Structure

InChI Key RHGYHLPFVJEAOC-FFNUKLMVSA-L
Smile O=C([O-])C[C@H](O)C[C@H](O)/C=C/c1c(C2CC2)nc2ccccc2c1-c1ccc(F)cc1.O=C([O-])C[C@H](O)C[C@H](O)/C=C/c1c(C2CC2)nc2ccccc2c1-c1ccc(F)cc1.[Ca+2]
InChI
InChI=1S/2C25H24FNO4.Ca/c2*26-17-9-7-15(8-10-17)24-20-3-1-2-4-22(20)27-25(16-5-6-16)21(24)12-11-18(28)13-19(29)14-23(30)31;/h2*1-4,7-12,16,18-19,28-29H,5-6,13-14H2,(H,30,31);/q;;+2/p-2/b2*12-11+;/t2*18-,19-;/m11./s1

Physicochemical Descriptors

Property Name Value
Molecular Formula C50H46CaF2N2O8
Molecular Weight 881.0
AlogP 4.52
Hydrogen Bond Acceptor 4.0
Hydrogen Bond Donor 3.0
Number of Rotational Bond 8.0
Polar Surface Area 90.65
Molecular species ACID
Aromatic Rings 3.0
Heavy Atoms 31.0

Pharmacology

Action Mechanism of Action Reference
INHIBITOR HMG-CoA reductase inhibitor FDA

Indications

Mesh Heading Maximum Phase Mesh ID Reference
Lipid Metabolism Disorders 3 D052439 ClinicalTrials
Hypercholesterolemia 3 D006937 ClinicalTrials

Related Entries

Scaffolds

Parent

Adverse Reactions

System Organ Classification (SOC)
Relative Frequency (%)
Musculoskeletal and connective tissue disorders
18.46
Nervous system disorders
11.32
General disorders and administration site conditions
11.27
Gastrointestinal disorders
9.3
Injury, poisoning and procedural complications
6.04
Skin and subcutaneous tissue disorders
5.96
Investigations
5.62
Respiratory, thoracic and mediastinal disorders
4.95
Psychiatric disorders
4.55
Cardiac disorders
4.1
Vascular disorders
3.88
Immune system disorders
2.47
Metabolism and nutrition disorders
2.22
Renal and urinary disorders
2.08

Cross References

Resources Reference
ChEBI 71258
ChEMBL CHEMBL1237061
EPA CompTox DTXSID4046448
FDA SRS IYD54XEG3W
KEGG D01862
PubChem 5282451
SureChEMBL SCHEMBL22720
ZINC ZINC01534965