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DNA Methyltransferase

DNA Methyltransferase

DNA methylation, which is the addition of a methyl group to the carbon atom five (C5) of cytosine, is carried out by a family of "writer" enzymes called DNA methyltransferases (DNMTs). De novo methyltransferases (DNMT3A-DNMT3B), DNMT1, DNMT2, DNMT3C, and DNMTL are the five DNMTs that mammals encode. The three active enzymes that maintain DNA methylation are DNMT1, DNMT3A, and DNMT3B. While DNMT2 functions as a tRNA transferase rather than a DNA methyltransferase, DNMT3L lacks catalytic activity and regulates DNMT3A and DNMT3B.
By regulating gene expression without altering the DNA sequence, DNA methylation is a crucial modification process in the control of genetic information. For transcription, post-replicative mismatch repair, DNA replication control, cell cycle control, bacterial virulence, and the distinction between self and non-self DNA in prokaryotes, DNA methylation is crucial. DNA methylation is essential for many important physiological processes in mammals, including imprinting, the inactivation of the X chromosome, the silencing of germline-specific genes, and the silencing of repetitive elements.

DNA Methyltransferase related products

Structure Cat No. Product Name CAS No. Product Description
HaeIII Methyltransferase (HaeIII) V75480 HaeIII Methyltransferase (HaeIII) 92228-40-5 HaeIII Methyltransferase (HaeIII) is a methyltransferase that covalently binds to DNA.
Hhal Methyltransferase (Hhal ) V75484 Hhal Methyltransferase (Hhal ) 91448-96-3 Hhal Methyltransferase (Hhal) is a DNA methyltransferase (recognition sequence: GCGC).
HpaII Methyltransferase (HpaII ) V86140 HpaII Methyltransferase (HpaII ) 85537-81-1
Levetiracetam (UCB-L 059, SIB-S 1) V0335 Levetiracetam (UCB-L 059, SIB-S 1) 102767-28-2 Levetiracetam (also known as UCB-L059, SIB-S1)is a potent and selective M2 muscarinic acetylcholine receptors (mAChR) inhibitor andan anticonvulsant medication used to treat epilepsy.
Levetiracetam-d3 (UCB L059-d3) V56178 Levetiracetam-d3 (UCB L059-d3) 1217851-16-5 Levetiracetam-d3 is the deuterium labelled form of Levetiracetam.
Levetiracetam-d6 (UCB L059-d6) V56177 Levetiracetam-d6 (UCB L059-d6) 1133229-29-4 Levetiracetam-d6 is the deuterated form of Levetiracetam.
Lomeguatrib (PaTrin2) V0409 Lomeguatrib (PaTrin2) 192441-08-0 Lomeguatrib (formerly PaTrin-2) is a novel, potentand selective inhibitor of MGMT (O6-alkylguanine-DNA-alkyltransferase) with anticancer activity.
METTL1-WDR4-IN-2 V85359 METTL1-WDR4-IN-2 2919742-07-5
MspI Methyltransferase (MspI ) V80846 MspI Methyltransferase (MspI ) MspI Methyltransferase (MspI) is a methyltransferase that recognizes the sequence CCGG and catalyzes the formation of 5-methylcytosine at the first C residue.
Procainamide (Procaine amide; SP 100) V52884 Procainamide (Procaine amide; SP 100) 51-06-9 Procainamide is a specific and potent inhibitor of DNA methyltransferase 1 (DNMT1).
Procainamide HCl V0410 Procainamide HCl 614-39-1 Procainamide HCl (known also as Procainamide hydrochloride; Procanbid; Procan) is an approved anti-arrhythmic drug that is used to treat cardiac arrhythmia by acting asa potent sodium channel blocker, and also a DNA methyltransferase inhibitor.
RG108 V0405 RG108 48208-26-0 RG108, also known asN-Phthalyl-L-tryptophan,is a novel non-nucleoside inhibitor of DNA methyltransferase ((DNMT)with potential antitumor activity.
SGI-1027 V0408 SGI-1027 1020149-73-8 SGI-1027 is a novel and potent inhibitorof DNA methyltransferase (DNMT) with antineoplastic activity.
Thioguanine (NSC-752; Tabloid) V0406 Thioguanine (NSC-752; Tabloid) 154-42-7 Thioguanine (6-Thioguanine; NSC752; Tabloid; 2-Amino-6-purinethiol; 6-TG), an FDA approved medication used for treating AML-acute myeloid leukemia, is an antimetabolite anticancer drug, specifically, an anti-leukemia and immunosuppressant agent.
Zebularine (NSC309132; 4-Deoxyuridine) V0407 Zebularine (NSC309132; 4-Deoxyuridine) 3690-10-6 Zebularine (formerly 4-Deoxyuridine; NSC-309132) is a selective and potent inhibitor of DNA methylation/methyltransferase with anticancer activity.
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