UCSF

ZINC36178968

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) 4.53 7.2 -38.25 1 3 -1 60 249.311 11
Hi High (pH 8-9.5) 4.53 8.32 -123.32 0 3 -2 63 248.303 11

Vendor Notes

Note Type Comments Provided By
Melting_Point 92-96? Alfa-Aesar
Melting_Point 92-96° Alfa-Aesar

Activity (Go SEA)

Clustered Target Annotations
Code Description Organism Class Affinity (nM) LE (kcal/mol/atom) Type
LPAR1-2-E Lysophosphatidic Acid Receptor Edg-2 (cluster #2 Of 2), Eukaryotic Eukaryotes 1270 0.52 Binding ≤ 10μM
LPAR2-1-E Lysophosphatidic Acid Receptor Edg-4 (cluster #1 Of 2), Eukaryotic Eukaryotes 1270 0.52 Binding ≤ 10μM
LPAR3-2-E Lysophosphatidic Acid Receptor Edg-7 (cluster #2 Of 2), Eukaryotic Eukaryotes 303 0.57 Binding ≤ 10μM
LPAR1-3-E Lysophosphatidic Acid Receptor Edg-2 (cluster #3 Of 4), Eukaryotic Eukaryotes 2638 0.49 Functional ≤ 10μM
LPAR2-2-E Lysophosphatidic Acid Receptor Edg-4 (cluster #2 Of 4), Eukaryotic Eukaryotes 2638 0.49 Functional ≤ 10μM
LPAR3-2-E Lysophosphatidic Acid Receptor Edg-7 (cluster #2 Of 3), Eukaryotic Eukaryotes 654 0.54 Functional ≤ 10μM
Z80390-7-O PC-3 (Prostate Carcinoma Cells) (cluster #7 Of 10), Other Other 2638 0.49 Functional ≤ 10μM
ChEMBL Target Annotations
Uniprot Swissprot Description Affinity (nM) LE (kcal/mol/atom) Type
LPAR3_HUMAN Q9UBY5 Lysophosphatidic Acid Receptor Edg-7, Human 303 0.57 Binding ≤ 1μM
LPAR1_HUMAN Q92633 Lysophosphatidic Acid Receptor Edg-2, Human 1270 0.52 Binding ≤ 10μM
LPAR2_HUMAN Q9HBW0 Lysophosphatidic Acid Receptor Edg-4, Human 1270 0.52 Binding ≤ 10μM
LPAR3_HUMAN Q9UBY5 Lysophosphatidic Acid Receptor Edg-7, Human 1270 0.52 Binding ≤ 10μM
LPAR1_HUMAN Q92633 Lysophosphatidic Acid Receptor Edg-2, Human 2638 0.49 Functional ≤ 10μM
LPAR2_HUMAN Q9HBW0 Lysophosphatidic Acid Receptor Edg-4, Human 2638 0.49 Functional ≤ 10μM
LPAR3_HUMAN Q9UBY5 Lysophosphatidic Acid Receptor Edg-7, Human 2638 0.49 Functional ≤ 10μM
Z80390 Z80390 PC-3 (Prostate Carcinoma Cells) 2638 0.49 Functional ≤ 10μM

Reactome Annotations from Targets (via Uniprot)

Description Species
G alpha (i) signalling events
G alpha (q) signalling events
Lysosphingolipid and LPA receptors

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