NP-MRD: Showing NP-Card for N-trans-feruloyloctopamine (NP0031586)

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Record Information

Version

2.0

Created at

2021-06-19 22:37:30 UTC

Updated at

2024-09-03 04:21:24 UTC

NP-MRD ID

NP0031586

Natural Product DOI

https://doi.org/10.57994/2474

Secondary Accession Numbers

None

Natural Product Identification

Common Name

N-trans-feruloyloctopamine

Provided By

JEOL Database JEOL Logo

Description

(R)-N-trans-feruloyloctopamine belongs to the class of organic compounds known as hydroxycinnamic acids and derivatives. Hydroxycinnamic acids and derivatives are compounds containing an cinnamic acid (or a derivative thereof) where the benzene ring is hydroxylated (R)-N-trans-feruloyloctopamine 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. N-trans-feruloyloctopamine is found in Antidesma membranaceum, Antidesma pentandrum, Capsicum annuum var.grossum , Pisonia aculeata, Salsola collina, Solanum tuberosum and Tribulus terrestris . N-trans-feruloyloctopamine was first documented in 2020 (PMID: 32980795). Based on a literature review very few articles have been published on (R)-N-trans-feruloyloctopamine.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306202100373D          

 43 44  0  0  0  0            999 V2000
    3.2094    2.9737    1.7194 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4975    2.6682    1.1981 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5563    1.6970    0.2311 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4787    0.9628   -0.2688 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6821   -0.0119   -1.2620 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5704   -0.7864   -1.8281 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5984   -1.3372   -1.0851 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5261   -2.1176   -1.7450 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4594   -2.2850   -2.9569 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4054   -2.6112   -0.8712 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5444   -3.3950   -1.3320 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6798   -2.5478   -1.9582 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2780   -1.9054   -3.1705 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2491   -1.5355   -0.9795 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1078   -1.9620    0.0476 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6164   -1.0499    0.9744 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2750    0.2929    0.8781 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7988    1.1497    1.8001 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4284    0.7415   -0.1287 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9155   -0.1728   -1.0522 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9727   -0.2228   -1.7672 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0535    0.5049   -1.2710 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8356    1.4510   -0.2792 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9120    2.1527    0.1914 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5457    3.3524    0.9351 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7724    2.1057    2.2240 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3302    3.7658    2.4645 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4707    1.1410    0.0893 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5853   -0.9221   -2.9087 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5769   -1.2455   -0.0073 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3540   -2.3873    0.1136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1749   -4.1127   -2.0738 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9117   -3.9559   -0.4660 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4901   -3.2282   -2.2471 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3390   -2.1321   -3.3388 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3927   -3.0084    0.1304 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2835   -1.3847    1.7636 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5507    2.0557    1.5531 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1588    1.7890   -0.2161 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2565    0.1842   -1.8421 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1482   -0.9622   -2.5459 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0553    0.3379   -1.6550 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5437    2.7591    0.8629 H   0  0  0  0  0  0  0  0  0  0  0  0
  5 21  2  0  0  0  0
  8  9  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 14 12  1  0  0  0  0
  5  6  1  0  0  0  0
 14 15  2  0  0  0  0
  3  4  2  0  0  0  0
 15 16  1  0  0  0  0
  6  7  2  0  0  0  0
 16 17  2  0  0  0  0
 17 19  1  0  0  0  0
  7  8  1  0  0  0  0
 19 20  2  0  0  0  0
 20 14  1  0  0  0  0
  4  5  1  0  0  0  0
 17 18  1  0  0  0  0
  8 10  1  0  0  0  0
 12 13  1  0  0  0  0
 23  3  1  0  0  0  0
 23 24  1  0  0  0  0
 10 11  1  0  0  0  0
  3  2  1  0  0  0  0
 11 12  1  0  0  0  0
  2  1  1  0  0  0  0
 22 42  1  0  0  0  0
  4 28  1  0  0  0  0
 21 41  1  0  0  0  0
  6 29  1  0  0  0  0
  7 30  1  0  0  0  0
 10 31  1  0  0  0  0
 11 32  1  0  0  0  0
 11 33  1  0  0  0  0
 12 34  1  0  0  0  0
 15 36  1  0  0  0  0
 16 37  1  0  0  0  0
 19 39  1  0  0  0  0
 20 40  1  0  0  0  0
 18 38  1  0  0  0  0
 13 35  1  0  0  0  0
 24 43  1  0  0  0  0
  1 25  1  0  0  0  0
  1 26  1  0  0  0  0
  1 27  1  0  0  0  0
M  END

