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N-feruloyl-3-methyldopamine

isolated from Cyathula officinalis; structure in first source

Also Known As:

N-trans-feruloyl-3-methyldopamine

Networked: 1 relevant articles (0 outcomes, 0 trials/studies)

Bio-Agent Context: Research Results

Organic Chemicals: 133
- Amines: 4871
  - Catecholamines: 15682
    - Dopamine: 23033
      - N-feruloyl-3-methyldopamine: 1
  - Biogenic Amines: 992
    - Biogenic Monoamines: 29
      - Dopamine: 23033
        N-feruloyl-3-methyldopamine: 1
- Hydrocarbons: 1713
  - Cyclic Hydrocarbons: 97
    - Aromatic Hydrocarbons: 291
      - Benzene Derivatives: 17
        Phenols: 677
        Catechols: 121
        Catecholamines: 15682
        Dopamine: 23033
        N-feruloyl-3-methyldopamine: 1

Experts

1.	Kim, Hyun Pyo: 1 article (09/2011)
2.	Kwon, Yong Soo: 1 article (09/2011)
3.	Lim, Hyun: 1 article (09/2011)
4.	Park, Hyun Young: 1 article (09/2011)

Related Diseases

1.

09/01/2011 - "officinalis Kuan as well as the N-hexane and chloroform soluble fractions were found to potently inhibit MMP-13 induction in IL-1 β-treated SW1353 cells, a human chondrosarcoma cell line, at 50-200 µg/mL. Activity-guided separation led to the isolation of six compounds, palmitic acid (1), β-sitosterol (2), α-spinasterol (3), atractylenolide I (4), 1,3-diacetoxy-tetradeca-6E,12E-dien-8,10-dyn (5), and N-trans-feruloyl-3-methyldopamine (6). "

Related Drugs and Biologics

1.	Palmitic Acid (Hexadecanoic Acid)
2.	Interleukin-1 (Interleukin 1)
3.	Chloroform (Trichloromethane)
4.	atractylenolide I
5.	spinasterol
6.	n-hexane
7.	gamma-sitosterol (beta-sitosterol)