UCSF

ZINC04006187

Draw Identity 99% 90% 80% 70%

Substance Information

In ZINC since Heavy atoms Benign functionality
November 1st, 2005 21 Yes

Popular Name: 3-(3-bromophenyl)-5H-indeno[1,2-c]pyridazin-5-one 3-(3-bromophenyl)-5H-indeno[1,2-…

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CAS Number: 147508-56-3

Other Names:

MFCD00561170

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) 4.47 0.45 -10.24 0 3 0 42 337.176 1 ↓

Vendor Notes

Note Type Comments Provided By
melting_point 234 - 236 KeyOrganics

Activity (Go SEA)

Clustered Target Annotations
Code Description Organism Class Affinity (nM) LE (kcal/mol/atom) Type
AOFA-2-E Monoamine Oxidase A (cluster #2 Of 8), Eukaryotic Eukaryotes 1000 0.40 Binding ≤ 10μM
AOFB-2-E Monoamine Oxidase B (cluster #2 Of 8), Eukaryotic Eukaryotes 660 0.41 Binding ≤ 10μM
ChEMBL Target Annotations
Uniprot Swissprot Description Affinity (nM) LE (kcal/mol/atom) Type
AOFA_RAT P21396 Monoamine Oxidase A, Rat 1000 0.40 Binding ≤ 1μM
AOFB_RAT P19643 Monoamine Oxidase B, Rat 660 0.41 Binding ≤ 1μM
AOFA_RAT P21396 Monoamine Oxidase A, Rat 1000 0.40 Binding ≤ 10μM
AOFB_RAT P19643 Monoamine Oxidase B, Rat 660 0.41 Binding ≤ 10μM

Reactome Annotations from Targets (via Uniprot)

Description Species
Monoamines are oxidized to aldehydes by MAOA and MAOB, producing NH3 and H2O2

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

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