     RDKit          3D

 43 44  0  0  0  0  0  0  0  0999 V2000
    3.2094    2.9737    1.7194 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4975    2.6682    1.1981 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5563    1.6970    0.2311 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4787    0.9628   -0.2688 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6821   -0.0119   -1.2620 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5704   -0.7864   -1.8281 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5984   -1.3372   -1.0851 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5261   -2.1176   -1.7450 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4594   -2.2850   -2.9569 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4054   -2.6112   -0.8712 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5444   -3.3950   -1.3320 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6798   -2.5478   -1.9582 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2780   -1.9054   -3.1705 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2491   -1.5355   -0.9795 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1078   -1.9620    0.0476 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6164   -1.0499    0.9744 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2750    0.2929    0.8781 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7988    1.1497    1.8001 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4284    0.7415   -0.1287 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9155   -0.1728   -1.0522 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9727   -0.2228   -1.7672 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0535    0.5049   -1.2710 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8356    1.4510   -0.2792 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9120    2.1527    0.1914 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5457    3.3524    0.9351 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7724    2.1057    2.2240 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3302    3.7658    2.4645 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4707    1.1410    0.0893 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5853   -0.9221   -2.9087 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5769   -1.2455   -0.0073 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3540   -2.3873    0.1136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1749   -4.1127   -2.0738 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9117   -3.9559   -0.4660 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4901   -3.2282   -2.2471 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3390   -2.1321   -3.3388 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3927   -3.0084    0.1304 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2835   -1.3847    1.7636 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5507    2.0557    1.5531 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1588    1.7890   -0.2161 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2565    0.1842   -1.8421 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1482   -0.9622   -2.5459 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0553    0.3379   -1.6550 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5437    2.7591    0.8629 H   0  0  0  0  0  0  0  0  0  0  0  0
  5 21  2  0
  8  9  2  0
 21 22  1  0
 22 23  2  0
 14 12  1  0
  5  6  1  0
 14 15  2  0
  3  4  2  0
 15 16  1  0
  6  7  2  0
 16 17  2  0
 17 19  1  0
  7  8  1  0
 19 20  2  0
 20 14  1  0
  4  5  1  0
 17 18  1  0
  8 10  1  0
 12 13  1  0
 23  3  1  0
 23 24  1  0
 10 11  1  0
  3  2  1  0
 11 12  1  0
  2  1  1  0
 22 42  1  0
  4 28  1  0
 21 41  1  0
  6 29  1  0
  7 30  1  0
 10 31  1  0
 11 32  1  0
 11 33  1  0
 12 34  1  0
 15 36  1  0
 16 37  1  0
 19 39  1  0
 20 40  1  0
 18 38  1  0
 13 35  1  0
 24 43  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
M  END


