NP-MRD: Showing NP-Card for (2z)-2-[(3s,6'r,7's,8'as)-6'-ethyl-2-hydroxy-3',5',6',7',8',8'a-hexahydro-2'h-spiro[indole-3,1'-indolizin]-7'-yl]-3-methoxyprop-2-enoic acid (NP0163974)

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Record Information

Version

2.0

Created at

2022-09-02 22:45:33 UTC

Updated at

2022-09-02 22:45:34 UTC

NP-MRD ID

NP0163974

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2z)-2-[(3s,6'r,7's,8'as)-6'-ethyl-2-hydroxy-3',5',6',7',8',8'a-hexahydro-2'h-spiro[indole-3,1'-indolizin]-7'-yl]-3-methoxyprop-2-enoic acid

Description

2-[(3S,6'R,7'S,8'aS)-6'-ethyl-2-hydroxy-3',5',6',7',8',8'a-hexahydro-2'H-spiro[indole-3,1'-indolizine]-7'-yl]-3-methoxyprop-2-enoic acid 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. (2z)-2-[(3s,6'r,7's,8'as)-6'-ethyl-2-hydroxy-3',5',6',7',8',8'a-hexahydro-2'h-spiro[indole-3,1'-indolizin]-7'-yl]-3-methoxyprop-2-enoic acid is found in Uncaria sinensis. Based on a literature review very few articles have been published on 2-[(3S,6'R,7'S,8'aS)-6'-ethyl-2-hydroxy-3',5',6',7',8',8'a-hexahydro-2'H-spiro[indole-3,1'-indolizine]-7'-yl]-3-methoxyprop-2-enoic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032200452D          

 27 30  0  0  1  0            999 V2000
    1.8079   -1.0420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6363   -0.2350    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2494    0.3170    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0779    1.1240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6910    1.6761    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.6910    2.5011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4756    2.7560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9605    2.0886    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4455    2.7560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1905    3.5406    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2301    2.5011    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.2301    1.6761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8432    1.1240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6716    0.3170    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8870    0.0621    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2739    0.6141    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4455    1.4211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4756    1.4211    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6471    0.6141    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0340    0.0621    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2056   -0.7449    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5925   -1.2969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7640   -2.1039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5486   -2.3588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9902   -0.9998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1617   -1.8068    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6033   -0.4478    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  1  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
  8  7  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 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
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 12 17  1  0  0  0  0
  8 17  1  0  0  0  0
  8 18  1  0  0  0  0
 18  5  1  6  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
  3 20  1  0  0  0  0
 20 21  1  6  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 21 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
M  END

     RDKit          3D

 53 56  0  0  0  0  0  0  0  0999 V2000
    1.5898   -3.6434    0.7306 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2405   -2.2365    0.8810 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1329   -1.2639    0.7055 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0424   -1.4210    1.7404 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6898   -0.2710    2.0375 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0192   -0.6145    2.5016 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9807    0.4000    1.9475 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2555    0.9190    0.7150 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6310    2.3139    0.4207 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3982    3.4096    1.2742 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1929    2.3450   -0.7234 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2637    1.0582   -1.3104 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7933    0.6576   -2.5385 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7549   -0.6582   -2.9142 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1866   -1.5721   -2.0609 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6780   -1.1607   -0.8722 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6899    0.1687   -0.4371 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8188    0.7759    1.1052 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1376    0.8015   -0.0447 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4283    0.1602    0.4938 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6071    0.5484   -0.2582 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5170    1.1686   -1.4564 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6650    1.5263   -2.1474 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9232    2.9018   -2.4010 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9639    0.3607    0.2212 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2321   -0.1827    1.3222 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0859    0.7777   -0.5090 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9291   -3.8190    1.5818 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3855   -4.4079    0.6599 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0531   -3.6283   -0.2348 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6978   -2.2192    1.8968 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9513   -2.1890    0.0631 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6166   -1.6065   -0.2727 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6293   -2.2694    1.5009 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5782   -1.7527    2.6803 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3263   -1.6214    2.1407 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0750   -0.6084    3.6136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9412   -0.0918    1.6655 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1771    1.2211    2.6773 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7594    4.1419    1.0672 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2442    1.3653   -3.2215 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1676   -0.9895   -3.8779 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1594   -2.6114   -2.3643 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2409   -1.8799   -0.2249 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5928    1.7236    1.6945 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2352    0.2601   -0.9132 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3913    1.8592   -0.3072 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5442    0.6022    1.5532 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5255    1.3724   -1.8520 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8657    3.0389   -2.9564 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1001    3.3356   -3.0061 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9735    3.4824   -1.4659 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7233    0.0226   -0.7842 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  1  0
 21 25  1  0
 25 27  1  0
 25 26  2  0
  8  9  1  6
  9 10  1  0
  9 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 20  3  1  0
 17 12  1  0
 18  5  1  0
 17  8  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  2 31  1  0
  2 32  1  0
  3 33  1  6
  4 34  1  0
  4 35  1  0
  6 36  1  0
  6 37  1  0
  7 38  1  0
  7 39  1  0
 18 45  1  1
 19 46  1  0
 19 47  1  0
 20 48  1  1
 22 49  1  0
 24 50  1  0
 24 51  1  0
 24 52  1  0
 27 53  1  0
 10 40  1  0
 13 41  1  0
 14 42  1  0
 15 43  1  0
 16 44  1  0
M  END


