NP-MRD: Showing NP-Card for Legioliulin (NP0005504)

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Record Information

Version

2.0

Created at

2020-12-09 02:44:15 UTC

Updated at

2021-07-15 16:52:12 UTC

NP-MRD ID

NP0005504

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Legioliulin

Provided By

NPAtlas

Description

Legioliulin is a secondary metabolite. Secondary metabolites are metabolically or physiologically non-essential metabolites that may serve a role as defense or signalling molecules. In some cases they are simply molecules that arise from the incomplete metabolism of other secondary metabolites. Legioliulin is found in Legionella and Legionella parisiensis. Legioliulin was first documented in 2004 (PMID: 15381093). Based on a literature review very few articles have been published on Legioliulin (PMID: 23821465).

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242118193D          

 36 38  0  0  0  0            999 V2000
    3.3784    2.7043   -0.3285 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2240    1.4658   -0.1228 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0071    0.9721   -0.0852 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6842   -0.2685    0.1143 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2873   -0.7287    0.1393 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7057    0.1236   -0.0445 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1161   -0.3307   -0.0211 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0828    0.5473   -0.2083 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5026    0.2469   -0.2115 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0031   -1.0154   -0.0151 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3798   -1.2621   -0.0259 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2802   -0.2468   -0.2340 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7845    1.0237   -0.4319 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4280    1.2510   -0.4186 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7144   -1.1559    0.3056 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0341   -0.7179    0.2815 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0805   -1.5659    0.4666 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3793   -1.1138    0.4393 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6367    0.2093    0.2231 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5821    1.1362    0.0242 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9134    2.4401   -0.1859 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2997    0.6369    0.0602 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0433   -1.7675    0.3073 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4595    1.1620   -0.2124 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3740   -1.3474    0.1426 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7751    1.5909   -0.3747 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3248   -1.8386    0.1516 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7729   -2.2583    0.1291 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3502   -0.4196   -0.2456 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4994    1.8387   -0.5986 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0827    2.2718   -0.5797 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5402   -2.2032    0.4778 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8723   -2.6179    0.6383 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2150   -1.7897    0.5869 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6529    0.5994    0.1955 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3766    3.2146   -0.3388 H   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  1  0  0  0  0
  5  6  2  0  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  2  0  0  0  0
  4 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
 20 22  2  0  0  0  0
 22  2  1  0  0  0  0
 14  9  1  0  0  0  0
 22 16  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
 10 27  1  0  0  0  0
 11 28  1  0  0  0  0
 12 29  1  0  0  0  0
 13 30  1  0  0  0  0
 14 31  1  0  0  0  0
 15 32  1  0  0  0  0
 17 33  1  0  0  0  0
 18 34  1  0  0  0  0
 19 35  1  0  0  0  0
 21 36  1  0  0  0  0
M  END

     RDKit          3D

 36 38  0  0  0  0  0  0  0  0999 V2000
    3.3784    2.7043   -0.3285 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2240    1.4658   -0.1228 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0071    0.9721   -0.0852 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6842   -0.2685    0.1143 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2873   -0.7287    0.1393 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7057    0.1236   -0.0445 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1161   -0.3307   -0.0211 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0828    0.5473   -0.2083 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5026    0.2469   -0.2115 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0031   -1.0154   -0.0151 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3798   -1.2621   -0.0259 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2802   -0.2468   -0.2340 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7845    1.0237   -0.4319 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4280    1.2510   -0.4186 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7144   -1.1559    0.3056 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0341   -0.7179    0.2815 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0805   -1.5659    0.4666 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3793   -1.1138    0.4393 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6367    0.2093    0.2231 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5821    1.1362    0.0242 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9134    2.4401   -0.1859 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2997    0.6369    0.0602 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0433   -1.7675    0.3073 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4595    1.1620   -0.2124 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3740   -1.3474    0.1426 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7751    1.5909   -0.3747 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3248   -1.8386    0.1516 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7729   -2.2583    0.1291 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3502   -0.4196   -0.2456 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4994    1.8387   -0.5986 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0827    2.2718   -0.5797 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5402   -2.2032    0.4778 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8723   -2.6179    0.6383 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2150   -1.7897    0.5869 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6529    0.5994    0.1955 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3766    3.2146   -0.3388 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  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  2  0
  4 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  1  0
 20 22  2  0
 22  2  1  0
 14  9  1  0
 22 16  1  0
  5 23  1  0
  6 24  1  0
  7 25  1  0
  8 26  1  0
 10 27  1  0
 11 28  1  0
 12 29  1  0
 13 30  1  0
 14 31  1  0
 15 32  1  0
 17 33  1  0
 18 34  1  0
 19 35  1  0
 21 36  1  0
M  END


