NP-MRD: Showing NP-Card for n-(2-aminoethyl)-4-[(4e)-5-{4-[3-(furan-3-yl)propyl]furan-2-yl}-4-methylpent-4-en-1-yl]furan-2-carboxamide (NP0237907)

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Record Information

Version

2.0

Created at

2022-09-06 21:11:05 UTC

Updated at

2022-09-06 21:11:05 UTC

NP-MRD ID

NP0237907

Secondary Accession Numbers

None

Natural Product Identification

Common Name

n-(2-aminoethyl)-4-[(4e)-5-{4-[3-(furan-3-yl)propyl]furan-2-yl}-4-methylpent-4-en-1-yl]furan-2-carboxamide

Description

Hippospongin E belongs to the class of organic compounds known as 2-heteroaryl carboxamides. 2-Heteroaryl carboxamides are compounds containing a heteroaromatic ring that carries a carboxamide group. Based on a literature review very few articles have been published on Hippospongin E.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062223112D          

 30 32  0  0  0  0            999 V2000
   -3.2726    0.0317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7877   -0.6357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1233   -1.3894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9437   -1.4757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3562   -2.1901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1632   -2.0186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7763   -2.5706    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5609   -2.3157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1740   -2.8677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9586   -2.6128    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6261   -3.0977    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2935   -2.6128    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0386   -1.8282    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2136   -1.8282    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2494   -1.1981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4958   -0.8626    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9672   -0.5495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6317    0.2042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8112    0.2904    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4756    1.0441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8881    1.7586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3361    2.3716    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4176    2.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1321    2.4486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1321    3.2736    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8465    2.0361    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.5610    2.4486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2755    2.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9899    2.4486    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.3314    1.2156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  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  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 10 14  2  0  0  0  0
  6 15  2  0  0  0  0
 15 16  1  0  0  0  0
  4 16  1  0  0  0  0
  2 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  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
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 23 30  2  0  0  0  0
 20 30  1  0  0  0  0
M  END

     RDKit          3D

 60 62  0  0  0  0  0  0  0  0999 V2000
   -0.6175   -0.4079    1.7368 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2216   -1.1349    0.4620 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9238   -1.0386   -0.6213 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1311   -0.2315   -0.7086 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3645   -0.4747   -0.2165 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1907    0.5645   -0.5486 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6310    0.7366   -0.2842 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9192    1.4780    0.9893 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4379    1.6666    1.1361 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1190    0.3769    1.1765 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5246   -0.3484    0.0871 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1018   -1.5028    0.5615 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0398   -1.4570    1.8672 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4692   -0.3708    2.2870 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3763    1.4471   -1.2655 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1988    0.9519   -1.3347 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0596   -1.9024    0.4977 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5333   -2.2363   -0.8904 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8515   -1.0204   -1.6802 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0748   -0.3104   -1.1864 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3030    0.5181   -0.1512 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5517    0.9529   -0.1801 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1797    0.4504   -1.1983 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6188    0.7002   -1.5813 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8101    0.5474   -2.8322 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5458    1.0372   -0.6678 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.5057    1.3862    0.2777 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7270    0.4790    0.3437 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3261   -0.8428    0.6484 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.3097   -0.3564   -1.8759 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8825   -1.1727    2.4735 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4577    0.2335    1.4738 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2368    0.2439    2.0278 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6507   -1.6122   -1.5307 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6418   -1.3713    0.3513 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0669    1.2576   -1.1650 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0432   -0.3175   -0.2213 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5235    0.9415    1.8719 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4577    2.4767    0.9926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8253    2.2644    0.2848 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5897    2.2706    2.0631 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4268   -0.1055   -0.9557 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5347   -2.3152   -0.0319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2977   -0.0991    3.3371 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7654    2.3653   -1.6554 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8269   -1.3166    1.0191 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8858   -2.8824    1.0349 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7585   -2.8445   -1.3925 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4600   -2.9024   -0.8094 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0073   -1.2971   -2.7748 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0514   -0.2499   -1.7352 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5571    0.7954    0.6059 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4904    1.1406   -1.6658 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0409    1.4129    1.3241 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8841    2.4413    0.1790 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.2869    0.5178   -0.6174 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.4294    0.8642    1.1150 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4949   -0.9518    1.2553 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1108   -1.3954    1.0496 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5123   -0.9171   -2.7516 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  1  0
 23 30  2  0
 23 24  1  0
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 24 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 14  2  0
 14 13  1  0
 13 12  1  0
 12 11  2  0
  6 15  2  0
 15 16  1  0
 30 20  1  0
 16  4  1  0
 11 10  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
 17 46  1  0
 17 47  1  0
 18 48  1  0
 18 49  1  0
 19 50  1  0
 19 51  1  0
 21 52  1  0
 30 60  1  0
 26 53  1  0
 27 54  1  0
 27 55  1  0
 28 56  1  0
 28 57  1  0
 29 58  1  0
 29 59  1  0
  3 34  1  0
  5 35  1  0
  7 36  1  0
  7 37  1  0
  8 38  1  0
  8 39  1  0
  9 40  1  0
  9 41  1  0
 14 44  1  0
 12 43  1  0
 11 42  1  0
 15 45  1  0
M  END


