SCHEMBL4423661

SCHEMBL4423661

COc1ccc(C2=C(C)c3ccc(OC)cc3C2c2ccccc2)cc1

nearest known ligand 0.41

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 4/20 0.41
MAPT P10636 3/20 0.41
NPC1 O15118 3/20 0.41
RAB9A P51151 3/20 0.41
HPGD P15428 2/20 0.41
TP53 P04637 1/20 0.41
MAOA P21397 1/20 0.41
PTGS2 P35354 1/20 0.41
MEN1 O00255 1/20 0.40
LMNA P02545 1/20 0.40
HTT P42858 1/20 0.40
KMT2A Q03164 1/20 0.40
NPSR1 Q6W5P4 1/20 0.40
ABL1 P00519 1/20 0.40
ABCB1 P08183 1/20 0.40
BCR P11274 1/20 0.40
BACE1 P56817 1/20 0.39
CYP1A1 P04798 1/20 0.39
CYP1A2 P05177 1/20 0.39
CYP2E1 P05181 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
SCHEMBL19305055 0.75 ESR1 (0.47) SMN1; SMN2MAPTNPC1RAB9AHPGD
SCHEMBL10109414 0.72 NOS3 (0.43) SMN1; SMN2MAPTNPC1RAB9AHPGD
Ammonia Solution, Strong SCHEMBL22730063 0.71 SLC6A2 (0.47) SMN1; SMN2MAPTNPC1RAB9AHPGD
SCHEMBL17765400 0.69 TP53 (0.44) TP53NPSR1CYP1A2CYP3A4CYP2D6
SCHEMBL17637160 0.67 ESR1 (0.54) ABCB1ALDH1A1
SCHEMBL1615072 0.67 ABL1 (0.63) SMN1; SMN2MAPTNPC1RAB9AHPGD
SCHEMBL11895545 0.66 MAPT (0.44) SMN1; SMN2MAPTNPC1RAB9AHPGD
SCHEMBL4423401 0.66 ESR2 (0.57) SMN1; SMN2MAPTNPC1RAB9AHPGD
SCHEMBL28414867 0.65 ESR2 (0.53) SMN1; SMN2MAPTNPC1RAB9AHPGD
SCHEMBL570649 0.64 KDM4E (0.67) LMNAABCB1CYP3A4CYP19A1MAOB

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 SMN1; SMN2 2790/4885MAPT 3272/4885NPC1 651/4885

“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.