  Mrv1652306202100373D          

 43 44  0  0  0  0            999 V2000
    3.2094    2.9737    1.7194 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4975    2.6682    1.1981 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5563    1.6970    0.2311 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4787    0.9628   -0.2688 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6821   -0.0119   -1.2620 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5704   -0.7864   -1.8281 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5984   -1.3372   -1.0851 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5261   -2.1176   -1.7450 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4594   -2.2850   -2.9569 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4054   -2.6112   -0.8712 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5444   -3.3950   -1.3320 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6798   -2.5478   -1.9582 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2780   -1.9054   -3.1705 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2491   -1.5355   -0.9795 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1078   -1.9620    0.0476 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6164   -1.0499    0.9744 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2750    0.2929    0.8781 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7988    1.1497    1.8001 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4284    0.7415   -0.1287 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9155   -0.1728   -1.0522 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9727   -0.2228   -1.7672 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0535    0.5049   -1.2710 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8356    1.4510   -0.2792 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9120    2.1527    0.1914 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5457    3.3524    0.9351 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7724    2.1057    2.2240 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3302    3.7658    2.4645 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4707    1.1410    0.0893 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5853   -0.9221   -2.9087 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5769   -1.2455   -0.0073 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3540   -2.3873    0.1136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1749   -4.1127   -2.0738 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9117   -3.9559   -0.4660 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4901   -3.2282   -2.2471 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3390   -2.1321   -3.3388 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3927   -3.0084    0.1304 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2835   -1.3847    1.7636 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5507    2.0557    1.5531 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1588    1.7890   -0.2161 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2565    0.1842   -1.8421 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1482   -0.9622   -2.5459 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0553    0.3379   -1.6550 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5437    2.7591    0.8629 H   0  0  0  0  0  0  0  0  0  0  0  0
  5 21  2  0  0  0  0
  8  9  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 14 12  1  0  0  0  0
  5  6  1  0  0  0  0
 14 15  2  0  0  0  0
  3  4  2  0  0  0  0
 15 16  1  0  0  0  0
  6  7  2  0  0  0  0
 16 17  2  0  0  0  0
 17 19  1  0  0  0  0
  7  8  1  0  0  0  0
 19 20  2  0  0  0  0
 20 14  1  0  0  0  0
  4  5  1  0  0  0  0
 17 18  1  0  0  0  0
  8 10  1  0  0  0  0
 12 13  1  0  0  0  0
 23  3  1  0  0  0  0
 23 24  1  0  0  0  0
 10 11  1  0  0  0  0
  3  2  1  0  0  0  0
 11 12  1  0  0  0  0
  2  1  1  0  0  0  0
 22 42  1  0  0  0  0
  4 28  1  0  0  0  0
 21 41  1  0  0  0  0
  6 29  1  0  0  0  0
  7 30  1  0  0  0  0
 10 31  1  0  0  0  0
 11 32  1  0  0  0  0
 11 33  1  0  0  0  0
 12 34  1  0  0  0  0
 15 36  1  0  0  0  0
 16 37  1  0  0  0  0
 19 39  1  0  0  0  0
 20 40  1  0  0  0  0
 18 38  1  0  0  0  0
 13 35  1  0  0  0  0
 24 43  1  0  0  0  0
  1 25  1  0  0  0  0
  1 26  1  0  0  0  0
  1 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0031586

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C([H])C([H])=C(C([H])=C1[H])[C@@]([H])(O[H])C([H])([H])N([H])C(=O)C(\[H])=C(/[H])C1=C([H])C([H])=C(O[H])C(OC([H])([H])[H])=C1[H]

> <INCHI_IDENTIFIER>
InChI=1S/C18H19NO5/c1-24-17-10-12(2-8-15(17)21)3-9-18(23)19-11-16(22)13-4-6-14(20)7-5-13/h2-10,16,20-22H,11H2,1H3,(H,19,23)/b9-3+/t16-/m0/s1

> <INCHI_KEY>
VJSCHQMOTSXAKB-CFZDNBDDSA-N

> <FORMULA>
C18H19NO5

> <MOLECULAR_WEIGHT>
329.352

> <EXACT_MASS>
329.126322716

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
43

> <JCHEM_AVERAGE_POLARIZABILITY>
34.34692593235859

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2E)-N-[(2R)-2-hydroxy-2-(4-hydroxyphenyl)ethyl]-3-(4-hydroxy-3-methoxyphenyl)prop-2-enamide

> <ALOGPS_LOGP>
1.61

> <JCHEM_LOGP>
1.8821559783333335

> <ALOGPS_LOGS>
-3.84

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.02941707966228

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.330861402907665

> <JCHEM_PKA_STRONGEST_BASIC>
-0.44932730655507636

> <JCHEM_POLAR_SURFACE_AREA>
99.02000000000001

> <JCHEM_REFRACTIVITY>
90.77890000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.75e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2E)-N-[(2R)-2-hydroxy-2-(4-hydroxyphenyl)ethyl]-3-(4-hydroxy-3-methoxyphenyl)prop-2-enamide

