NP-MRD: Showing NP-Card for Luteoalbusin A (NP0011178)

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Record Information

Version

2.0

Created at

2021-01-05 20:57:38 UTC

Updated at

2021-07-15 17:08:10 UTC

NP-MRD ID

NP0011178

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Luteoalbusin A

Provided By

NPAtlas

Description

(+)-Luteoalbusin A belongs to the class of organic compounds known as pyrroloindoles. Pyrroloindoles are compounds containing a pyrroloindole moiety, which is a tricyclic heterocycle which consists of a pyrrole ring fused to an indole. Pyrrole is 5-membered ring consisting of four carbon atoms and one nitrogen atom. Indole is a bicyclic compound consisting of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring. Luteoalbusin A is found in Acrostalagmus and Acrostalagmus luteoalbus. Based on a literature review very few articles have been published on (+)-Luteoalbusin A.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242107443D          

 52 58  0  0  0  0            999 V2000
    3.4952   -2.9828   -0.2038 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9864   -1.6316   -0.1552 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.7456   -1.3178   -0.7669 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0090   -2.2496   -1.1673 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3395    0.1047   -0.9231 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0349    0.3209   -1.3691 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7073    0.9788   -0.1362 C   0  0  2  0  0  0  0  0  0  0  0  0
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   -3.1014   -1.0543   -0.8900 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.3732    3.5876   -1.2283 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652306242107443D          

 52 58  0  0  0  0            999 V2000
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   -4.6503   -2.0703   -1.9737 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8599   -0.3878   -1.7320 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6282    1.6072   -0.6451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4293    3.7415   -1.4028 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7949    5.5704   -1.7577 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3927    5.1910   -1.3513 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5749    3.0936   -0.8103 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2703    2.0073    1.5472 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1198   -0.0954    1.9950 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2217   -1.5911    2.2761 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8401   -2.6727    1.4819 H   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
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  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  2  0  0  0  0
  7 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  1  0  0  0
 29 30  1  0  0  0  0
 28 31  1  0  0  0  0
 31 32  1  0  0  0  0
 28  2  1  0  0  0  0
 25  5  1  0  0  0  0
  5 32  1  6  0  0  0
 24  7  1  0  0  0  0
 16  8  1  0  0  0  0
 22 17  1  0  0  0  0
 16 11  1  0  0  0  0
  1 33  1  0  0  0  0
  1 34  1  0  0  0  0
  1 35  1  0  0  0  0
  6 36  1  0  0  0  0
  6 37  1  0  0  0  0
  9 38  1  0  0  0  0
 10 39  1  0  0  0  0
 12 40  1  0  0  0  0
 13 41  1  0  0  0  0
 14 42  1  0  0  0  0
 15 43  1  0  0  0  0
 18 44  1  0  0  0  0
 19 45  1  0  0  0  0
 20 46  1  0  0  0  0
 21 47  1  0  0  0  0
 23 48  1  0  0  0  0
 24 49  1  1  0  0  0
 29 50  1  0  0  0  0
 29 51  1  0  0  0  0
 30 52  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0011178

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC([H])([H])[C@]12SS[C@]3(N(C1=O)[C@@]1([H])N([H])C4=C([H])C([H])=C([H])C([H])=C4[C@@]1(C1=C([H])N([H])C4=C([H])C([H])=C([H])C([H])=C14)C3([H])[H])C(=O)N2C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C23H20N4O3S2/c1-26-19(29)22-11-21(15-10-24-16-8-4-2-6-13(15)16)14-7-3-5-9-17(14)25-18(21)27(22)20(30)23(26,12-28)32-31-22/h2-10,18,24-25,28H,11-12H2,1H3/t18-,21-,22+,23+/m1/s1

> <INCHI_KEY>
XHPIWHHLWCZQEF-QQUTXWOLSA-N

> <FORMULA>
C23H20N4O3S2

> <MOLECULAR_WEIGHT>
464.56

> <EXACT_MASS>
464.097682868

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
47.19834885722973

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,3R,11R,14S)-14-(hydroxymethyl)-3-(1H-indol-3-yl)-18-methyl-15,16-dithia-10,12,18-triazapentacyclo[12.2.2.0^{1,12}.0^{3,11}.0^{4,9}]octadeca-4,6,8-triene-13,17-dione

