SCHEMBL7205296

SCHEMBL7205296

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

nearest known ligand 0.68

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ PGR P06401 6/20 0.68
▸ AR P10275 6/20 0.68
▸ ADORA3 P0DMS8 2/20 0.68
▸ CHRM1 P11229 1/20 0.68
▸ ADRA1A P35348 1/20 0.68
▸ NR3C1 P04150 12/20 0.64
▸ CYP3A4 P08684 5/20 0.64
▸ HIF1A Q16665 4/20 0.64
▸ SMN1; SMN2 Q16637 2/20 0.64
▸ ALDH1A1 P00352 2/20 0.64
▸ CYP1A2 P05177 1/20 0.64
▸ NR3C2 P08235 2/20 0.62
▸ NR1I2 O75469 1/20 0.62
▸ ABCB11 O95342 1/20 0.57
▸ MAPT P10636 1/20 0.57
▸ RAB9A P51151 1/20 0.57
▸ CNR1 P21554 1/20 0.55
▸ PTGS1 P23219 1/20 0.55
▸ MEN1 O00255 1/20 0.52
▸ ALOX15 P16050 1/20 0.52

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
SCHEMBL7205448 0.94 PGR (0.69) PGRARADORA3CHRM1ADRA1A
SCHEMBL7204586 0.91 NR3C1 (0.68) PGRARADORA3CHRM1ADRA1A
SCHEMBL15325054 0.90 PGR (0.83) PGRARADORA3CHRM1ADRA1A
SCHEMBL7203073 0.90 PGR (0.65) PGRARADORA3CHRM1ADRA1A
SCHEMBL11286638 0.89 NR3C1 (0.70) PGRARADORA3CHRM1ADRA1A
SCHEMBL20589853 0.89 PGR (0.69) PGRARADORA3CHRM1ADRA1A
SCHEMBL8502918 0.89 PGR (0.69) PGRARADORA3CHRM1ADRA1A
SCHEMBL20589855 0.89 PGR (0.69) PGRARADORA3CHRM1ADRA1A
SCHEMBL11428349 0.89 NR3C1 (0.76) PGRARADORA3CHRM1ADRA1A
SCHEMBL7085618 0.88 PGR (0.67) PGRARADORA3CHRM1ADRA1A

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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