NP-MRD: Showing NP-Card for 15-ethylidene-13-(hydroxymethyl)-3,17-diazapentacyclo[12.3.1.0²,¹⁰.0⁴,⁹.0¹²,¹⁷]octadeca-2(10),4,6,8-tetraen-7-ol (NP0254255)

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Record Information

Version

2.0

Created at

2022-09-07 18:21:50 UTC

Updated at

2022-09-07 18:21:50 UTC

NP-MRD ID

NP0254255

Secondary Accession Numbers

None

Natural Product Identification

Common Name

15-ethylidene-13-(hydroxymethyl)-3,17-diazapentacyclo[12.3.1.0²,¹⁰.0⁴,⁹.0¹²,¹⁷]octadeca-2(10),4,6,8-tetraen-7-ol

Description

15-Ethylidene-13-(hydroxymethyl)-3,17-diazapentacyclo[12.3.1.0²,¹⁰.0⁴,⁹.0¹²,¹⁷]Octadeca-2(10),4(9),5,7-tetraen-7-ol belongs to the class of organic compounds known as macroline alkaloids. These are alkaloids with a structure that is based on the tetracyclic macroline skeleton. The macroline skeleton arises by scission of the C-21 to N-4 bond of the akuammilan skeleton, and mostly occurs in bisindole alkaloids. 15-ethylidene-13-(hydroxymethyl)-3,17-diazapentacyclo[12.3.1.0²,¹⁰.0⁴,⁹.0¹²,¹⁷]octadeca-2(10),4,6,8-tetraen-7-ol is found in Rauvolfia serpentina. 15-Ethylidene-13-(hydroxymethyl)-3,17-diazapentacyclo[12.3.1.0²,¹⁰.0⁴,⁹.0¹²,¹⁷]Octadeca-2(10),4(9),5,7-tetraen-7-ol is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 45 49  0  0  0  0  0  0  0  0999 V2000
   -4.8635    1.9883    0.9789 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2142    0.6382    0.7930 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0258    0.4693    0.3752 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0978    1.5498    0.0082 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7702    1.0272    0.0412 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4537    0.3827    1.3290 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2739   -0.8511    1.2786 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3847   -0.8439    0.1893 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7375   -0.6210   -1.2307 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6819   -2.0216   -1.8449 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1357   -2.8903   -0.8983 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4942   -0.1067   -0.8498 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7556    0.3280   -1.4303 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6263    0.2412   -0.1607 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0131    0.2509    1.0861 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0471    0.1393    1.9704 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.2077    0.0668    1.3364 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5385   -0.0520    1.7217 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5518   -0.1030    0.7868 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2775   -0.0376   -0.5638 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3235   -0.0911   -1.4998 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9647    0.0806   -0.9732 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9838    0.1288   -0.0356 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1069    2.7737    1.0965 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4380    2.2086    0.0339 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5340    1.9696    1.8674 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8898   -0.1979    1.0618 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1496    2.3270    0.7752 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2694    1.9490   -1.0102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6789    1.0562    2.1719 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9332   -0.7985    2.2110 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7893   -1.8116    1.3850 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9836   -1.7161    0.2343 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4116   -0.0503   -1.8723 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7122   -2.3576   -2.1252 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0234   -2.0117   -2.7433 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7166   -3.6855   -0.8096 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1053   -1.0553   -0.3184 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1535   -0.3984   -2.1705 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7412    1.3533   -1.8005 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9370    0.1147    3.0044 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7483   -0.1032    2.7897 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5793   -0.1952    1.0994 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7096    0.8218   -1.7490 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7162    0.1345   -2.0317 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 20 22  1  0
 22 23  2  0
 15  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
  8  3  1  0
  6  5  1  0
  9 12  1  0
 23 14  1  0
 23 17  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  2 27  1  0
  4 28  1  0
  4 29  1  0
 12 38  1  1
 13 39  1  0
 13 40  1  0
 16 41  1  0
 18 42  1  0
 19 43  1  0
 21 44  1  0
 22 45  1  0
  6 30  1  1
  7 31  1  0
  7 32  1  0
  8 33  1  6
  9 34  1  6
 10 35  1  0
 10 36  1  0
 11 37  1  0
M  END


