Raloxifene

Raloxifene

SCHEMBL3016712

C1CCOC1.Cl.O=C(c1ccc(OCCN2CCCCC2)cc1)c1c(-c2ccc(O)cc2)sc2cc(O)ccc12

nearest known ligand 0.90

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ESR1ESR2

The experimentally established mechanism targets of Raloxifene. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ESR1 known ✓ P03372 20/20 0.90
ESR2 known ✓ Q92731 18/20 0.90
MEN1 O00255 2/20 0.90
ALDH1A1 P00352 2/20 0.90
LMNA P02545 2/20 0.90
TP53 P04637 2/20 0.90
CYP3A4 P08684 2/20 0.90
MAPT P10636 2/20 0.90
ALOX15 P16050 2/20 0.90
KMT2A Q03164 2/20 0.90
HSD17B10 Q99714 2/20 0.90
TDP1 Q9NUW8 2/20 0.90
GMNN O75496 1/20 0.90
HLA-A P04439 1/20 0.90
HTT P42858 1/20 0.90
BLM P54132 1/20 0.90
UBE2N P61088 1/20 0.90
PMP22 Q01453 1/20 0.90
NPSR1 Q6W5P4 1/20 0.90
PLD2 O14939 1/20 0.88

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
Raloxifene SCHEMBL1665291 0.95 ESR1 (1.00) ESR1ESR2MEN1ALDH1A1LMNA
Hydrochloric Acid SCHEMBL9201404 0.95 ESR1 (1.00) ESR1ESR2MEN1ALDH1A1LMNA
Raloxifene SCHEMBL178172 0.95 ESR1 (1.00) ESR1ESR2MEN1ALDH1A1LMNA
Raloxifene SCHEMBL19077 0.95 ESR1 (1.00) ESR1ESR2MEN1ALDH1A1LMNA
Raloxifene SCHEMBL12485521 0.95 ESR1 (1.00) ESR1ESR2MEN1ALDH1A1LMNA
Raloxifene SCHEMBL975023 0.94 ESR1 (0.98) ESR1ESR2MEN1ALDH1A1LMNA
Hydrochloric Acid SCHEMBL7631648 0.94 ESR1 (0.98) ESR1ESR2MEN1ALDH1A1LMNA
Raloxifene SCHEMBL3162158 0.94 ESR1 (1.00) ESR1ESR2MEN1ALDH1A1LMNA
Ly-117018 SCHEMBL7080240 0.94 ESR1 (0.98) ESR1ESR2MEN1ALDH1A1LMNA
Raloxifene SCHEMBL9145135 0.94 ESR1 (1.00) ESR1ESR2MEN1ALDH1A1LMNA

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 9 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20100204470-A1 METHOD FOR SALT PREPARATION SANDOZ AG 2010-08-12 US claimed
EP-2032521-A2 NEW METHOD FOR SALT PREPARATION Sandoz AG (CH) 2009-03-11 EP claimed
WO-2008000418-A2 NEW METHOD FOR SALT PREPARATION SANDOZ AG (CH) 2008-01-03 WO claimed
EP-2145890-B1 Crystallization of hydrohalides of pharmaceutical compounds SANDOZ AG (CH) 2012-08-01 EP disclosed
US-20100204470-A1 METHOD FOR SALT PREPARATION SANDOZ AG 2010-08-12 US disclosed
EP-2145890-A2 Crystallization of hydrohalides of pharmaceutical compounds Sandoz AG (CH) 2010-01-20 EP disclosed
EP-2032521-B1 NEW METHOD FOR SALT PREPARATION SANDOZ AG (CH) 2009-10-28 EP disclosed
EP-2032521-A2 NEW METHOD FOR SALT PREPARATION Sandoz AG (CH) 2009-03-11 EP disclosed
WO-2008000418-A2 NEW METHOD FOR SALT PREPARATION SANDOZ AG (CH) 2008-01-03 WO disclosed