Details
Stereochemistry | RACEMIC |
Molecular Formula | C19H21NO5S |
Molecular Weight | 375.439 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC(OC)=C(C=C1)C2CC(=NCCS2)C3=C(O)C=C(C)OC3=O
InChI
InChIKey=NHFIAAAMCYVRIW-UHFFFAOYSA-N
InChI=1S/C19H21NO5S/c1-11-8-15(21)18(19(22)25-11)14-10-17(26-7-6-20-14)13-5-4-12(23-2)9-16(13)24-3/h4-5,8-9,17,21H,6-7,10H2,1-3H3
KF-38789 is a selective inhibitor of P-selectin-mediated cell adhesion (IC50 = 1.97 uM) that displays no effects on L-selectin- and E-selectin-mediated adhesion. KF-38789 inhibits P-selectin-dependent
cell adhesion, superoxide production by
human PMN and TG-induced cell migration into the murine
peritoneal cavity. It was also identified as a tubulin disruptor.
Originator
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL2455 Sources: https://www.ncbi.nlm.nih.gov/pubmed/11766994 |
1.97 µM [IC50] | ||
Target ID: CHEMBL2095182 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/11766994
Mice: KF-38789 (1 mg/kg) was injected intravenously prior to TG injection and at 3 h following initial injection. Intravenously injected KF-38789 significantly inhibited the TG-induced accumulation of leukocytes in the mouse peritoneal cavity.
Route of Administration:
Intravenous
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/11766994
KF-38789, inhibited the binding of U937 cells to immobilized P-selectin immunoglobulin G chimeric protein (P-selectin-Ig) with an IC50 value of 1.97 uM. Cell adhesion to both E-selectin-Ig and L-selectin-Ig were not affected even by 100 uM of KF-38789.
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SD6U8X7NAE
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257292-29-8
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135400439
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ACTIVE MOIETY