NP-MRD: Showing NP-Card for (+)-Dactylamide B (NP0068937)

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Record Information

Version

2.0

Created at

2022-04-28 14:12:28 UTC

Updated at

2022-04-28 14:12:28 UTC

NP-MRD ID

NP0068937

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(+)-Dactylamide B

Description

[(1S)-2-(7-hydroxy-1H-indol-3-yl)-1-{[(E)-2-(1H-indol-2-yl)ethenyl]-C-hydroxycarbonimidoyl}ethyl]trimethylazanium belongs to the class of organic compounds known as hydroxyindoles. These are organic compounds containing an indole moiety that carries a hydroxyl group. (+)-Dactylamide B is found in Aplysia dactylomela. Based on a literature review very few articles have been published on [(1S)-2-(7-hydroxy-1H-indol-3-yl)-1-{[(E)-2-(1H-indol-2-yl)ethenyl]-C-hydroxycarbonimidoyl}ethyl]trimethylazanium.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282216122D          

 30 33  0  0  1  0            999 V2000
   -1.4534   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8659    0.0165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6909    0.0165    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1034    0.7310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6909    1.4455    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9284    0.7310    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.3409    1.4455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1659    1.4455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6509    2.1129    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4355    1.8580    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4355    1.0330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6509    0.7780    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4793   -0.0289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0924   -0.5810    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8770   -0.3260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0486    0.4809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8332    0.7359    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3409    0.0165    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
   -5.0554    0.4290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6265   -0.3960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7534   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6284   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435   -1.3654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435   -0.0305    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  6  4  1  1  0  0  0
  6  7  1  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  1  0  0  0  0
 11 12  1  0  0  0  0
  8 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
 11 16  2  0  0  0  0
 16 17  1  0  0  0  0
  6 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 18 21  1  0  0  0  0
  1 22  1  0  0  0  0
 22 23  2  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
 22 26  1  0  0  0  0
 25 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 24 30  2  0  0  0  0
M  CHG  1  18   1
M  END

     RDKit          3D

 57 60  0  0  0  0  0  0  0  0999 V2000
   -3.5716   -2.2992   -0.6185 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3021   -2.4568    0.0122 N   0  0  1  0  0  4  0  0  0  0  0  0
   -2.6421   -2.8127    1.4080 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8549   -3.8207   -0.4924 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2754   -1.5673   -0.1859 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3871   -0.2301   -0.8048 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2432    0.7722   -0.1685 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8517    1.5200    0.9709 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8618    2.2840    1.3886 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9001    2.0635    0.5619 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1622    2.6192    0.5449 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5390    3.5597    1.5270 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0703    2.2682   -0.4225 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6926    1.3444   -1.3823 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4466    0.7737   -1.3915 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5375    1.1374   -0.4027 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4864   -1.2409    1.1324 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1487   -1.2494    2.1880 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8460   -0.9771    1.0434 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.1708   -0.7148    0.9558 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6462    0.3592    0.2999 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0662    0.6321    0.2161 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0954   -0.1402    0.7477 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2844    0.4915    0.4767 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5984    0.1889    0.7674 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6291    1.0471    0.3609 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3156    2.1969   -0.3329 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0093    2.5092   -0.6294 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9975    1.6489   -0.2201 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6655    1.6918   -0.3525 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1880   -1.6481    0.0001 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5500   -2.1399   -1.6884 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0892   -3.3171   -0.5108 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4193   -3.6465    1.2403 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2119   -2.0490    1.9234 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8462   -3.3301    1.9307 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2952   -4.3362    0.3096 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6966   -4.3857   -0.8753 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1397   -3.6276   -1.3176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4450   -2.0882   -0.7786 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3377    0.2089   -0.7668 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5558   -0.2755   -1.9215 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8765    1.4796    1.4336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8931    2.9409    2.1914 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4698    3.9366    1.4812 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0652    2.7228   -0.4140 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4412    1.0854   -2.1440 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1404    0.0613   -2.1508 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9433   -0.7081    2.3908 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9512   -1.3439    1.3815 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9245    1.0025   -0.1568 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9664   -1.0740    1.2777 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8720   -0.7053    1.3118 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6588    0.8481    0.5691 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0694    2.9034   -0.6756 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7734    3.4095   -1.1707 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1504    2.4775   -0.8537 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6
  2  3  1  0
  2  4  1  0
  2  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 11 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
  5 17  1  0
 17 18  2  0
 17 19  1  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  2  0
 23 24  1  0
 24 25  2  0
 25 26  1  0
 26 27  2  0
 27 28  1  0
 28 29  2  0
 29 30  1  0
 16  7  1  0
 30 22  1  0
 16 10  1  0
 29 24  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  3 34  1  0
  3 35  1  0
  3 36  1  0
  4 37  1  0
  4 38  1  0
  4 39  1  0
  5 40  1  6
  6 41  1  0
  6 42  1  0
  8 43  1  0
  9 44  1  0
 12 45  1  0
 13 46  1  0
 14 47  1  0
 15 48  1  0
 19 49  1  0
 20 50  1  0
 21 51  1  0
 23 52  1  0
 25 53  1  0
 26 54  1  0
 27 55  1  0
 28 56  1  0
 30 57  1  0
M  CHG  1   2   1
M  END


