NP-MRD: Showing NP-Card for 18-demethylgardneramine (NP0296243)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-10 05:42:27 UTC

Updated at

2022-09-10 05:42:28 UTC

NP-MRD ID

NP0296243

Secondary Accession Numbers

None

Natural Product Identification

Common Name

18-demethylgardneramine

Description

18-Demethylgardneramine 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. 18-demethylgardneramine is found in Gardneria multiflora. 18-demethylgardneramine was first documented in 2011 (PMID: 21425787). Based on a literature review very few articles have been published on 18-demethylgardneramine.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102207422D          

 29 34  0  0  1  0            999 V2000
    6.6610    0.9310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8517    0.7706    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3082    1.3912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5739    2.1723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0303    2.7929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2960    3.5739    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7525    4.1946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2211    2.6325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6775    3.2531    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8683    3.0927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9554    1.8514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4989    1.2308    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0920    0.5131    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.3029    0.7617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7116    0.1791    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9130    0.3650    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5362    1.1293    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0812    1.7654    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8828    2.2388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1109    1.6568    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1926    2.3227    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1520    2.2584    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7908    1.4582    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3918    2.1823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4304    2.2499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7830    2.9957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6053    3.0632    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9177    2.8496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7467    2.6863    0.0000 N   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  2  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
  5  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  8 11  1  0  0  0  0
 11 12  2  0  0  0  0
  3 12  1  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  1  0  0  0  0
 17 16  1  1  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 20 19  1  6  0  0  0
 14 20  1  0  0  0  0
 11 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 23 22  1  1  0  0  0
 17 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  1  0  0  0  0
 24 28  1  0  0  0  0
 28 29  1  0  0  0  0
 18 29  1  1  0  0  0
 21 29  1  6  0  0  0
M  END

     RDKit          3D

 55 60  0  0  0  0  0  0  0  0999 V2000
   -5.6245    2.8792   -0.2192 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2259    2.8004   -0.3782 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5675    1.5642   -0.3195 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2478    0.3871   -0.1066 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6241   -0.8335   -0.0452 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2890   -2.0381    0.1692 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6684   -2.1391    0.3463 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2326   -0.8532   -0.2103 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5697   -2.0659   -0.1497 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3272   -2.9529   -1.1895 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4936    0.3011   -0.4284 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1853    1.4929   -0.4775 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2564    2.5762   -0.6924 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0680    2.1220   -0.7757 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1132    2.8394   -0.9799 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2628    2.3739   -1.7233 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7603    1.0727   -1.1820 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9622   -0.1344   -1.4431 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5269    0.1313   -1.9272 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0771    0.6221   -0.6227 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8168    0.1256    0.4597 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7051    1.1576    1.0800 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0436    1.1628    0.3235 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6522   -0.1625    0.6684 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9036   -0.2932    1.0870 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4979   -1.6174    1.4273 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9198   -1.6562    2.7643 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7596   -1.3217    0.5102 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6103   -0.8831   -0.2249 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8898    2.7513    0.8467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0637    2.0743   -0.8613 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0396    3.8383   -0.5691 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3307    0.3912    0.0231 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2259   -2.2276   -0.6147 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8606   -3.0525    0.9667 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0639   -1.2818    0.9313 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2213   -3.0403   -1.3471 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8312   -2.5553   -2.1060 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7487   -3.9671   -0.9468 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0709    3.1191   -1.6090 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0498    2.2627   -2.7814 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7828    0.9169   -1.6386 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4638   -0.8493   -2.1202 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5305    0.9035   -2.7252 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1128   -0.8059   -2.2726 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2599   -0.4450    1.2521 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9218    0.7858    2.1285 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2803    2.1461    1.2161 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6694    2.0124    0.5856 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4881    0.6158    1.1737 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8224   -2.4521    1.1868 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4067   -1.7453    0.8029 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7267   -2.2213    2.8738 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2000   -2.1800   -0.0082 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4126   -1.6513    1.5040 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  5  8  2  0
  8  9  1  0
  9 10  1  0
  8 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 28  1  0
 28 29  1  0
 24 25  2  0
 25 26  1  0
 26 27  1  0
 12  3  1  0
 20 14  1  0
 29 21  1  0
 20 11  1  1
 23 17  1  0
 29 18  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  4 33  1  0
  7 34  1  0
  7 35  1  0
  7 36  1  0
 10 37  1  0
 10 38  1  0
 10 39  1  0
 16 40  1  0
 16 41  1  0
 17 42  1  6
 18 43  1  6
 19 44  1  0
 19 45  1  0
 21 46  1  1
 22 47  1  0
 22 48  1  0
 23 49  1  6
 28 54  1  0
 28 55  1  0
 25 50  1  0
 26 51  1  0
 26 52  1  0
 27 53  1  0
M  END


