NP-MRD: Showing NP-Card for (+)-16-Hydroxygalwesine (NP0069374)

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Record Information

Version

2.0

Created at

2022-04-28 14:43:33 UTC

Updated at

2022-04-28 14:43:33 UTC

NP-MRD ID

NP0069374

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(+)-16-Hydroxygalwesine

Description

(+)-16-Hydroxygalwesine belongs to the class of organic compounds known as homolycorine-type amaryllidaceae alkaloids. These are amaryllidaceae alkaloids compounds containing the homolycorine skeleton, made up of a [3,4-g]benzopyranone ring due to the oxidation of the hydroxyl group at the C6. They are biogenetically formed through a restructuring of lycorine-type alkaloids. (+)-16-Hydroxygalwesine is found in Galanthus elewesii and Galanthus elwesii. Based on a literature review very few articles have been published on (+)-16-Hydroxygalwesine.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282216432D          

 27 31  0  0  1  0            999 V2000
    4.8312    2.0036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3415    1.3554    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0353    0.5893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2188    0.4714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7084    1.1196    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0146    1.8857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8919    1.0018    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5857    0.2357    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0960   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9126   -0.2946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4229   -0.9429    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7692    0.1179    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2588    0.7661    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5650    1.5321    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3816    1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5218    2.4630    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.7919    2.8476    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2006    2.2723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2620    2.8274    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7485    1.4143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4630   -0.6482    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6464   -0.7661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1981    1.7679    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1581    1.4732    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4643    2.2393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1374    2.7696    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6271    3.4179    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
  5  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
  4 10  1  0  0  0  0
 10 11  2  0  0  0  0
  8 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
  7 15  1  0  0  0  0
 15 16  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 14 18  1  0  0  0  0
 16 19  1  0  0  0  0
 14 20  1  6  0  0  0
 13 20  1  6  0  0  0
 12 21  1  1  0  0  0
 21 22  1  0  0  0  0
  7 23  1  1  0  0  0
  2 24  1  0  0  0  0
 24 25  1  0  0  0  0
  1 26  1  0  0  0  0
 26 27  1  0  0  0  0
M  END

     RDKit          3D

 50 54  0  0  0  0  0  0  0  0999 V2000
    4.8346    2.8864    1.2861 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4279    1.5437    1.3350 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2039    1.1505    0.7756 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4058    2.0907    0.1789 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1931    1.7096   -0.3770 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7647    0.4014   -0.3460 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5877   -0.5139    0.2588 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8060   -0.1614    0.8231 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6287   -1.0975    1.4317 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3343   -2.4591    1.5424 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5202   -0.0193   -0.9319 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2145   -0.6667   -2.1469 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2360   -1.0405   -0.0798 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8159   -2.3946   -0.3556 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0128   -3.1866    0.8695 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7300   -2.9362   -1.3318 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9671   -2.0979   -1.3220 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7021   -1.0869   -0.2834 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5543   -0.8210    0.7608 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4333    0.1776   -0.1582 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4073    1.2762   -0.0087 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9430    2.5305    0.0666 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6028    3.2110    1.2331 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4647    1.1062   -1.2004 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8345    2.3160   -1.5472 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3720    2.7285   -1.0007 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7433    3.9221   -1.0391 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1527    3.5016    1.9144 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8906    2.9461    1.6154 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7223    3.2866    0.2407 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6914    3.1293    0.1260 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3027   -1.5335    0.3083 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2647   -3.0643    1.6402 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7824   -2.6152    2.5016 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7972   -2.8734    0.6676 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4571   -1.3651   -1.9136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9458   -0.8214    0.9799 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0939   -3.2366    1.0730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6035   -4.2008    0.6980 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4871   -2.7320    1.7276 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0418   -3.9879   -1.0741 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2523   -3.0161   -2.3368 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0133   -1.5755   -2.3210 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8982   -2.6815   -1.1965 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2427    0.3591   -0.8847 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8122    1.0757    0.8887 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4967    3.2947    1.2511 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8749    2.5409    2.0976 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0778    4.1900    1.3108 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0842    0.8102   -2.0950 H   0  0  0  0  0  0  0  0  0  0  0  0
 23 22  1  0
 22 21  1  0
 21 20  1  0
 20 19  1  0
 18 19  1  1
 18 17  1  0
 17 16  1  0
 16 14  1  0
 14 15  1  0
 14 13  1  0
 13 11  1  0
 11 12  1  6
 11 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  2  0
 26  5  1  0
  5  4  2  0
  4  3  1  0
  3  2  1  0
  2  1  1  0
  3  8  2  0
  8  9  1  0
  9 10  1  0
  8  7  1  0
  7  6  2  0
 24 21  1  0
  6  5  1  0
 18 20  1  0
 13 18  1  0
  6 11  1  0
 23 47  1  0
 23 48  1  0
 23 49  1  0
 21 46  1  1
 20 45  1  6
 17 43  1  0
 17 44  1  0
 16 41  1  0
 16 42  1  0
 15 38  1  0
 15 39  1  0
 15 40  1  0
 13 37  1  1
 12 36  1  0
 24 50  1  6
  4 31  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
 10 33  1  0
 10 34  1  0
 10 35  1  0
  7 32  1  0
M  END