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 43 44  0  0  0  0  0  0  0  0999 V2000
    3.2094    2.9737    1.7194 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4975    2.6682    1.1981 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5563    1.6970    0.2311 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4787    0.9628   -0.2688 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6821   -0.0119   -1.2620 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5704   -0.7864   -1.8281 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5984   -1.3372   -1.0851 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5261   -2.1176   -1.7450 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4594   -2.2850   -2.9569 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4054   -2.6112   -0.8712 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5444   -3.3950   -1.3320 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6798   -2.5478   -1.9582 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2780   -1.9054   -3.1705 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2491   -1.5355   -0.9795 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1078   -1.9620    0.0476 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6164   -1.0499    0.9744 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2750    0.2929    0.8781 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7988    1.1497    1.8001 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4284    0.7415   -0.1287 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9155   -0.1728   -1.0522 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9727   -0.2228   -1.7672 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0535    0.5049   -1.2710 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8356    1.4510   -0.2792 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9120    2.1527    0.1914 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5457    3.3524    0.9351 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7724    2.1057    2.2240 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3302    3.7658    2.4645 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4707    1.1410    0.0893 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5853   -0.9221   -2.9087 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5769   -1.2455   -0.0073 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3540   -2.3873    0.1136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1749   -4.1127   -2.0738 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9117   -3.9559   -0.4660 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4901   -3.2282   -2.2471 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3390   -2.1321   -3.3388 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3927   -3.0084    0.1304 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2835   -1.3847    1.7636 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5507    2.0557    1.5531 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1588    1.7890   -0.2161 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2565    0.1842   -1.8421 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1482   -0.9622   -2.5459 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0553    0.3379   -1.6550 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5437    2.7591    0.8629 H   0  0  0  0  0  0  0  0  0  0  0  0
  5 21  2  0
  8  9  2  0
 21 22  1  0
 22 23  2  0
 14 12  1  0
  5  6  1  0
 14 15  2  0
  3  4  2  0
 15 16  1  0
  6  7  2  0
 16 17  2  0
 17 19  1  0
  7  8  1  0
 19 20  2  0
 20 14  1  0
  4  5  1  0
 17 18  1  0
  8 10  1  0
 12 13  1  0
 23  3  1  0
 23 24  1  0
 10 11  1  0
  3  2  1  0
 11 12  1  0
  2  1  1  0
 22 42  1  0
  4 28  1  0
 21 41  1  0
  6 29  1  0
  7 30  1  0
 10 31  1  0
 11 32  1  0
 11 33  1  0
 12 34  1  0
 15 36  1  0
 16 37  1  0
 19 39  1  0
 20 40  1  0
 18 38  1  0
 13 35  1  0
 24 43  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
M  END

