UCSF

ZINC35143441

Substance Information

In ZINC since Heavy atoms Benign functionality
October 4th, 2009 13 Yes

Other Names:

MFCD06421446

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) 2.01 8.42 -7.26 0 2 0 18 172.231 2
Mid Mid (pH 6-8) 2.01 8.94 -32.74 1 2 1 19 173.239 2

Vendor Notes

Note Type Comments Provided By
Purity 97% Fluorochem
PUBCHEM_PATENT_ID EP1045846A1 IBM Patent Data

Activity (Go SEA)

Clustered Target Annotations
Code Description Organism Class Affinity (nM) LE (kcal/mol/atom) Type
C11B1-2-E Cytochrome P450 11B1 (cluster #2 Of 2), Eukaryotic Eukaryotes 48 0.79 Binding ≤ 10μM
C11B2-1-E Cytochrome P450 11B2 (cluster #1 Of 2), Eukaryotic Eukaryotes 110 0.75 Binding ≤ 10μM
ChEMBL Target Annotations
Uniprot Swissprot Description Affinity (nM) LE (kcal/mol/atom) Type
C11B1_HUMAN P15538 Cytochrome P450 11B1, Human 48 0.79 Binding ≤ 1μM
C11B2_HUMAN P19099 Cytochrome P450 11B2, Human 110 0.75 Binding ≤ 1μM
C11B1_HUMAN P15538 Cytochrome P450 11B1, Human 48 0.79 Binding ≤ 10μM
C11B2_HUMAN P19099 Cytochrome P450 11B2, Human 110 0.75 Binding ≤ 10μM

Reactome Annotations from Targets (via Uniprot)

Description Species
Endogenous sterols
Glucocorticoid biosynthesis
Mineralocorticoid biosynthesis

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