  Mrv1533004161518152D          

 23 27  0  0  0  0            999 V2000
   -1.4389   -0.5016    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0850    0.2436    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2627    0.3098    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2871    0.9480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0821    0.6214    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4501   -0.3360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2834   -0.5597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0240   -0.1521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7490    0.6257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4038    1.1276    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.0834    0.6599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8857    0.8521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4533    0.2534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2186   -0.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7861   -1.1363    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4163   -0.7297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8487   -0.1310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8938    0.6568    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1650    0.1181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3854   -0.2352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8279   -0.9407    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7294   -1.7598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3895   -2.2547    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  4  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  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  2  0  0  0  0
  9 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
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
  8 17  1  0  0  0  0
 11 17  1  0  0  0  0
  9 18  1  0  0  0  0
  5 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
  3 20  1  0  0  0  0
 20 21  1  0  0  0  0
  6 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0254255

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC=C1CN2C3CC4=C(NC5=CC=C(O)C=C45)C2CC1C3CO

> <INCHI_IDENTIFIER>
InChI=1S/C19H22N2O2/c1-2-10-8-21-17-7-14-13-5-11(23)3-4-16(13)20-19(14)18(21)6-12(10)15(17)9-22/h2-5,12,15,17-18,20,22-23H,6-9H2,1H3

> <INCHI_KEY>
VTVQHYQGTTVKDE-UHFFFAOYSA-N

> <FORMULA>
C19H22N2O2

> <MOLECULAR_WEIGHT>
310.397

> <EXACT_MASS>
310.168127956

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
35.241253761241964

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
15-ethylidene-13-(hydroxymethyl)-3,17-diazapentacyclo[12.3.1.0²,¹⁰.0⁴,⁹.0¹²,¹⁷]octadeca-2(10),4,6,8-tetraen-7-ol

> <ALOGPS_LOGP>
2.42

> <JCHEM_LOGP>
1.9048820460000004

> <ALOGPS_LOGS>
-2.94

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.39786924141723

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.553420067048988

> <JCHEM_PKA_STRONGEST_BASIC>
6.354593309949039

> <JCHEM_POLAR_SURFACE_AREA>
59.49000000000001

> <JCHEM_REFRACTIVITY>
91.30169999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.59e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
15-ethylidene-13-(hydroxymethyl)-3,17-diazapentacyclo[12.3.1.0²,¹⁰.0⁴,⁹.0¹²,¹⁷]octadeca-2(10),4,6,8-tetraen-7-ol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0      -2.686  -0.936   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.025   0.455   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.490   0.578   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.536   1.770   0.000  0.00  0.00           C+0
HETATM    5  N   UNK     0       2.020   1.160   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0       2.707  -0.627   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.262  -1.045   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.645  -0.284   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.131   1.168   0.000  0.00  0.00           C+0
HETATM   10  N   UNK     0       6.354   2.105   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0       7.622   1.232   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.120   1.591   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.180   0.473   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.741  -1.003   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      10.801  -2.121   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       8.244  -1.362   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.184  -0.244   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.535   1.226   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.175   0.220   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.719  -0.439   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.545  -1.756   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.362  -3.285   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       2.594  -4.209   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   20                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   18                                                  
CONECT    6    5    7   21                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   17                                                  
CONECT    9    8   10   18                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   17                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16    8   11                                                  
CONECT   18    9    5   19                                                  
CONECT   19   18   20                                                       
CONECT   20   19    3   21                                                  
CONECT   21   20    6   22                                                  
CONECT   22   21   23                                                       
CONECT   23   22                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   54    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₂₂N₂O₂

Average Mass

310.3970 Da

Monoisotopic Mass

310.16813 Da

IUPAC Name

15-ethylidene-13-(hydroxymethyl)-3,17-diazapentacyclo[12.3.1.0²,¹⁰.0⁴,⁹.0¹²,¹⁷]octadeca-2(10),4,6,8-tetraen-7-ol

Traditional Name

15-ethylidene-13-(hydroxymethyl)-3,17-diazapentacyclo[12.3.1.0²,¹⁰.0⁴,⁹.0¹²,¹⁷]octadeca-2(10),4,6,8-tetraen-7-ol

CAS Registry Number

Not Available

SMILES

CC=C1CN2C3CC4=C(NC5=CC=C(O)C=C45)C2CC1C3CO

InChI Identifier

InChI=1S/C19H22N2O2/c1-2-10-8-21-17-7-14-13-5-11(23)3-4-16(13)20-19(14)18(21)6-12(10)15(17)9-22/h2-5,12,15,17-18,20,22-23H,6-9H2,1H3

