SCHEMBL983874

SCHEMBL983874

CCCCCCCCCC(C)(C)c1ccccc1O

nearest known ligand 0.50

Predicted protein targets (top 7)

geneUniProtsupporting neighboursconfidence
CNR1 P21554 17/20 0.50
CNR2 P34972 16/20 0.50
ALDH1A1 P00352 1/20 0.48
TSHR P16473 1/20 0.48
TDP1 Q9NUW8 1/20 0.48
GPR18 Q14330 2/20 0.43
GPR55 Q9Y2T6 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
SCHEMBL1840803 1.00 CNR1 (0.50) CNR1CNR2ALDH1A1TSHRTDP1
SCHEMBL982789 1.00 CNR1 (0.50) CNR1CNR2ALDH1A1TSHRTDP1
SCHEMBL11782350 1.00 CNR1 (0.50) CNR1CNR2ALDH1A1TSHRTDP1
SCHEMBL983221 1.00 CNR1 (0.50) CNR1CNR2ALDH1A1TSHRTDP1
SCHEMBL678356 1.00 CNR1 (0.50) CNR1CNR2ALDH1A1TSHRTDP1
SCHEMBL11639019 1.00 CNR1 (0.50) CNR1CNR2ALDH1A1TSHRTDP1
SCHEMBL981356 1.00 CNR1 (0.50) CNR1CNR2ALDH1A1TSHRTDP1
SCHEMBL324567 0.98 ALDH1A1 (0.50) CNR1CNR2ALDH1A1TSHRTDP1
Tridecan-1-Ol SCHEMBL8500797 0.94 CNR1 (0.46) CNR1CNR2ALDH1A1TSHRTDP1
Formaldehyde SCHEMBL2496330 0.93 ALDH1A1 (0.46) CNR1CNR2ALDH1A1TSHRTDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20080090743-A1 COMPOUNDS AND METHODS OF MAKING THE COMPOUNDS AFTON CHEMICAL CORPORATION 2008-04-17 US claimed
US-20080090742-A1 Compound and method of making the compound AFTON CHEMICAL CORPORATION 2008-04-17 US claimed
US-6444836-B1 PURITY; DESORPTION USING AN INERT GAS; REACTING ALCOHOL WITH PHOSPHOROUS COMPOUND GENERAL ELECTRIC COMPANY 2002-09-03 US claimed
EP-0504320-B1 METHOD FOR PREPARING STERICALLY HINDERED ARYL PHOSPHITES UNIROYAL CHEM CO INC (US) 1994-09-21 EP claimed
US-5254709-A Catalytic reaction of phosphorus trihalide with a phenolic compound UNIROYAL CHEMICAL COMPANY, INC. (US) 1993-10-19 US claimed
EP-0504320-A1 METHOD FOR PREPARING STERICALLY HINDERED ARYL PHOSPHITES. UNIROYAL CHEM CO INC (US) 1992-09-23 EP claimed
WO-1991009040-A1 METHOD FOR PREPARING STERICALLY HINDERED ARYL PHOSPHITES UNIROYAL CHEMICAL COMPANY, INC. (US) 1991-06-27 WO claimed
JP-55048247-A None JP disclosed
CN-117631451-A Colored photosensitive resin composition, color filter and image display device 东友精细化工有限公司 2024-03-01 CN disclosed
EP-3293173-B1 METHOD FOR PRODUCING ISOCYANATE ASAHI CHEMICAL IND (JP) 2021-07-28 EP disclosed
EP-3838892-A1 METHOD FOR PRODUCING ISOCYANATE Asahi Kasei Kabushiki Kaisha (JP) 2021-06-23 EP disclosed
EP-2980066-B1 METHOD FOR PRODUCING ISOCYANATE ASAHI CHEMICAL IND (JP) 2021-04-21 EP disclosed
EP-2275405-B1 PROCESS FOR PRODUCING ISOCYANATE USING DIARYL CARBONATE ASAHI CHEMICAL IND (JP) 2019-04-24 EP disclosed
US-4224218-A Stabilized vinyl chloride polymer comprising a metal mono-organic phosphite ARGUS CHEMICAL CORPORATION (US) 1980-09-23 US disclosed
US-4221687-A BASIC INORGANIC SALT, 1,3-DIKETONE, VINYL CHLORIDE POLYMER ARGUS CHEMICAL CORP. (US) 1980-09-09 US disclosed
US-4217258-A THIOCARBONYL COMPOUND, ALKYLTIN COMPOUND, METAL CARBOXYLATE, HYDROCARBYLPHENOL ARGUS CHEMICAL CORP. (US) 1980-08-12 US disclosed
JP-S5548247-A CURABLE ASPHALT COMPOSITION SUMITOMO CHEM CO LTD 1980-04-05 JP disclosed
US-4134868-A Aromatic carboxylic acid ester stabilizers for PVC resins ARGUS CHEMICAL CORPORATION (US) 1979-01-16 US disclosed
US-4105627-A MERCAPTOHETEROCYCLIC RESIN STABILIZERS ARGUS CHEMICAL CORPORATION (US) 1978-08-08 US disclosed
US-3992308-A Lubricating oil composition containing sulfurized reaction product of mixed tertiary alkyl phenols with formaldehyde ETHYL CORPORATION (US) 1976-11-16 US disclosed