  Mrv1652306242118193D          

 36 38  0  0  0  0            999 V2000
    3.3784    2.7043   -0.3285 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2240    1.4658   -0.1228 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0071    0.9721   -0.0852 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6842   -0.2685    0.1143 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2873   -0.7287    0.1393 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7057    0.1236   -0.0445 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1161   -0.3307   -0.0211 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0828    0.5473   -0.2083 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5026    0.2469   -0.2115 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0031   -1.0154   -0.0151 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3798   -1.2621   -0.0259 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2802   -0.2468   -0.2340 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7845    1.0237   -0.4319 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4280    1.2510   -0.4186 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7144   -1.1559    0.3056 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0341   -0.7179    0.2815 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0805   -1.5659    0.4666 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3793   -1.1138    0.4393 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6367    0.2093    0.2231 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5821    1.1362    0.0242 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9134    2.4401   -0.1859 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2997    0.6369    0.0602 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0433   -1.7675    0.3073 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4595    1.1620   -0.2124 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3740   -1.3474    0.1426 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7751    1.5909   -0.3747 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3248   -1.8386    0.1516 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7729   -2.2583    0.1291 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3502   -0.4196   -0.2456 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4994    1.8387   -0.5986 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0827    2.2718   -0.5797 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5402   -2.2032    0.4778 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8723   -2.6179    0.6383 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2150   -1.7897    0.5869 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6529    0.5994    0.1955 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3766    3.2146   -0.3388 H   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  1  0  0  0  0
  5  6  2  0  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  2  0  0  0  0
  4 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
 20 22  2  0  0  0  0
 22  2  1  0  0  0  0
 14  9  1  0  0  0  0
 22 16  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
 10 27  1  0  0  0  0
 11 28  1  0  0  0  0
 12 29  1  0  0  0  0
 13 30  1  0  0  0  0
 14 31  1  0  0  0  0
 15 32  1  0  0  0  0
 17 33  1  0  0  0  0
 18 34  1  0  0  0  0
 19 35  1  0  0  0  0
 21 36  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0005504

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C2C(=O)OC(\C([H])=C(/[H])\C(\[H])=C(/[H])C3=C([H])C([H])=C([H])C([H])=C3[H])=C([H])C2=C([H])C([H])=C1[H]

> <INCHI_IDENTIFIER>
InChI=1S/C19H14O3/c20-17-12-6-10-15-13-16(22-19(21)18(15)17)11-5-4-9-14-7-2-1-3-8-14/h1-13,20H/b9-4+,11-5+

> <INCHI_KEY>
IFFMOWIJJAFQJN-HINBXAKRSA-N

> <FORMULA>
C19H14O3

> <MOLECULAR_WEIGHT>
290.318

> <EXACT_MASS>
290.094294311

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
36

> <JCHEM_AVERAGE_POLARIZABILITY>
32.28368535567792

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
8-hydroxy-3-[(1E,3E)-4-phenylbuta-1,3-dien-1-yl]-1H-isochromen-1-one