  Mrv1652304282216432D          

 27 31  0  0  1  0            999 V2000
    4.8312    2.0036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3415    1.3554    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0353    0.5893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2188    0.4714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7084    1.1196    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0146    1.8857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8919    1.0018    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5857    0.2357    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0960   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9126   -0.2946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4229   -0.9429    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7692    0.1179    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2588    0.7661    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5650    1.5321    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3816    1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5218    2.4630    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.7919    2.8476    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2006    2.2723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2620    2.8274    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7485    1.4143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4630   -0.6482    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6464   -0.7661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1981    1.7679    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1581    1.4732    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4643    2.2393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1374    2.7696    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6271    3.4179    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
  5  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
  4 10  1  0  0  0  0
 10 11  2  0  0  0  0
  8 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
  7 15  1  0  0  0  0
 15 16  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 14 18  1  0  0  0  0
 16 19  1  0  0  0  0
 14 20  1  6  0  0  0
 13 20  1  6  0  0  0
 12 21  1  1  0  0  0
 21 22  1  0  0  0  0
  7 23  1  1  0  0  0
  2 24  1  0  0  0  0
 24 25  1  0  0  0  0
  1 26  1  0  0  0  0
 26 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0069374

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CO[C@H]1[C@@H]2O[C@@]22CCN(C)[C@H]2[C@@]2(O)[C@@H]1OC(=O)C1=CC(OC)=C(OC)C=C21

> <INCHI_IDENTIFIER>
InChI=1S/C19H23NO7/c1-20-6-5-18-14(27-18)13(25-4)15-19(22,17(18)20)10-8-12(24-3)11(23-2)7-9(10)16(21)26-15/h7-8,13-15,17,22H,5-6H2,1-4H3/t13-,14-,15+,17+,18-,19-/m0/s1

> <INCHI_KEY>
GAIZQRCFAUCISE-GBHAUCNQSA-N

> <FORMULA>
C19H23NO7

> <MOLECULAR_WEIGHT>
377.393

> <EXACT_MASS>
377.147452085

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
50

> <JCHEM_AVERAGE_POLARIZABILITY>
38.05886612269903

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,2S,6R,8S,9S,10R)-1-hydroxy-9,15,16-trimethoxy-3-methyl-7,11-dioxa-3-azapentacyclo[8.8.0.0^{2,6}.0^{6,8}.0^{13,18}]octadeca-13,15,17-trien-12-one

> <ALOGPS_LOGP>
0.93

> <JCHEM_LOGP>
0.19872380000000056

> <ALOGPS_LOGS>
-1.94

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.168816038661447

> <JCHEM_PKA_STRONGEST_BASIC>
7.45758742355895

> <JCHEM_POLAR_SURFACE_AREA>
89.99000000000001

> <JCHEM_REFRACTIVITY>
92.72150000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.29e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2S,6R,8S,9S,10R)-1-hydroxy-9,15,16-trimethoxy-3-methyl-7,11-dioxa-3-azapentacyclo[8.8.0.0^{2,6}.0^{6,8}.0^{13,18}]octadeca-13,15,17-trien-12-one

> <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       9.018   3.740   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.971   2.530   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.399   1.100   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.875   0.880   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.922   2.090   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.494   3.520   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.398   1.870   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.827   0.440   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       5.779  -0.770   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       7.303  -0.550   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       8.256  -1.760   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       3.302   0.220   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.350   1.430   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.921   2.860   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.446   3.080   0.000  0.00  0.00           C+0
HETATM   16  N   UNK     0       4.707   4.598   0.000  0.00  0.00           N+0
HETATM   17  C   UNK     0       3.345   5.316   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.241   4.242   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.089   5.278   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       1.397   2.640   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       2.731  -1.210   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       1.207  -1.430   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       5.970   3.300   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0      11.495   2.750   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      12.067   4.180   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       9.590   5.170   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       8.637   6.380   0.000  0.00  0.00           C+0
CONECT    1    2    6   26                                                  
CONECT    2    1    3   24                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   10                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5    8   15   23                                             
CONECT    8    7    9   12                                                  
CONECT    9    8   10                                                       
CONECT   10    9    4   11                                                  
CONECT   11   10                                                            
CONECT   12    8   13   21                                                  
CONECT   13   12   14   20                                                  
CONECT   14   13   15   18   20                                             
CONECT   15   14    7   16                                                  
CONECT   16   15   17   19                                                  
CONECT   17   16   18                                                       
CONECT   18   17   14                                                       
CONECT   19   16                                                            
CONECT   20   14   13                                                       
CONECT   21   12   22                                                       
CONECT   22   21                                                            
CONECT   23    7                                                            
CONECT   24    2   25                                                       
CONECT   25   24                                                            
CONECT   26    1   27                                                       
CONECT   27   26                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   62    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₂₃NO₇

