NP-MRD: Showing NP-Card for 6-{[(4s,5r,6s,8s,10r)-6-hydroxy-5-methyl-2,11,12-triazatricyclo[6.3.1.0⁴,¹²]dodec-1-en-10-yl]methyl}pyrimidine-2,4-diol (NP0228689)

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Record Information

Version

2.0

Created at

2022-09-06 08:26:30 UTC

Updated at

2022-09-06 08:26:30 UTC

NP-MRD ID

NP0228689

Secondary Accession Numbers

None

Natural Product Identification

Common Name

6-{[(4s,5r,6s,8s,10r)-6-hydroxy-5-methyl-2,11,12-triazatricyclo[6.3.1.0⁴,¹²]dodec-1-en-10-yl]methyl}pyrimidine-2,4-diol

Description

7-Deoxy-desulfo-cylindrospermopsin belongs to the class of organic compounds known as pyridopyrimidines. Pyridopyrimidines are compounds containing a pyridopyrimidine, which consists of a pyridine fused to a pyrimidine. Pyridine is 6-membered ring consisting of five carbon atoms and a nitrogen atom. Pyrimidine is a 6-membered ring consisting of four carbon atoms and two nitrogen centers at the 1- and 3- ring positions. Based on a literature review very few articles have been published on 7-deoxy-desulfo-cylindrospermopsin.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 44 47  0  0  0  0  0  0  0  0999 V2000
   -4.5947    0.9777   -0.6762 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7665    0.4354    0.4648 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5328   -1.0173    0.2860 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.7589   -1.6011   -0.1031 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4645   -1.4535   -0.6412 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3109   -0.4959   -0.7958 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0277   -1.3348   -0.6906 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1570   -0.4195   -0.4383 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3795   -1.2810   -0.2902 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6309   -0.5247   -0.0869 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7477    0.8438   -0.1321 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9670    1.4567    0.0883 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1199    2.8370    0.0504 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0245    0.6905    0.3446 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.9411   -0.6438    0.3945 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0968   -1.3886    0.6697 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7650   -1.2180    0.1813 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.9927    0.3428    0.7837 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3217    0.8428    1.1263 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7893    1.5742    2.0858 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2041    1.7708    1.9431 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5044    1.2538    0.5714 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3499    0.4857    0.2505 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6267    0.2671   -1.5402 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6632    1.1381   -0.3646 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2267    1.9594   -1.0140 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3371    0.6023    1.4013 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3206   -1.4707    1.2981 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5358   -2.4388   -0.5555 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9107   -1.6039   -1.6457 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1139   -2.4831   -0.3396 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3505   -0.0168   -1.7900 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1226   -1.8450   -1.6426 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1024   -2.0241    0.1615 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2140    0.2431   -1.3287 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4598   -1.9499   -1.1752 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1985   -1.9157    0.6274 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9068    1.4525   -0.3477 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0179    3.3741   -0.8033 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1248   -2.0465    1.4480 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7339    0.5662    1.4608 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5078    2.8299    2.0856 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6790    1.1082    2.7107 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6005    2.1207   -0.1141 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2 22  1  0
 22 21  1  0
 21 20  1  0
 20 19  2  0
 19 18  1  0
 18  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 12 14  2  0
 14 15  1  0
 15 16  1  0
 15 17  2  0
  8  7  1  0
  7  6  1  0
  6  5  1  0
  5  3  1  0
  3  4  1  0
  6 23  1  0
  3  2  1  0
 23 22  1  0
 23 19  1  0
 17 10  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  2 27  1  1
 22 44  1  6
 21 42  1  0
 21 43  1  0
 18 41  1  0
  8 35  1  6
  9 36  1  0
  9 37  1  0
 11 38  1  0
 13 39  1  0
 16 40  1  0
  7 33  1  0
  7 34  1  0
  6 32  1  6
  5 30  1  0
  5 31  1  0
  3 28  1  1
  4 29  1  0
M  END


  Mrv1652309062210262D          

 23 26  0  0  1  0            999 V2000
    0.2702    0.1963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9377    0.6813    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8514    1.5017    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0978    1.8373    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5189    1.9867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2725    1.6511    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1987    1.9867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8661    1.5017    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6198    1.8373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2872    1.3524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0409    1.6879    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7084    1.2030    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4620    1.5386    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6221    0.3825    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.8684    0.0470    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7822   -0.7735    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2010    0.5319    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.7799    0.6813    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.0262    0.3457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7713   -0.4389    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9463   -0.4389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6913    0.3457    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3588    0.8306    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  3  4  1  1  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
 10 17  1  0  0  0  0
  8 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
  2 22  1  0  0  0  0
 22 23  1  6  0  0  0
 19 23  1  0  0  0  0
  6 23  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0228689

