SCHEMBL346325

SCHEMBL346325

Cc1ccc(C2CCCCC2)cc1

nearest known ligand 0.59

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 3/20 0.59
MAPT P10636 3/20 0.59
SMN1; SMN2 Q16637 3/20 0.59
ALDH1A1 P00352 2/20 0.59
TP53 P04637 1/20 0.59
ATM Q13315 1/20 0.59
SLC18A3 Q16572 1/20 0.55
HTT P42858 2/20 0.45
XBP1 P17861 1/20 0.45
NPC1 O15118 2/20 0.44
RAB9A P51151 2/20 0.44
HDAC1 Q13547 1/20 0.44
HDAC8 Q9BY41 1/20 0.44
HDAC6 Q9UBN7 1/20 0.44
HSP90AA1 P07900 1/20 0.43
GAA P10253 1/20 0.43
KMT2A Q03164 1/20 0.43
TDP1 Q9NUW8 1/20 0.43
NOTUM Q6P988 1/20 0.43
APOBEC3A P31941 1/20 0.42

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
SCHEMBL28722738 1.00 LMNA (0.59) LMNAMAPTSMN1; SMN2ALDH1A1TP53
SCHEMBL8025878 1.00 LMNA (0.59) LMNAMAPTSMN1; SMN2ALDH1A1TP53
SCHEMBL43080 0.97 SLC18A3 (0.56) LMNAMAPTSMN1; SMN2ALDH1A1TP53
SCHEMBL18117721 0.93 MAPT (0.54) LMNAMAPTSMN1; SMN2ALDH1A1TP53
SCHEMBL2537599 0.92 SLC18A3 (0.52) LMNAMAPTSMN1; SMN2ALDH1A1TP53
SCHEMBL1417522 0.89 LMNA (0.51) LMNAMAPTSMN1; SMN2ALDH1A1TP53
SCHEMBL4820760 0.88 MAPT (0.62) LMNAMAPTSMN1; SMN2ALDH1A1TP53
Acetic Acid SCHEMBL6347645 0.88 SMN1; SMN2 (0.54) LMNAMAPTSMN1; SMN2ALDH1A1TP53
SCHEMBL16216730 0.88 HAO1 (0.51) LMNAMAPTSMN1; SMN2ALDH1A1TP53
SCHEMBL558840 0.88 ALDH1A1 (0.50) LMNAMAPTSMN1; SMN2ALDH1A1TP53

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-10589256-B2 Selective hydrogenation catalyst and selective hydrogenation method using the same KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY (KR) 2020-03-17 US claimed
EP-3277649-B1 TRANSALKYLATED CYCLOHEXYLBENZYL AND BIPHENYL COMPOUNDS EXXONMOBIL CHEMICAL PATENTS INC (US) 2019-08-21 EP claimed
US-20190076826-A1 SELECTIVE HYDROGENATION CATALYST AND SELECTIVE HYDROGENATION METHOD USING THE SAME KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY (KR) 2019-03-14 US claimed
CN-106349000-B Heat-conducting fluid 1- phenyl -1- (cyclohexyl toluene) base ethane isomers and its synthetic method 江苏中能化学科技股份有限公司 2018-10-26 CN claimed
US-10017433-B2 Transalkylated cyclohexylbenzyl and biphenyl compounds EXXONMOBIL CHEMICAL PATENTS INC. (US) 2018-07-10 US claimed
US-20180050971-A1 Transalkylated Cyclohexylbenzyl and Biphenyl Compounds EXXONMOBIL CHEMICAL PATENTS INC. 2018-02-22 US claimed
EP-3277649-A1 TRANSALKYLATED CYCLOHEXYLBENZYL AND BIPHENYL COMPOUNDS ExxonMobil Chemical Patents Inc. (US) 2018-02-07 EP claimed
CN-107438590-A The cyclohexyl benzyl and biphenol compound of transfering alkylation 埃克森美孚化学专利公司 2017-12-05 CN claimed
US-9758447-B2 Activation of dehydrogenation catalysts EXXONMOBIL CHEMICAL PATENTS INC. (US) 2017-09-12 US claimed
CN-106349000-A 1-phenyl-1-(cyclohexyl methyl) base ethane isomer of heat conduction fluid and synthesis method of isomer 江苏中能化学有限公司 2017-01-25 CN claimed
WO-2016160084-A1 TRANSALKYLATED CYCLOHEXYLBENZYL AND BIPHENYL COMPOUNDS EXXONMOBIL CHEMICAL PATENTS INC. (US) 2016-10-06 WO claimed
US-20160115095-A1 Activation of Dehydrogenation Catalysts EXXONMOBIL CHEMICAL PATENTS INC. 2016-04-28 US claimed
US-20050215433-A1 Aromatic fluid as agricultural solvent EXXONMOBIL CHEMICAL PATENTS INC. 2005-09-29 US claimed
US-5183931-A Catalyzing with carboxylic acid medium in presence of palladium salt, metal persulfate, metal salt and tin salt PHILLIPS PETROLEUM COMPANY (US) 1993-02-02 US claimed
JP-8099914-A None JP disclosed
JP-51133238-A None JP disclosed
CN-121913901-A Preparation method and application of cyclohexyl benzoic acid 中国石油化工股份有限公司 2026-04-24 CN disclosed
US-4049629-A PREPARING POLYESTERS BY REACTING A DIACID HALIDE AND A SUBSTITUTED BISPHENOL AND A GLYCOL HOOKER CHEMICALS & PLASTICS CORPORATION (US) 1977-09-20 US disclosed
US-4010206-A Method for producing cyclohexanone and alkyl-substituted or unsubstituted phenol UBE INDUSTRIES, LTD. (JA) 1977-03-01 US disclosed
JP-S51133238-A PROCESS FOR PREPARATION OF P-CRESOL AND CYCLOHEXANONE UBE IND LTD 1976-11-18 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 (6 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-20190076826-A1 SELECTIVE HYDROGENATION CATALYST AND SELECTIVE HYDROGENATION METHOD USING THE SAME HRH4, HRH3, HRH2 LMNA 4590/4885MAPT 4540/4885SMN1; SMN2 3911/4885
US-10017433-B2 Transalkylated cyclohexylbenzyl and biphenyl compounds DDT, CYP2B6, AHR LMNA 2815/4885MAPT 4559/4885SMN1; SMN2 4840/4885
US-20180050971-A1 Transalkylated Cyclohexylbenzyl and Biphenyl Compounds DDT, CYP2B6, AHR LMNA 2815/4885MAPT 4559/4885SMN1; SMN2 4840/4885
US-10589256-B2 Selective hydrogenation catalyst and selective hydrogenation method using the same HRH4, HRH3, HRH2 LMNA 4590/4885MAPT 4540/4885SMN1; SMN2 3911/4885
US-20050215433-A1 Aromatic fluid as agricultural solvent DDT, AHR, ALB LMNA 2551/4885MAPT 640/4885SMN1; SMN2 3203/4885
US-20160115095-A1 Activation of Dehydrogenation Catalysts AHR, CYP1A1, CYP2E1 LMNA 1689/4885MAPT 3629/4885SMN1; SMN2 3377/4885

“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.