NP-MRD: Showing NP-Card for Glenthamine A (NP0333201)

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Record Information

Version

2.0

Created at

2024-05-12 13:24:16 UTC

Updated at

2024-09-03 04:21:33 UTC

NP-MRD ID

NP0333201

Natural Product DOI

https://doi.org/10.57994/2526

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Glenthamine A

Description

Glenthamine A belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. Glenthamine A was first documented in 2021 (PMID: 34652159). Based on a literature review very few articles have been published on Glenthamine A.

Structure

MOL SDF PDB SMILES InChI


  Mrv2104 01242316002D          

 56 62  0  0  1  0            999 V2000
    2.1190   -0.4347    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3069    0.5364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4520    0.8248    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2418   -0.2662    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9856    0.0907    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2592    0.8690    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9023    1.6128    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3681    2.2938    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1907    2.2310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5475    1.4871    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0818    0.8062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4387    0.0623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0725   -0.8926    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2613   -0.0005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7270    0.6805    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6545    0.6982    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3254    1.2385    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.0948    0.9407    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7374    1.4582    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5068    1.1604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6105    2.2734    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1986    2.0537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4292    2.3514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7866    1.8340    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3024    3.1666    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3701    1.4243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6282    0.7798    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2085    1.6131    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3802    1.5295    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1066    0.7512    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4635    0.0074    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3539    0.1189    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1098   -0.6484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9509   -0.6545    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3583   -1.3719    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3685    0.0570    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2193    2.1854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7694    2.2181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5737    2.0349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1346    2.6399    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0081    3.5545    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9390    2.4566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1825    1.6684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6217    1.0634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8652    0.2752    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1984    1.0299    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6460    0.0088    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.6340   -0.8161    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.2944   -1.3106    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1962   -2.1298    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0528   -0.9861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4931   -1.6290    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8458   -1.0596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3706   -0.3852    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8173    1.2466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1980    2.9254    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  3  2  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
  6 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 17 16  1  0  0  0  0
 17 18  1  1  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
 17 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  2  0  0  0  0
 15 26  2  0  0  0  0
 10 26  1  0  0  0  0
  3 27  1  1  0  0  0
  3 28  1  0  0  0  0
 28  7  1  6  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 31 30  1  0  0  0  0
  4 31  1  0  0  0  0
 31 32  1  1  0  0  0
 31 33  1  6  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  2  0  0  0  0
 29 37  1  1  0  0  0
 28 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  2  0  0  0  0
 40 41  1  0  0  0  0
 40 42  1  0  0  0  0
 42 43  2  0  0  0  0
 43 44  1  0  0  0  0
 45 44  1  6  0  0  0
 45 46  1  1  0  0  0
 45 47  1  0  0  0  0
 48 47  1  0  0  0  0
 48 49  1  6  0  0  0
 49 50  1  1  0  0  0
 49 51  1  0  0  0  0
 48 52  1  1  0  0  0
 48 53  1  0  0  0  0
 53 54  1  0  0  0  0
 45 54  1  0  0  0  0
 44 55  2  0  0  0  0
 39 55  1  0  0  0  0
  2 55  1  0  0  0  0
 38 56  2  0  0  0  0
M  END


