NP-MRD: Showing NP-Card for Noonindole K (NP0331480)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2023-02-01 04:00:33 UTC

Updated at

2024-09-03 04:15:52 UTC

NP-MRD ID

NP0331480

Natural Product DOI

https://doi.org/10.57994/0434

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Noonindole K

Description

Noonindole K belongs to the class of organic compounds known as sesterterpenoids. These are terpenes composed of five consecutive isoprene units. Noonindole K was first documented in 2023 (PMID: 36662567). Based on a literature review very few articles have been published on Noonindole K.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652302012305002D          

 47 53  0  0  1  0            999 V2000
    3.4402    0.7048    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4433   -0.1202    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3601   -0.9410    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1126   -0.6026    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5538   -1.1156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1957    0.2182    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2789    1.0390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0313    1.3773    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7005    0.8949    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.3698    0.4125    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6174    0.0741    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5342   -0.7467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2035   -1.2291    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2866   -0.4083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0390   -0.0699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1222    0.7509    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.8746    1.0893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2130    0.3368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6270    1.4276    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2963    0.9452    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.0487    1.2836    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.1319    2.1044    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.7179    0.8012    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.4704    1.1396    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.6348   -0.0196    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.3040   -0.5020    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.8824   -0.3580    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.7992   -1.1788    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0468   -1.5172    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2131    0.1244    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5362    1.8417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2054    1.5717    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4530    1.2333    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7083    0.8838    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8650   -0.2643    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9481    0.5565    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7818   -1.0851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0294   -1.4234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6884    0.2125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1386   -0.4026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3837   -0.0699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6313   -0.4083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0379    0.0741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0452    0.8949    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7976    1.2333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4669    0.7509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2732    0.9254    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  3  4  1  6  0  0  0
  3  5  1  0  0  0  0
  2  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  1  0  0  0
  9 11  1  0  0  0  0
 11 12  1  6  0  0  0
 12 13  1  0  0  0  0
 11 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  6  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 20 19  1  1  0  0  0
 20 21  1  0  0  0  0
 21 22  1  1  0  0  0
 21 23  1  0  0  0  0
 23 24  1  1  0  0  0
 23 25  1  0  0  0  0
 25 26  1  6  0  0  0
 25 27  1  0  0  0  0
 27 28  1  1  0  0  0
 28 29  1  0  0  0  0
 27 30  1  0  0  0  0
 20 30  1  0  0  0  0
 17 31  1  0  0  0  0
 16 32  1  1  0  0  0
 16 33  1  0  0  0  0
  9 33  1  0  0  0  0
  6 34  1  6  0  0  0
  6 35  1  0  0  0  0
 11 35  1  0  0  0  0
 35 36  1  1  0  0  0
 35 37  1  0  0  0  0
 37 38  1  0  0  0  0
  3 38  1  0  0  0  0
  2 39  1  0  0  0  0
 39 40  2  0  0  0  0
  5 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  2  0  0  0  0
 42 43  1  0  0  0  0
 43 44  2  0  0  0  0
 44 45  1  0  0  0  0
 45 46  2  0  0  0  0
 41 46  1  0  0  0  0
 46 47  1  0  0  0  0
 39 47  1  0  0  0  0
M  END