> <ALOGPS_LOGP>
3.56

> <JCHEM_LOGP>
3.0416418336666666

> <ALOGPS_LOGS>
-4.06

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.789686390445585

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.086627155582686

> <JCHEM_PKA_STRONGEST_BASIC>
1.6333835738013291

> <JCHEM_POLAR_SURFACE_AREA>
88.67

> <JCHEM_REFRACTIVITY>
135.98029999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.08e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,3R,11R,14S)-14-(hydroxymethyl)-3-(1H-indol-3-yl)-18-methyl-15,16-dithia-10,12,18-triazapentacyclo[12.2.2.0^{1,12}.0^{3,11}.0^{4,9}]octadeca-4,6,8-triene-13,17-dione

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 52 58  0  0  0  0  0  0  0  0999 V2000
    3.4952   -2.9828   -0.2038 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9864   -1.6316   -0.1552 N   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.0349    0.3209   -1.3691 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7073    0.9788   -0.1362 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3282   -0.0686    0.6565 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0294   -0.4392    1.9694 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8489   -1.4236    2.3253 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6890   -1.7431    1.3247 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6942   -2.6748    1.1719 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4154   -2.8199    0.0092 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0976   -1.9822   -1.0346 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.5310    2.1189   -0.5622 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8695    2.3637   -0.7977 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3732    3.5876   -1.2283 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4732    4.6077   -1.4274 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1198    4.3733   -1.1917 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6226    3.1704   -0.7676 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7088    2.7223   -0.4331 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.4689    1.6415    0.5489 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5404    0.7186    0.3844 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.6786    0.2866    1.1367 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8622    0.6066    2.3363 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7175   -0.5836    0.5066 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7311   -1.0180    1.4720 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7391   -1.8030    0.9805 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4146    0.4444   -0.8522 S   0  0  0  0  0  0  0  0  0  0  0  0
    2.6231    0.8618   -1.9979 S   0  0  0  0  0  0  0  0  0  0  0  0
    2.9062   -3.6325   -0.8824 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5445   -3.0149   -0.6205 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4538   -3.4738    0.7954 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5144   -0.6883   -1.5195 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1956    0.9147   -2.2732 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2376    0.0538    2.5312 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8644   -1.9111    3.2607 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9250   -3.3208    2.0057 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1992   -3.5422   -0.1187 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6503   -2.0703   -1.9737 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8599   -0.3878   -1.7320 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6282    1.6072   -0.6451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4293    3.7415   -1.4028 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7949    5.5704   -1.7577 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3927    5.1910   -1.3513 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5749    3.0936   -0.8103 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2703    2.0073    1.5472 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1198   -0.0954    1.9950 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2217   -1.5911    2.2761 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8401   -2.6727    1.4819 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
  3  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  1
  8  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
  7 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  2  0
 26 28  1  0
 28 29  1  1
 29 30  1  0
 28 31  1  0
 31 32  1  0
 28  2  1  0
 25  5  1  0
  5 32  1  6
 24  7  1  0
 16  8  1  0
 22 17  1  0
 16 11  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
  6 36  1  0
  6 37  1  0
  9 38  1  0
 10 39  1  0
 12 40  1  0
 13 41  1  0
 14 42  1  0
 15 43  1  0
 18 44  1  0
 19 45  1  0
 20 46  1  0
 21 47  1  0
 23 48  1  0
 24 49  1  1
 29 50  1  0
 29 51  1  0
 30 52  1  0
M  END

