M-Xylene

M-Xylene

SCHEMBL6838832

Cc1cccc(C)c1.Cl.Cl

nearest known ligand 0.92

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABL1ACEACHEACVR1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALKAVPR1AAVPR2BCHEBCRCA2CACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCASRCCR5CDK4CDK6CFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNA3CHRNA7CHRNB1CHRNB4CHRNDCHRNECHRNGCOXFA4COXFA4L2CRBNCSF1RCUL4ACYP19A1DDB1DPP4DRD1DRD2DRD3DRD4EDNRAEGFREML4ERBB2ERBB4ESR1ESR2FGFR1FGFR3FLT1FLT3FLT4GAAGABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGHSRGLAGNRHRGPD2GRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BGSTP1HCN4HCRTR1HCRTR2HDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HRH2HRH3HSD11B1HSP90AA1HSP90AB1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IMPDH1IMPDH2ITGA2BITGB3ITKJAK1JAK2KCNA1KCNA10KCNA2KCNA3KCNA4KCNA5KCNA6KCNA7KCNB1KCNB2KCNC1KCNC2KCNC3KCNC4KCND1KCND2KCND3KCNF1KCNG1KCNG2KCNG3KCNG4KCNH1KCNH2KCNH3KCNH4KCNH5KCNH6KCNH7KCNH8KCNJ2KCNJ3KCNJ5KCNK3KCNK9KCNQ1KCNQ2KCNQ3KCNQ4KCNQ5KCNS1KCNS2KCNS3KCNV1KCNV2KDRKITKLKB1LCKMMAOAMAOBMAPK14METMMP1MMP13MMP7MMP8MT-ND1MT-ND2MT-ND3MT-ND4MT-ND4LMT-ND5MT-ND6NDUFA1NDUFA10NDUFA11NDUFA12NDUFA13NDUFA2NDUFA3NDUFA5NDUFA6NDUFA7NDUFA8NDUFA9NDUFAB1NDUFAF1NDUFAF2NDUFAF3NDUFAF4NDUFB1NDUFB10NDUFB11NDUFB2NDUFB3NDUFB4NDUFB5NDUFB6NDUFB7NDUFB8NDUFB9NDUFC1NDUFC2NDUFS1NDUFS2NDUFS3NDUFS4NDUFS5NDUFS6NDUFS7NDUFS8NDUFV1NDUFV2NDUFV3NR3C1NS5ANTRK1NTRK2NTRK3ODC1OPRD1OPRK1OPRM1P2RY12PAHPARP1PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDE5APDE7APDE7BPDE8APDE8BPDGFRAPDGFRBPIK3CAPIK3CDPNPPOLA1POLA2POLD1POLD2POLD3POLD4POLEPOLE2POLE3PPARGPRIM1PRIM2PRKCAPRKCBPRKCDPRKCEPRKCGPRKCHPRKCIPRKCQPRKCZPRKD1PRKD3PTGS1PTGS2RBX1RENRETROCK1ROCK2RPE65RRM1RRM2RRM2BS1PR1S1PR2S1PR3S1PR4S1PR5SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC18A2SLC6A1SLC6A2SLC6A3SLC6A4SLC9A3SRCTACR1TOP1TOP2ATOP2BTTRTYMPdacAdacBdacCembAfolAftsIgyrAgyrBmrcAmrcBmrdAparCparEpolrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of M-Xylene. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ACHE known ✓ P22303 6/20 0.92
PARP1 known ✓ P09874 1/20 0.46
HTR3E known ✓ A5X5Y0 1/20 0.44
HTR3B known ✓ O95264 1/20 0.44
HTR3A known ✓ P46098 1/20 0.44
HTR3D known ✓ Q70Z44 1/20 0.44
HTR3C known ✓ Q8WXA8 1/20 0.44
ALDH1A1 P00352 2/20 0.58
MAPK1 P28482 1/20 0.58
TSHR P16473 2/20 0.50
LMNA P02545 1/20 0.50
ALOX12 P18054 1/20 0.50
TP53 P04637 1/20 0.50
TDP1 Q9NUW8 1/20 0.50
IDO1 P14902 1/20 0.48
CYP1A2 P05177 2/20 0.48
NPC1 O15118 1/20 0.48
CASP3 P42574 1/20 0.48
SENP8 Q96LD8 1/20 0.48
SENP7 Q9BQF6 1/20 0.48

