NP-MRD: Showing NP-Card for (+)-Thalrugosine (NP0067513)

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Record Information

Version

2.0

Created at

2022-04-28 12:21:54 UTC

Updated at

2022-04-28 12:21:55 UTC

NP-MRD ID

NP0067513

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(+)-Thalrugosine

Description

(+)-Thalrugosine is found in Cyclea barbata Miers , Cyclea peltata Diels , Limaciopsis loangensis Engl., Mahonia repens , Pycnarrhena novoguineensis, Stephania cephalantha, Stephania cepharantha Hayata , Stephania erecta Craib., Stephania japonica (Thumb.) Miers var.australis , Stephania pierrei, Stephania sasakii Hayata, Stephania sutchuenensis H.S.Lo, Thalictrum foetidum , Thalictrum lucidum, Thalictrum minus, Thalictrum rugosum and Tiliacora funifera Engl.ex Diels. Based on a literature review very few articles have been published on (1S,14R)-10,20,25-trimethoxy-15,30-dimethyl-8,23-dioxa-15,30-diazaheptacyclo[22.6.2.2⁹,¹².1³,⁷.1¹⁴,¹⁸.0²⁷,³¹.0²²,³³]Hexatriaconta-3(36),4,6,9,11,18,20,22(33),24,26,31,34-dodecaen-21-ol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282214212D          

 45 51  0  0  1  0            999 V2000
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   -1.4521   -0.1662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0516    0.4006    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8422    0.1647    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  2  0  0  0  0
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  4  5  1  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652304282214212D          

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    1.9532    1.0388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6906    0.5802    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4748   -0.2234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7670   -0.6141    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1337   -0.1233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3877   -0.4755    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3196   -1.2977    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9297   -0.8790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7237   -0.7554    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0210    0.0076    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5768    0.6937    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4817    0.6929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0923    0.0312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7391   -0.7463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0641   -1.5251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9077   -1.4755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3427   -0.7587    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9334   -0.0297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4869   -2.2139    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7544   -2.7215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3279   -3.4589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4835   -3.5052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9761   -2.8185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1481   -2.4864    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3412   -2.0914    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0022   -2.8613    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8138   -2.9889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3268   -2.3404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5051   -3.5153    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4098   -2.1116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2434   -2.0715    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7595   -4.1620    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3665   -4.8873    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8274   -0.1666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  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  1  0  0  0  0
  5  9  1  0  0  0  0
  4 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 11 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 14 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 22 21  1  1  0  0  0
 13 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 24 29  1  0  0  0  0
 26 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
  3 36  1  0  0  0  0
 36 37  1  1  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
  2 39  1  0  0  0  0
 37 40  1  0  0  0  0
 34 41  1  0  0  0  0
 41 42  2  0  0  0  0
 31 42  1  0  0  0  0
 32 43  1  0  0  0  0
 43 44  1  0  0  0  0
 21 45  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0067513

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC2=C3C=C1OC1=C4[C@@H](CC5=CC(OC)=C(OC6=CC=CC(C[C@@H]3N(C)CC2)=C6)C=C5)N(C)CCC4=CC(OC)=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C37H40N2O6/c1-38-13-11-24-19-32(42-4)33-21-27(24)28(38)16-22-7-6-8-26(15-22)44-30-10-9-23(18-31(30)41-3)17-29-35-25(12-14-39(29)2)20-34(43-5)36(40)37(35)45-33/h6-10,15,18-21,28-29,40H,11-14,16-17H2,1-5H3/t28-,29+/m0/s1

> <INCHI_KEY>
VJMBRWIHQHCVNM-URLMMPGGSA-N

> <FORMULA>
C37H40N2O6

> <MOLECULAR_WEIGHT>
608.735

> <EXACT_MASS>
608.288637016

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
85

> <JCHEM_AVERAGE_POLARIZABILITY>
67.09956081243801

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,14R)-10,20,25-trimethoxy-15,30-dimethyl-8,23-dioxa-15,30-diazaheptacyclo[22.6.2.2^{9,12}.1^{3,7}.1^{14,18}.0^{27,31}.0^{22,33}]hexatriaconta-3(36),4,6,9,11,18,20,22(33),24(32),25,27(31),34-dodecaen-21-ol