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  C   UNK     0       3.495  -2.983  -0.204  0.00  0.00           C+0
HETATM    2  N   UNK     0       2.986  -1.632  -0.155  0.00  0.00           N+0
HETATM    3  C   UNK     0       1.746  -1.318  -0.767  0.00  0.00           C+0
HETATM    4  O   UNK     0       1.009  -2.250  -1.167  0.00  0.00           O+0
HETATM    5  C   UNK     0       1.339   0.105  -0.923  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.035   0.321  -1.369  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.707   0.979  -0.136  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.328  -0.069   0.657  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.029  -0.439   1.969  0.00  0.00           C+0
HETATM   10  N   UNK     0      -1.849  -1.424   2.325  0.00  0.00           N+0
HETATM   11  C   UNK     0      -2.689  -1.743   1.325  0.00  0.00           C+0
HETATM   12  C   UNK     0      -3.694  -2.675   1.172  0.00  0.00           C+0
HETATM   13  C   UNK     0      -4.415  -2.820   0.009  0.00  0.00           C+0
HETATM   14  C   UNK     0      -4.098  -1.982  -1.035  0.00  0.00           C+0
HETATM   15  C   UNK     0      -3.101  -1.054  -0.890  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.364  -0.894   0.276  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.531   2.119  -0.562  0.00  0.00           C+0
HETATM   18  C   UNK     0      -2.869   2.364  -0.798  0.00  0.00           C+0
HETATM   19  C   UNK     0      -3.373   3.588  -1.228  0.00  0.00           C+0
HETATM   20  C   UNK     0      -2.473   4.608  -1.427  0.00  0.00           C+0
HETATM   21  C   UNK     0      -1.120   4.373  -1.192  0.00  0.00           C+0
HETATM   22  C   UNK     0      -0.623   3.170  -0.768  0.00  0.00           C+0
HETATM   23  N   UNK     0       0.709   2.722  -0.433  0.00  0.00           N+0
HETATM   24  C   UNK     0       0.469   1.642   0.549  0.00  0.00           C+0
HETATM   25  N   UNK     0       1.540   0.719   0.384  0.00  0.00           N+0
HETATM   26  C   UNK     0       2.679   0.287   1.137  0.00  0.00           C+0
HETATM   27  O   UNK     0       2.862   0.607   2.336  0.00  0.00           O+0
HETATM   28  C   UNK     0       3.717  -0.584   0.507  0.00  0.00           C+0
HETATM   29  C   UNK     0       4.731  -1.018   1.472  0.00  0.00           C+0
HETATM   30  O   UNK     0       5.739  -1.803   0.981  0.00  0.00           O+0
HETATM   31  S   UNK     0       4.415   0.444  -0.852  0.00  0.00           S+0
HETATM   32  S   UNK     0       2.623   0.862  -1.998  0.00  0.00           S+0
HETATM   33  H   UNK     0       2.906  -3.632  -0.882  0.00  0.00           H+0
HETATM   34  H   UNK     0       4.545  -3.015  -0.621  0.00  0.00           H+0
HETATM   35  H   UNK     0       3.454  -3.474   0.795  0.00  0.00           H+0
HETATM   36  H   UNK     0      -0.514  -0.688  -1.520  0.00  0.00           H+0
HETATM   37  H   UNK     0      -0.196   0.915  -2.273  0.00  0.00           H+0
HETATM   38  H   UNK     0      -0.238   0.054   2.531  0.00  0.00           H+0
HETATM   39  H   UNK     0      -1.864  -1.911   3.261  0.00  0.00           H+0
HETATM   40  H   UNK     0      -3.925  -3.321   2.006  0.00  0.00           H+0
HETATM   41  H   UNK     0      -5.199  -3.542  -0.119  0.00  0.00           H+0
HETATM   42  H   UNK     0      -4.650  -2.070  -1.974  0.00  0.00           H+0
HETATM   43  H   UNK     0      -2.860  -0.388  -1.732  0.00  0.00           H+0
HETATM   44  H   UNK     0      -3.628   1.607  -0.645  0.00  0.00           H+0
HETATM   45  H   UNK     0      -4.429   3.741  -1.403  0.00  0.00           H+0
HETATM   46  H   UNK     0      -2.795   5.570  -1.758  0.00  0.00           H+0
HETATM   47  H   UNK     0      -0.393   5.191  -1.351  0.00  0.00           H+0
HETATM   48  H   UNK     0       1.575   3.094  -0.810  0.00  0.00           H+0
HETATM   49  H   UNK     0       0.270   2.007   1.547  0.00  0.00           H+0
HETATM   50  H   UNK     0       5.120  -0.095   1.995  0.00  0.00           H+0
HETATM   51  H   UNK     0       4.222  -1.591   2.276  0.00  0.00           H+0
HETATM   52  H   UNK     0       5.840  -2.673   1.482  0.00  0.00           H+0
CONECT    1    2   33   34   35                                             
CONECT    2    1    3   28                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   25   32                                             
CONECT    6    5    7   36   37                                             
CONECT    7    6    8   17   24                                             
CONECT    8    7    9   16                                                  
CONECT    9    8   10   38                                                  
CONECT   10    9   11   39                                                  
CONECT   11   10   12   16                                                  
CONECT   12   11   13   40                                                  
CONECT   13   12   14   41                                                  
CONECT   14   13   15   42                                                  
CONECT   15   14   16   43                                                  
CONECT   16   15    8   11                                                  
CONECT   17    7   18   22                                                  
CONECT   18   17   19   44                                                  
CONECT   19   18   20   45                                                  
CONECT   20   19   21   46                                                  
CONECT   21   20   22   47                                                  
CONECT   22   21   23   17                                                  
CONECT   23   22   24   48                                                  
CONECT   24   23   25    7   49                                             
CONECT   25   24   26    5                                                  
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29   31    2                                             
CONECT   29   28   30   50   51                                             
CONECT   30   29   52                                                       
CONECT   31   28   32                                                       
CONECT   32   31    5                                                       
CONECT   33    1                                                            
CONECT   34    1                                                            
CONECT   35    1                                                            
CONECT   36    6                                                            
CONECT   37    6                                                            
CONECT   38    9                                                            
CONECT   39   10                                                            
CONECT   40   12                                                            
CONECT   41   13                                                            
CONECT   42   14                                                            
CONECT   43   15                                                            
CONECT   44   18                                                            
CONECT   45   19                                                            
CONECT   46   20                                                            
CONECT   47   21                                                            
CONECT   48   23                                                            
CONECT   49   24                                                            
CONECT   50   29                                                            
CONECT   51   29                                                            
CONECT   52   30                                                            
MASTER        0    0    0    0    0    0    0    0   52    0  116    0
END