  Mrv1652309032200452D          

 27 30  0  0  1  0            999 V2000
    1.8079   -1.0420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6363   -0.2350    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2494    0.3170    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0779    1.1240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6910    1.6761    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.6910    2.5011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4756    2.7560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9605    2.0886    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4455    2.7560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1905    3.5406    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2301    2.5011    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.2301    1.6761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8432    1.1240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6716    0.3170    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8870    0.0621    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2739    0.6141    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4455    1.4211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4756    1.4211    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6471    0.6141    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0340    0.0621    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2056   -0.7449    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5925   -1.2969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7640   -2.1039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5486   -2.3588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9902   -0.9998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1617   -1.8068    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6033   -0.4478    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  1  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
  8  7  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 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
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 12 17  1  0  0  0  0
  8 17  1  0  0  0  0
  8 18  1  0  0  0  0
 18  5  1  6  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
  3 20  1  0  0  0  0
 20 21  1  6  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 21 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0163974

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@H]1CN2CC[C@]3([C@@H]2C[C@@H]1\C(=C\OC)C(O)=O)C(O)=NC1=CC=CC=C31

> <INCHI_IDENTIFIER>
InChI=1S/C21H26N2O4/c1-3-13-11-23-9-8-21(16-6-4-5-7-17(16)22-20(21)26)18(23)10-14(13)15(12-27-2)19(24)25/h4-7,12-14,18H,3,8-11H2,1-2H3,(H,22,26)(H,24,25)/b15-12-/t13-,14-,18-,21-/m0/s1

> <INCHI_KEY>
IQSFEAHJUMVILC-FJGFRUQDSA-N

> <FORMULA>
C21H26N2O4

> <MOLECULAR_WEIGHT>
370.449

> <EXACT_MASS>
370.189257325

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
39.67252402282847

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2Z)-2-[(3S,6'R,7'S,8'aS)-6'-ethyl-2-hydroxy-3',5',6',7',8',8'a-hexahydro-2'H-spiro[indole-3,1'-indolizine]-7'-yl]-3-methoxyprop-2-enoic acid

> <ALOGPS_LOGP>
2.31

> <JCHEM_LOGP>
-0.07002302667184632

> <ALOGPS_LOGS>
-3.31

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
4.111473258778826

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.444961497578706

> <JCHEM_PKA_STRONGEST_BASIC>
11.25772363676287

> <JCHEM_POLAR_SURFACE_AREA>
82.36

> <JCHEM_REFRACTIVITY>
103.99199999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.83e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2Z)-2-[(3S,6'R,7'S,8'aS)-6'-ethyl-2-hydroxy-3',5',6',7',8',8'a-hexahydro-2'H-spiro[indole-3,1'-indolizine]-7'-yl]-3-methoxyprop-2-enoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0       3.375  -1.945   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.054  -0.439   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.199   0.592   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.879   2.098   0.000  0.00  0.00           C+0
HETATM    5  N   UNK     0       5.023   3.129   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0       5.023   4.669   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.488   5.145   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.393   3.899   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.298   5.145   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       7.822   6.609   0.000  0.00  0.00           O+0
HETATM   11  N   UNK     0       9.763   4.669   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0       9.763   3.129   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.907   2.098   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      10.587   0.592   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.122   0.116   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.978   1.146   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.298   2.653   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.488   2.653   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.808   1.146   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.664   0.116   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.984  -1.390   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.839  -2.421   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       5.159  -3.927   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       6.624  -4.403   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       7.448  -1.866   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       7.769  -3.373   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       8.593  -0.836   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   20                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   18                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   17   18                                             
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13   17                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   12    8                                                  
CONECT   18    8    5   19                                                  
CONECT   19   18   20                                                       
CONECT   20   19    3   21                                                  
CONECT   21   20   22   25                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23                                                            
CONECT   25   21   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
2-[(3S,6'r,7's,8'AS)-6'-ethyl-2-hydroxy-3',5',6',7',8',8'a-hexahydro-2'H-spiro[indole-3,1'-indolizine]-7'-yl]-3-methoxyprop-2-enoate	Generator

