Sugi Predict

Sugi Predict / Compounds / SCHEMBL361976

SCHEMBL361976

SCHEMBL361976

CC1(c2cccc(C3(C)CO3)c2)CO1

nearest known ligand 0.39

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
▸ CHRNB2 P17787 13/20 0.39
▸ SLC6A2 P23975 13/20 0.39
▸ CHRNB4 P30926 13/20 0.39
▸ CHRNA3 P32297 13/20 0.39
▸ CHRNA4 P43681 13/20 0.39
▸ SLC6A3 Q01959 13/20 0.39
▸ CHRNA1 P02708 12/20 0.39
▸ CHRNB1 P11230 12/20 0.39
▸ CHRNG P07510 10/20 0.39
▸ CHRND Q07001 10/20 0.39
▸ ALOX5 P09917 1/20 0.37
▸ SLC6A4 P31645 8/20 0.37
▸ OPRD1 P41143 1/20 0.32
▸ CYP1A2 P05177 1/20 0.32

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
SCHEMBL12852075 0.89 OPRD1 (0.42) CHRNB2SLC6A2CHRNB4CHRNA3CHRNA4
SCHEMBL30717245 0.87 CHRNA1 (0.53) CHRNB2SLC6A2CHRNB4CHRNA3CHRNA4
SCHEMBL17733690 0.84 ALOX5 (0.34) CHRNB2SLC6A2CHRNB4CHRNA3CHRNA4
SCHEMBL5855213 0.82 CHRNB2 (0.44) CHRNB2SLC6A2CHRNB4CHRNA3CHRNA4
SCHEMBL123189 0.82 CHRNB2 (0.44) CHRNB2SLC6A2CHRNB4CHRNA3CHRNA4
SCHEMBL11938179 0.82 CHRNB2 (0.44) CHRNB2SLC6A2CHRNB4CHRNA3CHRNA4
SCHEMBL11162269 0.82 SLC6A2 (0.55) CHRNB2SLC6A2CHRNB4CHRNA3CHRNA4
SCHEMBL5698966 0.80 KDM1A (0.51) SLC6A2SLC6A3SLC6A4
SCHEMBL5698913 0.80 KDM1A (0.51) SLC6A2SLC6A3SLC6A4
SCHEMBL1499359 0.80 CHRNB2 (0.38) CHRNB2SLC6A2CHRNB4CHRNA3CHRNA4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4025555-A1 METHOD OF MAKING A DIALDEYHDE Eastman Chemical Company (US) 2022-07-13 — — EP claimed
EP-4025553-A1 A PROCESS TO MAKE AROMATIC ENOL ETHERS AND OLEFIN ISOMERS OF AROMATIC ENOL ETHERS Eastman Chemical Company (US) 2022-07-13 — — EP claimed
EP-4025554-A1 METHOD OF MAKING A DIALDEYHDE EASTMAN CHEMICAL COMPANY (US) 2022-07-13 — — EP claimed
WO-2022076356-A1 METHOD FOR MAKING A DIALDEHYDE EASTMAN CHEMICAL COMPANY (US) 2022-04-14 — — WO claimed
US-10865171-B1 Process to make aromatic enol ethers and olefin isomers of aromatic enol ethers EASTMAN CHEMICAL COMPANY (US) 2020-12-15 — — US claimed
EP-3710159-A1 CATALYST COMPONENTS FOR PROPYLENE POLYMERIZATION W. R. Grace & Co. - Conn. (US) 2020-09-23 — — EP claimed
US-10550057-B1 Method of making a dialdeyhde EASTMAN CHEMICAL COMPANY (US) 2020-02-04 — — US claimed
US-10544076-B1 Method of making a dialdeyhde EASTMAN CHEMICAL COMPANY (US) 2020-01-28 — — US claimed
US-8344079-B2 Molar ratio modifications to larger polyolefin catalysts BASF CORPORATION (US) 2013-01-01 — — US claimed
US-20090171044-A1 MOLAR RATIO MODIFICATIONS TO LARGER POLYOLEFIN CATALYSTS BASF CATALYSTS LLC (US) 2009-07-02 — — US claimed
JP-11071364-A — — None — — JP disclosed
US-20260103548-A1 PROCESS FOR PRODUCING POLYPROPYLENE-ETHYLENE RANDOM COPOLYMER RESIN WITH SUSTAINABLE REACTOR OPERABILITY W. R. GRACE & CO.-CONN. 2026-04-16 — — US disclosed
US-20250235842-A1 GAS-PHASE PROCESS FOR MAKING POLYPROPYLENE RANDOM COPOLYMERS W.R. GRACE & CO.-CONN (US) 2025-07-24 — — US disclosed
US-20250145745-A1 HIGH MFR POLYPROPYLENE FOR MELTBLOWN NONWOVEN APPLICATIONS W. R. GRACE & CO.-CONN. 2025-05-08 — — US disclosed
US-12240925-B2 Process for preparing solid catalyst components for olefin polymerization W. R. GRACE & CO.- CONN. (US) 2025-03-04 — — US disclosed
EP-0972776-A1 A phosphine sulfide, a manufacturing process therefor and a use thereof Mitsui Chemicals, Inc. (JP) 2000-01-19 — — EP disclosed
EP-0950649-A1 A process for preparing oxyalkylene derivatives in the presence of phosphine oxides Mitsui Chemicals, Inc. (JP) 1999-10-20 — — EP disclosed
US-5962547-A STYRENE OXIDES; ADHESIVES, CATINGS Henkel IP & Holding GmbH (DE) 1999-10-05 — — US disclosed
JP-H1171364-A REACTIVE RADIATION-OR THERMALLY-INITIATED CATIONICALLY CURABLE EPOXIDE MONOMERS AND COMPOSITION PRODUCED FROM THE MONOMERS NATL STARCH & CHEM INVESTMENT HOLDING CORP 1999-03-16 — — JP disclosed
EP-0878472-A1 Reactive radiation- or thermally- initiated cationically-curable epoxide monomers and compositions made from those monomers National Starch and Chemical Investment Holding Corporation (US) 1998-11-18 — — 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 (5 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-12240925-B2 Process for preparing solid catalyst components for olefin polymerization POF1B, PPOX, OGFOD1 CHRNB2 4493/4885SLC6A2 4253/4885CHRNB4 4187/4885
US-10544076-B1 Method of making a dialdeyhde DERA, SORD, DDT CHRNB2 4026/4885SLC6A2 4489/4885CHRNB4 4034/4885
US-10865171-B1 Process to make aromatic enol ethers and olefin isomers of aromatic enol ethers ETV1, OSBPL8, ENY2 CHRNB2 104/4885SLC6A2 1645/4885CHRNB4 113/4885
US-20260103548-A1 PROCESS FOR PRODUCING POLYPROPYLENE-ETHYLENE RANDOM COPOLYMER RESIN WITH SUSTAINABLE REACTOR OPERABILITY CCT4, PTGER1, TCP1 CHRNB2 3341/4885SLC6A2 4673/4885CHRNB4 2439/4885
US-10550057-B1 Method of making a dialdeyhde ADH1C, DERA, DDT CHRNB2 3794/4885SLC6A2 3630/4885CHRNB4 3920/4885

“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.