NP-MRD: Showing NP-Card for siddiqui (NP0283759)

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Record Information

Version

2.0

Created at

2022-09-09 11:09:42 UTC

Updated at

2022-09-09 11:09:42 UTC

NP-MRD ID

NP0283759

Secondary Accession Numbers

None

Natural Product Identification

Common Name

siddiqui

Description

13-Ethyl-8-methyl-8,15-diazahexacyclo[14.2.1.0¹,⁹.0²,⁷.0¹⁰,¹⁵.0¹²,¹⁷]Nonadeca-2,4,6-triene-14,18-diol belongs to the class of organic compounds known as ajmaline-sarpagine alkaloids. These are organic compounds containing either of the ajmalan, sarpagan skeleton, or derivative thereof. The Sarpagine (Akuammidine) group, based on the sarpagan nucleus, arises from bond formation between C-16 and C-5 of the corynantheine precursor. Ajmaline alkaloids are based on a 17,19-secoyohimban skeleton (oxayohimban) which is invariably present as an ether. siddiqui is found in Rauvolfia caffra, Rauvolfia cubana, Rauvolfia verticillata, Rauvolfia serpentina, Rauvolfia tetraphylla, Rauvolfia viridis, Rauvolfia volkensii and Rauvolfia yunnanensis. 13-Ethyl-8-methyl-8,15-diazahexacyclo[14.2.1.0¹,⁹.0²,⁷.0¹⁰,¹⁵.0¹²,¹⁷]Nonadeca-2,4,6-triene-14,18-diol is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 50 55  0  0  0  0  0  0  0  0999 V2000
    5.0532    0.1463    0.7375 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9282   -0.7464    0.2705 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9931    0.1100   -0.5470 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4169    1.2778    0.1909 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9809    1.3155    1.4646 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9699    1.1511    0.3960 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8148   -0.1236    1.1156 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6523   -0.2111    1.4791 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2290   -0.6385    0.1426 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6596   -0.8487    0.1669 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4797   -1.9317    0.3943 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8563   -1.8568    0.3644 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4567   -0.6335    0.0924 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6365    0.4507   -0.1355 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2472    0.3733   -0.1051 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1981    1.3526   -0.3127 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3447    2.7522   -0.0716 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0972    0.5542   -0.7830 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2333    1.1637   -0.8332 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0181    0.3551   -1.8826 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8008   -0.6918   -1.0813 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0418   -1.2078    0.0931 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3450   -1.7356   -0.2704 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4206   -2.0772   -1.6126 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0018    0.2155    1.8455 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0041    1.1670    0.2818 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0136   -0.3313    0.4608 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3515   -1.4968   -0.4162 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4249   -1.2438    1.1107 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4996    0.5062   -1.4512 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6260    2.2538   -0.3179 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0740    2.2121    1.8297 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4790   -0.1438    1.9689 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7831   -0.9979    2.2568 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0289    0.7636    1.8185 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0674   -2.9253    0.6146 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4790   -2.7117    0.5442 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5316   -0.5476    0.0631 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0996    1.4042   -0.3464 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0482    3.1657   -0.8265 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7059    3.0221    0.9196 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3450    3.2334   -0.2002 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3912    0.1873   -1.8001 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1794    2.1996   -1.1963 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7141    1.0380   -2.3955 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3587   -0.1117   -2.6129 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1699   -1.4963   -1.7213 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6299   -2.0219    0.5408 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5322   -2.6211    0.3704 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1423   -3.0188   -1.6866 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3 21  1  0
 21 20  1  0
 20 19  1  0
 19 18  1  0
 18 16  1  0
 16 17  1  0
 16 15  1  0
 15 14  2  0
 14 13  1  0
 13 12  2  0
 12 11  1  0
 11 10  2  0
  9 10  1  1
  9  8  1  0
  8  7  1  0
  7 22  1  0
 22 23  1  0
 23 24  1  0
  7  6  1  0
  6  4  1  0
  4  5  1  0
  4  3  1  0
 22 21  1  0
  6 19  1  0
  9 18  1  0
 23  9  1  0
 10 15  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  2 28  1  0
  2 29  1  0
  3 30  1  6
 21 47  1  6
 20 45  1  0
 20 46  1  0
 19 44  1  6
 18 43  1  6
 17 40  1  0
 17 41  1  0
 17 42  1  0
 14 39  1  0
 13 38  1  0
 12 37  1  0
 11 36  1  0
  8 34  1  0
  8 35  1  0
  7 33  1  1
 22 48  1  1
 23 49  1  1
 24 50  1  0
  4 31  1  6
  5 32  1  0
M  END