Average Mass

377.3930 Da

Monoisotopic Mass

377.14745 Da

IUPAC Name

(1R,2S,6R,8S,9S,10R)-1-hydroxy-9,15,16-trimethoxy-3-methyl-7,11-dioxa-3-azapentacyclo[8.8.0.0^{2,6}.0^{6,8}.0^{13,18}]octadeca-13,15,17-trien-12-one

Traditional Name

(1R,2S,6R,8S,9S,10R)-1-hydroxy-9,15,16-trimethoxy-3-methyl-7,11-dioxa-3-azapentacyclo[8.8.0.0^{2,6}.0^{6,8}.0^{13,18}]octadeca-13,15,17-trien-12-one

CAS Registry Number

Not Available

SMILES

CO[C@H]1[C@@H]2O[C@@]22CCN(C)[C@H]2[C@@]2(O)[C@@H]1OC(=O)C1=CC(OC)=C(OC)C=C21

InChI Identifier

InChI=1S/C19H23NO7/c1-20-6-5-18-14(27-18)13(25-4)15-19(22,17(18)20)10-8-12(24-3)11(23-2)7-9(10)16(21)26-15/h7-8,13-15,17,22H,5-6H2,1-4H3/t13-,14-,15+,17+,18-,19-/m0/s1

InChI Key

GAIZQRCFAUCISE-GBHAUCNQSA-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
Galanthus elewesii	Plant	KNApSAcK
Galanthus elwesii	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as homolycorine-type amaryllidaceae alkaloids. These are amaryllidaceae alkaloids compounds containing the homolycorine skeleton, made up of a [3,4-g]benzopyranone ring due to the oxidation of the hydroxyl group at the C6. They are biogenetically formed through a restructuring of lycorine-type alkaloids.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Amaryllidaceae alkaloids

Sub Class

Homolycorine-type amaryllidaceae alkaloids

Direct Parent

Homolycorine-type amaryllidaceae alkaloids

Alternative Parents

Substituents

Homolycorine skeleton
Benzopyran
Isochromane
2-benzopyran
Indole or derivatives
Anisole
Alkyl aryl ether
Oxepane
Aralkylamine
N-alkylpyrrolidine
Benzenoid
Pyrrolidine
Tertiary alcohol
Cyclic alcohol
Tertiary amine
1,2-aminoalcohol
Lactone
Tertiary aliphatic amine
Carboxylic acid ester
Amino acid or derivatives
Oxacycle
Carboxylic acid derivative
Azacycle
Organoheterocyclic compound
Dialkyl ether
Oxirane
Ether
Monocarboxylic acid or derivatives
Alcohol
Organic nitrogen compound
Organic oxygen compound
Amine
Organopnictogen compound
Organic oxide
Organooxygen compound
Organonitrogen 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	0.93	ALOGPS
logP	0.2	ChemAxon
logS	-1.9	ALOGPS
pKa (Strongest Acidic)	12.17	ChemAxon
pKa (Strongest Basic)	7.46	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	89.99 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	92.72 m³·mol⁻¹	ChemAxon
Polarizability	38.06 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

101927636

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (+)-16-Hydroxygalwesine (NP0069374)

MOL for NP0069374 ((+)-16-Hydroxygalwesine)

3D MOL for NP0069374 ((+)-16-Hydroxygalwesine)

3D SDF for NP0069374 ((+)-16-Hydroxygalwesine)

3D-SDF for NP0069374 ((+)-16-Hydroxygalwesine)

PDB for NP0069374 ((+)-16-Hydroxygalwesine)

3D PDB for NP0069374 ((+)-16-Hydroxygalwesine)

SMILES for NP0069374 ((+)-16-Hydroxygalwesine)

INCHI for NP0069374 ((+)-16-Hydroxygalwesine)

Structure for NP0069374 ((+)-16-Hydroxygalwesine)

3D Structure for NP0069374 ((+)-16-Hydroxygalwesine)