SCHEMBL7205794

SCHEMBL7205794

CCCOC(=O)O[C@]1(C(=O)O)[C@H](C)C[C@H]2[C@@H]3C[C@H](F)C4=CC(=O)C=C[C@]4(C)[C@H]3[C@@H](O)C[C@@]21C

nearest known ligand 0.60

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ ABCB11 O95342 3/20 0.60
▸ PGR P06401 9/20 0.60
▸ AR P10275 5/20 0.60
▸ ADRA1A P35348 2/20 0.54
▸ ADORA3 P0DMS8 2/20 0.54
▸ CHRM1 P11229 1/20 0.54
▸ SLC6A2 P23975 1/20 0.54
▸ SLC6A3 Q01959 1/20 0.54
▸ KCNH2 Q12809 1/20 0.54
▸ CYP3A4 P08684 7/20 0.51
▸ NR3C1 P04150 7/20 0.51
▸ LMNA P02545 3/20 0.51
▸ HSD17B10 Q99714 2/20 0.51
▸ KDM4E B2RXH2 2/20 0.51
▸ CYP2C19 P33261 1/20 0.51
▸ HTR1A P08908 1/20 0.51
▸ ADRA2A P08913 1/20 0.51
▸ F2 P00734 1/20 0.44
▸ HIF1A Q16665 5/20 0.44
▸ NR1I2 O75469 3/20 0.44

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
SCHEMBL7210548 0.94 ABCB11 (0.62) ABCB11PGRARADRA1AADORA3
SCHEMBL7204631 0.91 ABCB11 (0.57) ABCB11PGRARADRA1AADORA3
SCHEMBL7208940 0.89 PGR (0.62) ABCB11PGRARADRA1AADORA3
SCHEMBL11230026 0.89 PGR (0.62) ABCB11PGRARADRA1AADORA3
SCHEMBL11236533 0.89 PGR (0.64) ABCB11PGRARADRA1AADORA3
SCHEMBL11237068 0.88 ABCB11 (0.67) ABCB11PGRARADRA1AADORA3
SCHEMBL7205320 0.87 PGR (0.60) ABCB11PGRARADRA1AADORA3
SCHEMBL10707938 0.87 ABCB11 (0.58) ABCB11PGRARADRA1AADORA3
SCHEMBL8505295 0.86 ABCB11 (0.61) ABCB11PGRARADRA1AADORA3
SCHEMBL10715139 0.86 PGR (0.63) ABCB11PGRARADRA1AADORA3

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 2 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6610675-B1 Identifying nontoxic therapeutically inactive metabolite of drug which elicits particular therapeutic response, converting inactive metabolite into activated structurally related drug species which cleaves in vivo to inactive metabolite Bodor, Nicholas S. 2003-08-26 — — US disclosed
US-4996335-A Soft steroids having anti-inflammatory activity Bodor, Nicholas S. (US) 1991-02-26 — — US disclosed
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