NP-MRD: Showing NP-Card for Triacsin B (NP0021243)

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Record Information

Version

2.0

Created at

2021-01-06 06:31:01 UTC

Updated at

2021-07-15 17:35:50 UTC

NP-MRD ID

NP0021243

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Triacsin B

Provided By

NPAtlas

Description

105201-47-6, Also known as triacsin b, belongs to the class of organic compounds known as organic n-nitroso compounds. These are organic compounds containing a n-nitroso group -NN=O. Triacsin B is found in Streptomyces. Based on a literature review very few articles have been published on 105201-47-6.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242120413D          

 30 29  0  0  0  0            999 V2000
   -5.9330    0.5305    2.2725 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5831    0.2773    0.8179 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.1668    0.5690    0.6062 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3460   -0.4444    0.2050 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9755   -0.1273    0.0079 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8081    0.1086   -0.1676 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4992    0.3867   -0.3609 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4013   -0.5679   -0.7716 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7751   -0.1798   -0.9457 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6777   -1.0741   -1.3596 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0752   -0.7182   -1.5454 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5006    0.4659   -1.3157 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.8627    0.7192   -1.5233 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.7372    0.3071   -0.5120 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.4558   -0.6975    0.2000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8292   -0.3989    2.8828 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2746    1.3323    2.6226 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9952    0.8327    2.3445 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8384   -0.7545    0.5790 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2418    0.9911    0.2522 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6944    1.5273    0.7410 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8273   -1.3726    0.0806 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6596   -1.4584   -0.3212 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0976    1.4494    0.2293 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9987    1.3680   -0.2311 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9851   -1.5360   -0.9257 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1214    0.7960   -0.7528 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2867   -2.0620   -1.5364 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7566   -1.4662   -1.8859 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1371    1.1967   -2.4008 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
  4  5  1  0  0  0  0
  5  6  2  3  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  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  1  0  0  0  0
 14 15  2  0  0  0  0
  1 16  1  0  0  0  0
  1 17  1  0  0  0  0
  1 18  1  0  0  0  0
  2 19  1  0  0  0  0
  2 20  1  0  0  0  0
  3 21  1  0  0  0  0
  4 22  1  0  0  0  0
  5 23  1  0  0  0  0
  6 24  1  0  0  0  0
  7 25  1  0  0  0  0
  8 26  1  0  0  0  0
  9 27  1  0  0  0  0
 10 28  1  0  0  0  0
 11 29  1  0  0  0  0
 13 30  1  0  0  0  0
M  END

     RDKit          3D

 30 29  0  0  0  0  0  0  0  0999 V2000
   -5.9330    0.5305    2.2725 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5831    0.2773    0.8179 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1668    0.5690    0.6062 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3460   -0.4444    0.2050 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9755   -0.1273    0.0079 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8081    0.1086   -0.1676 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4992    0.3867   -0.3609 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4013   -0.5679   -0.7716 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7751   -0.1798   -0.9457 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6777   -1.0741   -1.3596 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0752   -0.7182   -1.5454 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5006    0.4659   -1.3157 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.8627    0.7192   -1.5233 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.7372    0.3071   -0.5120 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.4558   -0.6975    0.2000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8292   -0.3989    2.8828 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2746    1.3323    2.6226 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9952    0.8327    2.3445 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8384   -0.7545    0.5790 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2418    0.9911    0.2522 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6944    1.5273    0.7410 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8273   -1.3726    0.0806 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6596   -1.4584   -0.3212 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0976    1.4494    0.2293 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9987    1.3680   -0.2311 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9851   -1.5360   -0.9257 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1214    0.7960   -0.7528 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2867   -2.0620   -1.5364 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7566   -1.4662   -1.8859 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1371    1.1967   -2.4008 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
  4  5  1  0
  5  6  2  3
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
  1 16  1  0
  1 17  1  0
  1 18  1  0
  2 19  1  0
  2 20  1  0
  3 21  1  0
  4 22  1  0
  5 23  1  0
  6 24  1  0
  7 25  1  0
  8 26  1  0
  9 27  1  0
 10 28  1  0
 11 29  1  0
 13 30  1  0
M  END