  Mrv1652309062223112D          

 30 32  0  0  0  0            999 V2000
   -3.2726    0.0317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7877   -0.6357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1233   -1.3894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9437   -1.4757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3562   -2.1901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1632   -2.0186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7763   -2.5706    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5609   -2.3157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1740   -2.8677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9586   -2.6128    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6261   -3.0977    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2935   -2.6128    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0386   -1.8282    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2136   -1.8282    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2494   -1.1981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4958   -0.8626    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9672   -0.5495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6317    0.2042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8112    0.2904    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4756    1.0441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8881    1.7586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3361    2.3716    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4176    2.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1321    2.4486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1321    3.2736    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8465    2.0361    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.5610    2.4486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2755    2.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9899    2.4486    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.3314    1.2156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  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  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 10 14  2  0  0  0  0
  6 15  2  0  0  0  0
 15 16  1  0  0  0  0
  4 16  1  0  0  0  0
  2 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  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
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 23 30  2  0  0  0  0
 20 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0237907

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C(CCCC1=COC(=C1)C(=O)NCCN)=C/C1=CC(CCCC2=COC=C2)=CO1

> <INCHI_IDENTIFIER>
InChI=1S/C24H30N2O4/c1-18(4-2-6-21-14-23(30-17-21)24(27)26-10-9-25)12-22-13-20(16-29-22)7-3-5-19-8-11-28-15-19/h8,11-17H,2-7,9-10,25H2,1H3,(H,26,27)/b18-12+

> <INCHI_KEY>
FRTYGMXWUOZBJW-LDADJPATSA-N

> <FORMULA>
C24H30N2O4

> <MOLECULAR_WEIGHT>
410.514

> <EXACT_MASS>
410.220557454

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
47.688800111440244

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
N-(2-aminoethyl)-4-[(4E)-5-{4-[3-(furan-3-yl)propyl]furan-2-yl}-4-methylpent-4-en-1-yl]furan-2-carboxamide

> <JCHEM_LOGP>
4.326456834666667

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.045546961221941

> <JCHEM_PKA_STRONGEST_BASIC>
9.163027655268605

> <JCHEM_POLAR_SURFACE_AREA>
94.53999999999999

> <JCHEM_REFRACTIVITY>
117.75709999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
N-(2-aminoethyl)-4-[(4E)-5-{4-[3-(furan-3-yl)propyl]furan-2-yl}-4-methylpent-4-en-1-yl]furan-2-carboxamide

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0      -6.109   0.059   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -5.204  -1.187   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -5.830  -2.594   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -7.362  -2.755   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -8.132  -4.088   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -9.638  -3.768   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0     -10.782  -4.799   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0     -12.247  -4.323   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0     -13.391  -5.353   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0     -14.856  -4.877   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0     -16.102  -5.782   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0     -17.348  -4.877   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0     -16.872  -3.413   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0     -15.332  -3.413   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -9.799  -2.236   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -8.392  -1.610   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -3.672  -1.026   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -3.046   0.381   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.514   0.542   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.888   1.949   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -1.658   3.283   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -0.627   4.427   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       0.780   3.801   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.113   4.571   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       2.113   6.111   0.000  0.00  0.00           O+0
HETATM   26  N   UNK     0       3.447   3.801   0.000  0.00  0.00           N+0
HETATM   27  C   UNK     0       4.781   4.571   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       6.114   3.801   0.000  0.00  0.00           C+0
HETATM   29  N   UNK     0       7.448   4.571   0.000  0.00  0.00           N+0
HETATM   30  C   UNK     0       0.619   2.269   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   17                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   16                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   15                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   14                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   10                                                       
CONECT   15    6   16                                                       
CONECT   16   15    4                                                       
CONECT   17    2   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   30                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   30                                                  
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28                                                            
CONECT   30   23   20                                                       
MASTER        0    0    0    0    0    0    0    0   30    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₃₀N₂O₄

