UCSF

ZINC08215403

Physical Representations

Type pH range xlogP Des A‑Pol Apolar desolvation (kcal/mol) Des Pol Polar desolvation (kcal/mol) H Don H-bond donors H Acc H-bond acceptors Chg Net charge tPSA (Ų) MWT Molecular weight (g/mol) RB Rotatable bonds DL

Vendor Notes

Note Type Comments Provided By
UniProt Database Links 2ENR_CLOTY; 3BHD_COMTE; 3BHS1_HUMAN; 3BHS1_MACMU; 3BHS1_MESAU; 3BHS1_MOUSE; 3BHS1_RAT; 3BHS2_HUMAN; 3BHS2_MESAU; 3BHS2_MOUSE; 3BHS2_RAT; 3BHS3_MOUSE; 3BHS4_RAT; 3BHS6_MOUSE; 3BHS7_HUMAN; 3BHS7_MOUSE; 3BHS7_RAT; 3BHS_BOVIN; 3BHS_CANFA; 3BHS_FOWPN; 3BHS_HOR ChEBI
UniProt Database Links 2ENR_CLOTY; 3BHS1_HUMAN; 3BHS1_MACMU; 3BHS1_MESAU; 3BHS1_MOUSE; 3BHS1_RAT; 3BHS2_HUMAN; 3BHS2_MESAU; 3BHS2_MOUSE; 3BHS2_RAT; 3BHS3_MOUSE; 3BHS4_RAT; 3BHS6_MOUSE; 3BHS7_HUMAN; 3BHS7_MOUSE; 3BHS7_RAT; 3BHS_BOVIN; 3BHS_CANFA; 3BHS_FOWPN; 3BHS_HORSE; 3BHS_MYC ChEBI
Patent Database Links EP1318200; EP1531180; EP1586325; EP1826267; EP1847606; EP1938841; EP1972629; EP1987836; US2003105347; US2003181492; US2004176570; US2004235124; US2005049313; US2005124040; US2005159401; US2005181443; US2005214885; US2005227336; US2005272136; US2005276870 ChEBI
Reactome Database Links REACT_10031; REACT_10053; REACT_10056; REACT_10065; REACT_10067; REACT_10090; REACT_1010; REACT_10115; REACT_1068; REACT_1077; REACT_1080; REACT_11169; REACT_11182; REACT_11216; REACT_1146; REACT_115982; REACT_116077; REACT_120926; REACT_121064; REACT_121 ChEBI

Activity (Go SEA)

Direct Reactome Annotations (via ChEBI)

Description Species
Abacavir metabolism
Abnormal metabolism in phenylketonuria
alpha-linolenic acid (ALA) metabolism
Alpha-oxidation of phytanate
Amino acid synthesis and interconversion (transamination)
Androgen biosynthesis
Beta oxidation of butanoyl-CoA to acetyl-CoA
Beta oxidation of decanoyl-CoA to octanoyl-CoA-CoA
Beta oxidation of hexanoyl-CoA to butanoyl-CoA
Beta oxidation of lauroyl-CoA to decanoyl-CoA-CoA
Beta oxidation of myristoyl-CoA to lauroyl-CoA
Beta oxidation of octanoyl-CoA to hexanoyl-CoA
Beta oxidation of palmitoyl-CoA to myristoyl-CoA
Beta-oxidation of pristanoyl-CoA
Beta-oxidation of very long chain fatty acids
Branched-chain amino acid catabolism
Carnitine synthesis
Cell redox homeostasis
Cholesterol biosynthesis
Chorismate via Shikimate Pathway
Citric acid cycle (TCA cycle)
Cobalamin (Cbl, vitamin B12) transport and metabolism
De novo synthesis of GMP
Degradation of cysteine and homocysteine
Degradation of GABA
Ethanol oxidation
Formation of the active cofactor, UDP-glucuronate
Glucocorticoid biosynthesis
Gluconeogenesis
Glycolysis
Glycosphingolipid metabolism
Hypusine synthesis from eIF5A-lysine
Linoleic acid (LA) metabolism
Lipid metabolism
Lysine catabolism
Metabolism of serotonin
Mineralocorticoid biosynthesis
mitochondrial fatty acid beta-oxidation of unsaturated fatty acids
Mycothiol-dependent detoxification
Phenylalanine and tyrosine catabolism
Proline catabolism
Purine ribonucleoside monophosphate biosynthesis
Pyruvate metabolism
Regulation of pyruvate dehydrogenase (PDH) complex
Respiratory electron transport
Serine biosynthesis
Sphingolipid de novo biosynthesis
Sphingolipid metabolism
Synthesis of 15-eicosatetraenoic acid derivatives
Synthesis of bile acids and bile salts via 24-hydroxycholesterol
Synthesis of bile acids and bile salts via 27-hydroxycholesterol
Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol
Synthesis of Ketone Bodies
Synthesis of Lipoxins (LX)
Synthesis of PA
Synthesis of Prostaglandins (PG) and Thromboxanes (TX)
The activation of arylsulfatases
The canonical retinoid cycle in rods (twilight vision)
The tricarboxylic acid cycle
Tolerance by Mtb to nitric oxide produced by macrophages
Triglyceride Biosynthesis
Tryptophan catabolism
Urate synthesis
Utilization of Ketone Bodies
Vitamin C (ascorbate) metabolism

Analogs ( Draw Identity 99% 90% 80% 70% )

No pre-computed analogs available. Try a structural similarity search.