  Mrv1652306242120413D          

 30 29  0  0  0  0            999 V2000
   -5.9330    0.5305    2.2725 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5831    0.2773    0.8179 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.1668    0.5690    0.6062 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3460   -0.4444    0.2050 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9755   -0.1273    0.0079 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8081    0.1086   -0.1676 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4992    0.3867   -0.3609 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4013   -0.5679   -0.7716 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7751   -0.1798   -0.9457 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6777   -1.0741   -1.3596 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0752   -0.7182   -1.5454 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5006    0.4659   -1.3157 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.8627    0.7192   -1.5233 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.7372    0.3071   -0.5120 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.4558   -0.6975    0.2000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8292   -0.3989    2.8828 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2746    1.3323    2.6226 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9952    0.8327    2.3445 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8384   -0.7545    0.5790 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2418    0.9911    0.2522 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6944    1.5273    0.7410 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8273   -1.3726    0.0806 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6596   -1.4584   -0.3212 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0976    1.4494    0.2293 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9987    1.3680   -0.2311 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9851   -1.5360   -0.9257 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1214    0.7960   -0.7528 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2867   -2.0620   -1.5364 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7566   -1.4662   -1.8859 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1371    1.1967   -2.4008 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
  4  5  1  0  0  0  0
  5  6  2  3  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  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  1  0  0  0  0
 14 15  2  0  0  0  0
  1 16  1  0  0  0  0
  1 17  1  0  0  0  0
  1 18  1  0  0  0  0
  2 19  1  0  0  0  0
  2 20  1  0  0  0  0
  3 21  1  0  0  0  0
  4 22  1  0  0  0  0
  5 23  1  0  0  0  0
  6 24  1  0  0  0  0
  7 25  1  0  0  0  0
  8 26  1  0  0  0  0
  9 27  1  0  0  0  0
 10 28  1  0  0  0  0
 11 29  1  0  0  0  0
 13 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0021243

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]N(N=O)\N=C(/[H])\C(\[H])=C(/[H])\C(\[H])=C(/[H])C([H])=C([H])C(\[H])=C(/[H])C([H])([H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C11H15N3O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15/h3-11H,2H2,1H3,(H,13,15)/b4-3+,6-5?,8-7+,10-9+,12-11+

> <INCHI_KEY>
UNHSVZVRFBRLAW-STAPSFGWSA-N

> <FORMULA>
C11H15N3O

> <MOLECULAR_WEIGHT>
205.261

> <EXACT_MASS>
205.121512115

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
30

> <JCHEM_AVERAGE_POLARIZABILITY>
24.319607218220547

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(E)-1-nitroso-2-[(2E,4E,8E)-undeca-2,4,6,8-tetraen-1-ylidene]hydrazine

> <ALOGPS_LOGP>
4.70

> <JCHEM_LOGP>
2.831943883666667

> <ALOGPS_LOGS>
-4.31

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.887268475679595

> <JCHEM_PKA_STRONGEST_BASIC>
1.1195127049738978

> <JCHEM_POLAR_SURFACE_AREA>
53.82

> <JCHEM_REFRACTIVITY>
68.3105

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.01e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(E)-1-nitroso-2-[(2E,4E,8E)-undeca-2,4,6,8-tetraen-1-ylidene]hydrazine

