NP-MRD: Showing NP-Card for (5z)-5-[(5-undecyl-1h-pyrrol-2-yl)methylidene]-1'h-2,2'-bipyrrole (NP0292026)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-09 23:21:59 UTC

Updated at

2022-09-09 23:21:59 UTC

NP-MRD ID

NP0292026

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(5z)-5-[(5-undecyl-1h-pyrrol-2-yl)methylidene]-1'h-2,2'-bipyrrole

Description

CHEMBL86046 belongs to the class of organic compounds known as dipyrrins. Dipyrrins are compounds containing two pyrrole rings fused via a methine (-C=) group. (5z)-5-[(5-undecyl-1h-pyrrol-2-yl)methylidene]-1'h-2,2'-bipyrrole is found in Streptomyces albidoflavus. Based on a literature review very few articles have been published on CHEMBL86046.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102201222D          

 27 29  0  0  0  0            999 V2000
    8.1709    2.1967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8853    2.6092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5998    2.1967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3143    2.6092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0287    2.1967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7432    2.6092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.4577    2.1967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.1722    2.6092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.8866    2.1967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.6011    2.6092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.3156    2.1967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.0300    2.6092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.1163    3.4297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.9233    3.6012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.3358    2.8867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.1562    2.8005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.4918    2.0468    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.2988    1.8753    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.3850    1.0548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.6313    0.7193    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.4598   -0.0877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.0118   -0.7008    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5993   -1.4153    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.7924   -1.2438    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.7061   -0.4233    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   18.0793    1.3324    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   16.7837    2.2736    0.0000 N   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  1  0  0  0  0
 10 11  1  0  0  0  0
 11 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
 16 17  2  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  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 21 25  1  0  0  0  0
 20 26  2  0  0  0  0
 17 26  1  0  0  0  0
 15 27  1  0  0  0  0
 12 27  1  0  0  0  0
M  END

     RDKit          3D

 60 62  0  0  0  0  0  0  0  0999 V2000
    8.2215   -0.3642   -0.8952 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6013    0.2466    0.3552 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1980   -0.8096    1.3421 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2574   -1.8448    0.9262 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8847   -1.5579    0.4925 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6293   -0.7230   -0.6865 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1443   -0.6481   -0.9823 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3825   -0.0555    0.1602 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8873    0.0518   -0.1647 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6124    0.9122   -1.3521 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8433    1.0556   -1.6631 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5962    1.7552   -0.6071 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1139    2.4311    0.4745 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2331    2.8906    1.1850 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3671    2.4846    0.5183 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7172    2.7933    0.9831 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7278    1.9730    0.8554 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1291    2.1660    1.2799 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7689    1.0618    0.9307 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8112    0.1489    0.2848 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1762   -1.1744   -0.2335 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3490   -2.0887   -0.8511 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0774   -3.2078   -1.1901 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3660   -2.9721   -0.7733 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3764   -1.7583   -0.2137 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6416    0.6860    0.2487 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9660    1.8082   -0.5493 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.9632   -1.1300   -0.6001 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4609   -0.7416   -1.6033 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7753    0.4438   -1.4046 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5050    0.8239    0.8039 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8981    1.0283    0.1384 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1796   -1.3481    1.5844 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9528   -0.3515    2.3427 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1550   -2.5579    1.8216 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7800   -2.5162    0.1774 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2512   -1.1682    1.3558 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3919   -2.5635    0.2933 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9429    0.3423   -0.6280 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0907   -1.1948   -1.6011 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7521   -1.7000   -1.1159 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9875   -0.0760   -1.9263 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7277    0.9164    0.5064 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4001   -0.8038    1.0033 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3890    0.4190    0.7299 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4901   -0.9894   -0.3645 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1174    1.9032   -1.2948 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0801    0.4121   -2.2485 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0074    1.5481   -2.6501 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2507    0.0113   -1.8122 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0928    2.6197    0.7578 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1300    3.4614    2.0951 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9053    3.7450    1.4590 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5094    3.0415    1.7700 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8079    0.8562    1.0871 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3042   -1.9716   -1.0470 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7709   -4.1219   -1.6822 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2319   -3.6455   -0.8754 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2350   -1.3269    0.1906 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6034    1.3741   -1.2532 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  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 27  1  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 26  2  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  2  0
 24 25  1  0
 27 12  1  0
 26 17  1  0
 25 21  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  2 31  1  0
  2 32  1  0
  3 33  1  0
  3 34  1  0
  4 35  1  0
  4 36  1  0
  5 37  1  0
  5 38  1  0
  6 39  1  0
  6 40  1  0
  7 41  1  0
  7 42  1  0
  8 43  1  0
  8 44  1  0
  9 45  1  0
  9 46  1  0
 10 47  1  0
 10 48  1  0
 11 49  1  0
 11 50  1  0
 13 51  1  0
 14 52  1  0
 27 60  1  0
 16 53  1  0
 18 54  1  0
 19 55  1  0
 22 56  1  0
 23 57  1  0
 24 58  1  0
 25 59  1  0
M  END


  Mrv1652309102201222D          

 27 29  0  0  0  0            999 V2000
    8.1709    2.1967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8853    2.6092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5998    2.1967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3143    2.6092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0287    2.1967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7432    2.6092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.4577    2.1967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.1722    2.6092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.8866    2.1967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.6011    2.6092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.3156    2.1967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.0300    2.6092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.1163    3.4297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.9233    3.6012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.3358    2.8867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.1562    2.8005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.4918    2.0468    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.2988    1.8753    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.3850    1.0548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.6313    0.7193    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.4598   -0.0877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.0118   -0.7008    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5993   -1.4153    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.7924   -1.2438    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.7061   -0.4233    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   18.0793    1.3324    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   16.7837    2.2736    0.0000 N   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  1  0  0  0  0
 10 11  1  0  0  0  0
 11 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
 16 17  2  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  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 21 25  1  0  0  0  0
 20 26  2  0  0  0  0
 17 26  1  0  0  0  0
 15 27  1  0  0  0  0
 12 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0292026

