Sugi Predict

Sugi Predict / Compounds / SCHEMBL851649

SCHEMBL851649

SCHEMBL851649

Cc1cc(C)c(-c2c(C)cc(C)cc2O)c(O)c1

nearest known ligand 0.55

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ SELL P14151 1/20 0.55
▸ SELP P16109 1/20 0.55
▸ SELE P16581 1/20 0.55
▸ ACHE P22303 1/20 0.55
▸ TDP1 Q9NUW8 3/20 0.48
▸ TP53 P04637 2/20 0.48
▸ PIM1 P11309 2/20 0.46
▸ ALDH1A1 P00352 8/20 0.44
▸ MAPT P10636 8/20 0.44
▸ KDM4E B2RXH2 7/20 0.44
▸ LMNA P02545 2/20 0.44
▸ GAA P10253 2/20 0.44
▸ TRPA1 O75762 1/20 0.43
▸ KMT2A Q03164 6/20 0.43
▸ MEN1 O00255 5/20 0.43
▸ ELANE P08246 3/20 0.43
▸ CYP3A4 P08684 3/20 0.43
▸ MAPK1 P28482 3/20 0.43
▸ ALOX15 P16050 3/20 0.43
▸ TSHR P16473 2/20 0.43

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
SCHEMBL29455292 1.00 SELL (0.55) SELLSELPSELEACHETDP1
SCHEMBL28099808 0.90 SELL (0.46) SELLSELPSELEACHETDP1
SCHEMBL26201039 0.86 PIM1 (0.47) SELLSELPSELEACHETDP1
SCHEMBL26769093 0.84 SELL (0.65) SELLSELPSELEACHETDP1
SCHEMBL9744550 0.81 ALDH1A1 (0.50) SELLSELPSELEACHETDP1
SCHEMBL4277100 0.79 CNR1 (0.44) SELLSELPSELEACHETDP1
SCHEMBL30522730 0.79 CNR1 (0.44) SELLSELPSELEACHETDP1
SCHEMBL18838191 0.78 PIM1 (0.45) SELLSELPSELEACHETDP1
SCHEMBL317299 0.77 RAPGEF4 (0.50) SELLSELPSELEACHETDP1
SCHEMBL28859756 0.77 ALDH1A1 (0.58) SELLSELPSELEACHETDP1

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 155 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8431223-B2 Low coefficient of thermal expansion (CTE) thermosetting resins for integrated circuit applications INTEL CORPORATION (US) 2013-04-30 — — US claimed
US-20120282462-A1 LOW COEFFICIENT OF THERMAL EXPANSION (CTE) THERMOSETTING RESINS FOR INTEGRATED CIRCUIT APPLICATIONS MATAYABAS JR JAMES C (US) 2012-11-08 — — US claimed
US-8242216-B2 Low coefficient of thermal expansion (CTE) thermosetting resins for integrated circuit applications INTEL CORPORATION (US) 2012-08-14 — — US claimed
EP-1868975-B1 IMPROVED METHOD FOR PRODUCING BIPHENOLS FROM MONOPHENOLS BASF SE (DE) 2012-06-13 — — EP claimed
US-20110250458-A1 LOW COEFFICIENT OF THERMAL EXPANSION (CTE) THERMOSETTING RESINS FOR INTEGRATED CIRCUIT APPLICATIONS MATAYABAS JR JAMES C 2011-10-13 — — US claimed
US-7737310-B2 for preparing phosphorus-comprising chelating ligands; a biphenol of high purity is in many cases obtained after only a single crystallization and simple filtration BASF SE (DE) 2010-06-15 — — US claimed
US-20080177113-A1 Method For Producing Biphenols From Monophenols BASF AKTIENGESELLSCHAFT (DE) 2008-07-24 — — US claimed
US-20050288454-A1 Low coefficient of thermal expansion (CTE) thermosetting resins for integrated circuit applications INTEL CORPORATION 2005-12-29 — — US claimed
US-6077979-A Manufacture of 3,3',5,5'-tetramethyl-2,2'-biphenol E. I. DU PONT DE NEMOURS AND COMPANY (US) 2000-06-20 — — US claimed
JP-9143113-A — — None — — JP disclosed
JP-4216854-A — — None — — JP disclosed
EP-4722199-A1 AZOLE COMPOUND, METHOD FOR SYNTHESIZING SAID AZOLE COMPOUND, AND USE THEREOF SHIKOKU CHEMICALS CORPORATION (JP) 2026-04-08 — — EP disclosed
US-20260022137-A1 METHOD FOR PREPARING CYCLIC PHOSPHATE COMPOUND AND DERIVATIVE THEREOF UNIV BEIJING (CN) 2026-01-22 — — US disclosed
US-20250289782-A1 THIOL COMPOUND AND USES THEREOF SHIKOKU CHEMICALS CORPORATION (JP) 2025-09-18 — — US disclosed
US-4978809-A Meta-halogenated dibenzylphenols THE DOW CHEMICAL COMPANY (US) 1990-12-18 — — US disclosed
US-4946872-A Polyisocyanate prepolymers prepared from rigid polyaromatic precursor materials, and polyurethanes prepared therefrom THE DOW CHEMICAL COMPANY (US) 1990-08-07 — — US disclosed
EP-0299462-A2 Polyisocyanate prepolymers prepared from rigid polyaromatic precursor materials, and polyurethanes prepared therefrom THE DOW CHEMICAL COMPANY (US) 1989-01-18 — — EP disclosed
US-4390731-A Polymeric phenolic benzylic ether compositions ICI AMERICAS INC. (US) 1983-06-28 — — US disclosed
US-4153621-A POLYEPOXIDES ICI AMERICAS INC. (US) 1979-05-08 — — US disclosed
US-4072656-A WITH P,P'-METHYLENEDIANILINE OR M-PHENYLENEDIAMINE CURING AGENT ICI AMERICAS INC. (US) 1978-02-07 — — US 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-20250289782-A1 THIOL COMPOUND AND USES THEREOF TMT1A, TXN, CTH SELL 1116/4885SELP 774/4885SELE 64/4885
US-20080177113-A1 Method For Producing Biphenols From Monophenols SQLE, CYP11B2, CYP11B1 SELL 3156/4885SELP 2986/4885SELE 1600/4885
US-20260022137-A1 METHOD FOR PREPARING CYCLIC PHOSPHATE COMPOUND AND DERIVATIVE THEREOF PNP, INPPL1, PHKA1 SELL 4747/4885SELP 3177/4885SELE 4836/4885

“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.