NP-MRD: Showing NP-Card for (3z)-dodec-3-en-1-yl({4-methoxy-1h,1'h-[2,2'-bipyrrol]-5-yl}methylidene)amine (NP0161740)

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Record Information

Version

2.0

Created at

2022-09-02 19:59:36 UTC

Updated at

2022-09-02 19:59:37 UTC

NP-MRD ID

NP0161740

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3z)-dodec-3-en-1-yl({4-methoxy-1h,1'h-[2,2'-bipyrrol]-5-yl}methylidene)amine

Description

[(3Z)-dodec-3-en-1-yl]({4-methoxy-1H,1'H-[2,2'-bipyrrole]-5-yl}methylidene)amine belongs to the class of organic compounds known as alkyl aryl ethers. These are organic compounds containing the alkyl aryl ether functional group with the generic formula R-O-R' , where R is an alkyl group and R' is an aryl group. (3z)-dodec-3-en-1-yl({4-methoxy-1h,1'h-[2,2'-bipyrrol]-5-yl}methylidene)amine is found in Pseudoalteromonas tunicata. Based on a literature review very few articles have been published on [(3Z)-dodec-3-en-1-yl]({4-methoxy-1H,1'H-[2,2'-bipyrrole]-5-yl}methylidene)amine.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022221592D          

 26 27  0  0  0  0            999 V2000
    2.9146  -11.0017    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6291  -10.5892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3436  -11.0017    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0580  -10.5892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7725  -11.0017    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4870  -10.5892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2014  -11.0017    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9159  -10.5892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6304  -11.0017    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3449  -10.5892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3449   -9.7642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0593   -9.3517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7738   -9.7642    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   11.4883   -9.3517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2027   -9.7642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9564   -9.4287    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   13.5085  -10.0417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.3289   -9.9555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.7414   -9.2410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.5484   -9.4126    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6346  -10.2330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.8810  -10.5686    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   13.0960  -10.7562    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2890  -10.5847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6759  -11.1367    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.8913  -10.8818    0.0000 C   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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 13 12  1  4  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 18 22  1  0  0  0  0
 17 23  2  0  0  0  0
 23 24  1  0  0  0  0
 15 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
M  END

     RDKit          3D

 59 60  0  0  0  0  0  0  0  0999 V2000
    7.0452   -1.4142    2.4358 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8310   -0.8546    1.0676 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4583    0.6131    1.0715 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2160    0.9088    1.8058 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9803    0.2396    1.4045 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3608    0.4112    0.0818 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0715    0.0072   -1.1459 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0527    0.2828   -2.3068 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8915   -0.5458   -2.0094 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7003   -0.0382   -1.8196 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3787    1.3816   -1.8778 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1766    1.8399   -0.5371 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3797    1.1221   -0.1772 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4976    1.3553   -0.7605 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7264    0.6543   -0.4257 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9536    0.7988   -0.9523 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8205   -0.0384   -0.3667 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2506   -0.1610   -0.6837 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1207   -1.0319   -0.0645 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3964   -0.8765   -0.6173 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2495    0.1138   -1.5817 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9642    0.5080   -1.5865 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1007   -0.7425    0.5736 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7851   -0.3341    0.5638 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7263   -0.7850    1.3508 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0064   -1.7964    2.2953 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0838   -1.7251    2.9058 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7105   -2.3156    2.3229 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5705   -0.7156    3.1038 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8060   -0.9255    0.5056 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0895   -1.4292    0.5146 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4659    1.0002    0.0635 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3373    1.1911    1.5682 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0440    2.0386    1.6807 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3675    0.8481    2.9301 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1712    0.5895    2.1560 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0072   -0.8783    1.6560 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3856   -0.1930    0.1186 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0084    1.4826   -0.0451 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3651   -1.0418   -1.1724 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9360    0.6467   -1.3979 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5753   -0.1275   -3.2098 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9425    1.3533   -2.3164 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0528   -1.6314   -1.9486 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1317   -0.7212   -1.5985 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4999    1.4823   -2.5925 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1259    2.0702   -2.2396 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5951    1.5947    0.2373 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3784    2.9221   -0.5937 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5259    2.1034   -1.5319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1461    1.4898   -1.7163 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9273   -1.7458    0.7232 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.2917   -1.4157   -0.3441 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0806    0.4598   -2.1913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5523    1.2504   -2.2162 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5259   -1.5021    1.2165 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2661   -1.8426    3.1141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0052   -1.5712    2.7699 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1408   -2.7784    1.7895 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 24  2  0
 24 25  1  0
 25 26  1  0
 24 23  1  0
 23 17  2  0
 17 16  1  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 16 15  1  0
 22 18  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  2 30  1  0
  2 31  1  0
  3 32  1  0
  3 33  1  0
  4 34  1  0
  4 35  1  0
  5 36  1  0
  5 37  1  0
  6 38  1  0
  6 39  1  0
  7 40  1  0
  7 41  1  0
  8 42  1  0
  8 43  1  0
  9 44  1  0
 10 45  1  0
 11 46  1  0
 11 47  1  0
 12 48  1  0
 12 49  1  0
 14 50  1  0
 26 57  1  0
 26 58  1  0
 26 59  1  0
 23 56  1  0
 16 51  1  0
 19 52  1  0
 20 53  1  0
 21 54  1  0
 22 55  1  0
M  END


