SCHEMBL411554

SCHEMBL411554

Cc1ccc(N(c2ccc(C)cc2)c2ccc(C(C)(c3ccc(O)cc3)c3ccc(O)cc3)cc2)cc1

nearest known ligand 0.53

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
▸ ESR1 P03372 11/20 0.53
▸ ESR2 Q92731 11/20 0.53
▸ ACHE P22303 1/20 0.50
▸ TSHR P16473 3/20 0.45
▸ CYP3A4 P08684 2/20 0.45
▸ LMNA P02545 1/20 0.45
▸ TYR P14679 1/20 0.45
▸ AR P10275 1/20 0.45
▸ HPGD P15428 1/20 0.45
▸ SLC6A2 P23975 1/20 0.45
▸ SLC6A4 P31645 1/20 0.45
▸ HTR6 P50406 1/20 0.45
▸ ESRRG P62508 1/20 0.45
▸ SLC6A3 Q01959 1/20 0.45
▸ HSD17B10 Q99714 1/20 0.45
▸ MEN1 O00255 1/20 0.44
▸ KMT2A Q03164 1/20 0.44
▸ ALDH1A1 P00352 2/20 0.39
▸ SHBG P04278 1/20 0.38

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
SCHEMBL8199516 0.89 ESR1 (0.56) ESR1ESR2ACHETSHRCYP3A4
SCHEMBL19018130 0.89 ESR1 (0.43) ESR1ESR2ACHETSHRCYP3A4
SCHEMBL12755222 0.89 ESR1 (0.61) ESR1ESR2ACHETSHRCYP3A4
SCHEMBL3143096 0.88 ESR2 (0.67) ESR1ESR2ACHETSHRCYP3A4
SCHEMBL13815221 0.88 ESR2 (0.67) ESR1ESR2ACHETSHRCYP3A4
SCHEMBL8211551 0.87 ESR1 (0.50) ESR1ESR2ACHETSHRCYP3A4
SCHEMBL16521520 0.87 ESR1 (0.46) ESR1ESR2ACHETSHRCYP3A4
SCHEMBL28032007 0.85 ACHE (0.68) ESR1ESR2ACHETSHRCYP3A4
SCHEMBL3743294 0.85 ACHE (0.68) ESR1ESR2ACHETSHRCYP3A4
SCHEMBL347583 0.85 ACHE (0.68) ESR1ESR2ACHETSHRCYP3A4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
JP-8134027-A — — None — — JP disclosed
US-9859505-B2 Charge-transporting molecular glass mixtures, luminescent molecular glass mixtures, or combinations thereof or organic light emitting diodes and other organic electronics and photonics applications MOLECULAR GLASSES, INC. (US) 2018-01-02 — — US disclosed
US-20150053894-A1 Charge-transporting Molecular Glass Mixtures, Luminescent Molecular Glass Mixtures, or Combinations Thereof for Organic Light Emitting Diodes and other Organic Electronics and Photonics Applications Molaire Consulting 2015-02-26 — — US disclosed
US-20150053894-A1 Charge-transporting Molecular Glass Mixtures, Luminescent Molecular Glass Mixtures, or Combinations Thereof for Organic Light Emitting Diodes and other Organic Electronics and Photonics Applications Molaire Consulting 2015-02-26 — — US disclosed
US-8481234-B2 Image bearing member RICOH COMPANY, LTD. (JP) 2013-07-09 — — US disclosed
US-8481234-B2 Image bearing member RICOH COMPANY, LTD. (JP) 2013-07-09 — — US disclosed
US-20120064444-A1 IMAGE BEARING MEMBER RICOH COMPANY, LTD. (JP) 2012-03-15 — — US disclosed
US-20120064444-A1 IMAGE BEARING MEMBER RICOH COMPANY, LTD. (JP) 2012-03-15 — — US disclosed
US-8017807-B2 Tetrahydroxy compound, method for preparing the tetrahydroxy compound, and photoreceptor using the tetrahydroxy compound RICOH COMPANY LIMITED (JP) 2011-09-13 — — US disclosed
US-8017807-B2 Tetrahydroxy compound, method for preparing the tetrahydroxy compound, and photoreceptor using the tetrahydroxy compound RICOH COMPANY LIMITED (JP) 2011-09-13 — — US disclosed
US-20070128530-A1 TETRAHYDROXY COMPOUND, METHOD FOR PREPARING THE TETRAHYDROXY COMPOUND, AND PHOTORECEPTOR USING THE TETRAHYDROXY COMPOUND RICOH COMPANY, LTD. (JP) 2007-06-07 — — US disclosed
US-20070128530-A1 TETRAHYDROXY COMPOUND, METHOD FOR PREPARING THE TETRAHYDROXY COMPOUND, AND PHOTORECEPTOR USING THE TETRAHYDROXY COMPOUND RICOH COMPANY, LTD. (JP) 2007-06-07 — — US disclosed
US-6093784-A (CO)POLYCARBONATE CONTAINING DIARYLAMINOPHENYL-SUBSTITUTED BISPHENOL UNITS; DURABILITY, HEAT RESISTANCE, RADIATION TRANSPARENCY RICOH COMPANY, LTD. (JP) 2000-07-25 — — US disclosed
US-5830980-A FROM (DIARYLAMINO)BENZYLIDENEDIPHENOLS AND BIS/CHLOROFORMATES RICOH COMPANY, LTD. (JP) 1998-11-03 — — US disclosed
US-5747204-A DURABILITY, PHOTOSENSITIVITY; COPIERS, PRINTERS RICOH COMPANY, LTD. (JP) 1998-05-05 — — US disclosed
JP-H08134027-A TERTIARY AMINE COMPOUND RICOH CO LTD 1996-05-28 — — JP 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-20070128530-A1 TETRAHYDROXY COMPOUND, METHOD FOR PREPARING THE TETRAHYDROXY COMPOUND, AND PHOTORECEPTOR USING THE TETRAHYDROXY COMPOUND ALDH1A2, SLC9B2, SLC18A2 ESR1 1345/4885ESR2 1776/4885ACHE 3985/4885

“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.

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