  Mrv1533004161519252D          

 24 29  0  0  0  0            999 V2000
   -1.2724    0.6461    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4772    0.8658    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1106    0.2870    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9791    0.1877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9515    1.0223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5871    0.4291    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4498    0.5739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0204    1.2285    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.9637    2.0515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6572    0.6743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4211    0.9859    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0729    0.4801    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9608   -0.3372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1969   -0.6488    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5451   -0.1430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6786   -0.2627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1182   -1.0762    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3140   -1.1684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7535   -0.4514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6022   -0.9752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9651   -1.7161    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0676   -0.3823    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.2173   -0.5325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2709   -1.1975    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  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  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 10 15  1  0  0  0  0
 15 16  1  0  0  0  0
  7 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
  4 19  1  0  0  0  0
 19 20  1  0  0  0  0
 16 20  1  0  0  0  0
 20 21  1  0  0  0  0
 18 22  1  0  0  0  0
  6 22  1  0  0  0  0
 22 23  1  0  0  0  0
  3 23  1  0  0  0  0
 23 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0283759

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC1C2CC3C4N(C)C5=CC=CC=C5C44CC(C2C4O)N3C1O

> <INCHI_IDENTIFIER>
InChI=1S/C20H26N2O2/c1-3-10-11-8-14-17-20(12-6-4-5-7-13(12)21(17)2)9-15(16(11)18(20)23)22(14)19(10)24/h4-7,10-11,14-19,23-24H,3,8-9H2,1-2H3

> <INCHI_KEY>
CJDRUOGAGYHKKD-UHFFFAOYSA-N

> <FORMULA>
C20H26N2O2

> <MOLECULAR_WEIGHT>
326.44

> <EXACT_MASS>
326.199428085

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
50

> <JCHEM_AVERAGE_POLARIZABILITY>
36.600250346919005

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
13-ethyl-8-methyl-8,15-diazahexacyclo[14.2.1.0¹,⁹.0²,⁷.0¹⁰,¹⁵.0¹²,¹⁷]nonadeca-2,4,6-triene-14,18-diol

> <ALOGPS_LOGP>
1.72

> <JCHEM_LOGP>
1.8508077869999995

> <ALOGPS_LOGS>
-1.90

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
14.329058596520166

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.28015557494178

> <JCHEM_PKA_STRONGEST_BASIC>
7.1953337407340285

> <JCHEM_POLAR_SURFACE_AREA>
46.94

> <JCHEM_REFRACTIVITY>
92.56580000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.09e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
siddiqui

> <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      -2.375   1.206   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.891   1.616   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.207   0.536   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.828   0.350   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.776   1.908   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.963   0.801   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.573   1.071   0.000  0.00  0.00           C+0
HETATM    8  N   UNK     0       5.638   2.293   0.000  0.00  0.00           N+0
HETATM    9  C   UNK     0       5.532   3.829   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.827   1.259   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.253   1.840   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.469   0.896   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.260  -0.629   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.834  -1.211   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.618  -0.267   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.000  -0.490   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.954  -2.009   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.453  -2.181   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.273  -0.843   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.857  -1.820   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       5.535  -3.203   0.000  0.00  0.00           O+0
HETATM   22  N   UNK     0       1.993  -0.714   0.000  0.00  0.00           N+0
HETATM   23  C   UNK     0       0.406  -0.994   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -0.506  -2.235   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   23                                                  
CONECT    4    3    5   19                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   22                                                  
CONECT    7    6    8   16                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   15                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   10   16                                                  
CONECT   16   15    7   17   20                                             
CONECT   17   16   18                                                       
CONECT   18   17   19   22                                                  
CONECT   19   18    4   20                                                  
CONECT   20   19   16   21                                                  
CONECT   21   20                                                            
CONECT   22   18    6   23                                                  
CONECT   23   22    3   24                                                  
CONECT   24   23                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   58    0
END

