M-Xylene

M-Xylene

SCHEMBL891494

Cc1cccc(C)c1.Cc1cccc(C)c1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ACHE P22303 6/20 1.00
ALDH1A1 P00352 2/20 0.61
MAPK1 P28482 1/20 0.61
TSHR P16473 2/20 0.53
LMNA P02545 1/20 0.53
ALOX12 P18054 1/20 0.53
TDP1 Q9NUW8 2/20 0.52
TP53 P04637 1/20 0.52
CYP1A2 P05177 2/20 0.50
NPC1 O15118 1/20 0.50
CASP3 P42574 1/20 0.50
SENP8 Q96LD8 1/20 0.50
SENP7 Q9BQF6 1/20 0.50
SENP6 Q9GZR1 1/20 0.50
CYP3A4 P08684 1/20 0.50
CYP2D6 P10635 1/20 0.50
MAPT P10636 1/20 0.50
CYP2C9 P11712 1/20 0.50
CYP2C19 P33261 1/20 0.50
HTT P42858 1/20 0.50

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
M-Xylene SCHEMBL28189 1.00
M-Xylene SCHEMBL6397624 1.00
M-Xylene SCHEMBL18890231 0.96 ACHE (0.92) ACHEALDH1A1MAPK1TSHRLMNA
M-Xylene SCHEMBL358508 0.96
M-Xylene SCHEMBL18045662 0.96
M-Xylene SCHEMBL4596533 0.96 ACHE (0.92) ACHEALDH1A1MAPK1TSHRLMNA
M-Xylene SCHEMBL78260 0.96 ACHE (0.92) ACHEALDH1A1MAPK1TSHRLMNA
M-Xylene SCHEMBL6838834 0.96
M-Xylene SCHEMBL5179379 0.96
M-Xylene SCHEMBL2292576 0.96 ACHE (0.92) ACHEALDH1A1MAPK1TSHRLMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2023120923-A1 HEAT DISSIPATION MATERIAL, COMPOSITION INCLUDING SAME, AND PREPARATION METHOD THEREFOR 한국세라믹기술원 2023-06-29 WO claimed
CN-111259543-B Design method of SVE process parameters in petroleum pollution sites 生态环境部土壤与农业农村生态环境监管技术中心 2024-01-23 CN disclosed
CN-112763642-A High performance liquid detection method for benzene pollutants in water body 中国石油天然气集团有限公司 2021-05-07 CN disclosed
CN-111259543-A Design method of SVE (singular value analysis) process parameters in petroleum-polluted site 生态环境部土壤与农业农村生态环境监管技术中心 2020-06-09 CN disclosed
US-10626256-B2 Solution polymerization process NOVA CHEMICALS (INTERNATIONAL) S.A. (CH) 2020-04-21 US disclosed
EP-2108032-B1 UNLEADED FUEL COMPOSITIONS SHELL INT RESEARCH (NL) 2018-09-12 EP disclosed
US-10000630-B2 Ethylene interpolymers having improved color NOVA CHEMICALS (INTERNATIONAL) S.A. (CH) 2018-06-19 US disclosed
US-9512282-B2 Dilution index NOVA CHEMICALS (INTERNATIONAL) S.A. (CH) 2016-12-06 US disclosed
US-20160108221-A1 SOLUTION POLYMERIZATION PROCESS NOVA CHEMICALS (INTERNATIONAL) S.A. (CH) 2016-04-21 US disclosed
US-20160108222-A1 ETHYLENE INTERPOLYMERS HAVING IMPROVED COLOR NOVA CHEMICALS (INTERNATIONAL) S.A. (CH) 2016-04-21 US disclosed
CN-100431651-C Multiple-chamber device for fractionated evaporation and separation of a solution JOINT INDUSTRIAL PROCESSORS FOR ELECTRONICS (FR) 2008-11-12 CN disclosed
WO-2008073118-A1 UNLEADED FUEL COMPOSITIONS SHELL INTERNATIONALE RESEARCH MAATSCHAPPIJ B.V. (NL) 2008-06-19 WO disclosed
US-20080134571-A1 UNLEADED FUEL COMPOSITIONS SHELL OIL COMPANY 2008-06-12 US disclosed
EP-1542958-A1 PROCESS FOR PRODUCING AROMATIC DICARBOXYLIC ACIDS UNDER SUPERCRITICAL CONDITIONS Invista Technologies S.à.r.l. (US) 2005-06-22 EP disclosed
CN-1549738-A Multiple-chamber device for fractionated evaporation and separation of a solution �������Ȼ��Ʒ��ҵ���޹�˾ 2004-11-24 CN disclosed
WO-2004005235-A1 PROCESS FOR PRODUCING AROMATIC DICARBOXYLIC ACIDS UNDER SUPERCRITICAL CONDITIONS INVISTA TECHNOLOGIES S.À.R.L. (US) 2004-01-15 WO disclosed
CN-1116277-C Process for preparing carbocyclic or heterocyclic nitriles by vapor phase ammoxidation MITSUBISHI RAYON CO (JP) 2003-07-30 CN disclosed
US-6506740-B1 Compounds that can be substituted at the 7, 8, and/or 9 positions and methods for preparing the 4- dedimethylamino tetracycline compounds. Other tetracycline compounds are the 4-dedimethylaminotetracycline derivatives with an oxime GALDERMA LABORATORIES INC. 2003-01-14 US disclosed
CN-1188104-A Process for preparing carbocyclic or heterocyclic nitriles by vapor phase ammoxidation NITTO CHEMICAL INDUSTRY CO LTD (JP) 1998-07-22 CN disclosed
CN-1172846-A Branched polyolefin polymers as additives in fuel and lubricating oil compositions DSM COPOLYMER INC (US) 1998-02-11 CN disclosed