  Mrv1652302012305002D          

 47 53  0  0  1  0            999 V2000
    3.4402    0.7048    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4433   -0.1202    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3601   -0.9410    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1126   -0.6026    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5538   -1.1156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1957    0.2182    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2789    1.0390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0313    1.3773    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7005    0.8949    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.3698    0.4125    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6174    0.0741    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5342   -0.7467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2035   -1.2291    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2866   -0.4083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0390   -0.0699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1222    0.7509    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.8746    1.0893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2130    0.3368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6270    1.4276    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2963    0.9452    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.0487    1.2836    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.1319    2.1044    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.7179    0.8012    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.4704    1.1396    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.6348   -0.0196    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.3040   -0.5020    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.8824   -0.3580    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.7992   -1.1788    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0468   -1.5172    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2131    0.1244    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5362    1.8417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2054    1.5717    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4530    1.2333    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7083    0.8838    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8650   -0.2643    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9481    0.5565    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7818   -1.0851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0294   -1.4234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6884    0.2125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1386   -0.4026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3837   -0.0699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6313   -0.4083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0379    0.0741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0452    0.8949    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7976    1.2333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4669    0.7509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2732    0.9254    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  3  4  1  6  0  0  0
  3  5  1  0  0  0  0
  2  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  1  0  0  0
  9 11  1  0  0  0  0
 11 12  1  6  0  0  0
 12 13  1  0  0  0  0
 11 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  6  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 20 19  1  1  0  0  0
 20 21  1  0  0  0  0
 21 22  1  1  0  0  0
 21 23  1  0  0  0  0
 23 24  1  1  0  0  0
 23 25  1  0  0  0  0
 25 26  1  6  0  0  0
 25 27  1  0  0  0  0
 27 28  1  1  0  0  0
 28 29  1  0  0  0  0
 27 30  1  0  0  0  0
 20 30  1  0  0  0  0
 17 31  1  0  0  0  0
 16 32  1  1  0  0  0
 16 33  1  0  0  0  0
  9 33  1  0  0  0  0
  6 34  1  6  0  0  0
  6 35  1  0  0  0  0
 11 35  1  0  0  0  0
 35 36  1  1  0  0  0
 35 37  1  0  0  0  0
 37 38  1  0  0  0  0
  3 38  1  0  0  0  0
  2 39  1  0  0  0  0
 39 40  2  0  0  0  0
  5 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  2  0  0  0  0
 42 43  1  0  0  0  0
 43 44  2  0  0  0  0
 44 45  1  0  0  0  0
 45 46  2  0  0  0  0
 41 46  1  0  0  0  0
 46 47  1  0  0  0  0
 39 47  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0331480

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H][C@]12CC3=C(NC4=CC=CC=C34)[C@]1(C)[C@@]1(C)CC[C@]3([H])O[C@@]([H])(CC[C@@]3(CO)[C@]1([H])CC2)C(C)(C)O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C34H49NO8/c1-31(2,43-30-28(40)27(39)26(38)22(16-36)41-30)24-12-14-34(17-37)23-10-9-18-15-20-19-7-5-6-8-21(19)35-29(20)33(18,4)32(23,3)13-11-25(34)42-24/h5-8,18,22-28,30,35-40H,9-17H2,1-4H3/t18-,22+,23+,24-,25-,26+,27-,28-,30-,32-,33+,34+/m0/s1

> <INCHI_KEY>
ZXLLAVVXCSIHAT-CGSQOTMISA-N

> <FORMULA>
C34H49NO8

> <MOLECULAR_WEIGHT>
599.765

> <EXACT_MASS>
599.345817542

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
92

> <JCHEM_AVERAGE_POLARIZABILITY>
68.07235951270582

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,3S,4S,5S,6S)-2-(hydroxymethyl)-6-({2-[(1S,2S,5S,7S,10S,11R,14S)-10-(hydroxymethyl)-1,2-dimethyl-6-oxa-23-azahexacyclo[12.10.0.0^{2,11}.0^{5,10}.0^{16,24}.0^{17,22}]tetracosa-16(24),17,19,21-tetraen-7-yl]propan-2-yl}oxy)oxane-3,4,5-triol

