UCSF

ZINC13675663

Draw Identity 99% 90% 80% 70%

Substance Information

In ZINC since Heavy atoms Benign functionality
June 23rd, 2008 34 Yes

Popular Name: N-[6-[(6-chloro-1,2,3,4-tetrahydroacridin-9-yl)amino]hexyl]-1H-indole-3-carboxamide N-[6-[(6-chloro-1,2,3,4-tetrahyd…

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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) 6.60 12.3 -41.19 4 5 1 71 476.044 9 ↓

Activity (Go SEA)

Clustered Target Annotations
Code Description Organism Class Affinity (nM) LE (kcal/mol/atom) Type
ACES-1-E Acetylcholinesterase (cluster #1 Of 12), Eukaryotic Eukaryotes 33 0.31 Binding ≤ 10μM
CHLE-1-E Butyrylcholinesterase (cluster #1 Of 7), Eukaryotic Eukaryotes 2 0.36 Binding ≤ 10μM
ChEMBL Target Annotations
Uniprot Swissprot Description Affinity (nM) LE (kcal/mol/atom) Type
ACES_BOVIN P23795 Acetylcholinesterase, Bovin 33 0.31 Binding ≤ 1μM
ACES_HUMAN P22303 Acetylcholinesterase, Human 33 0.31 Binding ≤ 1μM
CHLE_HUMAN P06276 Butyrylcholinesterase, Human 1.7 0.36 Binding ≤ 1μM
ACES_BOVIN P23795 Acetylcholinesterase, Bovin 33 0.31 Binding ≤ 10μM
ACES_HUMAN P22303 Acetylcholinesterase, Human 33 0.31 Binding ≤ 10μM
CHLE_HUMAN P06276 Butyrylcholinesterase, Human 1.7 0.36 Binding ≤ 10μM

Reactome Annotations from Targets (via Uniprot)

Description Species
Neurotransmitter Clearance In The Synaptic Cleft
Synthesis of PC
Synthesis, secretion, and deacylation of Ghrelin

Rings

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

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