NP-MRD: Showing NP-Card for 9-methoxy-4-methyl-11-oxa-4-azatetracyclo[8.6.1.0¹,¹².0⁶,¹⁷]heptadeca-6,8,10(17),15-tetraen-14-yl 3-hydroxybutanoate (NP0258060)

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Record Information

Version

2.0

Created at

2022-09-07 23:21:22 UTC

Updated at

2022-09-07 23:21:22 UTC

NP-MRD ID

NP0258060

Secondary Accession Numbers

None

Natural Product Identification

Common Name

9-methoxy-4-methyl-11-oxa-4-azatetracyclo[8.6.1.0¹,¹².0⁶,¹⁷]heptadeca-6,8,10(17),15-tetraen-14-yl 3-hydroxybutanoate

Description

9-Methoxy-4-methyl-11-oxa-4-azatetracyclo[8.6.1.0¹,¹².0⁶,¹⁷]Heptadeca-6(17),7,9,15-tetraen-14-yl 3-hydroxybutanoate belongs to the class of organic compounds known as galanthamine-type amaryllidaceae alkaloids. These are amaryllidaceae alkaloids with a structure characterized a tetracyclic skeleton with two ortho aromatic protons in ring A. 9-methoxy-4-methyl-11-oxa-4-azatetracyclo[8.6.1.0¹,¹².0⁶,¹⁷]heptadeca-6,8,10(17),15-tetraen-14-yl 3-hydroxybutanoate is found in Galanthus elwesii. 9-Methoxy-4-methyl-11-oxa-4-azatetracyclo[8.6.1.0¹,¹².0⁶,¹⁷]Heptadeca-6(17),7,9,15-tetraen-14-yl 3-hydroxybutanoate is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004231522222D          

 27 30  0  0  0  0            999 V2000
    0.2864   -0.5910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0930   -0.4177    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3462    0.3675    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7929    0.9793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0461    1.7645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8903    1.9698    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9598    2.7694    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4806    3.4230    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3019    4.2284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2363    3.0474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1140    2.1983    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2310    1.3277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7817    1.9420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5891    1.7723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8457    0.9882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2950    0.3739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4877    0.5437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8213    0.0573    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1528    0.5408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4060    1.3259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6531    0.8184    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9097    0.0344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3590   -0.5799    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7171   -0.1354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9737   -0.9194    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7811   -1.0892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4230   -1.5337    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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  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  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
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 12 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
  3 19  1  0  0  0  0
 19 20  2  0  0  0  0
  6 20  1  0  0  0  0
 12 20  1  0  0  0  0
 15 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
M  END

     RDKit          3D

 54 57  0  0  0  0  0  0  0  0999 V2000
   -4.6780    4.7646    0.6998 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5309    3.9824    0.6624 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4333    2.6858    0.2849 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5778    1.9921   -0.1264 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5396    0.6660   -0.5216 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3409    0.0043   -0.5135 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2066    0.6627   -0.1198 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2346    1.9761    0.2786 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9495    2.3759    0.6388 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0821    1.4642    0.1509 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2084    1.1344    0.7845 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9163    0.2468   -0.2115 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7213   -0.7248    0.4139 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0912   -0.7634    0.3454 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6419    0.1620   -0.3422 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9281   -1.7883    1.0059 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3877   -1.5154    0.7126 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.7100   -1.5420   -0.7461 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8173   -0.3295    1.2860 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0995   -0.3023   -1.3040 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2252   -0.3535   -1.3020 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8405    0.2101   -0.0614 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8000   -0.8581    1.0116 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3976   -2.0951    0.3314 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7958   -2.1575    0.2457 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5104   -2.0013    1.4695 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4369   -1.4716   -0.8669 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5176    4.3035    1.2607 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5440    5.7723    1.0835 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0517    4.8605   -0.3553 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5107    2.5340   -0.1259 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4389    0.1746   -0.8269 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2097    1.8366   -0.8981 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1257    0.6595    1.7839 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8276    2.0374    0.9479 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6683    0.9248   -0.7396 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6388   -2.8163    0.8023 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8045   -1.6341    2.1131 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9567   -2.3346    1.2431 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9422   -0.5323   -1.1407 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8404   -1.9729   -1.2845 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5765   -2.2192   -0.9867 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4742   -0.2551    2.2227 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6635   -0.6968   -2.1859 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7735   -0.7587   -2.1199 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1927   -1.1277    1.3585 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4203   -0.5321    1.8580 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9629   -2.1949   -0.6856 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0363   -2.9897    0.9007 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4713   -2.5852    1.3682 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7962   -0.9631    1.6834 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9512   -2.4716    2.2777 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8985   -1.7011   -1.7865 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4898   -1.7418   -0.8667 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  2  0
  6 27  1  0
 27 25  1  0
 25 26  1  0
 25 24  1  0
 24 23  1  0
 23 22  1  0
 22 21  1  6
 21 20  2  0
 20 12  1  0
 12 11  1  0
 11 10  1  0
 10  9  1  0
  9  8  1  0
  8  7  2  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 14 16  1  0
 16 17  1  0
 17 18  1  0
 17 19  1  0
  8  3  1  0
  7  6  1  0
 10 22  1  0
  7 22  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  4 31  1  0
  5 32  1  0
 27 53  1  0
 27 54  1  0
 26 50  1  0
 26 51  1  0
 26 52  1  0
 24 48  1  0
 24 49  1  0
 23 46  1  0
 23 47  1  0
 21 45  1  0
 20 44  1  0
 12 36  1  6
 11 34  1  0
 11 35  1  0
 10 33  1  6
 16 37  1  0
 16 38  1  0
 17 39  1  1
 18 40  1  0
 18 41  1  0
 18 42  1  0
 19 43  1  0
M  END