> <JCHEM_LOGP>
2.584315337333332

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.193978879926679

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.209381498958729

> <JCHEM_PKA_STRONGEST_BASIC>
-2.789449285075439

> <JCHEM_POLAR_SURFACE_AREA>
144.63

> <JCHEM_REFRACTIVITY>
159.21469999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3S,4S,5S,6S)-2-(hydroxymethyl)-6-({2-[(1S,2S,5S,7S,10S,11R,14S)-10-(hydroxymethyl)-1,2-dimethyl-6-oxa-23-azahexacyclo[12.10.0.0^{2,11}.0^{5,10}.0^{16,24}.0^{17,22}]tetracosa-16(24),17,19,21-tetraen-7-yl]propan-2-yl}oxy)oxane-3,4,5-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 01-FEB-23   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   01-FEB-23         0                                  
HETATM    1  C   UNK     0       6.422   1.316   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.428  -0.224   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.272  -1.757   0.000  0.00  0.00           C+0
HETATM    4  H   UNK     0       7.677  -1.125   0.000  0.00  0.00           H+0
HETATM    5  C   UNK     0       4.767  -2.082   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.832   0.407   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.987   1.939   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.392   2.571   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      10.641   1.671   0.000  0.00  0.00           C+0
HETATM   10  H   UNK     0      11.890   0.770   0.000  0.00  0.00           H+0
HETATM   11  C   UNK     0      10.486   0.138   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.331  -1.394   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      11.580  -2.294   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      11.735  -0.762   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      13.140  -0.131   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      13.295   1.402   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      14.699   2.033   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      15.331   0.629   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      16.104   2.665   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      17.353   1.764   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      18.758   2.396   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      18.913   3.928   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      20.007   1.496   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      21.411   2.127   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      19.852  -0.037   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      21.101  -0.937   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      18.447  -0.668   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      18.292  -2.200   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      16.887  -2.832   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0      17.198   0.232   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      14.068   3.438   0.000  0.00  0.00           C+0
HETATM   32  H   UNK     0      13.450   2.934   0.000  0.00  0.00           H+0
HETATM   33  O   UNK     0      12.046   2.302   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       6.922   1.650   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       9.081  -0.493   0.000  0.00  0.00           C+0
HETATM   36  H   UNK     0       9.237   1.039   0.000  0.00  0.00           H+0
HETATM   37  C   UNK     0       8.926  -2.025   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       7.522  -2.657   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       5.018   0.397   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       3.992  -0.752   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       2.583  -0.131   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       1.178  -0.762   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      -0.071   0.138   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       0.084   1.671   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       1.489   2.302   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       2.738   1.402   0.000  0.00  0.00           C+0
HETATM   47  N   UNK     0       4.243   1.727   0.000  0.00  0.00           N+0
CONECT    1    2                                                            
CONECT    2    1    3    6   39                                             
CONECT    3    2    4    5   38                                             
CONECT    4    3                                                            
CONECT    5    3   40                                                       
CONECT    6    2    7   34   35                                             
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11   33                                             
CONECT   10    9                                                            
CONECT   11    9   12   14   35                                             
CONECT   12   11   13                                                       
CONECT   13   12                                                            
CONECT   14   11   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   32   33                                             
CONECT   17   16   18   19   31                                             
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21   30                                                  
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   30                                                  
CONECT   28   27   29                                                       
CONECT   29   28                                                            
CONECT   30   27   20                                                       
CONECT   31   17                                                            
CONECT   32   16                                                            
CONECT   33   16    9                                                       
CONECT   34    6                                                            
CONECT   35    6   11   36   37                                             
CONECT   36   35                                                            
CONECT   37   35   38                                                       
CONECT   38   37    3                                                       
CONECT   39    2   40   47                                                  
CONECT   40   39    5   41                                                  
CONECT   41   40   42   46                                                  
CONECT   42   41   43                                                       
CONECT   43   42   44                                                       
CONECT   44   43   45                                                       
CONECT   45   44   46                                                       
CONECT   46   45   41   47                                                  
CONECT   47   46   39                                                       
MASTER        0    0    0    0    0    0    0    0   47    0  106    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₄H₄₉NO₈

Average Mass

599.7650 Da

Monoisotopic Mass

599.34582 Da

IUPAC Name

(2R,3S,4S,5S,6S)-2-(hydroxymethyl)-6-({2-[(1S,2S,5S,7S,10S,11R,14S)-10-(hydroxymethyl)-1,2-dimethyl-6-oxa-23-azahexacyclo[12.10.0.0^{2,11}.0^{5,10}.0^{16,24}.0^{17,22}]tetracosa-16(24),17,19,21-tetraen-7-yl]propan-2-yl}oxy)oxane-3,4,5-triol

