In ZINC since | Heavy atoms | Benign functionality |
---|---|---|
November 7th, 2005 | 31 | No |
Popular Name: Friedelin Friedelin
Find On: PubMed — Wikipedia — Google
CAS Numbers: 559-74-0 , [559-74-0]
(-)-friedelin; D:A-friedooleanan-3-one; Friedelin; friedelan-3-one; friedelin; friedeline
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 |
---|---|---|---|---|---|---|---|---|---|---|
Ref Reference (pH 7) | 7.85 | 14.3 | -3.64 | 0 | 1 | 0 | 17 | 426.729 | 0 | ↓ |
Note Type | Comments | Provided By |
---|---|---|
UniProt Database Links | FRIES_KALDA; SHS1_ASTTA | ChEBI |
Code | Description | Organism Class | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
NR1H4-2-E | Bile Acid Receptor FXR (cluster #2 Of 2), Eukaryotic | Eukaryotes | 0 | 0.00 | Functional ≤ 10μM |
Uniprot | Swissprot | Description | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
NR1H4_HUMAN | Q96RI1 | Bile Acid Receptor FXR, Human | 0.1 | 0.45 | Functional ≤ 10μM |
Description | Species |
---|---|
Endogenous sterols | |
PPARA activates gene expression | |
Recycling of bile acids and salts | |
Synthesis of bile acids and bile salts | |
Synthesis of bile acids and bile salts via 27-hydroxycholesterol | |
Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol |