Free shipping on all orders over $ 500

ADH-6 

Cat. No. M29381
ADH-6  Structure
Size Price Availability Quantity
Free Delivery on orders over USD 500 Bulk Inquiry?

Quality Control & Documentation
Biological Activity

ADH-6 is a tripyridylamide compound. ADH-6 abrogates self-assembly of the aggregation-nucleating subdomain of mutant p53 DBD. ADH-6 targets and dissociates mutant p53 aggregates in human cancer cells, which restores p53's transcriptional activity, leading to cell cycle arrest and apoptosis. ADH-6 has the potential for the research of cancer diseases.

Chemical Information
Molecular Weight 640.64
Formula C29H36N8O9
CAS Number 2227429-65-2
Storage Please store the product under the recommended conditions in the Certificate of Analysis.
Conversion of different model animals based on BSA (PMID: 27057123)
Species Mouse Rat Rabbit Guinea pig Hamster Dog
Weight (kg) 0.02 0.15 1.8 0.4 0.08 10
Body Surface Area (m2) 0.007 0.025 0.15 0.05 0.02 0.5
Km factor 3 6 12 8 5 20
Animal A (mg/kg) = Animal B (mg/kg) multiplied by  Animal B Km
Animal A Km

For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.

References

[1] L Palanikumar, et al. Nat Commun. Protein mimetic amyloid inhibitor potently abrogates cancer-associated mutant p53 aggregation and restores tumor suppressor function

[2] Michael Zaleski, et al. Ann Diagn Pathol. Should we excise? Are there any clinical or histologic features that predict upgrade in papillomas, incidental or non-incidental?

[3] Erna Guo, et al. Oncol Lett. Prognostic value of alcohol dehydrogenase mRNA expression in gastric cancer

[4] Shalini Arora, et al. Ann Surg Oncol. Atypical ductal hyperplasia at margin of breast biopsy--is re-excision indicated?

[5] T Matsushima. Nihon Rinsho. [ADH isoenzymes]

Related p53 Products
SCH529074

SCH529074 is an orally active, potent activator of mutant p53, which binds p53 DNA binding domain (DBD), restores growth-suppressive function to mutant p53 and interrupts HDM2-mediated ubiquitination of wild type p53.

BAY 1892005

BAY 1892005, a p53 protein modulator, is active on p53 condensates and does not lead to mutant p53 reactivation.

FOXO4-DRI

FOXO4-DRI is a cell-permeable peptide antagonist that blocks the interaction of FOXO4 and p53.

p53 (17-26)

p53 (17-26) is amino acids 17 to 26 fragment of p53.

Azurin p28 peptide

Azurin p28 peptide is a tumor-penetrated antitumor peptide.

  Catalog
Abmole Inhibitor Catalog




Keywords: ADH-6  supplier, p53, inhibitors, activators


Products are for research use only. Not for human use. We do not sell to patients.
© Copyright 2010-2023 AbMole BioScience. All Rights Reserved.