ADT-OHADT-OH - High-quality laboratory reagent available from Gentaur. Catalog: 804-HY-109582-01.804-HY-109582-01804-HY-109582-01Business & Industrial > Science & LaboratoryADT-OH
Gentaur
EUR12027-02-23

ADT-OH

CAT:
804-HY-109582-01
Size:
5 mg
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
ADT-OH - image 1

ADT-OH

  • Description:

    ADT-OH is a hydrogen sulfide-releasing donor. ADT-OH induces apoptosis and upregulates FADD. ADT-OH inhibits FAK/Paxillin. ADT-OH has the potential for the research of cancer diseases[1][5].
  • Product Name Alternative:

    5- (4-Hydroxyphenyl) -3H-1,2-dithiole-3-thione; ACS 1
  • UNSPSC:

    12352005
  • Hazard Statement:

    H302, H315, H319, H335
  • Target:

    Apoptosis; FAK
  • Type:

    Reference compound
  • Related Pathways:

    Apoptosis; Protein Tyrosine Kinase/RTK
  • Applications:

    Cancer-programmed cell death
  • Field of Research:

    Cancer
  • Assay Protocol:

    https://www.medchemexpress.com/adt-oh.html
  • Concentration:

    10mM
  • Purity:

    98.55
  • Solubility:

    DMSO : 125 mg/mL (ultrasonic)
  • Smiles:

    S=C1SSC(C2=CC=C(O)C=C2)=C1
  • Molecular Formula:

    C9H6OS3
  • Molecular Weight:

    226.35
  • Precautions:

    H302, H315, H319, H335
  • References & Citations:

    [1]Cai F, et al. ADT-OH, a hydrogen sulfide-releasing donor, induces apoptosis and inhibits the development of melanoma in vivo by upregulating FADD. Cell Death Dis. 2020;11 (1) :33.|[2]Yu S, et al. ADT-OH exhibits anti-metastatic activity on triple-negative breast cancer by combinatorial targeting of autophagy and mitochondrial fission. Cell Death Dis. 2024 Jun 28;15 (6) :463. |[3]Xu H, et al. ADT-OH synergistically enhanced the antitumor activity of celecoxib in human colorectal cancer cells. Cancer Med. 2023 Aug;12 (16) :17193-17211.|[4]Wei SW, et al. Role of the hydrogen sulfide-releasing donor ADT-OH in the regulation of mammal neural precursor cells. J Cell Physiol. 2022 Jul;237 (7) :2877-2887.|[5]Li CY, et al. Gambogic acid exhibits anti-metastatic activity on malignant melanoma mainly through inhibition of PI3K/Akt and ERK signaling pathways. Eur J Pharmacol. 2019 Dec 1;864:172719.
  • Shipping Conditions:

    Room Temperature
  • Storage Conditions:

    -20°C, 3 years; 4°C, 2 years (Powder)
  • Scientific Category:

    Reference compound1
  • Clinical Information:

    No Development Reported
  • CAS Number:

    [18274-81-2]