RDKit          3D

52 58  0  0  0  0  0  0  0  0999 V2000
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M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₂₃H₂₀N₄O₃S₂

Average Mass

464.5600 Da

Monoisotopic Mass

464.09768 Da

IUPAC Name

(1S,3R,11R,14S)-14-(hydroxymethyl)-3-(1H-indol-3-yl)-18-methyl-15,16-dithia-10,12,18-triazapentacyclo[12.2.2.0^{1,12}.0^{3,11}.0^{4,9}]octadeca-4,6,8-triene-13,17-dione

Traditional Name

(1S,3R,11R,14S)-14-(hydroxymethyl)-3-(1H-indol-3-yl)-18-methyl-15,16-dithia-10,12,18-triazapentacyclo[12.2.2.0^{1,12}.0^{3,11}.0^{4,9}]octadeca-4,6,8-triene-13,17-dione

CAS Registry Number

Not Available

SMILES

CN1C(=O)[C@@]23C[C@]4([C@H](NC5=CC=CC=C45)N2C(=O)[C@]1(CO)SS3)C1=CNC2=CC=CC=C12

InChI Identifier

InChI=1S/C23H20N4O3S2/c1-26-19(29)22-11-21(15-10-24-16-8-4-2-6-13(15)16)14-7-3-5-9-17(14)25-18(21)27(22)20(30)23(26,12-28)32-31-22/h2-10,18,24-25,28H,11-12H2,1H3/t18-,21-,22+,23+/m1/s1

InChI Key

XHPIWHHLWCZQEF-QQUTXWOLSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Acrostalagmus	NPAtlas	23079524
Acrostalagmus luteoalbus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyrroloindoles. Pyrroloindoles are compounds containing a pyrroloindole moiety, which is a tricyclic heterocycle which consists of a pyrrole ring fused to an indole. Pyrrole is 5-membered ring consisting of four carbon atoms and one nitrogen atom. Indole is a bicyclic compound consisting of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Pyrroloindoles

Direct Parent

Pyrroloindoles

Alternative Parents

Substituents

Pyrroloindole
Alpha-amino acid or derivatives
Epipolythiodioxopiperazine
3-alkylindole
Indole
Dihydroindole
Thiodioxopiperazine
Dioxopiperazine
2,5-dioxopiperazine
N-methylpiperazine
N-alkylpiperazine
1,4-diazinane
Dithiazinane
Piperazine
Substituted pyrrole
Benzenoid
Pyrrolidine
Pyrrole
Tertiary carboxylic acid amide
Heteroaromatic compound
Carboxamide group
Organic disulfide
Lactam
Azacycle
Carboxylic acid derivative
Carbonyl group
Organic nitrogen compound
Organic oxide
Organic oxygen compound
Alcohol
Hydrocarbon derivative
Organonitrogen compound
Organooxygen compound
Amine
Primary 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	3.56	ALOGPS
logP	3.04	ChemAxon
logS	-4.1	ALOGPS
pKa (Strongest Acidic)	14.09	ChemAxon
pKa (Strongest Basic)	1.63	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	88.67 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	135.98 m³·mol⁻¹	ChemAxon
Polarizability	47.2 Å³	ChemAxon
Number of Rings	7	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

NPAtlas ID

NPA009066

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

28533884

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

71497282

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Luteoalbusin A (NP0011178)

MOL for NP0011178 (Luteoalbusin A)

3D MOL for NP0011178 (Luteoalbusin A)

3D SDF for NP0011178 (Luteoalbusin A)

3D-SDF for NP0011178 (Luteoalbusin A)

PDB for NP0011178 (Luteoalbusin A)

3D PDB for NP0011178 (Luteoalbusin A)

SMILES for NP0011178 (Luteoalbusin A)

INCHI for NP0011178 (Luteoalbusin A)

Structure for NP0011178 (Luteoalbusin A)

3D Structure for NP0011178 (Luteoalbusin A)