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CAS 4159-20-0

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3,4-Didehydroretinoic acid

Description:
3,4-Didehydroretinoic acid is a derivative of retinoic acid, which is a metabolite of vitamin A and plays a crucial role in various biological processes, including vision, cell growth, and differentiation. This compound is characterized by its unique structure, which features a series of conjugated double bonds that contribute to its biological activity and stability. It is known to interact with nuclear receptors, influencing gene expression and cellular functions. The compound is typically a yellow to orange solid and is soluble in organic solvents, reflecting its hydrophobic nature. Its chemical properties include a relatively high melting point and specific reactivity patterns typical of retinoids. 3,4-Didehydroretinoic acid has been studied for its potential therapeutic applications, particularly in dermatology and oncology, due to its ability to modulate cellular processes. However, like other retinoids, it may also exhibit side effects, necessitating careful consideration in its use. Overall, this compound exemplifies the complex interplay between structure and function in bioactive molecules.
Formula:C20H26O2
InChI:InChI=1S/C20H26O2/c1-15(8-6-9-16(2)14-19(21)22)11-12-18-17(3)10-7-13-20(18,4)5/h6-12,14H,13H2,1-5H3,(H,21,22)/b9-6+,12-11+,15-8+,16-14+
InChI key:InChIKey=SYESMXTWOAQFET-YCNIQYBTSA-N
SMILES:C(=C/C(=C/C=C/C(=C/C(O)=O)/C)/C)\C=1C(C)(C)CC=CC1C
Synonyms:
  • (all-E)-3,7-Dimethyl-9-(2,6,6-trimethyl-1,3-cyclohexadien-1-yl)-2,4,6,8-nonatetraenoic acid
  • 3,4-Didehydro-all-trans-retinoic acid
  • 3-Dehydroretinoic acid
  • Retinoic Acid, 3,4-Didehydro-
  • Retinoic acid, 3,4-didehydro-, all-trans-
  • Ro 8-7057
  • Vitamin A<sub>2</sub> acid
  • Vitamin A<sub>2</sub> acid, all-trans-
  • all-trans-Vitamin A<sub>2</sub> acid
  • all-trans-Vitamin A2 acid
  • 3,4-Didehydroretinoic acid
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