SCHEMBL7204579

SCHEMBL7204579

CCOC(=O)O[C@@H]1C[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@]2(C)[C@@]1(OC(=O)OCC)C(=O)OCCl

nearest known ligand 0.52

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ PGR P06401 9/20 0.52
▸ NR3C1 P04150 6/20 0.52
▸ ABCB11 O95342 4/20 0.52
▸ NR1I2 O75469 3/20 0.52
▸ ABCC3 O15438 1/20 0.52
▸ AR P10275 4/20 0.51
▸ CYP3A4 P08684 7/20 0.50
▸ LMNA P02545 4/20 0.50
▸ ADRA1A P35348 3/20 0.50
▸ HSD17B10 Q99714 2/20 0.50
▸ KDM4E B2RXH2 2/20 0.50
▸ CYP2C19 P33261 1/20 0.50
▸ HTR1A P08908 1/20 0.50
▸ ADRA2A P08913 1/20 0.50
▸ ADORA3 P0DMS8 2/20 0.47
▸ CHRM1 P11229 2/20 0.47
▸ SLC6A2 P23975 1/20 0.47
▸ SLC6A3 Q01959 1/20 0.47
▸ KCNH2 Q12809 1/20 0.47
▸ HIF1A Q16665 5/20 0.41

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
SCHEMBL7209821 0.91 ABCB11 (0.59) PGRNR3C1ABCB11NR1I2ABCC3
SCHEMBL7204631 0.85 ABCB11 (0.57) PGRNR3C1ABCB11NR1I2ABCC3
SCHEMBL7204614 0.84 ABCB11 (0.60) PGRNR3C1ABCB11NR1I2ABCC3
SCHEMBL7210548 0.83 ABCB11 (0.62) PGRNR3C1ABCB11NR1I2ABCC3
SCHEMBL7209170 0.82 ABCB11 (0.57) PGRNR3C1ABCB11NR1I2ABCC3
SCHEMBL8502593 0.81 ABCB11 (0.60) PGRNR3C1ABCB11NR1I2ABCC3
SCHEMBL8504524 0.79 ABCB11 (0.60) PGRNR3C1ABCB11NR1I2AR
SCHEMBL7205794 0.77 ABCB11 (0.60) PGRNR3C1ABCB11NR1I2AR
SCHEMBL7598319 0.75 PGR (0.61) PGRNR3C1ABCB11NR1I2ABCC3
SCHEMBL11328916 0.75 PGR (0.62) PGRNR3C1ABCB11NR1I2AR

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 3 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
EP-0137212-A2 Ointment bases and ointments OTSUKA PHARMACEUTICAL CO., LTD. (JP) 1985-04-17 — — EP disclosed
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