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  2. Dihydroxyanthraquinone - Wikipedia

    en.wikipedia.org/wiki/Dihydroxyanthraquinone

    A dihydroxyanthraquinone is any of several isomeric organic compounds with formula (C 12 H 6 (OH) 2)(CO) 2, formally derived from 9,10-anthraquinone by replacing two hydrogen atoms by hydroxyl groups. Dihyroxyantraquinones have been studied since the early 1900s, and include some compounds of historical and current importance.

  3. 1,3-Dihydroxyanthraquinone - Wikipedia

    en.wikipedia.org/wiki/1,3-Dihydroxyanthraquinone

    It is one of ten dihydroxyanthraquinone isomers. Its molecular structure can be viewed as being derived from anthraquinone by replacement of two hydrogen atoms (H) by hydroxyl groups (-OH). Xanthopurpurin occurs in small amounts (as a glycoside ) in the root of the common madder plant, Rubia tinctorum , together with alizarin , purpurin and ...

  4. 1,5-Dihydroxyanthraquinone - Wikipedia

    en.wikipedia.org/wiki/1,5-Dihydroxyanthraquinone

    1,5-Dihydroxyanthraquinone is an organic compound with the formula (C 6 H 3 OH) 2 (CO) 2. It is one of several isomers of dihydroxyanthraquinone . An orange solid, it is a component of traditional Chinese medications. [ 3 ]

  5. 1,4-Dihydroxyanthraquinone - Wikipedia

    en.wikipedia.org/wiki/1,4-dihydroxyanthraquinone

    1,4-Dihydroxyanthraquinone, also called quinizarin or Solvent Orange 86, is an organic compound derived from anthroquinone. Quinizarin is an orange or red-brown crystalline powder. It is formally derived from anthraquinone by replacement of two hydrogen atoms by hydroxyl (OH) groups.

  6. Damage-associated molecular pattern - Wikipedia

    en.wikipedia.org/wiki/Damage-associated...

    They are also known as danger signals, and alarmins because they serve as warning signs to alert the organism to any damage or infection to its cells. DAMPs are endogenous danger signals that are discharged to the extracellular space in response to damage to the cell from mechanical trauma or a pathogen. [ 3 ]

  7. Anthraquinones - Wikipedia

    en.wikipedia.org/wiki/Anthraquinones

    A type II polyketide synthase is responsible for anthraquinone biosynthesis in the bacterium Photorhabdus luminescens. [3] Chorismate, formed by isochorismate synthase in the shikimate pathway, is a precursor of anthraquinones in Morinda citrifolia. [4] Tests for anthraquinones in natural extracts have been established. [5] Senna glycosides ...

  8. Bone morphogenetic protein - Wikipedia

    en.wikipedia.org/wiki/Bone_morphogenetic_protein

    Bone morphogenetic proteins (BMPs) are a group of growth factors also known as cytokines and as metabologens. [1] Professor Marshall Urist and Professor Hari Reddi discovered their ability to induce the formation of bone and cartilage, BMPs are now considered to constitute a group of pivotal morphogenetic signals, orchestrating tissue architecture throughout the body.

  9. JAK-STAT signaling pathway - Wikipedia

    en.wikipedia.org/wiki/JAK-STAT_signaling_pathway

    The JAK-STAT system consists of three main components: (1) a receptor (green), which penetrates the cell membrane; (2) Janus kinase (JAK) (yellow), which is bound to the receptor, and; (3) Signal Transducer and Activator of Transcription (STAT) (blue), which carries the signal into the nucleus and DNA. The red dots are phosphates.