  Mrv1533004231522222D          

 27 30  0  0  0  0            999 V2000
    0.2864   -0.5910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0930   -0.4177    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3462    0.3675    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7929    0.9793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0461    1.7645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8903    1.9698    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9598    2.7694    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4806    3.4230    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3019    4.2284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2363    3.0474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1140    2.1983    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2310    1.3277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7817    1.9420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5891    1.7723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8457    0.9882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2950    0.3739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4877    0.5437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8213    0.0573    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1528    0.5408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4060    1.3259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6531    0.8184    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9097    0.0344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3590   -0.5799    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7171   -0.1354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9737   -0.9194    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7811   -1.0892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4230   -1.5337    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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  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  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
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 12 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
  3 19  1  0  0  0  0
 19 20  2  0  0  0  0
  6 20  1  0  0  0  0
 12 20  1  0  0  0  0
 15 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0258060

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C2CN(C)CCC34C=CC(CC3OC1=C24)OC(=O)CC(C)O

> <INCHI_IDENTIFIER>
InChI=1S/C21H27NO5/c1-13(23)10-18(24)26-15-6-7-21-8-9-22(2)12-14-4-5-16(25-3)20(19(14)21)27-17(21)11-15/h4-7,13,15,17,23H,8-12H2,1-3H3

> <INCHI_KEY>
MJSGJSLIEXDCKY-UHFFFAOYSA-N

> <FORMULA>
C21H27NO5

> <MOLECULAR_WEIGHT>
373.449

> <EXACT_MASS>
373.188922973

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
41.03056131111726

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
9-methoxy-4-methyl-11-oxa-4-azatetracyclo[8.6.1.0¹,¹².0⁶,¹⁷]heptadeca-6,8,10(17),15-tetraen-14-yl 3-hydroxybutanoate

> <ALOGPS_LOGP>
1.92

> <JCHEM_LOGP>
1.4405079289999994

> <ALOGPS_LOGS>
-2.97

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.407199790345835

> <JCHEM_PKA_STRONGEST_BASIC>
8.738997824452202

> <JCHEM_POLAR_SURFACE_AREA>
68.23

> <JCHEM_REFRACTIVITY>
102.2768

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.03e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
9-methoxy-4-methyl-11-oxa-4-azatetracyclo[8.6.1.0¹,¹².0⁶,¹⁷]heptadeca-6,8,10(17),15-tetraen-14-yl 3-hydroxybutanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 23-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-APR-15         0                                  
HETATM    1  C   UNK     0       0.535  -1.103   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       2.040  -0.780   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       2.513   0.686   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.480   1.828   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.953   3.294   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.528   3.677   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.658   5.169   0.000  0.00  0.00           C+0
HETATM    8  N   UNK     0       4.631   6.390   0.000  0.00  0.00           N+0
HETATM    9  C   UNK     0       4.297   7.893   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.041   5.688   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.813   4.103   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.031   2.478   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.059   3.625   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.566   3.308   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.045   1.845   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.017   0.698   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.510   1.015   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       5.266   0.107   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       4.019   1.009   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.491   2.475   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      10.552   1.528   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      11.032   0.064   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      10.004  -1.083   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      12.539  -0.253   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      13.018  -1.716   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      14.525  -2.033   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      11.990  -2.863   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   19                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   20                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   17   20                                             
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   21                                                  
CONECT   16   15   17                                                       
CONECT   17   16   12   18                                                  
CONECT   18   17   19                                                       
CONECT   19   18    3   20                                                  
CONECT   20   19    6   12                                                  
CONECT   21   15   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   60    0
END

View in JSmol

Synonyms

Value	Source
9-Methoxy-4-methyl-11-oxa-4-azatetracyclo[8.6.1.0,.0,]heptadeca-6(17),7,9,15-tetraen-14-yl 3-hydroxybutanoic acid	Generator
9-Methoxy-4-methyl-11-oxa-4-azatetracyclo[8.6.1.0¹,¹².0⁶,¹⁷]heptadeca-6(17),7,9,15-tetraen-14-yl 3-hydroxybutanoic acid	Generator

Chemical Formula

C₂₁H₂₇NO₅

Average Mass

373.4490 Da

Monoisotopic Mass

373.18892 Da

IUPAC Name

9-methoxy-4-methyl-11-oxa-4-azatetracyclo[8.6.1.0¹,¹².0⁶,¹⁷]heptadeca-6,8,10(17),15-tetraen-14-yl 3-hydroxybutanoate

