SCHEMBL6718488

SCHEMBL6718488

O=C(c1ccccc1)N1Cc2cc(O)ccc2C(c2ccc(O)cc2)C1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
ESR1 P03372 5/20 1.00
ESR2 Q92731 5/20 1.00
KIF11 P52732 6/20 0.54
GRIN1 Q05586 1/20 0.49
GRIN2B Q13224 1/20 0.49
SLC6A2 P23975 3/20 0.44
SLC6A4 P31645 3/20 0.44
SLC6A3 Q01959 3/20 0.44
MGLL Q99685 2/20 0.41
DRD1 P21728 2/20 0.41
NAMPT P43490 1/20 0.41
HTR2A P28223 1/20 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
SCHEMBL6713506 0.79 ESR1 (1.00) ESR1ESR2KIF11SLC6A2SLC6A4
SCHEMBL6718303 0.77 ESR2 (0.63) ESR1ESR2KIF11SLC6A2SLC6A4
SCHEMBL22461292 0.76 ESR2 (0.61) ESR1ESR2KIF11SLC6A2SLC6A4
SCHEMBL6716517 0.74 ESR2 (1.00) ESR1ESR2SLC6A2SLC6A4SLC6A3
SCHEMBL11639888 0.73 SLC6A2 (0.72) ESR1ESR2SLC6A2SLC6A4SLC6A3
Hydrochloric Acid SCHEMBL11640224 0.72 SLC6A2 (0.70) ESR1ESR2SLC6A2SLC6A4SLC6A3
SCHEMBL2473773 0.70 ESR1 (0.54) ESR1ESR2GRIN1GRIN2BMGLL
SCHEMBL16523571 0.70 CA1 (0.61) ESR1ESR2GRIN1GRIN2BNAMPT
SCHEMBL3056380 0.70 CA1 (0.68) ESR1ESR2GRIN1GRIN2BNAMPT
SCHEMBL20425694 0.68 ESR1 (0.52) ESR1ESR2KIF11

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20040192685-A1 Tetrahydroisoquinoline compounds as estrogen agonists/antagonists CAMERON KIMBERLY O (US) 2004-09-30 US disclosed
US-20030220494-A1 Tetrahydroisoquinoline compounds as estrogen agonists/antagonists CAMERON KIMBERLY O (US) 2003-11-27 US disclosed
US-6608203-B2 Devoid of unwanted side effects PFIZER INC. 2003-08-19 US disclosed
US-20010039285-A1 Tetrahydroisoquinoline compounds as estrogen agonists/antagonists CAMERON KIMBERLY O (US) 2001-11-08 US disclosed
EP-1113007-A1 Tetrahydroisoquinoline compounds as estrogen agonists/antagonists PFIZER INC. (US) 2001-07-04 EP 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 (3 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-20010039285-A1 Tetrahydroisoquinoline compounds as estrogen agonists/antagonists GPER1, ESR1, ESR2 ESR1 2/4885ESR2 3/4885KIF11 4404/4885
US-20030220494-A1 Tetrahydroisoquinoline compounds as estrogen agonists/antagonists GPER1, ESR1, ESR2 ESR1 2/4885ESR2 3/4885KIF11 4404/4885
US-20040192685-A1 Tetrahydroisoquinoline compounds as estrogen agonists/antagonists GPER1, ESR1, ESR2 ESR1 2/4885ESR2 3/4885KIF11 4404/4885

“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.