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 SCHEMBL6838834 1.00
M-Xylene SCHEMBL31500493 1.00 ACHE (0.92) ACHEALDH1A1MAPK1TSHRLMNA
M-Xylene SCHEMBL1833203 1.00 ACHE (0.92) ACHEALDH1A1MAPK1TSHRLMNA
M-Xylene SCHEMBL1833208 1.00 ACHE (0.92) ACHEALDH1A1MAPK1TSHRLMNA
M-Xylene SCHEMBL8140418 1.00 ACHE (0.92) ACHEALDH1A1MAPK1TSHRLMNA
M-Xylene SCHEMBL28365822 0.96 ACHE (0.86) ACHEALDH1A1MAPK1TSHRLMNA
M-Xylene SCHEMBL6019078 0.96 ACHE (0.86) ACHEALDH1A1MAPK1TSHRLMNA
M-Xylene SCHEMBL11598111 0.96 ACHE (0.86) ACHEALDH1A1MAPK1TSHRLMNA
M-Xylene SCHEMBL891494 0.96 ACHE (1.00) ACHEALDH1A1MAPK1TSHRLMNA
M-Xylene SCHEMBL6397624 0.96

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-116637603-A Method for preparing porous adsorbent by using floccules produced by coagulation 重庆工商大学 2023-08-25 CN claimed
CN-1269819-A Food cleaning compositions containing cyclodextrin PROCTER & GAMBLE (US) 2000-10-11 CN claimed
US-20250195445-A1 LONG-LASTING ANTIMICROBIAL COMPOSITIONS CONTAINING CATIONIC ACTIVE AGENTS AND ANIONIC EXCIPIENTS AND USES UNIVERSIDADE FEDERAL DE MINAS GERAIS - UFMG (BR) 2025-06-19 US disclosed
EP-4477217-A1 LONG-LASTING ANTIMICROBIAL COMPOSITIONS CONTAINING CATIONIC ACTIVE AGENTS AND ANIONIC EXCIPIENTS AND USES Universidade Federal De Minas Gerais - UFMG (BR) 2024-12-18 EP disclosed
CN-118401587-A Curable resin composition, resin sheet, and cured product thereof 日本化药株式会社 2024-07-26 CN disclosed
WO-2024031162-A1 SPORICIDAL ANTIMICROBIAL COMPOSITIONS AND USES THEREOF DA SILVA, Tasso Pereira (BR) 2024-02-15 WO disclosed
CN-116637603-A Method for preparing porous adsorbent by using floccules produced by coagulation 重庆工商大学 2023-08-25 CN disclosed
CN-116637603-A Method for preparing porous adsorbent by using floccules produced by coagulation 重庆工商大学 2023-08-25 CN disclosed
CN-112105673-B Aromatic amine resin having N-alkyl group, curable resin composition, and cured product thereof 日本化药株式会社 2023-03-14 CN disclosed
CN-112105673-A Aromatic amine resin having N-alkyl group, curable resin composition, and cured product thereof 日本化药株式会社 2020-12-18 CN disclosed
CN-107446131-B Energy-saving and environment-friendly meta-aramid polymerization process 广东彩艳股份有限公司 2020-03-24 CN disclosed
CN-1322265-A Wrinkle reducing composition PROCTER & GAMBLE (US) 2001-11-14 CN disclosed
CN-1269819-A Food cleaning compositions containing cyclodextrin PROCTER & GAMBLE (US) 2000-10-11 CN disclosed
CN-1268874-A Method and composition for cleaning food products to reduce microorganisms PROCTER & GAMBLE (US) 2000-10-04 CN disclosed
US-6046299-A MAKING A DYE FIXING AGENT QUATERNARY CATIONIC POLYMER BY REACTING DI-TERTIARY AMINE(S) WITH XYLENE DIHALIDE(S) OF GIVEN FORMULAS; EXCELLENT INK DYE FIXABILITY, AND IMPROVES WATER RESISTANCE OF THE PRINTED MATTER NICCA CHEMICAL CO., LTD. (JP) 2000-04-04 US disclosed
EP-0424144-B1 Diethylenically unsaturated monomer and use thereof MITSUBISHI PETROCHEMICAL CO (JP) 1994-03-16 EP disclosed
US-5225508-A With sulfide linkages MITSUBISHI PETROCHEMICAL COMPANY LIMITED (JP) 1993-07-06 US disclosed
US-5180577-A Mouthwashes, stabilizer is betaine surfactant COLGATE-PALMOLIVE (US) 1993-01-19 US disclosed
EP-0431398-A2 Heating device with a phase change temperature controller MILES INC. (US) 1991-06-12 EP disclosed
US-3975448-A THERMAL STABILITY, CHEMICAL RESISTANCE TESSENDERLO CHEMIE S.A. (BE) 1976-08-17 US disclosed