  Mrv1652309102207422D          

 29 34  0  0  1  0            999 V2000
    6.6610    0.9310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8517    0.7706    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3082    1.3912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5739    2.1723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0303    2.7929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2960    3.5739    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7525    4.1946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2211    2.6325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6775    3.2531    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8683    3.0927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9554    1.8514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4989    1.2308    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0920    0.5131    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.3029    0.7617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7116    0.1791    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9130    0.3650    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5362    1.1293    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0812    1.7654    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8828    2.2388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1109    1.6568    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1926    2.3227    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1520    2.2584    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7908    1.4582    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3918    2.1823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4304    2.2499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7830    2.9957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6053    3.0632    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9177    2.8496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7467    2.6863    0.0000 N   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  2  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
  5  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  8 11  1  0  0  0  0
 11 12  2  0  0  0  0
  3 12  1  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  1  0  0  0  0
 17 16  1  1  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 20 19  1  6  0  0  0
 14 20  1  0  0  0  0
 11 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 23 22  1  1  0  0  0
 17 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  1  0  0  0  0
 24 28  1  0  0  0  0
 28 29  1  0  0  0  0
 18 29  1  1  0  0  0
 21 29  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0296243

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(OC)=C(OC)C2=C1N=C1OC[C@@H]3[C@@H]4C[C@]21[C@@H]1C[C@H]3\C(CN41)=C\CO

> <INCHI_IDENTIFIER>
InChI=1S/C22H26N2O5/c1-26-15-7-16(27-2)20(28-3)18-19(15)23-21-22(18)8-14-13(10-29-21)12-6-17(22)24(14)9-11(12)4-5-25/h4,7,12-14,17,25H,5-6,8-10H2,1-3H3/b11-4+/t12-,13-,14-,17-,22-/m0/s1

> <INCHI_KEY>
SGRASRCZUGHSHN-HTEZAAIQSA-N

> <FORMULA>
C22H26N2O5

> <MOLECULAR_WEIGHT>
398.459

> <EXACT_MASS>
398.184171945

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
42.71020107405094

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-[(1R,12S,13S,16Z,17R,19S)-3,4,6-trimethoxy-10-oxa-8,14-diazahexacyclo[11.6.1.0^{1,9}.0^{2,7}.0^{12,17}.0^{14,19}]icosa-2(7),3,5,8-tetraen-16-ylidene]ethan-1-ol

> <JCHEM_LOGP>
0.9657225983333334

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.623916405313214

> <JCHEM_PKA_STRONGEST_BASIC>
8.168417802332899

> <JCHEM_POLAR_SURFACE_AREA>
72.75

> <JCHEM_REFRACTIVITY>
109.28609999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
2-[(1R,12S,13S,16Z,17R,19S)-3,4,6-trimethoxy-10-oxa-8,14-diazahexacyclo[11.6.1.0^{1,9}.0^{2,7}.0^{12,17}.0^{14,19}]icosa-2(7),3,5,8-tetraen-16-ylidene]ethanol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0      12.434   1.738   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      10.923   1.438   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       9.909   2.597   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.405   4.055   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.390   5.213   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       9.886   6.671   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       8.871   7.830   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.879   4.914   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       6.865   6.072   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       5.354   5.773   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.383   3.456   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.398   2.298   0.000  0.00  0.00           C+0
HETATM   13  N   UNK     0       7.638   0.958   0.000  0.00  0.00           N+0
HETATM   14  C   UNK     0       6.165   1.422   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       5.062   0.334   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       3.571   0.681   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.868   2.108   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.885   3.295   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.381   4.179   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.807   3.093   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.093   4.336   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.150   4.216   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.476   2.722   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.731   4.074   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -0.803   4.200   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -1.462   5.592   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -2.997   5.718   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       1.713   5.319   0.000  0.00  0.00           C+0
HETATM   29  N   UNK     0       3.261   5.014   0.000  0.00  0.00           N+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   12                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    8                                                  
CONECT    6    5    7                                                       
CONECT    7    6                                                            
CONECT    8    5    9   11                                                  
CONECT    9    8   10                                                       
CONECT   10    9                                                            
CONECT   11    8   12   20                                                  
CONECT   12   11    3   13                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   20                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   23                                                  
CONECT   18   17   19   29                                                  
CONECT   19   18   20                                                       
CONECT   20   19   14   11   21                                             
CONECT   21   20   22   29                                                  
CONECT   22   21   23                                                       
CONECT   23   22   17   24                                                  
CONECT   24   23   25   28                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26                                                            
CONECT   28   24   29                                                       
CONECT   29   28   18   21                                                  
MASTER        0    0    0    0    0    0    0    0   29    0   68    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₂₆N₂O₅