> <ALOGPS_LOGP>
4.95

> <JCHEM_LOGP>
5.106694229

> <ALOGPS_LOGS>
-4.84

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.551056684896839

> <JCHEM_PKA_STRONGEST_BASIC>
-4.306786847732732

> <JCHEM_POLAR_SURFACE_AREA>
46.53

> <JCHEM_REFRACTIVITY>
89.78720000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.15e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
8-hydroxy-3-[(1E,3E)-4-phenylbuta-1,3-dien-1-yl]isochromen-1-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 36 38  0  0  0  0  0  0  0  0999 V2000
    3.3784    2.7043   -0.3285 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2240    1.4658   -0.1228 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0071    0.9721   -0.0852 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6842   -0.2685    0.1143 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2873   -0.7287    0.1393 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7057    0.1236   -0.0445 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1161   -0.3307   -0.0211 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0828    0.5473   -0.2083 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5026    0.2469   -0.2115 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0031   -1.0154   -0.0151 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3798   -1.2621   -0.0259 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2802   -0.2468   -0.2340 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7845    1.0237   -0.4319 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4280    1.2510   -0.4186 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7144   -1.1559    0.3056 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0341   -0.7179    0.2815 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0805   -1.5659    0.4666 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3793   -1.1138    0.4393 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6367    0.2093    0.2231 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5821    1.1362    0.0242 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9134    2.4401   -0.1859 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2997    0.6369    0.0602 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0433   -1.7675    0.3073 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4595    1.1620   -0.2124 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3740   -1.3474    0.1426 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7751    1.5909   -0.3747 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3248   -1.8386    0.1516 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7729   -2.2583    0.1291 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3502   -0.4196   -0.2456 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.0827    2.2718   -0.5797 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5402   -2.2032    0.4778 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8723   -2.6179    0.6383 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2150   -1.7897    0.5869 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6529    0.5994    0.1955 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3766    3.2146   -0.3388 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
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  4 15  2  0
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 22  2  1  0
 14  9  1  0
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  5 23  1  0
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 11 28  1  0
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 13 30  1  0
 14 31  1  0
 15 32  1  0
 17 33  1  0
 18 34  1  0
 19 35  1  0
 21 36  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  O   UNK     0       3.378   2.704  -0.329  0.00  0.00           O+0
HETATM    2  C   UNK     0       3.224   1.466  -0.123  0.00  0.00           C+0
HETATM    3  O   UNK     0       2.007   0.972  -0.085  0.00  0.00           O+0
HETATM    4  C   UNK     0       1.684  -0.269   0.114  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.287  -0.729   0.139  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.706   0.124  -0.045  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.116  -0.331  -0.021  0.00  0.00           C+0
HETATM    8  C   UNK     0      -3.083   0.547  -0.208  0.00  0.00           C+0
HETATM    9  C   UNK     0      -4.503   0.247  -0.212  0.00  0.00           C+0
HETATM   10  C   UNK     0      -5.003  -1.015  -0.015  0.00  0.00           C+0
HETATM   11  C   UNK     0      -6.380  -1.262  -0.026  0.00  0.00           C+0
HETATM   12  C   UNK     0      -7.280  -0.247  -0.234  0.00  0.00           C+0
HETATM   13  C   UNK     0      -6.785   1.024  -0.432  0.00  0.00           C+0
HETATM   14  C   UNK     0      -5.428   1.251  -0.419  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.714  -1.156   0.306  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.034  -0.718   0.282  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.080  -1.566   0.467  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.379  -1.114   0.439  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.637   0.209   0.223  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.582   1.136   0.024  0.00  0.00           C+0
HETATM   21  O   UNK     0       5.913   2.440  -0.186  0.00  0.00           O+0
HETATM   22  C   UNK     0       4.300   0.637   0.060  0.00  0.00           C+0
HETATM   23  H   UNK     0       0.043  -1.768   0.307  0.00  0.00           H+0
HETATM   24  H   UNK     0      -0.460   1.162  -0.212  0.00  0.00           H+0
HETATM   25  H   UNK     0      -2.374  -1.347   0.143  0.00  0.00           H+0
HETATM   26  H   UNK     0      -2.775   1.591  -0.375  0.00  0.00           H+0
HETATM   27  H   UNK     0      -4.325  -1.839   0.152  0.00  0.00           H+0
HETATM   28  H   UNK     0      -6.773  -2.258   0.129  0.00  0.00           H+0
HETATM   29  H   UNK     0      -8.350  -0.420  -0.246  0.00  0.00           H+0
HETATM   30  H   UNK     0      -7.499   1.839  -0.599  0.00  0.00           H+0
HETATM   31  H   UNK     0      -5.083   2.272  -0.580  0.00  0.00           H+0
HETATM   32  H   UNK     0       2.540  -2.203   0.478  0.00  0.00           H+0
HETATM   33  H   UNK     0       4.872  -2.618   0.638  0.00  0.00           H+0
HETATM   34  H   UNK     0       7.215  -1.790   0.587  0.00  0.00           H+0
HETATM   35  H   UNK     0       7.653   0.599   0.196  0.00  0.00           H+0
HETATM   36  H   UNK     0       5.377   3.215  -0.339  0.00  0.00           H+0
CONECT    1    2                                                            
CONECT    2    1    3   22                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   15                                                  
CONECT    5    4    6   23                                                  
CONECT    6    5    7   24                                                  
CONECT    7    6    8   25                                                  
CONECT    8    7    9   26                                                  
CONECT    9    8   10   14                                                  
CONECT   10    9   11   27                                                  
CONECT   11   10   12   28                                                  
CONECT   12   11   13   29                                                  
CONECT   13   12   14   30                                                  
CONECT   14   13    9   31                                                  
CONECT   15    4   16   32                                                  
CONECT   16   15   17   22                                                  
CONECT   17   16   18   33                                                  
CONECT   18   17   19   34                                                  
CONECT   19   18   20   35                                                  
CONECT   20   19   21   22                                                  
CONECT   21   20   36                                                       
CONECT   22   20    2   16                                                  
CONECT   23    5                                                            
CONECT   24    6                                                            
CONECT   25    7                                                            
CONECT   26    8                                                            
CONECT   27   10                                                            
CONECT   28   11                                                            
CONECT   29   12                                                            
CONECT   30   13                                                            
CONECT   31   14                                                            
CONECT   32   15                                                            
CONECT   33   17                                                            
CONECT   34   18                                                            
CONECT   35   19                                                            
CONECT   36   21                                                            
MASTER        0    0    0    0    0    0    0    0   36    0   76    0
END