  Mrv2104 01242316002D          

 56 62  0  0  1  0            999 V2000
    2.1190   -0.4347    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3069    0.5364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4520    0.8248    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2418   -0.2662    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9856    0.0907    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2592    0.8690    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9023    1.6128    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3681    2.2938    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1907    2.2310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5475    1.4871    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0818    0.8062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4387    0.0623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0725   -0.8926    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2613   -0.0005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7270    0.6805    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6545    0.6982    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3254    1.2385    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.0948    0.9407    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7374    1.4582    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5068    1.1604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6105    2.2734    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1986    2.0537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4292    2.3514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7866    1.8340    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3024    3.1666    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3701    1.4243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6282    0.7798    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2085    1.6131    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3802    1.5295    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1066    0.7512    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4635    0.0074    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3539    0.1189    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1098   -0.6484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9509   -0.6545    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3583   -1.3719    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3685    0.0570    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2193    2.1854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7694    2.2181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5737    2.0349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1346    2.6399    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0081    3.5545    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9390    2.4566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1825    1.6684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6217    1.0634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8652    0.2752    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1984    1.0299    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6460    0.0088    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.6340   -0.8161    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.2944   -1.3106    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1962   -2.1298    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0528   -0.9861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4931   -1.6290    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8458   -1.0596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3706   -0.3852    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8173    1.2466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1980    2.9254    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  3  2  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
  6 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 17 16  1  0  0  0  0
 17 18  1  1  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
 17 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  2  0  0  0  0
 15 26  2  0  0  0  0
 10 26  1  0  0  0  0
  3 27  1  1  0  0  0
  3 28  1  0  0  0  0
 28  7  1  6  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 31 30  1  0  0  0  0
  4 31  1  0  0  0  0
 31 32  1  1  0  0  0
 31 33  1  6  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  2  0  0  0  0
 29 37  1  1  0  0  0
 28 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  2  0  0  0  0
 40 41  1  0  0  0  0
 40 42  1  0  0  0  0
 42 43  2  0  0  0  0
 43 44  1  0  0  0  0
 45 44  1  6  0  0  0
 45 46  1  1  0  0  0
 45 47  1  0  0  0  0
 48 47  1  0  0  0  0
 48 49  1  6  0  0  0
 49 50  1  1  0  0  0
 49 51  1  0  0  0  0
 48 52  1  1  0  0  0
 48 53  1  0  0  0  0
 53 54  1  0  0  0  0
 45 54  1  0  0  0  0
 44 55  2  0  0  0  0
 39 55  1  0  0  0  0
  2 55  1  0  0  0  0
 38 56  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0333201

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H][C@]1(CC[C@@]([H])(N1)C1=C2C(=O)[C@]3([H])[C@@H]4OC5=C(C=CC6=C5C(O)=CC(C[C@@H](CC(O)=O)OC(C)=O)=C6)[C@]3([C@H](C)O[C@@]4([H])CC(O)=O)C(=O)C2=C(O)C=C1)[C@@H](C)O

> <INCHI_IDENTIFIER>
InChI=1S/C38H39NO13/c1-15(40)23-7-8-24(39-23)21-5-9-25(42)32-31(21)34(48)33-36-27(14-29(46)47)50-16(2)38(33,37(32)49)22-6-4-19-10-18(12-26(43)30(19)35(22)52-36)11-20(13-28(44)45)51-17(3)41/h4-6,9-10,12,15-16,20,23-24,27,33,36,39-40,42-43H,7-8,11,13-14H2,1-3H3,(H,44,45)(H,46,47)/t15-,16+,20+,23+,24-,27+,33-,36-,38+/m1/s1

> <INCHI_KEY>
HQJXALLBGUWTSH-GILRLZENSA-N

> <FORMULA>
C38H39NO13

> <MOLECULAR_WEIGHT>
717.724

> <EXACT_MASS>
717.24214032

> <JCHEM_ACCEPTOR_COUNT>
13

> <JCHEM_ATOM_COUNT>
91

> <JCHEM_AVERAGE_POLARIZABILITY>
73.01355340089876

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3S)-3-(acetyloxy)-4-[(1R,13S,14S,23S,25S)-25-(carboxymethyl)-9,20-dihydroxy-17-[(2R,5S)-5-[(1R)-1-hydroxyethyl]pyrrolidin-2-yl]-23-methyl-15,22-dioxo-12,24-dioxahexacyclo[11.9.3.0^{1,14}.0^{2,11}.0^{5,10}.0^{16,21}]pentacosa-2(11),3,5(10),6,8,16,18,20-octaen-7-yl]butanoic acid