View in JSmol

Synonyms

Value	Source
ASTA medica brand OF ajmaline	MeSH
Ajmaline	MeSH
Ajmaline forest brand	MeSH
Ajmaline giulini brand	MeSH
Ajmaline hydrochloride	MeSH
Ajmaline lacer brand	MeSH
Ajmaline protea brand	MeSH
Ajmaline servier brand	MeSH
Ajmaline solvay brand	MeSH
Cardiorythmine	MeSH
Forest brand OF ajmaline	MeSH
Gilurtymal	MeSH
Giulini brand OF ajmaline	MeSH
Hydrochloride, ajmaline	MeSH
Lacer brand OF ajmaline	MeSH
Protea brand OF ajmaline	MeSH
Rauverid	MeSH
Serenol	MeSH
Servier brand OF ajmaline	MeSH
Solvay brand OF ajmaline	MeSH
Tachmalin	MeSH
Wolfina	MeSH

Chemical Formula

C₂₀H₂₆N₂O₂

Average Mass

326.4400 Da

Monoisotopic Mass

326.19943 Da

IUPAC Name

13-ethyl-8-methyl-8,15-diazahexacyclo[14.2.1.0¹,⁹.0²,⁷.0¹⁰,¹⁵.0¹²,¹⁷]nonadeca-2,4,6-triene-14,18-diol

Traditional Name

siddiqui

CAS Registry Number

Not Available

SMILES

CCC1C2CC3C4N(C)C5=CC=CC=C5C44CC(C2C4O)N3C1O

InChI Identifier

InChI=1S/C20H26N2O2/c1-3-10-11-8-14-17-20(12-6-4-5-7-13(12)21(17)2)9-15(16(11)18(20)23)22(14)19(10)24/h4-7,10-11,14-19,23-24H,3,8-9H2,1-2H3

InChI Key

CJDRUOGAGYHKKD-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 caffra	LOTUS Database	35616633
Rauvolfia cubana	LOTUS Database	35616633
Rauvolfia latifrons	LOTUS Database	35616633
Rauvolfia serpentina	LOTUS Database	35616633
Rauvolfia tetraphylla	LOTUS Database	35616633
Rauvolfia viridis	LOTUS Database	35616633
Rauvolfia volkensii	LOTUS Database	35616633
Rauvolfia yunnanensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as ajmaline-sarpagine alkaloids. These are organic compounds containing either of the ajmalan, sarpagan skeleton, or derivative thereof. The Sarpagine (Akuammidine) group, based on the sarpagan nucleus, arises from bond formation between C-16 and C-5 of the corynantheine precursor. Ajmaline alkaloids are based on a 17,19-secoyohimban skeleton (oxayohimban) which is invariably present as an ether.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Ajmaline-sarpagine alkaloids

Sub Class

Not Available

Direct Parent

Ajmaline-sarpagine alkaloids

Alternative Parents

Substituents

Sarpagine-skeleton
Beta-carboline
Pyridoindole
Quinolizidine
Indole or derivatives
Dialkylarylamine
Quinuclidine
Tertiary aliphatic/aromatic amine
Azepane
Aralkylamine
Benzenoid
Piperidine
Cyclic alcohol
Secondary alcohol
Tertiary amine
Hemiaminal
Organoheterocyclic compound
Azacycle
Alkanolamine
Alcohol
Organopnictogen compound
Organonitrogen compound
Organic oxygen compound
Organic nitrogen compound
Amine
Organooxygen compound
Hydrocarbon derivative
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	1.72	ALOGPS
logP	1.85	ChemAxon
logS	-1.9	ALOGPS
pKa (Strongest Acidic)	13.28	ChemAxon
pKa (Strongest Basic)	7.2	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	46.94 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	92.57 m³·mol⁻¹	ChemAxon
Polarizability	36.6 Å³	ChemAxon
Number of Rings	6	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

2073

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for siddiqui (NP0283759)

MOL for NP0283759 (siddiqui)

3D MOL for NP0283759 (siddiqui)

3D SDF for NP0283759 (siddiqui)

3D-SDF for NP0283759 (siddiqui)

PDB for NP0283759 (siddiqui)

3D PDB for NP0283759 (siddiqui)

SMILES for NP0283759 (siddiqui)

INCHI for NP0283759 (siddiqui)

Structure for NP0283759 (siddiqui)

3D Structure for NP0283759 (siddiqui)