RDKit          3D

36 38  0  0  0  0  0  0  0  0999 V2000
    3.3784    2.7043   -0.3285 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2240    1.4658   -0.1228 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0071    0.9721   -0.0852 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6842   -0.2685    0.1143 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2873   -0.7287    0.1393 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7057    0.1236   -0.0445 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1161   -0.3307   -0.0211 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0828    0.5473   -0.2083 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5026    0.2469   -0.2115 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0031   -1.0154   -0.0151 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3798   -1.2621   -0.0259 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2802   -0.2468   -0.2340 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7845    1.0237   -0.4319 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4280    1.2510   -0.4186 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7144   -1.1559    0.3056 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0341   -0.7179    0.2815 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0805   -1.5659    0.4666 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3793   -1.1138    0.4393 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6367    0.2093    0.2231 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5821    1.1362    0.0242 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9134    2.4401   -0.1859 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2997    0.6369    0.0602 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0433   -1.7675    0.3073 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4595    1.1620   -0.2124 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3740   -1.3474    0.1426 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7751    1.5909   -0.3747 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3248   -1.8386    0.1516 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7729   -2.2583    0.1291 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3502   -0.4196   -0.2456 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4994    1.8387   -0.5986 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0827    2.2718   -0.5797 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5402   -2.2032    0.4778 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8723   -2.6179    0.6383 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2150   -1.7897    0.5869 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6529    0.5994    0.1955 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3766    3.2146   -0.3388 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  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  2  0
  4 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  1  0
 20 22  2  0
 22  2  1  0
 14  9  1  0
 22 16  1  0
  5 23  1  0
  6 24  1  0
  7 25  1  0
  8 26  1  0
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 11 28  1  0
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 13 30  1  0
 14 31  1  0
 15 32  1  0
 17 33  1  0
 18 34  1  0
 19 35  1  0
 21 36  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
8-Hydroxy-3-[(1E,3E)-4-phenyl-1,3-butadienyl]-1H-2-benzopyran-1-one	ChEBI
8-Hydroxy-3-[(1E,3E)-4-phenylbuta-1,3-dien-1-yl]-1H-2-benzopyran-1-one	ChEBI

