NP-MRD: Showing NP-Card for (-)-14-O-Acetylindolactam-V (NP0068875)

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Record Information

Version

2.0

Created at

2022-04-28 14:08:45 UTC

Updated at

2022-04-28 14:08:45 UTC

NP-MRD ID

NP0068875

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(-)-14-O-Acetylindolactam-V

Description

[(10S,13R)-11-hydroxy-9-methyl-10-(propan-2-yl)-3,9,12-triazatricyclo[6.6.1.0⁴,¹⁵]Pentadeca-1,4(15),5,7,11-pentaen-13-yl]methyl acetate belongs to the class of organic compounds known as 3-alkylindoles. 3-Alkylindoles are compounds containing an indole moiety that carries an alkyl chain at the 3-position. (-)-14-O-Acetylindolactam-V is found in Streptomyces blastmyceticum NA34-17. Based on a literature review very few articles have been published on [(10S,13R)-11-hydroxy-9-methyl-10-(propan-2-yl)-3,9,12-triazatricyclo[6.6.1.0⁴,¹⁵]Pentadeca-1,4(15),5,7,11-pentaen-13-yl]methyl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 50 52  0  0  0  0  0  0  0  0999 V2000
    5.8253   -2.2298    1.3644 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0605   -1.2586    0.5384 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7268   -0.4697   -0.1758 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6896   -1.1770    0.5128 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0762   -0.2011   -0.3224 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5608   -0.2691   -0.2119 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0213    0.7512   -1.1547 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5497    1.9602   -0.4873 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3513    3.0669   -0.1371 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5132    4.0053    0.3188 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7543    3.5673    0.2812 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9821    4.1662    0.5949 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1611    3.4824    0.4081 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1234    2.1996   -0.0875 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8834    1.5798   -0.4054 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7411    2.2761   -0.2211 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9626    0.1814   -0.7886 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8346   -0.1187   -1.8958 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2540   -0.8628   -0.0659 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1997   -1.6818    0.7870 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2786   -2.3924    0.0580 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4432   -2.7000    1.6180 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3313   -1.6935   -0.8436 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7130   -2.5219   -1.7381 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1014   -1.6164   -0.6292 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.3822   -2.9616    0.7575 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6109   -1.6180    1.8950 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2104   -2.6836    2.1596 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4366   -0.3421   -1.3444 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3636    0.8123    0.0173 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3247   -0.1596    0.8380 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7828    1.0032   -1.9658 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2038    0.2605   -1.7405 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4214    3.1283   -0.2248 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8118    4.9548    0.6590 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9620    5.1777    0.9858 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1016    3.9398    0.6447 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0507    1.6735   -0.2572 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8837    0.1595   -1.6039 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8332   -1.2083   -2.1440 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5501    0.4116   -2.8296 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6196   -0.3227    0.7216 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7098   -0.9895    1.5202 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7240   -3.1229    0.8133 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1363   -1.7920   -0.2565 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8845   -3.0909   -0.7275 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0232   -3.0252    2.4953 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4985   -2.2598    2.0144 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1336   -3.5802    1.0090 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7490   -2.4084   -0.7536 H   0  0  0  0  0  0  0  0  0  0  0  0
 21 20  1  0
 20 22  1  0
 20 19  1  0
 19 17  1  0
 17 18  1  0
 17 15  1  0
 15 16  2  0
 16  8  1  0
  8  7  1  0
  7  6  1  0
  6  5  1  0
  5  4  1  0
  4  2  1  0
  2  1  1  0
  2  3  2  0
  6 25  1  0
 25 23  1  0
 23 24  2  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 23 19  1  0
 14 15  1  0
 11 16  1  0
 21 44  1  0
 21 45  1  0
 21 46  1  0
 20 43  1  1
 22 47  1  0
 22 48  1  0
 22 49  1  0
 19 42  1  1
 18 39  1  0
 18 40  1  0
 18 41  1  0
  7 32  1  0
  7 33  1  0
  6 31  1  1
  5 29  1  0
  5 30  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
 25 50  1  0
  9 34  1  0
 10 35  1  0
 12 36  1  0
 13 37  1  0
 14 38  1  0
M  END


  Mrv1652304282216082D          

 25 27  0  0  1  0            999 V2000
    0.8481   -0.3370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8039   -1.1608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2426   -1.6313    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5047   -1.2817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5756   -0.4597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1008    0.0126    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2024    0.8313    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.0125    0.9877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4115    0.2657    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2305    0.3652    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9218   -0.0850    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1620   -0.8743    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8387   -1.6333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4414   -2.1967    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1032   -2.0069    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2996   -1.8203    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8493   -2.5116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2027   -2.8259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5432   -3.3215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9617   -3.1492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5813    0.4106    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4818    1.2296    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1413    1.7253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0418    2.5442    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9003    1.4020    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
  8  9  2  0  0  0  0
  1  9  1  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  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
  2 16  1  0  0  0  0
 16 17  1  0  0  0  0
 15 18  1  6  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 11 21  1  6  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0068875

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)[C@@H]1N(C)C2=C3C(C[C@H](COC(C)=O)NC1=O)=CNC3=CC=C2

> <INCHI_IDENTIFIER>
InChI=1S/C19H25N3O3/c1-11(2)18-19(24)21-14(10-25-12(3)23)8-13-9-20-15-6-5-7-16(17(13)15)22(18)4/h5-7,9,11,14,18,20H,8,10H2,1-4H3,(H,21,24)/t14-,18+/m1/s1