HEADER    PROTEIN                                 20-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-JUN-21         0                                  
HETATM    1  C   UNK     0       3.209   2.974   1.719  0.00  0.00           C+0
HETATM    2  O   UNK     0       4.497   2.668   1.198  0.00  0.00           O+0
HETATM    3  C   UNK     0       4.556   1.697   0.231  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.479   0.963  -0.269  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.682  -0.012  -1.262  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.570  -0.786  -1.828  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.598  -1.337  -1.085  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.526  -2.118  -1.745  0.00  0.00           C+0
HETATM    9  O   UNK     0       0.459  -2.285  -2.957  0.00  0.00           O+0
HETATM   10  N   UNK     0      -0.405  -2.611  -0.871  0.00  0.00           N+0
HETATM   11  C   UNK     0      -1.544  -3.395  -1.332  0.00  0.00           C+0
HETATM   12  C   UNK     0      -2.680  -2.548  -1.958  0.00  0.00           C+0
HETATM   13  O   UNK     0      -2.278  -1.905  -3.171  0.00  0.00           O+0
HETATM   14  C   UNK     0      -3.249  -1.536  -0.980  0.00  0.00           C+0
HETATM   15  C   UNK     0      -4.108  -1.962   0.048  0.00  0.00           C+0
HETATM   16  C   UNK     0      -4.616  -1.050   0.974  0.00  0.00           C+0
HETATM   17  C   UNK     0      -4.275   0.293   0.878  0.00  0.00           C+0
HETATM   18  O   UNK     0      -4.799   1.150   1.800  0.00  0.00           O+0
HETATM   19  C   UNK     0      -3.428   0.742  -0.129  0.00  0.00           C+0
HETATM   20  C   UNK     0      -2.916  -0.173  -1.052  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.973  -0.223  -1.767  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.053   0.505  -1.271  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.836   1.451  -0.279  0.00  0.00           C+0
HETATM   24  O   UNK     0       6.912   2.153   0.191  0.00  0.00           O+0
HETATM   25  H   UNK     0       2.546   3.352   0.935  0.00  0.00           H+0
HETATM   26  H   UNK     0       2.772   2.106   2.224  0.00  0.00           H+0
HETATM   27  H   UNK     0       3.330   3.766   2.465  0.00  0.00           H+0
HETATM   28  H   UNK     0       2.471   1.141   0.089  0.00  0.00           H+0
HETATM   29  H   UNK     0       2.585  -0.922  -2.909  0.00  0.00           H+0
HETATM   30  H   UNK     0       1.577  -1.246  -0.007  0.00  0.00           H+0
HETATM   31  H   UNK     0      -0.354  -2.387   0.114  0.00  0.00           H+0
HETATM   32  H   UNK     0      -1.175  -4.113  -2.074  0.00  0.00           H+0
HETATM   33  H   UNK     0      -1.912  -3.956  -0.466  0.00  0.00           H+0
HETATM   34  H   UNK     0      -3.490  -3.228  -2.247  0.00  0.00           H+0
HETATM   35  H   UNK     0      -1.339  -2.132  -3.339  0.00  0.00           H+0
HETATM   36  H   UNK     0      -4.393  -3.008   0.130  0.00  0.00           H+0
HETATM   37  H   UNK     0      -5.284  -1.385   1.764  0.00  0.00           H+0
HETATM   38  H   UNK     0      -4.551   2.056   1.553  0.00  0.00           H+0
HETATM   39  H   UNK     0      -3.159   1.789  -0.216  0.00  0.00           H+0
HETATM   40  H   UNK     0      -2.256   0.184  -1.842  0.00  0.00           H+0
HETATM   41  H   UNK     0       5.148  -0.962  -2.546  0.00  0.00           H+0
HETATM   42  H   UNK     0       7.055   0.338  -1.655  0.00  0.00           H+0
HETATM   43  H   UNK     0       6.544   2.759   0.863  0.00  0.00           H+0
CONECT    1    2   25   26   27                                             
CONECT    2    3    1                                                       
CONECT    3    4   23    2                                                  
CONECT    4    3    5   28                                                  
CONECT    5   21    6    4                                                  
CONECT    6    5    7   29                                                  
CONECT    7    6    8   30                                                  
CONECT    8    9    7   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   31                                                  
CONECT   11   10   12   32   33                                             
CONECT   12   14   13   11   34                                             
CONECT   13   12   35                                                       
CONECT   14   12   15   20                                                  
CONECT   15   14   16   36                                                  
CONECT   16   15   17   37                                                  
CONECT   17   16   19   18                                                  
CONECT   18   17   38                                                       
CONECT   19   17   20   39                                                  
CONECT   20   19   14   40                                                  
CONECT   21    5   22   41                                                  
CONECT   22   21   23   42                                                  
CONECT   23   22    3   24                                                  
CONECT   24   23   43                                                       
CONECT   25    1                                                            
CONECT   26    1                                                            
CONECT   27    1                                                            
CONECT   28    4                                                            
CONECT   29    6                                                            
CONECT   30    7                                                            
CONECT   31   10                                                            
CONECT   32   11                                                            
CONECT   33   11                                                            
CONECT   34   12                                                            
CONECT   35   13                                                            
CONECT   36   15                                                            
CONECT   37   16                                                            
CONECT   38   18                                                            
CONECT   39   19                                                            
CONECT   40   20                                                            
CONECT   41   21                                                            
CONECT   42   22                                                            
CONECT   43   24                                                            
MASTER        0    0    0    0    0    0    0    0   43    0   88    0
END