  Mrv1652304282216122D          

 30 33  0  0  1  0            999 V2000
   -1.4534   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8659    0.0165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6909    0.0165    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1034    0.7310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6909    1.4455    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9284    0.7310    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.3409    1.4455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1659    1.4455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6509    2.1129    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4355    1.8580    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4355    1.0330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6509    0.7780    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4793   -0.0289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0924   -0.5810    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8770   -0.3260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0486    0.4809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8332    0.7359    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3409    0.0165    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
   -5.0554    0.4290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6265   -0.3960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7534   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6284   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435   -1.3654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435   -0.0305    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  6  4  1  1  0  0  0
  6  7  1  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  1  0  0  0  0
 11 12  1  0  0  0  0
  8 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
 11 16  2  0  0  0  0
 16 17  1  0  0  0  0
  6 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 18 21  1  0  0  0  0
  1 22  1  0  0  0  0
 22 23  2  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
 22 26  1  0  0  0  0
 25 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 24 30  2  0  0  0  0
M  CHG  1  18   1
M  END
> <DATABASE_ID>
NP0068937

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[N+](C)(C)[C@@H](CC1=CNC2=C(O)C=CC=C12)C(=O)N\C=C\C1=CC2=CC=CC=C2N1

> <INCHI_IDENTIFIER>
InChI=1S/C24H26N4O2/c1-28(2,3)21(14-17-15-26-23-19(17)8-6-10-22(23)29)24(30)25-12-11-18-13-16-7-4-5-9-20(16)27-18/h4-13,15,21,26-27H,14H2,1-3H3,(H-,25,29,30)/p+1/b12-11+/t21-/m0/s1

> <INCHI_KEY>
NMRYPTMIPHJQLC-VIOKTNGOSA-O

> <FORMULA>
C24H27N4O2

> <MOLECULAR_WEIGHT>
403.505

> <EXACT_MASS>
403.212852546

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
57

> <JCHEM_AVERAGE_POLARIZABILITY>
44.498670238926884

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
1

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[(1S)-2-(7-hydroxy-1H-indol-3-yl)-1-{[(E)-2-(1H-indol-2-yl)ethenyl]carbamoyl}ethyl]trimethylazanium

> <ALOGPS_LOGP>
1.44

> <JCHEM_LOGP>
-0.9305866251384118

> <ALOGPS_LOGS>
-6.27

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
13.384756070393799

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.596503792108084

> <JCHEM_PKA_STRONGEST_BASIC>
-5.7645992143073785

> <JCHEM_POLAR_SURFACE_AREA>
80.91

> <JCHEM_REFRACTIVITY>
131.3102

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.34e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
[(1S)-2-(7-hydroxy-1H-indol-3-yl)-1-{[(E)-2-(1H-indol-2-yl)ethenyl]carbamoyl}ethyl]trimethylazanium

