UCSF

ZINC03870415

Substance Information

In ZINC since Heavy atoms Benign functionality
October 4th, 2005 33 No

Download: MOL2 SDF SMILES Flexibase

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
Ref Reference (pH 7) 2.25 -6.74 -19.53 8 11 0 197 458.375 4
Hi High (pH 8-9.5) 2.25 -5.71 -50 7 11 -1 200 457.367 4
Hi High (pH 8-9.5) 2.25 -5.84 -52.28 7 11 -1 200 457.367 4

Vendor Notes

Note Type Comments Provided By
Target Tyrosine-protein kinase Fyn(P06241)&Transcription factor p65(Q04206)&Inhibitor of nuclear factor kappa-B kinase subunit beta(O14920)&Interferon regulatory factor 3(Q14653)&Serine/threonine-protein kinase TBK1(Q9UHD2)&Angiotensinogen(P01019)&Epidermal grow Herbal Ingredients Targets

Activity (Go SEA)

Clustered Target Annotations
Code Description Organism Class Affinity (nM) LE (kcal/mol/atom) Type
BACE1-2-E Beta-secretase 1 (cluster #2 Of 4), Eukaryotic Eukaryotes 210 0.28 Binding ≤ 10μM
KCNH2-1-E HERG (cluster #1 Of 5), Eukaryotic Eukaryotes 6026 0.22 Binding ≤ 10μM
ChEMBL Target Annotations
Uniprot Swissprot Description Affinity (nM) LE (kcal/mol/atom) Type
BACE1_HUMAN P56817 Beta-secretase 1, Human 210 0.28 Binding ≤ 1μM
BACE1_HUMAN P56817 Beta-secretase 1, Human 1600 0.25 Binding ≤ 10μM
KCNH2_HUMAN Q12809 HERG, Human 6025.59586 0.22 Binding ≤ 10μM

Reactome Annotations from Targets (via Uniprot)

Description Species
Voltage gated Potassium channels

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