Avobenzone-d3
CAT:
804-HY-B0316S1
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- Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
- Dry Ice Shipment: No

Avobenzone-d3
- CAS Number: 2518100-58-6
- UNSPSC Description: Avobenzone-d3 is deuterium labeled Avobenzone. Avobenzone, a dibenzoylmethane compound, is one of the most widely used filters in sunscreens for skin photoprotection in the UVA band. Avobenzone is an endocrine disruptor that directly binds to estrogen receptor β and acts as an estrogen agonist[1][2][3].
- Target Antigen: Apoptosis; Estrogen Receptor/ERR; Isotope-Labeled Compounds
- Type: Isotope-Labeled Compounds
- Related Pathways: Apoptosis;Others;Vitamin D Related/Nuclear Receptor
- Field of Research: Others
- Smiles: O=C(C1=CC=C(C=C1)OC([2H])([2H])[2H])CC(C2=CC=C(C=C2)C(C)(C)C)=O
- Molecular Weight: 313.41
- References & Citations: [1]Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019 Feb;53(2):211-216.|[2]Kojić M, et al. A new insight into the photochemistry of avobenzone in gas phase and acetonitrile from ab initio calculations. Phys Chem Chem Phys. 2016;18(32):22168-22178.|[3]Ahn S, An S, et al. A long-wave UVA filter avobenzone induces obesogenic phenotypes in normal human epidermal keratinocytes and mesenchymal stem cells. Arch Toxicol. 2019;93(7):1903-1915.|[4]Yang C, et al. Avobenzone suppresses proliferative activity of human trophoblast cells and induces apoptosis mediated by mitochondrial disruption. Reprod Toxicol. 2018;81:50-57.|[5]Schreurs RH, et al. Interaction of polycyclic musks and UV filters with the estrogen receptor (ER), androgen receptor (AR), and progesterone receptor (PR) in reporter gene bioassays. Toxicol Sci. 2005;83(2):264-272.
- Shipping Conditions: Room temperature
- Clinical Information: No Development Reported