Chemical Formula

C₁₉H₁₄O₃

Average Mass

290.3180 Da

Monoisotopic Mass

290.09429 Da

IUPAC Name

8-hydroxy-3-[(1E,3E)-4-phenylbuta-1,3-dien-1-yl]-1H-isochromen-1-one

Traditional Name

8-hydroxy-3-[(1E,3E)-4-phenylbuta-1,3-dien-1-yl]isochromen-1-one

CAS Registry Number

Not Available

SMILES

OC1=CC=CC2=C1C(=O)OC(\C=C\C=C\C1=CC=CC=C1)=C2

InChI Identifier

InChI=1S/C19H14O3/c20-17-12-6-10-15-13-16(22-19(21)18(15)17)11-5-4-9-14-7-2-1-3-8-14/h1-13,20H/b9-4+,11-5+

InChI Key

IFFMOWIJJAFQJN-HINBXAKRSA-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
Legionella	NPAtlas	15381093
Legionella parisiensis	LOTUS Database	35616633

Chemical Taxonomy

Classification

Not classified

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	4.95	ALOGPS
logP	5.11	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Acidic)	9.55	ChemAxon
pKa (Strongest Basic)	-4.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	46.53 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	89.79 m³·mol⁻¹	ChemAxon
Polarizability	32.28 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

NPAtlas ID

NPA000480

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

9348884

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11173792

PDB ID

Not Available

ChEBI ID

156300

Good Scents ID

Not Available

References

General References

Amemura-Maekawa J, Hayakawa Y, Sugie H, Moribayashi A, Kura F, Chang B, Wada A, Watanabe H: Legioliulin, a new isocoumarin compound responsible for blue-white autofluorescence in Legionella (Fluoribacter) dumoffii under long-wavelength UV light. Biochem Biophys Res Commun. 2004 Oct 22;323(3):954-9. doi: 10.1016/j.bbrc.2004.08.180. [PubMed:15381093 ]
Ahrendt T, Miltenberger M, Haneburger I, Kirchner F, Kronenwerth M, Brachmann AO, Hilbi H, Bode HB: Biosynthesis of the natural fluorophore legioliulin from legionella. Chembiochem. 2013 Aug 19;14(12):1415-8. doi: 10.1002/cbic.201300373. Epub 2013 Jul 2. [PubMed:23821465 ]

Showing NP-Card for Legioliulin (NP0005504)

MOL for NP0005504 (Legioliulin)

3D MOL for NP0005504 (Legioliulin)

3D SDF for NP0005504 (Legioliulin)

3D-SDF for NP0005504 (Legioliulin)

PDB for NP0005504 (Legioliulin)

3D PDB for NP0005504 (Legioliulin)

SMILES for NP0005504 (Legioliulin)

INCHI for NP0005504 (Legioliulin)

Structure for NP0005504 (Legioliulin)

3D Structure for NP0005504 (Legioliulin)