> <JCHEM_LOGP>
0.2497987373689337

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
3.7695043809697313

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.0761718393753807

> <JCHEM_PKA_STRONGEST_BASIC>
9.551793481856462

> <JCHEM_POLAR_SURFACE_AREA>
226.22

> <JCHEM_REFRACTIVITY>
180.364

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(3S)-3-(acetyloxy)-4-[(1R,13S,14S,23S,25S)-25-(carboxymethyl)-9,20-dihydroxy-17-[(2R,5S)-5-[(1R)-1-hydroxyethyl]pyrrolidin-2-yl]-23-methyl-15,22-dioxo-12,24-dioxahexacyclo[11.9.3.0^{1,14}.0^{2,11}.0^{5,10}.0^{16,21}]pentacosa-2(11),3,5(10),6,8,16,18,20-octaen-7-yl]butanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-JAN-23   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JAN-23         0                                  
HETATM    1  O   UNK     0       3.955  -0.811   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       4.306   1.001   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.710   1.540   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.318  -0.497   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       3.706   0.169   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       4.217   1.622   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.551   3.011   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.420   4.282   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.956   4.164   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.622   2.776   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.753   1.505   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.419   0.116   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       5.735  -1.666   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       7.954  -0.001   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.824   1.270   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      10.555   1.303   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      11.807   2.312   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      13.244   1.756   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      14.443   2.722   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      15.879   2.166   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      14.206   4.244   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      11.571   3.834   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      10.134   4.389   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       8.935   3.423   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0       9.898   5.911   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       8.158   2.659   0.000  0.00  0.00           C+0
HETATM   27  H   UNK     0       1.173   1.456   0.000  0.00  0.00           H+0
HETATM   28  C   UNK     0       2.256   3.011   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       0.710   2.855   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       0.199   1.402   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       0.865   0.014   0.000  0.00  0.00           C+0
HETATM   32  H   UNK     0      -0.661   0.222   0.000  0.00  0.00           H+0
HETATM   33  C   UNK     0      -0.205  -1.210   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -1.775  -1.222   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      -2.535  -2.561   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0      -2.555   0.106   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      -0.409   4.079   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       3.303   4.140   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       4.804   3.798   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       5.851   4.928   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0       5.615   6.635   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0       7.353   4.586   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       7.807   3.114   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       6.760   1.985   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       7.215   0.514   0.000  0.00  0.00           C+0
HETATM   46  H   UNK     0       7.837   1.922   0.000  0.00  0.00           H+0
HETATM   47  N   UNK     0       8.673   0.017   0.000  0.00  0.00           N+0
HETATM   48  C   UNK     0       8.650  -1.523   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0       9.883  -2.447   0.000  0.00  0.00           C+0
HETATM   50  O   UNK     0       9.700  -3.976   0.000  0.00  0.00           O+0
HETATM   51  C   UNK     0      11.299  -1.841   0.000  0.00  0.00           C+0
HETATM   52  H   UNK     0       8.387  -3.041   0.000  0.00  0.00           H+0
HETATM   53  C   UNK     0       7.179  -1.978   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0       6.292  -0.719   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0       5.259   2.327   0.000  0.00  0.00           C+0
HETATM   56  O   UNK     0       2.236   5.461   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   55                                                  
CONECT    3    2    4   27   28                                             
CONECT    4    3    5   31                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   11                                                  
CONECT    7    6    8   28                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   26                                                  
CONECT   11   10    6   12                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16   26                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   22                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19                                                            
CONECT   22   17   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23                                                            
CONECT   26   15   10                                                       
CONECT   27    3                                                            
CONECT   28    3    7   29   38                                             
CONECT   29   28   30   37                                                  
CONECT   30   29   31                                                       
CONECT   31   30    4   32   33                                             
CONECT   32   31                                                            
CONECT   33   31   34                                                       
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34                                                            
CONECT   37   29                                                            
CONECT   38   28   39   56                                                  
CONECT   39   38   40   55                                                  
CONECT   40   39   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40   43                                                       
CONECT   43   42   44                                                       
CONECT   44   43   45   55                                                  
CONECT   45   44   46   47   54                                             
CONECT   46   45                                                            
CONECT   47   45   48                                                       
CONECT   48   47   49   52   53                                             
CONECT   49   48   50   51                                                  
CONECT   50   49                                                            
CONECT   51   49                                                            
CONECT   52   48                                                            
CONECT   53   48   54                                                       
CONECT   54   53   45                                                       
CONECT   55   44   39    2                                                  
CONECT   56   38                                                            
MASTER        0    0    0    0    0    0    0    0   56    0  124    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₈H₃₉NO₁₃

Average Mass

717.7240 Da

Monoisotopic Mass

717.24214 Da

IUPAC Name

(3S)-3-(acetyloxy)-4-[(1R,13S,14S,23S,25S)-25-(carboxymethyl)-9,20-dihydroxy-17-[(2R,5S)-5-[(1R)-1-hydroxyethyl]pyrrolidin-2-yl]-23-methyl-15,22-dioxo-12,24-dioxahexacyclo[11.9.3.0^{1,14}.0^{2,11}.0^{5,10}.0^{16,21}]pentacosa-2(11),3,5(10),6,8,16,18,20-octaen-7-yl]butanoic acid