Traditional Name

CAS Registry Number

Not Available

SMILES

[H][C@]12CC3=C(NC4=CC=CC=C34)[C@]1(C)[C@@]1(C)CC[C@]3([H])O[C@@]([H])(CC[C@@]3(CO)[C@]1([H])CC2)C(C)(C)O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]1O

InChI Identifier

InChI=1S/C34H49NO8/c1-31(2,43-30-28(40)27(39)26(38)22(16-36)41-30)24-12-14-34(17-37)23-10-9-18-15-20-19-7-5-6-8-21(19)35-29(20)33(18,4)32(23,3)13-11-25(34)42-24/h5-8,18,22-28,30,35-40H,9-17H2,1-4H3/t18-,22+,23+,24-,25-,26+,27-,28-,30-,32-,33+,34+/m0/s1

InChI Key

ZXLLAVVXCSIHAT-CGSQOTMISA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
HSQC NMR	[¹H, ¹³C] NMR Spectrum (2D, 600 MHz, CD3OD, experimental)	s.kankanamge@imb.uq.edu.au	Not Available	Not Available	2024-05-11	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, CD3OD, experimental)	s.kankanamge@imb.uq.edu.au	Not Available	Not Available	2024-05-11	View Spectrum
COSY NMR	[¹H, ¹H] NMR Spectrum (2D, 600 MHz, CD3OD, experimental)	s.kankanamge@imb.uq.edu.au	Not Available	Not Available	2024-05-11	View Spectrum
HMBC NMR	[¹H, ¹³C] NMR Spectrum (2D, 600 MHz, CD3OD, experimental)	s.kankanamge@imb.uq.edu.au	Not Available	Not Available	2024-05-11	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CD3OD, experimental)	s.kankanamge@imb.uq.edu.au	Not Available	Not Available	2024-05-11	View Spectrum
ROESY NMR	[¹H, ¹H] NMR Spectrum (2D, 600 MHz, CD3OD, experimental)	s.kankanamge@imb.uq.edu.au	Not Available	Not Available	2024-05-11	View Spectrum

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
noonimiae		Not Available

Chemical Taxonomy

Description

This compound belongs to the class of organic compounds known as sesterterpenoids. These are terpenes composed of five consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesterterpenoids

Direct Parent

Sesterterpenoids

Alternative Parents

Substituents

Sesterterpenoid
Fatty acyl glycoside of mono- or disaccharide
Fatty acyl glycoside
Naphthopyran
Alkyl glycoside
Naphthalene
Indole or derivatives
Indole
Fatty acyl
Benzenoid
Pyran
Oxane
Monosaccharide
Heteroaromatic compound
Pyrroline
Pyrrole
Secondary alcohol
Oxacycle
Azacycle
Organoheterocyclic compound
Secondary amine
Ether
Secondary aliphatic amine
Dialkyl ether
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Amine
Alcohol
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	2.58	ChemAxon
pKa (Strongest Acidic)	12.21	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	144.63 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	159.21 m³·mol⁻¹	ChemAxon
Polarizability	68.07 Å³	ChemAxon
Number of Rings	7	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

171358508

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Noonindole K (NP0331480)

MOL for NP0331480 (Noonindole K)

3D MOL for NP0331480 (Noonindole K)

3D SDF for NP0331480 (Noonindole K)

3D-SDF for NP0331480 (Noonindole K)

PDB for NP0331480 (Noonindole K)

3D PDB for NP0331480 (Noonindole K)

SMILES for NP0331480 (Noonindole K)

INCHI for NP0331480 (Noonindole K)

Structure for NP0331480 (Noonindole K)

3D Structure for NP0331480 (Noonindole K)