UCSF

ZINC05570003

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Substance Information

In ZINC since Heavy atoms Benign functionality
February 5th, 2006 12 No

Popular Name: N-hydroxy-4-iodo-benzenesulfonamide N-hydroxy-4-iodo-benzenesulfonamide

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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) 1.77 -0.56 -9.4 2 4 0 66 299.089 2 ↓
Hi High (pH 8-9.5) 1.77 0.45 -43.47 1 4 -1 69 298.081 2 ↓

Activity (Go SEA)

Clustered Target Annotations
Code Description Organism Class Affinity (nM) LE (kcal/mol/atom) Type
CAH2-6-E Carbonic Anhydrase II (cluster #6 Of 15), Eukaryotic Eukaryotes 13 0.92 Binding ≤ 10μM
CAH4-16-E Carbonic Anhydrase IV (cluster #16 Of 16), Eukaryotic Eukaryotes 45 0.86 Binding ≤ 10μM
ChEMBL Target Annotations
Uniprot Swissprot Description Affinity (nM) LE (kcal/mol/atom) Type
CAH2_HUMAN P00918 Carbonic Anhydrase II, Human 13 0.92 Binding ≤ 1μM
CAH4_BOVIN Q95323 Carbonic Anhydrase IV, Bovin 45 0.86 Binding ≤ 1μM
CAH2_HUMAN P00918 Carbonic Anhydrase II, Human 13 0.92 Binding ≤ 10μM
CAH4_BOVIN Q95323 Carbonic Anhydrase IV, Bovin 45 0.86 Binding ≤ 10μM

Reactome Annotations from Targets (via Uniprot)

Description Species
Erythrocytes take up carbon dioxide and release oxygen
Erythrocytes take up oxygen and release carbon dioxide
Reversible hydration of carbon dioxide

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

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