Traditional Name

9-methoxy-4-methyl-11-oxa-4-azatetracyclo[8.6.1.0¹,¹².0⁶,¹⁷]heptadeca-6,8,10(17),15-tetraen-14-yl 3-hydroxybutanoate

CAS Registry Number

Not Available

SMILES

COC1=CC=C2CN(C)CCC34C=CC(CC3OC1=C24)OC(=O)CC(C)O

InChI Identifier

InChI=1S/C21H27NO5/c1-13(23)10-18(24)26-15-6-7-21-8-9-22(2)12-14-4-5-16(25-3)20(19(14)21)27-17(21)11-15/h4-7,13,15,17,23H,8-12H2,1-3H3

InChI Key

MJSGJSLIEXDCKY-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
Galanthus elwesii	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as galanthamine-type amaryllidaceae alkaloids. These are amaryllidaceae alkaloids with a structure characterized a tetracyclic skeleton with two ortho aromatic protons in ring A.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Amaryllidaceae alkaloids

Sub Class

Galanthamine-type amaryllidaceae alkaloids

Direct Parent

Galanthamine-type amaryllidaceae alkaloids

Alternative Parents

Substituents

Galanthamine-type amaryllidaceae alkaloid
Benzazepine
Coumaran
Anisole
Alkyl aryl ether
Azepine
Beta-hydroxy acid
Fatty acid ester
Aralkylamine
Fatty acyl
Benzenoid
Hydroxy acid
Carboxylic acid ester
Amino acid or derivatives
Tertiary aliphatic amine
Tertiary amine
Secondary alcohol
Oxacycle
Azacycle
Carboxylic acid derivative
Ether
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Organic oxide
Carbonyl group
Amine
Organic oxygen compound
Alcohol
Organic nitrogen compound
Hydrocarbon derivative
Organopnictogen compound
Organooxygen compound
Organonitrogen compound
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	1.92	ALOGPS
logP	1.44	ChemAxon
logS	-3	ALOGPS
pKa (Strongest Acidic)	15.41	ChemAxon
pKa (Strongest Basic)	8.74	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	68.23 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	102.28 m³·mol⁻¹	ChemAxon
Polarizability	41.03 Å³	ChemAxon
Number of Rings	4	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 9-methoxy-4-methyl-11-oxa-4-azatetracyclo[8.6.1.0¹,¹².0⁶,¹⁷]heptadeca-6,8,10(17),15-tetraen-14-yl 3-hydroxybutanoate (NP0258060)

MOL for NP0258060 (9-methoxy-4-methyl-11-oxa-4-azatetracyclo[8.6.1.0¹,¹².0⁶,¹⁷]heptadeca-6,8,10(17),15-tetraen-14-yl 3-hydroxybutanoate)

3D MOL for NP0258060 (9-methoxy-4-methyl-11-oxa-4-azatetracyclo[8.6.1.0¹,¹².0⁶,¹⁷]heptadeca-6,8,10(17),15-tetraen-14-yl 3-hydroxybutanoate)

3D SDF for NP0258060 (9-methoxy-4-methyl-11-oxa-4-azatetracyclo[8.6.1.0¹,¹².0⁶,¹⁷]heptadeca-6,8,10(17),15-tetraen-14-yl 3-hydroxybutanoate)

3D-SDF for NP0258060 (9-methoxy-4-methyl-11-oxa-4-azatetracyclo[8.6.1.0¹,¹².0⁶,¹⁷]heptadeca-6,8,10(17),15-tetraen-14-yl 3-hydroxybutanoate)

PDB for NP0258060 (9-methoxy-4-methyl-11-oxa-4-azatetracyclo[8.6.1.0¹,¹².0⁶,¹⁷]heptadeca-6,8,10(17),15-tetraen-14-yl 3-hydroxybutanoate)

3D PDB for NP0258060 (9-methoxy-4-methyl-11-oxa-4-azatetracyclo[8.6.1.0¹,¹².0⁶,¹⁷]heptadeca-6,8,10(17),15-tetraen-14-yl 3-hydroxybutanoate)

SMILES for NP0258060 (9-methoxy-4-methyl-11-oxa-4-azatetracyclo[8.6.1.0¹,¹².0⁶,¹⁷]heptadeca-6,8,10(17),15-tetraen-14-yl 3-hydroxybutanoate)

INCHI for NP0258060 (9-methoxy-4-methyl-11-oxa-4-azatetracyclo[8.6.1.0¹,¹².0⁶,¹⁷]heptadeca-6,8,10(17),15-tetraen-14-yl 3-hydroxybutanoate)

Structure for NP0258060 (9-methoxy-4-methyl-11-oxa-4-azatetracyclo[8.6.1.0¹,¹².0⁶,¹⁷]heptadeca-6,8,10(17),15-tetraen-14-yl 3-hydroxybutanoate)

3D Structure for NP0258060 (9-methoxy-4-methyl-11-oxa-4-azatetracyclo[8.6.1.0¹,¹².0⁶,¹⁷]heptadeca-6,8,10(17),15-tetraen-14-yl 3-hydroxybutanoate)