Target intelligence / Profile preview

Guanine nucleobase (G)

Target
G
Molecular classification
Nucleobase, Purine base, Nitrogenous base
01

Overview

Guanine is a **purine nucleobase** (chemical formula C₅H₅N₅O) and serves as one of the four principal bases in DNA and RNA, designated by the symbol **G**. In DNA, guanine pairs with cytosine via three hydrogen bonds, contributing to the stability and information encoding of the double helix. It is a planar, aromatic, double-ring structure forming part of the nucleic acid backbone, and also participates in cellular energy metabolism as a component of guanosine triphosphate (GTP). Guanine is susceptible to chemical modifications such as oxidation and alkylation, which can lead to mutagenesis and play roles in disease and therapeutic contexts [1][2][3][4][5][6][7][8].

Other names
GuanineG2-amino-1,7-dihydro-6H-purin-6-onePurine nucleobase G
02

Mechanism of action

Alkylation or modification of guanine bases disrupts base pairing, triggering cell cycle arrest or apoptosis; Intercalation between guanine bases disrupts DNA replication and transcription; Platinum agents form adducts with N7 of guanine, causing DNA crosslinking and double-strand breaks

03

Biological functions

Encoding genetic informationBase pairing with cytosine in DNA and RNAStructural maintenance of DNA helixPrecursor in nucleic acid biosynthesisComponent of energy-transfer molecules (as guanosine in GTP)
04

Disease associations

Mutagenesis (guanine oxidation, mispairing)Cancer (DNA mutation hotspots)Hereditary disorders of purine metabolism
05

Safety considerations

DNA mutation risks from guanine-targeting agentsResistance via repair enzymes (e.g., MGMT for O6-methylguanine)Off-target cytotoxicity in dividing tissues
06

Interacting drugs

Alkylating agents (e.g., temozolomide, dacarbazine)

3 more in the full profile.

07

Biomarkers

8-oxo-guanine (marker of oxidative DNA damage)O6-methylguanine (monitoring DNA alkylation)

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