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCCC1=CC=C(N1)\C=C1\C=CC(=N1)C1=CC=CN1

> <INCHI_IDENTIFIER>
InChI=1S/C24H33N3/c1-2-3-4-5-6-7-8-9-10-12-20-14-15-21(26-20)19-22-16-17-24(27-22)23-13-11-18-25-23/h11,13-19,25-26H,2-10,12H2,1H3/b22-19-

> <INCHI_KEY>
MTEMKDFDIADHNU-QOCHGBHMSA-N

> <FORMULA>
C24H33N3

> <MOLECULAR_WEIGHT>
363.549

> <EXACT_MASS>
363.267448075

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
46.390841017034134

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(5'Z)-5'-[(5-undecyl-1H-pyrrol-2-yl)methylidene]-1H,5'H-2,2'-bipyrrole

> <JCHEM_LOGP>
6.694281792333333

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
16.59850923628786

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.502257058345815

> <JCHEM_PKA_STRONGEST_BASIC>
8.024547555131818

> <JCHEM_POLAR_SURFACE_AREA>
43.94

> <JCHEM_REFRACTIVITY>
118.13570000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(5Z)-5-[(5-undecyl-1H-pyrrol-2-yl)methylidene]-1'H-2,2'-bipyrrole

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0      15.252   4.101   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      16.586   4.871   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      17.920   4.101   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      19.253   4.871   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      20.587   4.101   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      21.921   4.871   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      23.254   4.101   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      24.588   4.871   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      25.922   4.101   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      27.255   4.871   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      28.589   4.101   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      29.923   4.871   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      30.084   6.402   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      31.590   6.722   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      32.360   5.389   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      33.892   5.228   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      34.518   3.821   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      36.024   3.501   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      36.185   1.969   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      34.778   1.343   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      34.458  -0.164   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      35.489  -1.308   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      34.719  -2.642   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      33.212  -2.322   0.000  0.00  0.00           C+0
HETATM   25  N   UNK     0      33.051  -0.790   0.000  0.00  0.00           N+0
HETATM   26  N   UNK     0      33.748   2.487   0.000  0.00  0.00           N+0
HETATM   27  N   UNK     0      31.330   4.244   0.000  0.00  0.00           N+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   27                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   27                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   26                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   26                                                  
CONECT   21   20   22   25                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   21                                                       
CONECT   26   20   17                                                       
CONECT   27   15   12                                                       
MASTER        0    0    0    0    0    0    0    0   27    0   58    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₃₃N₃

Average Mass

363.5490 Da

Monoisotopic Mass

363.26745 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCC1=CC=C(N1)\C=C1\C=CC(=N1)C1=CC=CN1

InChI Identifier

InChI=1S/C24H33N3/c1-2-3-4-5-6-7-8-9-10-12-20-14-15-21(26-20)19-22-16-17-24(27-22)23-13-11-18-25-23/h11,13-19,25-26H,2-10,12H2,1H3/b22-19-

InChI Key

MTEMKDFDIADHNU-QOCHGBHMSA-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
Streptomyces albidoflavus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as dipyrrins. Dipyrrins are compounds containing two pyrrole rings fused via a methine (-C=) group.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Pyrroles

Sub Class

Substituted pyrroles

Direct Parent

Dipyrrins

Alternative Parents

Substituents

Dipyrrin
Heteroaromatic compound
Ketimine
Azacycle
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
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

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

59702810

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

135476167

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (5z)-5-[(5-undecyl-1h-pyrrol-2-yl)methylidene]-1'h-2,2'-bipyrrole (NP0292026)

MOL for NP0292026 ((5z)-5-[(5-undecyl-1h-pyrrol-2-yl)methylidene]-1'h-2,2'-bipyrrole)

3D MOL for NP0292026 ((5z)-5-[(5-undecyl-1h-pyrrol-2-yl)methylidene]-1'h-2,2'-bipyrrole)

3D SDF for NP0292026 ((5z)-5-[(5-undecyl-1h-pyrrol-2-yl)methylidene]-1'h-2,2'-bipyrrole)

3D-SDF for NP0292026 ((5z)-5-[(5-undecyl-1h-pyrrol-2-yl)methylidene]-1'h-2,2'-bipyrrole)

PDB for NP0292026 ((5z)-5-[(5-undecyl-1h-pyrrol-2-yl)methylidene]-1'h-2,2'-bipyrrole)

3D PDB for NP0292026 ((5z)-5-[(5-undecyl-1h-pyrrol-2-yl)methylidene]-1'h-2,2'-bipyrrole)

SMILES for NP0292026 ((5z)-5-[(5-undecyl-1h-pyrrol-2-yl)methylidene]-1'h-2,2'-bipyrrole)

INCHI for NP0292026 ((5z)-5-[(5-undecyl-1h-pyrrol-2-yl)methylidene]-1'h-2,2'-bipyrrole)

Structure for NP0292026 ((5z)-5-[(5-undecyl-1h-pyrrol-2-yl)methylidene]-1'h-2,2'-bipyrrole)

3D Structure for NP0292026 ((5z)-5-[(5-undecyl-1h-pyrrol-2-yl)methylidene]-1'h-2,2'-bipyrrole)