General Information of the Drug (ID: M6APDG01104)
Name
Fluvastatin sodium
Synonyms
Fluindostatin sodium; Fluvastatin (sodium); Fluvastatin sodium (Lescol); Fluvastatin sodium salt; Fluyastatin Sodium Salt; Fractal; Lescol XL; Lipaxan; Lochol; Prestwick_1032; Sri 62320; Sri-62320; Vastin; XU 62-320; XU-62-320; Xilep XL; 93957-55-2; 94061-80-0; AB01274723-01; C24H25FNNaO4; CAS-93957-55-2; CHEBI:77602; Canef; DSSTox_CID_24758; DSSTox_GSID_44758; DSSTox_RID_80451; Locol; SMR000550480; Sodium (3R,5S,E)-7-(3-(4-fluorophenyl)-1-isopropyl-1H-indol-2-yl)-3,5-dihydroxyhept-6-enoate; FLUVASTATIN SODIUM; Fluvastatin [INN:BAN]; XU 62320; XU-62320; fluvastatin; (+)-(3R,5S)-fluvastatin; (3R,5S)-fluvastatin; (3R,5S,6E)-7-[3-(4-fluorophenyl)-1-(1-methylethyl)-1H-indol-2-yl]-3,5-dihydroxyhept-6-enoic acid; (3R,5S,6E)-7-[3-(4-fluorophenyl)-1-(propan-2-yl)-1H-indol-2-yl]-3,5-dihydroxyhept-6-enoic acid; (3R,5S,6E)-7-[3-(4-fluorophenyl)-1-isopropyl-1H-indol-2-yl]-3,5-dihydroxyhept-6-enoic acid; 93957-54-1; C24H26FNO4; CHEBI:38565; EN300-51915; CHEMBL1078
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Status
Approved
Structure
3D MOL
Formula
C24H25FNNaO4
InChI
1S/C24H26FNO4.Na/c1-15(2)26-21-6-4-3-5-20(21)24(16-7-9-17(25)10-8-16)22(26)12-11-18(27)13-19(28)14-23(29)30;/h3-12,15,18-19,27-28H,13-14H2,1-2H3,(H,29,30);/q;+1/p-1/b12-11+;/t18-,19-;/m1./s1
InChIKey
ZGGHKIMDNBDHJB-NRFPMOEYSA-M
PubChem CID
23663976
INTEDE Drug ID
DR0738
Target Gene(s) and Their Upstream m6A Regulator, Together with the Effect of Target Gene(s) in Drug Response
The target genes involved in drug-target interaction (such as drug-metabolizing enzymes, drug transporters and therapeutic targets) and drug-mediated cell death signaling (including modulating DNA damage and repair capacity, escaping from drug-induced apoptosis, autophagy, cellular metabolic reprogramming, oncogenic bypass signaling, cell microenvironment, cell stemness, etc.) could be regulated by m6A regulator(s) and affected their corresponding drug response. You can browse detailed information on drug-related target gene(s) mediated by m6A regulators.
Cytochrome P450 2C8 (CYP2C8)
Fat mass and obesity-associated protein (FTO)
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Fluvastatin sodium. The Fat mass and obesity-associated protein (FTO) has potential in affecting the response of Fluvastatin sodium through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [1], [2]
Methyltransferase-like 14 (METTL14)
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Fluvastatin sodium. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Fluvastatin sodium through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [1], [2]
Methyltransferase-like 3 (METTL3)
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Fluvastatin sodium. The Methyltransferase-like 3 (METTL3) has potential in affecting the response of Fluvastatin sodium through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [1], [2]
YTH domain-containing protein 2 (YTHDC2)
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Fluvastatin sodium. The YTH domain-containing protein 2 (YTHDC2) has potential in affecting the response of Fluvastatin sodium through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [1], [2]
References
Ref 1 Methylation of adenosine at the N(6) position post-transcriptionally regulates hepatic P450s expression. Biochem Pharmacol. 2020 Jan;171:113697. doi: 10.1016/j.bcp.2019.113697. Epub 2019 Nov 7.
Ref 2 Comparison of 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitors (statins) as inhibitors of cytochrome P450 2C8. Basic Clin Pharmacol Toxicol. 2005 Aug;97(2):104-8. doi: 10.1111/j.1742-7843.2005.pto_134.x.