19  1  0  0  0  0
 15 20  1  1  0  0  0
 20 21  1  0  0  0  0
 15 22  1  6  0  0  0
  1 23  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0082813

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)C1=C(O)C2=C(C=C1)[C@@]1(C)CCC(=O)[C@](C)(CO)[C@@H]1CC2

> <INCHI_IDENTIFIER>
InChI=1S/C20H28O3/c1-12(2)13-5-7-15-14(18(13)23)6-8-16-19(15,3)10-9-17(22)20(16,4)11-21/h5,7,12,16,21,23H,6,8-11H2,1-4H3/t16-,19-,20-/m1/s1

> <INCHI_KEY>
TZJRHFCKOBGRSH-NSISKUIASA-N

> <FORMULA>
C20H28O3

> <MOLECULAR_WEIGHT>
316.441

> <EXACT_MASS>
316.203844762

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
51

> <JCHEM_AVERAGE_POLARIZABILITY>
36.650778694256005

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,4aS,10aR)-8-hydroxy-1-(hydroxymethyl)-1,4a-dimethyl-7-(propan-2-yl)-1,2,3,4,4a,9,10,10a-octahydrophenanthren-2-one

> <ALOGPS_LOGP>
3.98

> <JCHEM_LOGP>
4.305452289333333

> <ALOGPS_LOGS>
-4.43

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.954341128463152

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.220121104086322

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8187267092996375

> <JCHEM_POLAR_SURFACE_AREA>
57.53

> <JCHEM_REFRACTIVITY>
92.17559999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.18e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,4aS,10aR)-8-hydroxy-1-(hydroxymethyl)-7-isopropyl-1,4a-dimethyl-4,9,10,10a-tetrahydro-3H-phenanthren-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  C   UNK     0       4.414   0.770   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.184   2.104   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.414   3.437   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.874   3.437   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.104   2.104   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.874   0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.104  -0.564   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.564  -0.564   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.206   0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.564   2.104   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -0.206   3.437   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -1.746   0.770   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.516   2.104   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.516  -0.564   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.724   2.104   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.494   0.770   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       9.034   0.770   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       6.724  -0.564   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.184  -0.564   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.777   3.643   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       8.137   4.366   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       8.030   2.920   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.644  -0.564   0.000  0.00  0.00           C+0
CONECT    1    2    6   19   23                                             
CONECT    2    1    3   15                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   10                                                  
CONECT    6    5    1    7                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   12                                                  
CONECT   10    9    5   11                                                  
CONECT   11   10                                                            
CONECT   12    9   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15    2   16   20   22                                             
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18    1                                                       
CONECT   20   15   21                                                       
CONECT   21   20                                                            
CONECT   22   15                                                            
CONECT   23    1                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   50    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₂₈O₃

Average Mass

316.4410 Da

Monoisotopic Mass

316.20384 Da

IUPAC Name

(1S,4aS,10aR)-8-hydroxy-1-(hydroxymethyl)-1,4a-dimethyl-7-(propan-2-yl)-1,2,3,4,4a,9,10,10a-octahydrophenanthren-2-one

Traditional Name

(1S,4aS,10aR)-8-hydroxy-1-(hydroxymethyl)-7-isopropyl-1,4a-dimethyl-4,9,10,10a-tetrahydro-3H-phenanthren-2-one

CAS Registry Number

Not Available

SMILES

CC(C)C1=C(O)C2=C(C=C1)[C@@]1(C)CCC(=O)[C@](C)(CO)[C@@H]1CC2

InChI Identifier

InChI=1S/C20H28O3/c1-12(2)13-5-7-15-14(18(13)23)6-8-16-19(15,3)10-9-17(22)20(16,4)11-21/h5,7,12,16,21,23H,6,8-11H2,1-4H3/t16-,19-,20-/m1/s1

InChI Key

TZJRHFCKOBGRSH-NSISKUIASA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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 hypoglaucum	LOTUS Database	35616633
Tripterygium wilfordii	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hydroxysteroids. Hydroxysteroids are compounds containing an steroid backbone, with at least one hydrogen substituted by a hydroxyl group.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Hydroxysteroids

Direct Parent

Hydroxysteroids

Alternative Parents

Substituents

Abietane diterpenoid
Diterpenoid
4-hydroxysteroid
Hydroxysteroid
Hydrophenanthrene
Phenanthrene
Tetralin
1-hydroxy-4-unsubstituted benzenoid
Benzenoid
Cyclic ketone
Ketone
Primary alcohol
Alcohol
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Carbonyl group
Organooxygen compound
Aromatic homopolycyclic compound

Molecular Framework

Aromatic 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
logP	3.98	ALOGPS
logP	4.31	ChemAxon
logS	-4.4	ALOGPS
pKa (Strongest Acidic)	10.22	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	57.53 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	92.18 m³·mol⁻¹	ChemAxon
Polarizability	36.65 Å³	ChemAxon
Number of Rings	3	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

C00049755

Chemspider ID

58827400

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

15762008

PDB ID

Not Available

ChEBI ID

132349

Good Scents ID

Not Available

References

General References

Showing NP-Card for Triptobenzene A (NP0082813)

MOL for NP0082813 (Triptobenzene A)

3D MOL for NP0082813 (Triptobenzene A)

3D SDF for NP0082813 (Triptobenzene A)

3D-SDF for NP0082813 (Triptobenzene A)

PDB for NP0082813 (Triptobenzene A)

3D PDB for NP0082813 (Triptobenzene A)

SMILES for NP0082813 (Triptobenzene A)

INCHI for NP0082813 (Triptobenzene A)

Structure for NP0082813 (Triptobenzene A)

3D Structure for NP0082813 (Triptobenzene A)