  Mrv1652309022221592D          

 26 27  0  0  0  0            999 V2000
    2.9146  -11.0017    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6291  -10.5892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3436  -11.0017    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0580  -10.5892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7725  -11.0017    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4870  -10.5892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2014  -11.0017    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9159  -10.5892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6304  -11.0017    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3449  -10.5892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3449   -9.7642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0593   -9.3517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7738   -9.7642    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   11.4883   -9.3517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2027   -9.7642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9564   -9.4287    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   13.5085  -10.0417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.3289   -9.9555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.7414   -9.2410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.5484   -9.4126    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6346  -10.2330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.8810  -10.5686    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   13.0960  -10.7562    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2890  -10.5847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6759  -11.1367    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.8913  -10.8818    0.0000 C   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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 13 12  1  4  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 18 22  1  0  0  0  0
 17 23  2  0  0  0  0
 23 24  1  0  0  0  0
 15 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0161740

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCC\C=C/CCN=CC1=C(OC)C=C(N1)C1=CC=CN1

> <INCHI_IDENTIFIER>
InChI=1S/C22H33N3O/c1-3-4-5-6-7-8-9-10-11-12-15-23-18-21-22(26-2)17-20(25-21)19-14-13-16-24-19/h10-11,13-14,16-18,24-25H,3-9,12,15H2,1-2H3/b11-10-,23-18?

> <INCHI_KEY>
CHBHMVCOGQWJJP-JUXBKNRKSA-N

> <FORMULA>
C22H33N3O

> <MOLECULAR_WEIGHT>
355.526

> <EXACT_MASS>
355.262362695

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
44.56647349241181

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[(3Z)-dodec-3-en-1-yl]({4-methoxy-1H,1'H-[2,2'-bipyrrole]-5-yl}methylidene)amine

> <ALOGPS_LOGP>
6.62

> <JCHEM_LOGP>
5.849938110333333

> <ALOGPS_LOGS>
-6.53

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
16.92916086447077

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.042602168632243

> <JCHEM_PKA_STRONGEST_BASIC>
6.679991838558097

> <JCHEM_POLAR_SURFACE_AREA>
53.17

> <JCHEM_REFRACTIVITY>
112.14350000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.05e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3Z)-dodec-3-en-1-yl({4-methoxy-1H,1'H-[2,2'-bipyrrole]-5-yl}methylidene)amine

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0       5.441 -20.537   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.774 -19.767   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.108 -20.537   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.442 -19.767   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.775 -20.537   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      12.109 -19.767   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      13.443 -20.537   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      14.776 -19.767   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      16.110 -20.537   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      17.444 -19.767   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      17.444 -18.227   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      18.777 -17.457   0.000  0.00  0.00           C+0
HETATM   13  N   UNK     0      20.111 -18.227   0.000  0.00  0.00           N+0
HETATM   14  C   UNK     0      21.445 -17.457   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      22.778 -18.227   0.000  0.00  0.00           C+0
HETATM   16  N   UNK     0      24.185 -17.600   0.000  0.00  0.00           N+0
HETATM   17  C   UNK     0      25.216 -18.745   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      26.747 -18.584   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      27.517 -17.250   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      29.024 -17.570   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      29.185 -19.102   0.000  0.00  0.00           C+0
HETATM   22  N   UNK     0      27.778 -19.728   0.000  0.00  0.00           N+0
HETATM   23  C   UNK     0      24.446 -20.078   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      22.939 -19.758   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      21.795 -20.789   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      20.330 -20.313   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   24                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   23                                                  
CONECT   18   17   19   22                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   18                                                       
CONECT   23   17   24                                                       
CONECT   24   23   15   25                                                  
CONECT   25   24   26                                                       
CONECT   26   25                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   54    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₃₃N₃O