Average Mass

398.4590 Da

Monoisotopic Mass

398.18417 Da

IUPAC Name

2-[(1R,12S,13S,16Z,17R,19S)-3,4,6-trimethoxy-10-oxa-8,14-diazahexacyclo[11.6.1.0^{1,9}.0^{2,7}.0^{12,17}.0^{14,19}]icosa-2(7),3,5,8-tetraen-16-ylidene]ethan-1-ol

Traditional Name

2-[(1R,12S,13S,16Z,17R,19S)-3,4,6-trimethoxy-10-oxa-8,14-diazahexacyclo[11.6.1.0^{1,9}.0^{2,7}.0^{12,17}.0^{14,19}]icosa-2(7),3,5,8-tetraen-16-ylidene]ethanol

CAS Registry Number

Not Available

SMILES

COC1=CC(OC)=C(OC)C2=C1N=C1OC[C@@H]3[C@@H]4C[C@]21[C@@H]1C[C@H]3\C(CN41)=C\CO

InChI Identifier

InChI=1S/C22H26N2O5/c1-26-15-7-16(27-2)20(28-3)18-19(15)23-21-22(18)8-14-13(10-29-21)12-6-17(22)24(14)9-11(12)4-5-25/h4,7,12-14,17,25H,5-6,8-10H2,1-3H3/b11-4+/t12-,13-,14-,17-,22-/m0/s1

InChI Key

SGRASRCZUGHSHN-HTEZAAIQSA-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
Gardneria multiflora	LOTUS Database	35616633

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
Indolizidine
Anisole
Quinuclidine
Alkyl aryl ether
Oxepane
Aralkylamine
Piperidine
N-alkylpyrrolidine
Benzenoid
Pyrrolidine
Tertiary amine
Tertiary aliphatic amine
Organic 1,3-dipolar compound
Azacycle
Oxacycle
Ether
Propargyl-type 1,3-dipolar organic compound
Alcohol
Primary alcohol
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Organopnictogen compound
Organic oxygen compound
Amine
Organic nitrogen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

tropane alkaloid (CHEBI:67517 )

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	0.97	ChemAxon
pKa (Strongest Acidic)	15.62	ChemAxon
pKa (Strongest Basic)	8.17	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	72.75 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	109.29 m³·mol⁻¹	ChemAxon
Polarizability	42.71 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

35518046

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

70697905

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Li XN, Cai XH, Feng T, Li Y, Liu YP, Luo XD: Monoterpenoid indole alkaloids from Gardneria ovata. J Nat Prod. 2011 May 27;74(5):1073-8. doi: 10.1021/np2000254. Epub 2011 Mar 22. [PubMed:21425787 ]
LOTUS database [Link]

Showing NP-Card for 18-demethylgardneramine (NP0296243)

MOL for NP0296243 (18-demethylgardneramine)

3D MOL for NP0296243 (18-demethylgardneramine)

3D SDF for NP0296243 (18-demethylgardneramine)

3D-SDF for NP0296243 (18-demethylgardneramine)

PDB for NP0296243 (18-demethylgardneramine)

3D PDB for NP0296243 (18-demethylgardneramine)

SMILES for NP0296243 (18-demethylgardneramine)

INCHI for NP0296243 (18-demethylgardneramine)

Structure for NP0296243 (18-demethylgardneramine)

3D Structure for NP0296243 (18-demethylgardneramine)