UCSF

ZINC08214722

Draw Identity 99% 90% 80% 70%

Substance Information

In ZINC since Heavy atoms Benign functionality
July 4th, 2006 30 No

Popular Name: Solasodine Solasodine

Find On: PubMed — Wikipedia — Google

CAS Number: 126-17-0

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) 5.73 -2.49 -38.24 3 3 1 46 414.654 0 ↓

Vendor Notes

Note Type Comments Provided By
biological_use Antiandrogenic IBScreen Bioactives
biological_use Antiinflammatory IBScreen Bioactives
biological_use Antineoplastic agent IBScreen Bioactives IBScreen Bioactives
biological_use Antispermatogenic props. IBScreen Bioactives
PUBCHEM_PATENT_ID EP0515386A1; EP0515386B1; US3960839; US3992315; US4246346; US5241063; US5274088; US5614408; US5958770; US5959180; WO1991010743A1; WO1998034471A1; WO1999043837A1; WO1999059578A1; WO2000061153A1 IBM Patent Data
mechanism Inhibitor of spermatogenesis and sperm motility IBScreen Bioactives IBScreen Bioactives
mechanism Inhibitor of testosterone release IBScreen Bioactives
mechanism Regulations of TNFR I and II expression IBScreen Bioactives

Activity (Go SEA)

Clustered Target Annotations
Code Description Organism Class Affinity (nM) LE (kcal/mol/atom) Type
SGMR1-3-E Sigma Opioid Receptor (cluster #3 Of 6), Eukaryotic Eukaryotes 207 0.31 Binding ≤ 10μM
ERG2-1-F C-8 Sterol Isomerase (cluster #1 Of 2), Fungal Fungi 1170 0.28 Binding ≤ 10μM
ChEMBL Target Annotations
Uniprot Swissprot Description Affinity (nM) LE (kcal/mol/atom) Type
SGMR1_HUMAN Q99720 Sigma Opioid Receptor, Human 207 0.31 Binding ≤ 1μM
ERG2_YEAST P32352 C-8 Sterol Isomerase, Yeast 1170 0.28 Binding ≤ 10μM
SGMR1_HUMAN Q99720 Sigma Opioid Receptor, Human 207 0.31 Binding ≤ 10μM

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