InChI Key

VTVQHYQGTTVKDE-UHFFFAOYSA-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
Rauvolfia serpentina	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as macroline alkaloids. These are alkaloids with a structure that is based on the tetracyclic macroline skeleton. The macroline skeleton arises by scission of the C-21 to N-4 bond of the akuammilan skeleton, and mostly occurs in bisindole alkaloids.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Macroline alkaloids

Sub Class

Not Available

Direct Parent

Macroline alkaloids

Alternative Parents

Substituents

Macroline skeleton
Sarpagine-skeleton
Vobasan skeleton
Beta-carboline
Pyridoindole
Hydroxyindole
3-alkylindole
Indole
Indole or derivatives
Quinuclidine
1-hydroxy-2-unsubstituted benzenoid
Phenol
Aralkylamine
Benzenoid
Piperidine
1,3-aminoalcohol
Pyrrole
Heteroaromatic compound
Tertiary aliphatic amine
Tertiary amine
Azacycle
Organoheterocyclic compound
Primary alcohol
Organonitrogen compound
Hydrocarbon derivative
Organic oxygen compound
Organooxygen compound
Amine
Organic nitrogen compound
Alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

a small molecule (CPD-4243 )

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	2.42	ALOGPS
logP	1.9	ChemAxon
logS	-2.9	ALOGPS
pKa (Strongest Acidic)	9.55	ChemAxon
pKa (Strongest Basic)	6.35	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	59.49 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	91.3 m³·mol⁻¹	ChemAxon
Polarizability	35.24 Å³	ChemAxon
Number of Rings	5	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

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

5089092

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 15-ethylidene-13-(hydroxymethyl)-3,17-diazapentacyclo[12.3.1.0²,¹⁰.0⁴,⁹.0¹²,¹⁷]octadeca-2(10),4,6,8-tetraen-7-ol (NP0254255)

MOL for NP0254255 (15-ethylidene-13-(hydroxymethyl)-3,17-diazapentacyclo[12.3.1.0²,¹⁰.0⁴,⁹.0¹²,¹⁷]octadeca-2(10),4,6,8-tetraen-7-ol)

3D MOL for NP0254255 (15-ethylidene-13-(hydroxymethyl)-3,17-diazapentacyclo[12.3.1.0²,¹⁰.0⁴,⁹.0¹²,¹⁷]octadeca-2(10),4,6,8-tetraen-7-ol)

3D SDF for NP0254255 (15-ethylidene-13-(hydroxymethyl)-3,17-diazapentacyclo[12.3.1.0²,¹⁰.0⁴,⁹.0¹²,¹⁷]octadeca-2(10),4,6,8-tetraen-7-ol)

3D-SDF for NP0254255 (15-ethylidene-13-(hydroxymethyl)-3,17-diazapentacyclo[12.3.1.0²,¹⁰.0⁴,⁹.0¹²,¹⁷]octadeca-2(10),4,6,8-tetraen-7-ol)

PDB for NP0254255 (15-ethylidene-13-(hydroxymethyl)-3,17-diazapentacyclo[12.3.1.0²,¹⁰.0⁴,⁹.0¹²,¹⁷]octadeca-2(10),4,6,8-tetraen-7-ol)

3D PDB for NP0254255 (15-ethylidene-13-(hydroxymethyl)-3,17-diazapentacyclo[12.3.1.0²,¹⁰.0⁴,⁹.0¹²,¹⁷]octadeca-2(10),4,6,8-tetraen-7-ol)

SMILES for NP0254255 (15-ethylidene-13-(hydroxymethyl)-3,17-diazapentacyclo[12.3.1.0²,¹⁰.0⁴,⁹.0¹²,¹⁷]octadeca-2(10),4,6,8-tetraen-7-ol)

INCHI for NP0254255 (15-ethylidene-13-(hydroxymethyl)-3,17-diazapentacyclo[12.3.1.0²,¹⁰.0⁴,⁹.0¹²,¹⁷]octadeca-2(10),4,6,8-tetraen-7-ol)

Structure for NP0254255 (15-ethylidene-13-(hydroxymethyl)-3,17-diazapentacyclo[12.3.1.0²,¹⁰.0⁴,⁹.0¹²,¹⁷]octadeca-2(10),4,6,8-tetraen-7-ol)

3D Structure for NP0254255 (15-ethylidene-13-(hydroxymethyl)-3,17-diazapentacyclo[12.3.1.0²,¹⁰.0⁴,⁹.0¹²,¹⁷]octadeca-2(10),4,6,8-tetraen-7-ol)