Traditional Name

CAS Registry Number

Not Available

SMILES

[H][C@]1(CC[C@@]([H])(N1)C1=C2C(=O)[C@]3([H])[C@@H]4OC5=C(C=CC6=C5C(O)=CC(C[C@@H](CC(O)=O)OC(C)=O)=C6)[C@]3([C@H](C)O[C@@]4([H])CC(O)=O)C(=O)C2=C(O)C=C1)[C@@H](C)O

InChI Identifier

InChI=1S/C38H39NO13/c1-15(40)23-7-8-24(39-23)21-5-9-25(42)32-31(21)34(48)33-36-27(14-29(46)47)50-16(2)38(33,37(32)49)22-6-4-19-10-18(12-26(43)30(19)35(22)52-36)11-20(13-28(44)45)51-17(3)41/h4-6,9-10,12,15-16,20,23-24,27,33,36,39-40,42-43H,7-8,11,13-14H2,1-3H3,(H,44,45)(H,46,47)/t15-,16+,20+,23+,24-,27+,33-,36-,38+/m1/s1

InChI Key

HQJXALLBGUWTSH-GILRLZENSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
ROESY NMR	[¹H, ¹H] NMR Spectrum (2D, 600 MHz, C2D6OS, experimental)	taizong.wu@uq.edu.au	Not Available	Not Available	2024-05-12	View Spectrum
HSQC NMR	[¹H, ¹³C] NMR Spectrum (2D, 600 MHz, C2D6OS, experimental)	taizong.wu@uq.edu.au	Not Available	Not Available	2024-05-12	View Spectrum
HMBC NMR	[¹H, ¹³C] NMR Spectrum (2D, 600 MHz, C2D6OS, experimental)	taizong.wu@uq.edu.au	Not Available	Not Available	2024-05-12	View Spectrum
COSY NMR	[¹H, ¹H] NMR Spectrum (2D, 600 MHz, C2D6OS, experimental)	taizong.wu@uq.edu.au	Not Available	Not Available	2024-05-12	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, C2D6OS, experimental)	taizong.wu@uq.edu.au	Not Available	Not Available	2024-05-12	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, C2D6OS, experimental)	taizong.wu@uq.edu.au	Not Available	Not Available	2024-05-12	View Spectrum
HMBC NMR	[¹H, ¹³C] NMR Spectrum (2D, 600 MHz, C2D6OS, experimental)	taizong.wu@uq.edu.au	Not Available	Not Available	2024-05-12	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
Streptomyces sp. CMB-PB042		Not Available

Chemical Taxonomy

Description

This compound belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Diterpenoids

Alternative Parents

Substituents

Diterpenoid
Naphthopyranone
Naphthopyran
Naphthoquinone
2-phenylpyrrolidine
1-naphthol
Secoiridoid-skeleton
1-benzopyran
Tetralin
Naphthalene
Benzopyran
Chromane
Tricarboxylic acid or derivatives
Aryl alkyl ketone
Aryl ketone
Quinone
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Pyranone
Alkyl aryl ether
Alpha-branched alpha,beta-unsaturated-ketone
Benzenoid
Pyran
Oxane
Vinylogous acid
Alpha,beta-unsaturated ketone
Pyrrolidine
Pyrrole
Enone
Acryloyl-group
Amino acid
Secondary alcohol
Ketone
Carboxylic acid ester
Amino acid or derivatives
Oxacycle
Azacycle
Organoheterocyclic compound
Secondary amine
Ether
Secondary aliphatic amine
Dialkyl ether
Carboxylic acid
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
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	0.25	ChemAxon
pKa (Strongest Acidic)	3.08	ChemAxon
pKa (Strongest Basic)	9.55	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	13	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	226.22 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	180.36 m³·mol⁻¹	ChemAxon
Polarizability	73.01 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	Yes	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

DOI: 10.1021/acs.orglett.1c02954

Showing NP-Card for Glenthamine A (NP0333201)

MOL for NP0333201 (Glenthamine A)

3D MOL for NP0333201 (Glenthamine A)

3D SDF for NP0333201 (Glenthamine A)

3D-SDF for NP0333201 (Glenthamine A)

PDB for NP0333201 (Glenthamine A)

3D PDB for NP0333201 (Glenthamine A)

SMILES for NP0333201 (Glenthamine A)

INCHI for NP0333201 (Glenthamine A)

Structure for NP0333201 (Glenthamine A)

3D Structure for NP0333201 (Glenthamine A)