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0      -2.713  -1.303   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -3.483   0.031   0.000  0.00  0.00           C+0
HETATM    3  N   UNK     0      -5.023   0.031   0.000  0.00  0.00           N+0
HETATM    4  C   UNK     0      -5.793   1.365   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -5.023   2.698   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -7.333   1.365   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -8.103   2.698   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -9.643   2.698   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0     -10.548   3.944   0.000  0.00  0.00           C+0
HETATM   10  N   UNK     0     -12.013   3.468   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0     -12.013   1.928   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0     -10.548   1.452   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0     -10.228  -0.054   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0     -11.373  -1.084   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0     -12.837  -0.609   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0     -13.157   0.898   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0     -14.622   1.374   0.000  0.00  0.00           O+0
HETATM   18  N   UNK     0      -8.103   0.031   0.000  0.00  0.00           N+1
HETATM   19  C   UNK     0      -9.437   0.801   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -6.769  -0.739   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -8.873  -1.303   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -1.173  -1.303   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -0.268  -2.549   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.197  -2.073   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.197  -0.533   0.000  0.00  0.00           C+0
HETATM   26  N   UNK     0      -0.268  -0.057   0.000  0.00  0.00           N+0
HETATM   27  C   UNK     0       2.530   0.237   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       3.864  -0.533   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       3.864  -2.073   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       2.530  -2.843   0.000  0.00  0.00           C+0
CONECT    1    2   22                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7   18                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   12                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   16                                                  
CONECT   12   11    8   13                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   11   17                                                  
CONECT   17   16                                                            
CONECT   18    6   19   20   21                                             
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   18                                                            
CONECT   22    1   23   26                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   30                                                  
CONECT   25   24   26   27                                                  
CONECT   26   25   22                                                       
CONECT   27   25   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   24                                                       
MASTER        0    0    0    0    0    0    0    0   30    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₂₇N₄O₂

Average Mass

403.5050 Da

Monoisotopic Mass

403.21285 Da

IUPAC Name

[(1S)-2-(7-hydroxy-1H-indol-3-yl)-1-{[(E)-2-(1H-indol-2-yl)ethenyl]carbamoyl}ethyl]trimethylazanium

Traditional Name

[(1S)-2-(7-hydroxy-1H-indol-3-yl)-1-{[(E)-2-(1H-indol-2-yl)ethenyl]carbamoyl}ethyl]trimethylazanium

CAS Registry Number

Not Available

SMILES

C[N+](C)(C)[C@@H](CC1=CNC2=C(O)C=CC=C12)C(=O)N\C=C\C1=CC2=CC=CC=C2N1

InChI Identifier

InChI=1S/C24H26N4O2/c1-28(2,3)21(14-17-15-26-23-19(17)8-6-10-22(23)29)24(30)25-12-11-18-13-16-7-4-5-9-20(16)27-18/h4-13,15,21,26-27H,14H2,1-3H3,(H-,25,29,30)/p+1/b12-11+/t21-/m0/s1

InChI Key

NMRYPTMIPHJQLC-VIOKTNGOSA-O

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
Aplysia dactylomela	Animalia	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hydroxyindoles. These are organic compounds containing an indole moiety that carries a hydroxyl group.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Hydroxyindoles

Direct Parent

Hydroxyindoles

Alternative Parents

Substituents

Hydroxyindole
3-alkylindole
Indole
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Aralkylamine
Benzenoid
Substituted pyrrole
Tetraalkylammonium salt
Heteroaromatic compound
Quaternary ammonium salt
Pyrrole
Azacycle
Carboximidic acid derivative
Carboximidic acid
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Hydrocarbon derivative
Organic salt
Organooxygen compound
Organonitrogen compound
Amine
Organic cation
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	1.44	ALOGPS
logP	-0.93	ChemAxon
logS	-6.3	ALOGPS
pKa (Strongest Acidic)	9.6	ChemAxon
pKa (Strongest Basic)	-5.8	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	80.91 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	131.31 m³·mol⁻¹	ChemAxon
Polarizability	44.5 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	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

163189047

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (+)-Dactylamide B (NP0068937)

MOL for NP0068937 ((+)-Dactylamide B)

3D MOL for NP0068937 ((+)-Dactylamide B)

3D SDF for NP0068937 ((+)-Dactylamide B)

3D-SDF for NP0068937 ((+)-Dactylamide B)

PDB for NP0068937 ((+)-Dactylamide B)

3D PDB for NP0068937 ((+)-Dactylamide B)

SMILES for NP0068937 ((+)-Dactylamide B)

INCHI for NP0068937 ((+)-Dactylamide B)

Structure for NP0068937 ((+)-Dactylamide B)

3D Structure for NP0068937 ((+)-Dactylamide B)