Average Mass

355.5260 Da

Monoisotopic Mass

355.26236 Da

IUPAC Name

[(3Z)-dodec-3-en-1-yl]({4-methoxy-1H,1'H-[2,2'-bipyrrole]-5-yl}methylidene)amine

Traditional Name

(3Z)-dodec-3-en-1-yl({4-methoxy-1H,1'H-[2,2'-bipyrrole]-5-yl}methylidene)amine

CAS Registry Number

Not Available

SMILES

CCCCCCCC\C=C/CCN=CC1=C(OC)C=C(N1)C1=CC=CN1

InChI Identifier

InChI=1S/C22H33N3O/c1-3-4-5-6-7-8-9-10-11-12-15-23-18-21-22(26-2)17-20(25-21)19-14-13-16-24-19/h10-11,13-14,16-18,24-25H,3-9,12,15H2,1-2H3/b11-10-,23-18?

InChI Key

CHBHMVCOGQWJJP-JUXBKNRKSA-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, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, 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
Pseudoalteromonas tunicata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as alkyl aryl ethers. These are organic compounds containing the alkyl aryl ether functional group with the generic formula R-O-R' , where R is an alkyl group and R' is an aryl group.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Ethers

Direct Parent

Alkyl aryl ethers

Alternative Parents

Substituents

Alkyl aryl ether
Substituted pyrrole
Heteroaromatic compound
Pyrrole
Shiff base
Azacycle
Organoheterocyclic compound
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Aldimine
Organic nitrogen compound
Organopnictogen compound
Hydrocarbon derivative
Organonitrogen compound
Imine
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic 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	6.62	ALOGPS
logP	5.85	ChemAxon
logS	-6.5	ALOGPS
pKa (Strongest Acidic)	14.04	ChemAxon
pKa (Strongest Basic)	6.68	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	53.17 Å²	ChemAxon
Rotatable Bond Count	13	ChemAxon
Refractivity	112.14 m³·mol⁻¹	ChemAxon
Polarizability	44.57 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

135577882

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3z)-dodec-3-en-1-yl({4-methoxy-1h,1'h-[2,2'-bipyrrol]-5-yl}methylidene)amine (NP0161740)

MOL for NP0161740 ((3z)-dodec-3-en-1-yl({4-methoxy-1h,1'h-[2,2'-bipyrrol]-5-yl}methylidene)amine)

3D MOL for NP0161740 ((3z)-dodec-3-en-1-yl({4-methoxy-1h,1'h-[2,2'-bipyrrol]-5-yl}methylidene)amine)

3D SDF for NP0161740 ((3z)-dodec-3-en-1-yl({4-methoxy-1h,1'h-[2,2'-bipyrrol]-5-yl}methylidene)amine)

3D-SDF for NP0161740 ((3z)-dodec-3-en-1-yl({4-methoxy-1h,1'h-[2,2'-bipyrrol]-5-yl}methylidene)amine)

PDB for NP0161740 ((3z)-dodec-3-en-1-yl({4-methoxy-1h,1'h-[2,2'-bipyrrol]-5-yl}methylidene)amine)

3D PDB for NP0161740 ((3z)-dodec-3-en-1-yl({4-methoxy-1h,1'h-[2,2'-bipyrrol]-5-yl}methylidene)amine)

SMILES for NP0161740 ((3z)-dodec-3-en-1-yl({4-methoxy-1h,1'h-[2,2'-bipyrrol]-5-yl}methylidene)amine)

INCHI for NP0161740 ((3z)-dodec-3-en-1-yl({4-methoxy-1h,1'h-[2,2'-bipyrrol]-5-yl}methylidene)amine)

Structure for NP0161740 ((3z)-dodec-3-en-1-yl({4-methoxy-1h,1'h-[2,2'-bipyrrol]-5-yl}methylidene)amine)

3D Structure for NP0161740 ((3z)-dodec-3-en-1-yl({4-methoxy-1h,1'h-[2,2'-bipyrrol]-5-yl}methylidene)amine)