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 30 29  0  0  0  0  0  0  0  0999 V2000
   -5.9330    0.5305    2.2725 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5831    0.2773    0.8179 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1668    0.5690    0.6062 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3460   -0.4444    0.2050 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9755   -0.1273    0.0079 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8081    0.1086   -0.1676 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4992    0.3867   -0.3609 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4013   -0.5679   -0.7716 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7751   -0.1798   -0.9457 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6777   -1.0741   -1.3596 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0752   -0.7182   -1.5454 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5006    0.4659   -1.3157 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.8627    0.7192   -1.5233 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.7372    0.3071   -0.5120 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.4558   -0.6975    0.2000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8292   -0.3989    2.8828 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2746    1.3323    2.6226 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9952    0.8327    2.3445 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8384   -0.7545    0.5790 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2418    0.9911    0.2522 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6944    1.5273    0.7410 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8273   -1.3726    0.0806 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6596   -1.4584   -0.3212 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0976    1.4494    0.2293 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9987    1.3680   -0.2311 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9851   -1.5360   -0.9257 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1214    0.7960   -0.7528 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2867   -2.0620   -1.5364 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7566   -1.4662   -1.8859 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1371    1.1967   -2.4008 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
  4  5  1  0
  5  6  2  3
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
  1 16  1  0
  1 17  1  0
  1 18  1  0
  2 19  1  0
  2 20  1  0
  3 21  1  0
  4 22  1  0
  5 23  1  0
  6 24  1  0
  7 25  1  0
  8 26  1  0
  9 27  1  0
 10 28  1  0
 11 29  1  0
 13 30  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      -5.933   0.531   2.272  0.00  0.00           C+0
HETATM    2  C   UNK     0      -5.583   0.277   0.818  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.167   0.569   0.606  0.00  0.00           C+0
HETATM    4  C   UNK     0      -3.346  -0.444   0.205  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.976  -0.127   0.008  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.808   0.109  -0.168  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.499   0.387  -0.361  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.401  -0.568  -0.772  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.775  -0.180  -0.946  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.678  -1.074  -1.360  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.075  -0.718  -1.545  0.00  0.00           C+0
HETATM   12  N   UNK     0       5.501   0.466  -1.316  0.00  0.00           N+0
HETATM   13  N   UNK     0       6.863   0.719  -1.523  0.00  0.00           N+0
HETATM   14  N   UNK     0       7.737   0.307  -0.512  0.00  0.00           N+0
HETATM   15  O   UNK     0       7.456  -0.698   0.200  0.00  0.00           O+0
HETATM   16  H   UNK     0      -5.829  -0.399   2.883  0.00  0.00           H+0
HETATM   17  H   UNK     0      -5.275   1.332   2.623  0.00  0.00           H+0
HETATM   18  H   UNK     0      -6.995   0.833   2.345  0.00  0.00           H+0
HETATM   19  H   UNK     0      -5.838  -0.755   0.579  0.00  0.00           H+0
HETATM   20  H   UNK     0      -6.242   0.991   0.252  0.00  0.00           H+0
HETATM   21  H   UNK     0      -3.694   1.527   0.741  0.00  0.00           H+0
HETATM   22  H   UNK     0      -3.827  -1.373   0.081  0.00  0.00           H+0
HETATM   23  H   UNK     0      -1.660  -1.458  -0.321  0.00  0.00           H+0
HETATM   24  H   UNK     0      -1.098   1.449   0.229  0.00  0.00           H+0
HETATM   25  H   UNK     0       0.999   1.368  -0.231  0.00  0.00           H+0
HETATM   26  H   UNK     0       0.985  -1.536  -0.926  0.00  0.00           H+0
HETATM   27  H   UNK     0       3.121   0.796  -0.753  0.00  0.00           H+0
HETATM   28  H   UNK     0       3.287  -2.062  -1.536  0.00  0.00           H+0
HETATM   29  H   UNK     0       5.757  -1.466  -1.886  0.00  0.00           H+0
HETATM   30  H   UNK     0       7.137   1.197  -2.401  0.00  0.00           H+0
CONECT    1    2   16   17   18                                             
CONECT    2    1    3   19   20                                             
CONECT    3    2    4   21                                                  
CONECT    4    3    5   22                                                  
CONECT    5    4    6   23                                                  
CONECT    6    5    7   24                                                  
CONECT    7    6    8   25                                                  
CONECT    8    7    9   26                                                  
CONECT    9    8   10   27                                                  
CONECT   10    9   11   28                                                  
CONECT   11   10   12   29                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   30                                                  
CONECT   14   13   15                                                       
CONECT   15   14                                                            
CONECT   16    1                                                            
CONECT   17    1                                                            
CONECT   18    1                                                            
CONECT   19    2                                                            
CONECT   20    2                                                            
CONECT   21    3                                                            
CONECT   22    4                                                            
CONECT   23    5                                                            
CONECT   24    6                                                            
CONECT   25    7                                                            
CONECT   26    8                                                            
CONECT   27    9                                                            
CONECT   28   10                                                            
CONECT   29   11                                                            
CONECT   30   13                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   58    0
END