Average Mass

410.5140 Da

Monoisotopic Mass

410.22056 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C\C(CCCC1=COC(=C1)C(=O)NCCN)=C/C1=CC(CCCC2=COC=C2)=CO1

InChI Identifier

InChI=1S/C24H30N2O4/c1-18(4-2-6-21-14-23(30-17-21)24(27)26-10-9-25)12-22-13-20(16-29-22)7-3-5-19-8-11-28-15-19/h8,11-17H,2-7,9-10,25H2,1H3,(H,26,27)/b18-12+

InChI Key

FRTYGMXWUOZBJW-LDADJPATSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 2-heteroaryl carboxamides. 2-Heteroaryl carboxamides are compounds containing a heteroaromatic ring that carries a carboxamide group.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Carboxylic acid derivatives

Direct Parent

2-heteroaryl carboxamides

Alternative Parents

Substituents

2-heteroaryl carboxamide
Furoic acid or derivatives
Furan
Heteroaromatic compound
Amino acid or derivatives
Secondary carboxylic acid amide
Organoheterocyclic compound
Oxacycle
Amine
Hydrocarbon derivative
Organic oxide
Primary amine
Organooxygen compound
Organonitrogen compound
Primary aliphatic amine
Organic oxygen compound
Organic nitrogen compound
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

8868276

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10692931

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for n-(2-aminoethyl)-4-[(4e)-5-{4-[3-(furan-3-yl)propyl]furan-2-yl}-4-methylpent-4-en-1-yl]furan-2-carboxamide (NP0237907)

MOL for NP0237907 (n-(2-aminoethyl)-4-[(4e)-5-{4-[3-(furan-3-yl)propyl]furan-2-yl}-4-methylpent-4-en-1-yl]furan-2-carboxamide)

3D MOL for NP0237907 (n-(2-aminoethyl)-4-[(4e)-5-{4-[3-(furan-3-yl)propyl]furan-2-yl}-4-methylpent-4-en-1-yl]furan-2-carboxamide)

3D SDF for NP0237907 (n-(2-aminoethyl)-4-[(4e)-5-{4-[3-(furan-3-yl)propyl]furan-2-yl}-4-methylpent-4-en-1-yl]furan-2-carboxamide)

3D-SDF for NP0237907 (n-(2-aminoethyl)-4-[(4e)-5-{4-[3-(furan-3-yl)propyl]furan-2-yl}-4-methylpent-4-en-1-yl]furan-2-carboxamide)

PDB for NP0237907 (n-(2-aminoethyl)-4-[(4e)-5-{4-[3-(furan-3-yl)propyl]furan-2-yl}-4-methylpent-4-en-1-yl]furan-2-carboxamide)

3D PDB for NP0237907 (n-(2-aminoethyl)-4-[(4e)-5-{4-[3-(furan-3-yl)propyl]furan-2-yl}-4-methylpent-4-en-1-yl]furan-2-carboxamide)

SMILES for NP0237907 (n-(2-aminoethyl)-4-[(4e)-5-{4-[3-(furan-3-yl)propyl]furan-2-yl}-4-methylpent-4-en-1-yl]furan-2-carboxamide)

INCHI for NP0237907 (n-(2-aminoethyl)-4-[(4e)-5-{4-[3-(furan-3-yl)propyl]furan-2-yl}-4-methylpent-4-en-1-yl]furan-2-carboxamide)

Structure for NP0237907 (n-(2-aminoethyl)-4-[(4e)-5-{4-[3-(furan-3-yl)propyl]furan-2-yl}-4-methylpent-4-en-1-yl]furan-2-carboxamide)

3D Structure for NP0237907 (n-(2-aminoethyl)-4-[(4e)-5-{4-[3-(furan-3-yl)propyl]furan-2-yl}-4-methylpent-4-en-1-yl]furan-2-carboxamide)