> <INCHI_KEY>
WJBVMJYASZWGBL-KDOFPFPSSA-N

> <FORMULA>
C19H25N3O3

> <MOLECULAR_WEIGHT>
343.427

> <EXACT_MASS>
343.189591677

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
50

> <JCHEM_AVERAGE_POLARIZABILITY>
36.49315699860848

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
[(10S,13R)-9-methyl-11-oxo-10-(propan-2-yl)-3,9,12-triazatricyclo[6.6.1.0^{4,15}]pentadeca-1,4,6,8(15)-tetraen-13-yl]methyl acetate

> <ALOGPS_LOGP>
2.76

> <JCHEM_LOGP>
2.381706866333334

> <ALOGPS_LOGS>
-3.28

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
17.370288503711663

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.919362959957631

> <JCHEM_PKA_STRONGEST_BASIC>
-0.5900473453623286

> <JCHEM_POLAR_SURFACE_AREA>
74.43

> <JCHEM_REFRACTIVITY>
96.2897

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.80e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
[(10S,13R)-10-isopropyl-9-methyl-11-oxo-3,9,12-triazatricyclo[6.6.1.0^{4,15}]pentadeca-1,4,6,8(15)-tetraen-13-yl]methyl acetate

> <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       1.583  -0.629   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.501  -2.167   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.453  -3.045   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.942  -2.392   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.074  -0.858   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.188   0.024   0.000  0.00  0.00           C+0
HETATM    7  N   UNK     0       0.378   1.552   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0       1.890   1.844   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.635   0.496   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.164   0.682   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.454  -0.159   0.000  0.00  0.00           C+0
HETATM   12  N   UNK     0       5.902  -1.632   0.000  0.00  0.00           N+0
HETATM   13  C   UNK     0       5.299  -3.049   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       6.424  -4.101   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       3.926  -3.746   0.000  0.00  0.00           C+0
HETATM   16  N   UNK     0       2.426  -3.398   0.000  0.00  0.00           N+0
HETATM   17  C   UNK     0       1.585  -4.688   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.112  -5.275   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.881  -6.200   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.528  -5.879   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.685   0.767   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       6.499   2.295   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       7.730   3.221   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       7.545   4.749   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       9.147   2.617   0.000  0.00  0.00           C+0
CONECT    1    2    6    9                                                  
CONECT    2    1    3   16                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    1    7                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8    1   10                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   21                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   18                                                  
CONECT   16   15    2   17                                                  
CONECT   17   16                                                            
CONECT   18   15   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   11   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   54    0
END

View in JSmol

Synonyms

Value	Source
[(10S,13R)-11-Hydroxy-9-methyl-10-(propan-2-yl)-3,9,12-triazatricyclo[6.6.1.0,]pentadeca-1,4(15),5,7,11-pentaen-13-yl]methyl acetic acid	Generator

Chemical Formula

C₁₉H₂₅N₃O₃

Average Mass

343.4270 Da

Monoisotopic Mass

343.18959 Da

IUPAC Name

[(10S,13R)-9-methyl-11-oxo-10-(propan-2-yl)-3,9,12-triazatricyclo[6.6.1.0^{4,15}]pentadeca-1,4,6,8(15)-tetraen-13-yl]methyl acetate

Traditional Name

[(10S,13R)-10-isopropyl-9-methyl-11-oxo-3,9,12-triazatricyclo[6.6.1.0^{4,15}]pentadeca-1,4,6,8(15)-tetraen-13-yl]methyl acetate

CAS Registry Number

Not Available

SMILES

CC(C)[C@@H]1N(C)C2=C3C(C[C@H](COC(C)=O)NC1=O)=CNC3=CC=C2

InChI Identifier

InChI=1S/C19H25N3O3/c1-11(2)18-19(24)21-14(10-25-12(3)23)8-13-9-20-15-6-5-7-16(17(13)15)22(18)4/h5-7,9,11,14,18,20H,8,10H2,1-4H3,(H,21,24)/t14-,18+/m1/s1

InChI Key

WJBVMJYASZWGBL-KDOFPFPSSA-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
Streptomyces blastmyceticum NA34-17	Bacteria	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 3-alkylindoles. 3-Alkylindoles are compounds containing an indole moiety that carries an alkyl chain at the 3-position.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Indoles

Direct Parent

3-alkylindoles

Alternative Parents

Substituents

3-alkylindole
Dialkylarylamine
Tertiary aliphatic/aromatic amine
Benzenoid
Heteroaromatic compound
Cyclic carboximidic acid
Pyrrole
Tertiary amine
Carboxylic acid ester
Amino acid or derivatives
Azacycle
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Amine
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	2.76	ALOGPS
logP	2.38	ChemAxon
logS	-3.3	ALOGPS
pKa (Strongest Acidic)	12.92	ChemAxon
pKa (Strongest Basic)	-0.59	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	74.43 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	96.29 m³·mol⁻¹	ChemAxon
Polarizability	36.49 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

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

162893368

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (-)-14-O-Acetylindolactam-V (NP0068875)

MOL for NP0068875 ((-)-14-O-Acetylindolactam-V)

3D MOL for NP0068875 ((-)-14-O-Acetylindolactam-V)

3D SDF for NP0068875 ((-)-14-O-Acetylindolactam-V)

3D-SDF for NP0068875 ((-)-14-O-Acetylindolactam-V)

PDB for NP0068875 ((-)-14-O-Acetylindolactam-V)

3D PDB for NP0068875 ((-)-14-O-Acetylindolactam-V)

SMILES for NP0068875 ((-)-14-O-Acetylindolactam-V)

INCHI for NP0068875 ((-)-14-O-Acetylindolactam-V)

Structure for NP0068875 ((-)-14-O-Acetylindolactam-V)

3D Structure for NP0068875 ((-)-14-O-Acetylindolactam-V)