RDKit          3D

30 29  0  0  0  0  0  0  0  0999 V2000
   -5.9330    0.5305    2.2725 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5831    0.2773    0.8179 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1668    0.5690    0.6062 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3460   -0.4444    0.2050 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9755   -0.1273    0.0079 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8081    0.1086   -0.1676 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4992    0.3867   -0.3609 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4013   -0.5679   -0.7716 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7751   -0.1798   -0.9457 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6777   -1.0741   -1.3596 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0752   -0.7182   -1.5454 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5006    0.4659   -1.3157 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.8627    0.7192   -1.5233 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.7372    0.3071   -0.5120 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.4558   -0.6975    0.2000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8292   -0.3989    2.8828 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2746    1.3323    2.6226 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9952    0.8327    2.3445 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8384   -0.7545    0.5790 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2418    0.9911    0.2522 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6944    1.5273    0.7410 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8273   -1.3726    0.0806 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6596   -1.4584   -0.3212 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0976    1.4494    0.2293 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9987    1.3680   -0.2311 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9851   -1.5360   -0.9257 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1214    0.7960   -0.7528 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2867   -2.0620   -1.5364 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7566   -1.4662   -1.8859 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1371    1.1967   -2.4008 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
  4  5  1  0
  5  6  2  3
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
  1 16  1  0
  1 17  1  0
  1 18  1  0
  2 19  1  0
  2 20  1  0
  3 21  1  0
  4 22  1  0
  5 23  1  0
  6 24  1  0
  7 25  1  0
  8 26  1  0
  9 27  1  0
 10 28  1  0
 11 29  1  0
 13 30  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
Triacsin b	MeSH

Chemical Formula

C₁₁H₁₅N₃O

Average Mass

205.2610 Da

Monoisotopic Mass

205.12151 Da

IUPAC Name

(E)-1-nitroso-2-[(2E,4E,8E)-undeca-2,4,6,8-tetraen-1-ylidene]hydrazine

Traditional Name

(E)-1-nitroso-2-[(2E,4E,8E)-undeca-2,4,6,8-tetraen-1-ylidene]hydrazine

CAS Registry Number

Not Available

SMILES

CC\C=C\C=C\C=C\C=C\C=N\NN=O

InChI Identifier

InChI=1S/C11H15N3O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15/h3-11H,2H2,1H3,(H,13,15)/b4-3+,6-5+,8-7+,10-9+,12-11+

InChI Key

UNHSVZVRFBRLAW-STAPSFGWSA-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
Streptomyces	NPAtlas	3781919

Species Where Detected

Species Name	Source	Reference
Streptomyces sp. SK-1894	KNApSAcK Database	22123792

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as organic n-nitroso compounds. These are organic compounds containing a n-nitroso group -NN=O.

Kingdom

Organic compounds

Super Class

Organic nitrogen compounds

Class

Organonitrogen compounds

Sub Class

Organic nitroso compounds

Direct Parent

Organic N-nitroso compounds

Alternative Parents

Substituents

Organic n-nitroso compound
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic 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	4.7	ALOGPS
logP	2.83	ChemAxon
logS	-4.3	ALOGPS
pKa (Strongest Acidic)	7.89	ChemAxon
pKa (Strongest Basic)	1.12	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	53.82 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	68.31 m³·mol⁻¹	ChemAxon
Polarizability	24.32 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

NPAtlas ID

NPA020841

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00017801

Chemspider ID

7852319

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

9577955

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Triacsin B (NP0021243)

MOL for NP0021243 (Triacsin B)

3D MOL for NP0021243 (Triacsin B)

3D SDF for NP0021243 (Triacsin B)

3D-SDF for NP0021243 (Triacsin B)

PDB for NP0021243 (Triacsin B)

3D PDB for NP0021243 (Triacsin B)

SMILES for NP0021243 (Triacsin B)

INCHI for NP0021243 (Triacsin B)

Structure for NP0021243 (Triacsin B)

3D Structure for NP0021243 (Triacsin B)