RDKit          3D

43 44  0  0  0  0  0  0  0  0999 V2000
    3.2094    2.9737    1.7194 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4975    2.6682    1.1981 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5563    1.6970    0.2311 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4787    0.9628   -0.2688 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6821   -0.0119   -1.2620 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5704   -0.7864   -1.8281 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5984   -1.3372   -1.0851 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5261   -2.1176   -1.7450 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4594   -2.2850   -2.9569 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4054   -2.6112   -0.8712 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5444   -3.3950   -1.3320 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6798   -2.5478   -1.9582 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2780   -1.9054   -3.1705 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2491   -1.5355   -0.9795 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1078   -1.9620    0.0476 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6164   -1.0499    0.9744 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2750    0.2929    0.8781 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7988    1.1497    1.8001 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4284    0.7415   -0.1287 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9155   -0.1728   -1.0522 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9727   -0.2228   -1.7672 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0535    0.5049   -1.2710 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8356    1.4510   -0.2792 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9120    2.1527    0.1914 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5457    3.3524    0.9351 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7724    2.1057    2.2240 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3302    3.7658    2.4645 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4707    1.1410    0.0893 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5853   -0.9221   -2.9087 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5769   -1.2455   -0.0073 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3540   -2.3873    0.1136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1749   -4.1127   -2.0738 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9117   -3.9559   -0.4660 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4901   -3.2282   -2.2471 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3390   -2.1321   -3.3388 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3927   -3.0084    0.1304 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2835   -1.3847    1.7636 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5507    2.0557    1.5531 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1588    1.7890   -0.2161 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2565    0.1842   -1.8421 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1482   -0.9622   -2.5459 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0553    0.3379   -1.6550 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5437    2.7591    0.8629 H   0  0  0  0  0  0  0  0  0  0  0  0
  5 21  2  0
  8  9  2  0
 21 22  1  0
 22 23  2  0
 14 12  1  0
  5  6  1  0
 14 15  2  0
  3  4  2  0
 15 16  1  0
  6  7  2  0
 16 17  2  0
 17 19  1  0
  7  8  1  0
 19 20  2  0
 20 14  1  0
  4  5  1  0
 17 18  1  0
  8 10  1  0
 12 13  1  0
 23  3  1  0
 23 24  1  0
 10 11  1  0
  3  2  1  0
 11 12  1  0
  2  1  1  0
 22 42  1  0
  4 28  1  0
 21 41  1  0
  6 29  1  0
  7 30  1  0
 10 31  1  0
 11 32  1  0
 11 33  1  0
 12 34  1  0
 15 36  1  0
 16 37  1  0
 19 39  1  0
 20 40  1  0
 18 38  1  0
 13 35  1  0
 24 43  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
M  END

View in JSmol

Synonyms

Value	Source
(2S,e)-N-[2-Hydroxy-2-(4-hydroxyphenyl)ethyl]ferulamide	ChEBI
N-[2-(R)-Hydroxy-2-(4-hydroxy-phenyl)ethyl]-3-(4-hydroxy-3-methoxy-phenyl)acrylamide	ChEBI

Chemical Formula

C₁₈H₁₉NO₅

Average Mass

329.3520 Da

Monoisotopic Mass

329.12632 Da

IUPAC Name

(2E)-N-[(2R)-2-hydroxy-2-(4-hydroxyphenyl)ethyl]-3-(4-hydroxy-3-methoxyphenyl)prop-2-enamide

Traditional Name

(2E)-N-[(2R)-2-hydroxy-2-(4-hydroxyphenyl)ethyl]-3-(4-hydroxy-3-methoxyphenyl)prop-2-enamide

CAS Registry Number

Not Available

SMILES

[H]OC1=C([H])C([H])=C(C([H])=C1[H])[C@@]([H])(O[H])C([H])([H])N([H])C(=O)C(\[H])=C(/[H])C1=C([H])C([H])=C(O[H])C(OC([H])([H])[H])=C1[H]

InChI Identifier

InChI=1S/C18H19NO5/c1-24-17-10-12(2-8-15(17)21)3-9-18(23)19-11-16(22)13-4-6-14(20)7-5-13/h2-10,16,20-22H,11H2,1H3,(H,19,23)/b9-3+/t16-/m0/s1

