SCHEMBL4423375

SCHEMBL4423375

COc1cc(C)cc(C(O)c2ccccc2)c1

nearest known ligand 0.56

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
BRD4 O60885 6/20 0.56
CREBBP Q92793 5/20 0.56
TACR1 P25103 2/20 0.48
CNR2 P34972 1/20 0.48
ACHE P22303 1/20 0.41
PDE10A Q9Y233 1/20 0.41
ACP3 P15309 2/20 0.40
AOC3 Q16853 2/20 0.40
CA4 P22748 1/20 0.39
L3MBTL1 Q9Y468 1/20 0.39
SLC6A2 P23975 1/20 0.39
SLC6A4 P31645 1/20 0.39
SLC6A3 Q01959 1/20 0.39

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
SCHEMBL4819668 0.89 BRD4 (0.57) BRD4CREBBPTACR1CNR2ACP3
SCHEMBL11914197 0.87 ALDH1A1 (0.46) BRD4CREBBPTACR1ACHEAOC3
SCHEMBL13027665 0.83 TACR1 (0.46) BRD4CREBBPTACR1CNR2ACP3
SCHEMBL30655591 0.81 BRD4 (0.51) BRD4CREBBPTACR1CNR2PDE10A
SCHEMBL27686957 0.80 AOC3 (0.54) BRD4CREBBPCNR2AOC3CA4
SCHEMBL477338 0.80 AOC3 (0.54) BRD4CREBBPCNR2AOC3CA4
SCHEMBL4428549 0.79 TACR1 (0.48) BRD4CREBBPTACR1ACHEACP3
SCHEMBL477389 0.77 ACP3 (0.61) CNR2ACP3CA4L3MBTL1
SCHEMBL477621 0.77 ACP3 (0.61) CNR2ACP3CA4L3MBTL1
SCHEMBL477466 0.77 ACP3 (0.61) CNR2ACP3CA4L3MBTL1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20090326018-A1 2-Phenyl indene derivatives useful as estrogen receptor ligands KARO BIO AB (SE) 2009-12-31 US disclosed
US-20090326018-A1 2-Phenyl indene derivatives useful as estrogen receptor ligands KARO BIO AB (SE) 2009-12-31 US disclosed
US-20090326018-A1 2-Phenyl indene derivatives useful as estrogen receptor ligands KARO BIO AB (SE) 2009-12-31 US disclosed
EP-2074102-A1 2-PHENYL INDENE DERIVATIVES USEFUL AS ESTROGEN RECEPTOR LIGANDS KARO BIO AB (SE) 2009-07-01 EP disclosed
WO-2008043567-A1 2-PHENYL INDENE DERIVATIVES USEFUL AS ESTROGEN RECEPTOR LIGANDS KARO BIO AB (SE) 2008-04-17 WO disclosed
WO-2008043567-A1 2-PHENYL INDENE DERIVATIVES USEFUL AS ESTROGEN RECEPTOR LIGANDS KARO BIO AB (SE) 2008-04-17 WO disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20090326018-A1 2-Phenyl indene derivatives useful as estrogen receptor ligands ESR1, GPER1, ESR2 BRD4 1096/4885CREBBP 2660/4885TACR1 87/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.