Chemical Formula

C₂₁H₂₆N₂O₄

Average Mass

370.4490 Da

Monoisotopic Mass

370.18926 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC[C@H]1CN2CC[C@]3([C@@H]2C[C@@H]1\C(=C\OC)C(O)=O)C(O)=NC1=CC=CC=C31

InChI Identifier

InChI=1S/C21H26N2O4/c1-3-13-11-23-9-8-21(16-6-4-5-7-17(16)22-20(21)26)18(23)10-14(13)15(12-27-2)19(24)25/h4-7,12-14,18H,3,8-11H2,1-2H3,(H,22,26)(H,24,25)/b15-12-/t13-,14-,18-,21-/m0/s1

InChI Key

IQSFEAHJUMVILC-FJGFRUQDSA-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
Uncaria sinensis	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
Aralkylamine
Benzenoid
N-alkylpyrrolidine
Piperidine
Vinylogous ester
Cyclic carboximidic acid
Pyrrolidine
Amino acid
Tertiary aliphatic amine
Tertiary amine
Amino acid or derivatives
Azacycle
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Amine
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source

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

114544604

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

134715415

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2z)-2-[(3s,6'r,7's,8'as)-6'-ethyl-2-hydroxy-3',5',6',7',8',8'a-hexahydro-2'h-spiro[indole-3,1'-indolizin]-7'-yl]-3-methoxyprop-2-enoic acid (NP0163974)

MOL for NP0163974 ((2z)-2-[(3s,6'r,7's,8'as)-6'-ethyl-2-hydroxy-3',5',6',7',8',8'a-hexahydro-2'h-spiro[indole-3,1'-indolizin]-7'-yl]-3-methoxyprop-2-enoic acid)

3D MOL for NP0163974 ((2z)-2-[(3s,6'r,7's,8'as)-6'-ethyl-2-hydroxy-3',5',6',7',8',8'a-hexahydro-2'h-spiro[indole-3,1'-indolizin]-7'-yl]-3-methoxyprop-2-enoic acid)

3D SDF for NP0163974 ((2z)-2-[(3s,6'r,7's,8'as)-6'-ethyl-2-hydroxy-3',5',6',7',8',8'a-hexahydro-2'h-spiro[indole-3,1'-indolizin]-7'-yl]-3-methoxyprop-2-enoic acid)

3D-SDF for NP0163974 ((2z)-2-[(3s,6'r,7's,8'as)-6'-ethyl-2-hydroxy-3',5',6',7',8',8'a-hexahydro-2'h-spiro[indole-3,1'-indolizin]-7'-yl]-3-methoxyprop-2-enoic acid)

PDB for NP0163974 ((2z)-2-[(3s,6'r,7's,8'as)-6'-ethyl-2-hydroxy-3',5',6',7',8',8'a-hexahydro-2'h-spiro[indole-3,1'-indolizin]-7'-yl]-3-methoxyprop-2-enoic acid)

3D PDB for NP0163974 ((2z)-2-[(3s,6'r,7's,8'as)-6'-ethyl-2-hydroxy-3',5',6',7',8',8'a-hexahydro-2'h-spiro[indole-3,1'-indolizin]-7'-yl]-3-methoxyprop-2-enoic acid)

SMILES for NP0163974 ((2z)-2-[(3s,6'r,7's,8'as)-6'-ethyl-2-hydroxy-3',5',6',7',8',8'a-hexahydro-2'h-spiro[indole-3,1'-indolizin]-7'-yl]-3-methoxyprop-2-enoic acid)

INCHI for NP0163974 ((2z)-2-[(3s,6'r,7's,8'as)-6'-ethyl-2-hydroxy-3',5',6',7',8',8'a-hexahydro-2'h-spiro[indole-3,1'-indolizin]-7'-yl]-3-methoxyprop-2-enoic acid)

Structure for NP0163974 ((2z)-2-[(3s,6'r,7's,8'as)-6'-ethyl-2-hydroxy-3',5',6',7',8',8'a-hexahydro-2'h-spiro[indole-3,1'-indolizin]-7'-yl]-3-methoxyprop-2-enoic acid)

3D Structure for NP0163974 ((2z)-2-[(3s,6'r,7's,8'as)-6'-ethyl-2-hydroxy-3',5',6',7',8',8'a-hexahydro-2'h-spiro[indole-3,1'-indolizin]-7'-yl]-3-methoxyprop-2-enoic acid)