SCHEMBL981302

SCHEMBL981302

CCCCCCc1c(O)cccc1CC

nearest known ligand 0.59

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
BID P55957 6/20 0.59
MCL1 Q07820 6/20 0.59
BCL2L1 Q07817 5/20 0.59
BAK1 Q16611 5/20 0.59
KAT8 Q9H7Z6 3/20 0.59
EP300 Q09472 2/20 0.59
KAT5 Q92993 2/20 0.59
SAE1 Q9UBE0 2/20 0.59
PPARG P37231 1/20 0.59
PPARA Q07869 1/20 0.59
KAT2A Q92830 1/20 0.59
KAT2B Q92831 1/20 0.59
F7 P08709 3/20 0.51
F3 P13726 3/20 0.51
MMP2 P08253 2/20 0.51
MAPT P10636 2/20 0.51
KDM4E B2RXH2 1/20 0.51
ALOX15 P16050 1/20 0.51
ECE1 P42892 1/20 0.51
SGMS1 Q86VZ5 1/20 0.51

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
SCHEMBL981550 1.00 BID (0.59) BIDMCL1BCL2L1BAK1KAT8
SCHEMBL984542 1.00 BID (0.59) BIDMCL1BCL2L1BAK1KAT8
SCHEMBL983837 1.00 BID (0.59) BIDMCL1BCL2L1BAK1KAT8
SCHEMBL984316 1.00 BID (0.59) BIDMCL1BCL2L1BAK1KAT8
SCHEMBL983628 1.00 BID (0.59) BIDMCL1BCL2L1BAK1KAT8
Water SCHEMBL27333005 0.98 BID (0.58) BIDMCL1BCL2L1BAK1KAT8
SCHEMBL980887 0.98 BID (0.57) BIDMCL1BCL2L1BAK1KAT8
Phosphoric Acid SCHEMBL29256469 0.94 BID (0.54) BIDMCL1BCL2L1BAK1KAT8
SCHEMBL982521 0.93 BID (0.50) BIDMCL1BCL2L1BAK1KAT8
SCHEMBL1003820 0.91 BID (0.61) BIDMCL1BCL2L1BAK1KAT8

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-116157494-A Phosphorus-free oil-soluble molybdenum complexes as high temperature scale inhibitors 埃科莱布美国股份有限公司 2023-05-23 CN disclosed
CN-116057155-A Phosphorus-free oil-soluble molybdenum complex for high-temperature naphthenic acid corrosion inhibition 埃科莱布美国股份有限公司 2023-05-02 CN disclosed
WO-2022118751-A1 AMINE RESISTANCE IMPARTING AGENT FOR VINYL CHLORIDE RESIN 株式会社ADEKA 2022-06-09 WO disclosed
EP-2275405-B1 PROCESS FOR PRODUCING ISOCYANATE USING DIARYL CARBONATE ASAHI CHEMICAL IND (JP) 2019-04-24 EP disclosed
EP-2275406-B1 PROCESS FOR PRODUCING ISOCYANATE ASAHI CHEMICAL IND (JP) 2018-11-28 EP disclosed
EP-2792673-B1 Carbamic acid ester derivatives for the production of isocyanate and aromatic hydroxy compounds ASAHI CHEMICAL IND (JP) 2018-07-25 EP disclosed
EP-3320065-A1 COMPOSITION AND METHOD FOR PREVENTING OR REDUCING ENGINE KNOCK AND PRE-IGNITION IN HIGH COMPRESSION SPARK IGNITION ENGINES ExxonMobil Research and Engineering Company (US) 2018-05-16 EP disclosed
CN-107001566-A Polyurethane-polyurea, its manufacture method and the cosmetic combination comprising the polyurethane-polyurea 株式会社ADEKA 2017-08-01 CN disclosed
US-9637445-B2 Isocyanate production process using composition containing carbamic acid ester and aromatic hydroxy compound, and composition for transfer and storage of carbamic acid ester ASAHI KASEI CHEMICALS CORPORATION (JP) 2017-05-02 US disclosed
WO-2017007669-A1 COMPOSITION AND METHOD FOR PREVENTING OR REDUCING ENGINE KNOCK AND PRE-IGNITION IN HIGH COMPRESSION SPARK IGNITION ENGINES EXXONMPBIL RESEARCH AND ENGINEERING COMPANY (US) 2017-01-12 WO disclosed
EP-2213658-A1 METHOD FOR PRODUCTION OF ISOCYANATE AND AROMATIC HYDROXY COMPOUND Asahi Kasei Chemicals Corporation (JP) 2010-08-04 EP disclosed
US-20100113823-A1 ISOCYANATE PRODUCTION PROCESS USING COMPOSITION CONTAINING CARBAMIC ACID ESTER AND AROMATIC HYDROXY COMPOUND, AND COMPOSITION FOR TRANSFER AND STORAGE OF CARBAMIC ACID ESTER ASAHI KASEI CHEMICALS CORPORATION (JP) 2010-05-06 US disclosed
EP-2147909-A1 METHOD FOR PRODUCTION OF ISOCYANATE USING COMPOSITION COMPRISING CARBAMIC ACID ESTER AND AROMATIC HYDROXY COMPOUND, AND COMPOSITION FOR TRANSPORT OR STORAGE OF CARBAMIC ACID ESTER Asahi Kasei Chemicals Corporation (JP) 2010-01-27 EP disclosed
EP-0220400-B1 WET ABRASION RESISTANT YARN AND CORDAGE AlliedSignal Inc. (US) 1992-03-04 EP disclosed
US-4960431-A TREATING THE YARN AFTER DRAWING WITH OXIDZED POLYETHYLENE NEUTRALIZED WITH AMMONIUM HYDROXIDE AND EMULSIFIED WITH A NON-NITROGEN, NONIONIC EMULSIFIER ALLIED-SIGNAL INC. (US) 1990-10-02 US disclosed
US-4767646-A OXIDIZED AND NEUTRALIZED POLYETHYLENE; NONIONIC EMULSIFIER; SILOXANE COPOLYMER WITH 3-((2-AMINOETHYL)AMINOPROPYL) GROUPS OR AMIDE MELAMINE WAX ALLIED CORPORATION (US) 1988-08-30 US disclosed
EP-0220400-A2 Wet abrasion resistant yarn and cordage AlliedSignal Inc. (US) 1987-05-06 EP disclosed
US-4371658-A Polyamide yarn spin finish containing a glyceride and oxidized polyethylene ALLIED CORPORATION (US) 1983-02-01 US disclosed
US-4293460-A Polyamide yarn spin finish containing a rearranged glyceride and oxidized polyethylene ALLIED CHEMICAL CORPORATION (US) 1981-10-06 US disclosed
US-4077917-A SURFACTANTS ALCOLAC, INC. (US) 1978-03-07 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 (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-20100113823-A1 ISOCYANATE PRODUCTION PROCESS USING COMPOSITION CONTAINING CARBAMIC ACID ESTER AND AROMATIC HYDROXY COMPOUND, AND COMPOSITION FOR TRANSFER AND STORAGE OF CARBAMIC ACID ESTER PAH, APEH, CPS1 BID 2510/4885MCL1 4012/4885BCL2L1 3887/4885

“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.