3-Deazaneplanocin A (hydrochloride)
CAT:
804-HY-12186-04
Size:
10 mg
Price:
Ask
- Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
- Dry Ice Shipment: No

3-Deazaneplanocin A (hydrochloride)
- Product Name Alternative: DZNep hydrochloride; NSC 617989 hydrochloride; 3-Deazaneplanocin hydrochloride
- CAS Number: 120964-45-6
- UNSPSC Description: 3-Deazaneplanocin A hydrochloride (DZNep hydrochloride) is a potent histone methyltransferase EZH2 inhibitor[1][2]. 3-Deazaneplanocin A hydrochlorideis a potent S-adenosylhomocysteine hydrolase (AHCY) inhibitor[6]. 3-Deazaneplanocin A hydrochloride also has anti-orthopoxvirus and anti-variola activities[7].
- Target Antigen: Histone Methyltransferase; Orthopoxvirus
- Type: Reference compound
- Related Pathways: Anti-infection;Epigenetics
- Field of Research: Cancer; Infection
- Assay Protocol: https://www.medchemexpress.com/3-Deazaneplanocin-A-hydrochloride.html
- Purity: 99.98
- Solubility: H2O : 50 mg/mL (ultrasonic)
- Smiles: O[C@@H]1[C@H](O)C(CO)=C[C@H]1N2C=NC3=C2C=CN=C3N.[H]Cl
- Molecular Weight: 298.73
- References & Citations: [1]Fiskus W, et al. Combined epigenetic therapy with the histone methyltransferase EZH2 inhibitor 3-deazaneplanocin A and the histone deacetylase inhibitor LBH589 against human AML cells. Blood, 2009, 114(13), 2733-2743.|[2]Avan A, et al. Molecular mechanisms involved in the synergistic interaction of the EZH2 inhibitor 3-deazaneplanocin A with LY 188011 in pancreatic cancer cells. Mol Cancer Ther. 2012 Aug;11(8):1735-46.|[3]Kikuchi J, et al. Epigenetic therapy with 3-deazaneplanocin A, an inhibitor of the histone methyltransferase EZH2, inhibits growth of non-small cell lung cancer cells. Lung Cancer. 2012 Nov;78(2):138-43.|[4]Sun F, et al. Preclinical pharmacokinetic studies of 3-deazaneplanocin A, a potent epigenetic anticancer agent, and its human pharmacokinetic prediction using GastroPlus?. Eur J Pharm Sci. 2015 Sep 18;77:290-302.|[5]Noriko Uchiyama, et al. Aristeromycin and DZNeP cause growth inhibition of prostate cancer via induction of mir-26a. Eur J Pharmacol. 2017 Oct 5;812:138-146.|[6]Robert O Baker, et al. Potential antiviral therapeutics for smallpox, monkeypox and other orthopoxvirus infections. Antiviral Res. 2003 Jan;57(1-2):13-23. Apoptosis. 2020 Oct;25(9-10):697-714.|Biochem Biophys Res Commun. 2018 Sep 10;503(3):2061-2067.|bioRxiv. 2023 Apr 21.|bioRxiv. 2024 May 18.|Cell Signal. 2023 Dec 30:115:111029.|Exp Mol Pathol. 2020 Feb;112:104344.|J Pharmacol Exp Ther. 2019 Sep;370(3):490-503.|Nat Commun. 2022 Jan 10;13(1):12.|Università degli Studi di CAGLIARI. Dipartimento di Scienze Biomediche. 2021 May.|bioRxiv. 2024 July 27.|Cancers (Basel). 2022 Jul 23;14(15):3600.|Cell Death Dis. 2020 Oct 23;11(10):906.|Cell Death Discov. 2024 Jul 28;10(1):341.|Cell Rep. 2023 May 23;42(6):112550.|Cell Reprogram. 2017 Dec;19(6):363-371.|Cells Tissues Organs. 2021 Jan 18;1-9.|Genes. 2024 Sep 13.|Int Immunopharmacol. 2022 Feb 19;106:108612.|J Am Soc Nephrol. 2016 Jul;27(7):2021-34. |J Immunother Cancer. 2019 Nov 14;7(1):300. |J Mol Cell Cardiol. 2019 Oct;135:119-133.|Lab Invest. 2021 Mar 10.|Nat Commun. 2021 Feb 23;12(1):1237.|Patent. US20180263995A1.|Research Square Preprint. 2020 May.|Research Square Print. September 13th, 2022.
- Shipping Conditions: Room Temperature
- Storage Conditions: 4°C (Powder, sealed storage, away from moisture)
- Clinical Information: No Development Reported