In ZINC since | Heavy atoms | Benign functionality |
---|---|---|
December 11th, 2008 | 22 | No |
Popular Name: alfa-oxo[(Phenylmethoxy) carbonyl]-1-piperidine acetic acid methyl ester alfa-oxo[(Phenylmethoxy) carbony…
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CAS Number: 409366-76-3
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) | 1.88 | 9.05 | -11.92 | 0 | 6 | 0 | 73 | 305.33 | 6 | ↓ |
Code | Description | Organism Class | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
FKB1A-1-E | FK506-binding Protein 1A (cluster #1 Of 1), Eukaryotic | Eukaryotes | 8000 | 0.32 | Binding ≤ 10μM |
Uniprot | Swissprot | Description | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
FKB1A_HUMAN | P62942 | FK506-binding Protein 1A, Human | 8000 | 0.32 | Binding ≤ 10μM |
Description | Species |
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TGF-beta receptor signaling activates SMADs | |
TGF-beta receptor signaling in EMT (epithelial to mesenchymal transition) | |
TGFBR1 KD Mutants in Cancer | |
TGFBR1 LBD Mutants in Cancer | |
TGFBR2 Kinase Domain Mutants in Cancer |
No pre-computed analogs available. Try a structural similarity search.