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1[C@H]2CN=C3N[C@@H](CC4=CC(O)=NC(O)=N4)C[C@@H](C[C@@H]1O)N23

> <INCHI_IDENTIFIER>
InChI=1S/C15H21N5O3/c1-7-11-6-16-14-17-8(3-10(20(11)14)5-12(7)21)2-9-4-13(22)19-15(23)18-9/h4,7-8,10-12,21H,2-3,5-6H2,1H3,(H,16,17)(H2,18,19,22,23)/t7-,8+,10+,11-,12+/m1/s1

> <INCHI_KEY>
HKUZFYRVEQYWCO-GATYQTQLSA-N

> <FORMULA>
C15H21N5O3

> <MOLECULAR_WEIGHT>
319.365

> <EXACT_MASS>
319.164439556

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
44

> <JCHEM_AVERAGE_POLARIZABILITY>
32.95898460495027

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
6-{[(4S,5R,6S,8S,10R)-6-hydroxy-5-methyl-2,11,12-triazatricyclo[6.3.1.0^{4,12}]dodec-1-en-10-yl]methyl}pyrimidine-2,4-diol

> <JCHEM_LOGP>
0.05419137513849813

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
14.047371073539445

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.16725779895624

> <JCHEM_PKA_STRONGEST_BASIC>
10.797644999149533

> <JCHEM_POLAR_SURFACE_AREA>
114.10000000000001

> <JCHEM_REFRACTIVITY>
82.9386

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
6-{[(4S,5R,6S,8S,10R)-6-hydroxy-5-methyl-2,11,12-triazatricyclo[6.3.1.0^{4,12}]dodec-1-en-10-yl]methyl}pyrimidine-2,4-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0       0.504   0.366   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.750   1.272   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.589   2.803   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       0.182   3.430   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       2.835   3.708   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.242   3.082   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.971   3.708   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.217   2.803   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.624   3.430   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.870   2.524   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      11.276   3.151   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      12.522   2.246   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      13.929   2.872   0.000  0.00  0.00           O+0
HETATM   14  N   UNK     0      12.361   0.714   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0      10.954   0.088   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      10.793  -1.444   0.000  0.00  0.00           O+0
HETATM   17  N   UNK     0       9.709   0.993   0.000  0.00  0.00           N+0
HETATM   18  N   UNK     0       7.056   1.272   0.000  0.00  0.00           N+0
HETATM   19  C   UNK     0       5.649   0.645   0.000  0.00  0.00           C+0
HETATM   20  N   UNK     0       5.173  -0.819   0.000  0.00  0.00           N+0
HETATM   21  C   UNK     0       3.633  -0.819   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.157   0.645   0.000  0.00  0.00           C+0
HETATM   23  N   UNK     0       4.403   1.550   0.000  0.00  0.00           N+0
CONECT    1    2                                                            
CONECT    2    1    3   22                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7   23                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   18                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   17                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   10                                                       
CONECT   18    8   19                                                       
CONECT   19   18   20   23                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21    2   23                                                  
CONECT   23   22   19    6                                                  
MASTER        0    0    0    0    0    0    0    0   23    0   52    0
END

View in JSmol

Synonyms

Value	Source
7-Deoxy-desulphO-cylindrospermopsin	Generator

Chemical Formula

C₁₅H₂₁N₅O₃

Average Mass

319.3650 Da

Monoisotopic Mass

319.16444 Da

IUPAC Name

6-{[(4S,5R,6S,8S,10R)-6-hydroxy-5-methyl-2,11,12-triazatricyclo[6.3.1.0^{4,12}]dodec-1-en-10-yl]methyl}pyrimidine-2,4-diol

Traditional Name

6-{[(4S,5R,6S,8S,10R)-6-hydroxy-5-methyl-2,11,12-triazatricyclo[6.3.1.0^{4,12}]dodec-1-en-10-yl]methyl}pyrimidine-2,4-diol

CAS Registry Number

Not Available

SMILES

C[C@@H]1[C@H]2CN=C3N[C@@H](CC4=CC(O)=NC(O)=N4)C[C@@H](C[C@@H]1O)N23

InChI Identifier

InChI=1S/C15H21N5O3/c1-7-11-6-16-14-17-8(3-10(20(11)14)5-12(7)21)2-9-4-13(22)19-15(23)18-9/h4,7-8,10-12,21H,2-3,5-6H2,1H3,(H,16,17)(H2,18,19,22,23)/t7-,8+,10+,11-,12+/m1/s1

InChI Key

HKUZFYRVEQYWCO-GATYQTQLSA-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 pyridopyrimidines. Pyridopyrimidines are compounds containing a pyridopyrimidine, which consists of a pyridine fused to a pyrimidine. Pyridine is 6-membered ring consisting of five carbon atoms and a nitrogen atom. Pyrimidine is a 6-membered ring consisting of four carbon atoms and two nitrogen centers at the 1- and 3- ring positions.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Pyridopyrimidines

Sub Class

Not Available

Direct Parent

Pyridopyrimidines

Alternative Parents

Substituents

Pyridopyrimidine
Imidazopyrimidine
Pyrimidone
1,3-diazinane
Hydropyrimidine
Piperidine
Pyridine
Pyrimidine
Heteroaromatic compound
Vinylogous amide
2-imidazoline
Urea
Secondary alcohol
Guanidine
Lactam
Propargyl-type 1,3-dipolar organic compound
Carboximidamide
Azacycle
Organic 1,3-dipolar compound
Hydrocarbon derivative
Organonitrogen compound
Organic nitrogen compound
Organooxygen compound
Amine
Alcohol
Organic oxygen compound
Organic oxide
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	0.054	ChemAxon
pKa (Strongest Acidic)	12.17	ChemAxon
pKa (Strongest Basic)	10.8	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	114.1 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	82.94 m³·mol⁻¹	ChemAxon
Polarizability	32.96 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

9422531

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11247498

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 6-{[(4s,5r,6s,8s,10r)-6-hydroxy-5-methyl-2,11,12-triazatricyclo[6.3.1.0⁴,¹²]dodec-1-en-10-yl]methyl}pyrimidine-2,4-diol (NP0228689)

MOL for NP0228689 (6-{[(4s,5r,6s,8s,10r)-6-hydroxy-5-methyl-2,11,12-triazatricyclo[6.3.1.0⁴,¹²]dodec-1-en-10-yl]methyl}pyrimidine-2,4-diol)

3D MOL for NP0228689 (6-{[(4s,5r,6s,8s,10r)-6-hydroxy-5-methyl-2,11,12-triazatricyclo[6.3.1.0⁴,¹²]dodec-1-en-10-yl]methyl}pyrimidine-2,4-diol)

3D SDF for NP0228689 (6-{[(4s,5r,6s,8s,10r)-6-hydroxy-5-methyl-2,11,12-triazatricyclo[6.3.1.0⁴,¹²]dodec-1-en-10-yl]methyl}pyrimidine-2,4-diol)

3D-SDF for NP0228689 (6-{[(4s,5r,6s,8s,10r)-6-hydroxy-5-methyl-2,11,12-triazatricyclo[6.3.1.0⁴,¹²]dodec-1-en-10-yl]methyl}pyrimidine-2,4-diol)

PDB for NP0228689 (6-{[(4s,5r,6s,8s,10r)-6-hydroxy-5-methyl-2,11,12-triazatricyclo[6.3.1.0⁴,¹²]dodec-1-en-10-yl]methyl}pyrimidine-2,4-diol)

3D PDB for NP0228689 (6-{[(4s,5r,6s,8s,10r)-6-hydroxy-5-methyl-2,11,12-triazatricyclo[6.3.1.0⁴,¹²]dodec-1-en-10-yl]methyl}pyrimidine-2,4-diol)

SMILES for NP0228689 (6-{[(4s,5r,6s,8s,10r)-6-hydroxy-5-methyl-2,11,12-triazatricyclo[6.3.1.0⁴,¹²]dodec-1-en-10-yl]methyl}pyrimidine-2,4-diol)

INCHI for NP0228689 (6-{[(4s,5r,6s,8s,10r)-6-hydroxy-5-methyl-2,11,12-triazatricyclo[6.3.1.0⁴,¹²]dodec-1-en-10-yl]methyl}pyrimidine-2,4-diol)

Structure for NP0228689 (6-{[(4s,5r,6s,8s,10r)-6-hydroxy-5-methyl-2,11,12-triazatricyclo[6.3.1.0⁴,¹²]dodec-1-en-10-yl]methyl}pyrimidine-2,4-diol)

3D Structure for NP0228689 (6-{[(4s,5r,6s,8s,10r)-6-hydroxy-5-methyl-2,11,12-triazatricyclo[6.3.1.0⁴,¹²]dodec-1-en-10-yl]methyl}pyrimidine-2,4-diol)