> <ALOGPS_LOGP>
5.55

> <JCHEM_LOGP>
6.06926457977928

> <ALOGPS_LOGS>
-4.83

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
2

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.06689879866094

> <JCHEM_PKA_STRONGEST_BASIC>
9.245794056938415

> <JCHEM_POLAR_SURFACE_AREA>
72.86

> <JCHEM_REFRACTIVITY>
175.63229999999993

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
8.99e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,14R)-10,20,25-trimethoxy-15,30-dimethyl-8,23-dioxa-15,30-diazaheptacyclo[22.6.2.2^{9,12}.1^{3,7}.1^{14,18}.0^{27,31}.0^{22,33}]hexatriaconta-3(36),4,6,9,11,18,20,22(33),24(32),25,27(31),34-dodecaen-21-ol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0      -3.060  -1.812   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.934  -2.906   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.389  -2.567   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.078  -0.932   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.241   0.120   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.710  -0.310   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -3.830   0.748   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -5.305   0.307   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -0.897   1.621   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0       0.734   0.515   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       2.162   1.306   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.646   1.939   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.023   1.083   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.620  -0.417   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.298  -1.146   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.116  -0.230   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       0.724  -0.888   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       0.597  -2.422   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.469  -1.641   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.951  -1.410   0.000  0.00  0.00           C+0
HETATM   21  N   UNK     0       7.506   0.014   0.000  0.00  0.00           N+0
HETATM   22  C   UNK     0       6.677   1.295   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.366   1.293   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       9.506   0.058   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       8.846  -1.393   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       9.453  -2.847   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      11.028  -2.754   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      11.840  -1.416   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      11.076  -0.055   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       8.376  -4.133   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       7.008  -5.080   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       6.212  -6.457   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       4.636  -6.543   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       3.689  -5.261   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       2.143  -4.641   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       0.637  -3.904   0.000  0.00  0.00           C+0
HETATM   37  N   UNK     0       0.004  -5.341   0.000  0.00  0.00           N+0
HETATM   38  C   UNK     0      -1.519  -5.579   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      -2.477  -4.369   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       0.943  -6.562   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       4.498  -3.942   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       6.054  -3.867   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0       7.018  -7.769   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0       6.284  -9.123   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       9.011  -0.311   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3   39                                                  
CONECT    3    2    4   36                                                  
CONECT    4    3    5   10                                                  
CONECT    5    4    6    9                                                  
CONECT    6    5    1    7                                                  
CONECT    7    6    8                                                       
CONECT    8    7                                                            
CONECT    9    5                                                            
CONECT   10    4   11                                                       
CONECT   11   10   12   16                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   22                                                  
CONECT   14   13   15   19                                                  
CONECT   15   14   16                                                       
CONECT   16   15   11   17                                                  
CONECT   17   16   18                                                       
CONECT   18   17                                                            
CONECT   19   14   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   45                                                  
CONECT   22   21   13   23                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   29                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   30                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   24                                                       
CONECT   30   26   31                                                       
CONECT   31   30   32   42                                                  
CONECT   32   31   33   43                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35   41                                                  
CONECT   35   34   36                                                       
CONECT   36   35    3   37                                                  
CONECT   37   36   38   40                                                  
CONECT   38   37   39                                                       
CONECT   39   38    2                                                       
CONECT   40   37                                                            
CONECT   41   34   42                                                       
CONECT   42   41   31                                                       
CONECT   43   32   44                                                       
CONECT   44   43                                                            
CONECT   45   21                                                            
MASTER        0    0    0    0    0    0    0    0   45    0  102    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₇H₄₀N₂O₆

Average Mass

608.7350 Da

Monoisotopic Mass

608.28864 Da

IUPAC Name

(1S,14R)-10,20,25-trimethoxy-15,30-dimethyl-8,23-dioxa-15,30-diazaheptacyclo[22.6.2.2^{9,12}.1^{3,7}.1^{14,18}.0^{27,31}.0^{22,33}]hexatriaconta-3(36),4,6,9,11,18,20,22(33),24(32),25,27(31),34-dodecaen-21-ol

Traditional Name

CAS Registry Number

Not Available

SMILES

COC1=CC2=C3C=C1OC1=C4[C@@H](CC5=CC(OC)=C(OC6=CC=CC(C[C@@H]3N(C)CC2)=C6)C=C5)N(C)CCC4=CC(OC)=C1O

InChI Identifier

InChI=1S/C37H40N2O6/c1-38-13-11-24-19-32(42-4)33-21-27(24)28(38)16-22-7-6-8-26(15-22)44-30-10-9-23(18-31(30)41-3)17-29-35-25(12-14-39(29)2)20-34(43-5)36(40)37(35)45-33/h6-10,15,18-21,28-29,40H,11-14,16-17H2,1-5H3/t28-,29+/m0/s1

InChI Key

VJMBRWIHQHCVNM-URLMMPGGSA-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
Cyclea barbata	Plant	KNApSAcK
Cyclea peltata Diels	Plant	KNApSAcK
Limaciopsis loangensis Engl.	Plant	KNApSAcK
Mahonia repens	Plant	KNApSAcK
Pycnarrhena novoguineensis	Plant	KNApSAcK
Stephania cephalantha	LOTUS Database	35616633
Stephania cepharantha Hayata	Plant	KNApSAcK
Stephania erecta Craib.	Plant	KNApSAcK
Stephania japonica (Thumb.) Miers var.australis	Plant	KNApSAcK
Stephania pierrei	LOTUS Database	35616633
Stephania sasakii Hayata	Plant	KNApSAcK
Stephania sutchuenensis H.S.Lo	Plant	KNApSAcK
Thalictrum foetidum	Plant	KNApSAcK
Thalictrum lucidum	Plant	KNApSAcK
Thalictrum minus	Plant	KNApSAcK
Thalictrum rugosum	Plant	KNApSAcK
Tiliacora funifera Engl.ex Diels	Plant	KNApSAcK

Chemical Taxonomy

Classification

Not classified

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	5.55	ALOGPS
logP	6.07	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Acidic)	8.07	ChemAxon
pKa (Strongest Basic)	9.25	ChemAxon
Physiological Charge	2	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	72.86 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	175.63 m³·mol⁻¹	ChemAxon
Polarizability	67.1 Å³	ChemAxon
Number of Rings	7	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

161315820

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (+)-Thalrugosine (NP0067513)

MOL for NP0067513 ((+)-Thalrugosine)

3D MOL for NP0067513 ((+)-Thalrugosine)

3D SDF for NP0067513 ((+)-Thalrugosine)

3D-SDF for NP0067513 ((+)-Thalrugosine)

PDB for NP0067513 ((+)-Thalrugosine)

3D PDB for NP0067513 ((+)-Thalrugosine)

SMILES for NP0067513 ((+)-Thalrugosine)

INCHI for NP0067513 ((+)-Thalrugosine)

Structure for NP0067513 ((+)-Thalrugosine)

3D Structure for NP0067513 ((+)-Thalrugosine)