InChI Key

VJSCHQMOTSXAKB-CFZDNBDDSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, CD3OD, experimental)	hxkuang@hljucm.net	Not Available	Not Available	2024-05-11	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View

Chemical Shift Submissions

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹H NMR Spectrum (1D, simulated)	Not Available	Not Available	Not Available	2024-05-11	View Spectrum

Species

Species of Origin

Species Name	Source	Reference
Antidesma membranaceum	LOTUS Database	35616633
Antidesma pentandrum	LOTUS Database	35616633
Capsicum annuum	FooDB	Dr. Duke's Phytochemical and Ethnobotanical Databases
Capsicum annuum var.grossum	Plant	KNApSAcK
Datura metel		Not Available
Pisonia aculeata	LOTUS Database	35616633
Salsola collina	LOTUS Database	35616633
Solanum melongena	FooDB	Dr. Duke's Phytochemical and Ethnobotanical Databases
Solanum tuberosum	JEOL database	King, R. R., et al, Phytochemistry 66, 2468 (2005)
Tribulus terrestris	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hydroxycinnamic acids and derivatives. Hydroxycinnamic acids and derivatives are compounds containing an cinnamic acid (or a derivative thereof) where the benzene ring is hydroxylated.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Cinnamic acids and derivatives

Sub Class

Hydroxycinnamic acids and derivatives

Direct Parent

Hydroxycinnamic acids and derivatives

Alternative Parents

Substituents

Cinnamic acid amide
Hydroxycinnamic acid or derivatives
Methoxyphenol
Anisole
Phenoxy compound
Phenol ether
Styrene
Methoxybenzene
Alkyl aryl ether
1-hydroxy-2-unsubstituted benzenoid
Phenol
Benzenoid
Monocyclic benzene moiety
Secondary carboxylic acid amide
Secondary alcohol
Carboxamide group
Carboxylic acid derivative
Ether
Organic oxygen compound
Aromatic alcohol
Organic nitrogen compound
Organic oxide
Organooxygen compound
Carbonyl group
Alcohol
Hydrocarbon derivative
Organopnictogen compound
Organonitrogen compound
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

phenols (CHEBI:67373 )
monomethoxybenzene (CHEBI:67373 )
cinnamamides (CHEBI:67373 )

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	1.61	ALOGPS
logP	1.88	ChemAxon
logS	-3.8	ALOGPS
pKa (Strongest Acidic)	9.33	ChemAxon
pKa (Strongest Basic)	-0.45	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	99.02 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	90.78 m³·mol⁻¹	ChemAxon
Polarizability	34.35 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

9326730

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

67373

Good Scents ID

Not Available

References

General References

Ayanlowo AG, Garadi Z, Boldizsar I, Darcsi A, Nedves AN, Varjas B, Simon A, Alberti A, Riethmuller E: UHPLC-DPPH method reveals antioxidant tyramine and octopamine derivatives in Celtis occidentalis. J Pharm Biomed Anal. 2020 Nov 30;191:113612. doi: 10.1016/j.jpba.2020.113612. Epub 2020 Sep 9. [PubMed:32980795 ]
King, R. R., et al. (2005). King, R. R., et al, Phytochemistry 66, 2468 (2005). Phytochem..
DOI: 10.1016/j.phytol.2022.04.008
PII: s1874390022000866

Showing NP-Card for N-trans-feruloyloctopamine (NP0031586)

MOL for NP0031586 (N-trans-feruloyloctopamine)

3D MOL for NP0031586 (N-trans-feruloyloctopamine)

3D SDF for NP0031586 (N-trans-feruloyloctopamine)

3D-SDF for NP0031586 (N-trans-feruloyloctopamine)

PDB for NP0031586 (N-trans-feruloyloctopamine)

3D PDB for NP0031586 (N-trans-feruloyloctopamine)

SMILES for NP0031586 (N-trans-feruloyloctopamine)

INCHI for NP0031586 (N-trans-feruloyloctopamine)

Structure for NP0031586 (N-trans-feruloyloctopamine)

3D Structure for NP0031586 (N-trans-feruloyloctopamine)