1-Methylimidazole

1-Methylimidazole

SCHEMBL459534

CS(=O)(=O)O.Cn1ccnc1

nearest known ligand 0.68

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Known targets — ChEMBL curated mechanism

ABL1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB2AGTR1BCL2BCL2A1BCL2L1BCL2L10BCL2L2BCRBRAFCHRM1CHRNA10CHRNA9DRD1DRD2DRD3DRD4DRD5EGFRF2FLT1FLT4GCKGHSRGNRHRGRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BHTR1AHTR1BHTR1DHTR2AHTR2CHTR3AIDH2KDRKITMAOBMCL1MTTPPP4HBPDGFRBPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PIKFYVEROCK1ROCK2SLC18A2SLC6A2SLC6A3SLC6A4TACR1TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8gyrAgyrBparCparEpol

The experimentally established mechanism targets of 1-Methylimidazole. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
QPCT Q16769 2/20 0.68
NFKB1 P19838 1/20 0.68
HSD17B10 Q99714 1/20 0.68
QPCTL Q9NXS2 1/20 0.68
HTT P42858 3/20 0.41
EGLN3 Q9H6Z9 1/20 0.35
ALDH1A1 P00352 3/20 0.33
CYP19A1 P11511 1/20 0.33
LMNA P02545 1/20 0.33
TP53 P04637 1/20 0.33
TSHR P16473 1/20 0.33
TBXAS1 P24557 3/20 0.32
NPC1 O15118 1/20 0.32
GAA P10253 1/20 0.32
MAPT P10636 1/20 0.32
RAB9A P51151 1/20 0.32
SMN1; SMN2 Q16637 1/20 0.32
CYP3A4 P08684 1/20 0.32
BAZ2B Q9UIF8 1/20 0.32

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
1-Methylimidazole SCHEMBL28194536 1.00 QPCT (0.68) QPCTNFKB1HSD17B10QPCTLHTT
1-Methylimidazole SCHEMBL29110568 0.98 NFKB1 (0.65) QPCTNFKB1HSD17B10QPCTLHTT
1-Methylimidazole SCHEMBL15295407 0.94 NFKB1 (0.60) QPCTNFKB1HSD17B10QPCTLHTT
1-Methylimidazole SCHEMBL693786 0.93 NFKB1 (0.71) QPCTNFKB1HSD17B10QPCTLHTT
1-Methylimidazole SCHEMBL4955404 0.93 NFKB1 (0.71) QPCTNFKB1HSD17B10QPCTLHTT
1-Methylimidazole SCHEMBL27681653 0.93 NFKB1 (0.71) QPCTNFKB1HSD17B10QPCTLHTT
1-Methylimidazole SCHEMBL27724089 0.91 NFKB1 (0.68) QPCTNFKB1HSD17B10QPCTLHTT
1-Methylimidazole SCHEMBL27993647 0.91 NFKB1 (0.68) QPCTNFKB1HSD17B10QPCTLHTT
1-Methylimidazole SCHEMBL28175971 0.89 NFKB1 (0.65) QPCTNFKB1HSD17B10QPCTLHTT
1-Methylimidazole SCHEMBL28339216 0.89 NFKB1 (0.65) QPCTNFKB1HSD17B10QPCTLHTT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240133117-A1 DYE RECYCLING METHODS IMPERIAL COLLEGE INNOVATIONS LIMITED (GB) 2024-04-25 US claimed
WO-2023247987-A1 IONIC LIQUID ENCAPSULATED METAL ORGANIC FRAMEWORK BASED THIN FILM NANOCOMPOSITE MEMBRANE FOR METAL IONS SEPARATION COMMISSARIAT A L'ENERGIE ATOMIQUE ET AUX ENERGIES ALTERNATIVES (FR) 2023-12-28 WO claimed
EP-4294977-A1 DYE RECYCLING METHODS Imperial College Innovations Limited (GB) 2023-12-27 EP claimed
CN-116917568-A Method for recovering dye 帝国理工学院创新有限公司 2023-10-20 CN claimed
WO-2022175559-A1 DYE RECYCLING METHODS IMPERIAL COLLEGE INNOVATIONS LIMITED (GB) 2022-08-25 WO claimed
EP-3512905-B1 METHOD FOR PRODUCING A POLYBENZAZOL POLYMER (P) BASF SE (DE) 2022-08-24 EP claimed
CN-109790292-B Process for preparing polybenzazole polymer (P) 巴斯夫欧洲公司 2022-05-31 CN claimed
CN-106694007-B A kind of single dispersion metal atom/graphene composite catalyst and its preparation method and application 中国科学院山西煤炭化学研究所 2019-09-10 CN claimed
EP-3512905-A1 METHOD FOR PRODUCING A POLYBENZAZOL POLYMER (P) BASF SE (DE) 2019-07-24 EP claimed
CN-110041631-A A kind of wear-resistant plastic of modification and preparation method thereof 王德秀 2019-07-23 CN claimed
US-7659430-B2 Method for separating hydrogen chloride and phosgene BASF AKTIENGESELLSCHAFT (DE) 2010-02-09 US claimed
EP-1789160-B1 METHOD FOR SEPARATING HYDROGEN CHLORIDE AND PHOSGENE BASF SE (DE) 2009-11-18 EP claimed
CN-100430356-C Method for producing haloalkanes from alcohols BASF AG (DE) 2008-11-05 CN claimed
WO-2008022983-A2 CONDUCTIVE POLYMER GELS BASF SE (DE) 2008-02-28 WO claimed
US-20070293707-A1 Method for Separating Hydrogen Chloride and Phosgene BASF AKTIENGESELLSCHAFT (DE) 2007-12-20 US claimed
EP-1789160-A1 METHOD FOR SEPARATING HYDROGEN CHLORIDE AND PHOSGENE BASF AKTIENGESELLSCHAFT (DE) 2007-05-30 EP claimed
EP-1663921-B1 METHOD FOR PRODUCING HALOALKANES FROM ALCOHOLS BASF AG (DE) 2007-05-02 EP claimed
US-20070055084-A1 Method for producing haloalkanes from alcohols BASF AKTIENGESELLSCHAFT (DE) 2007-03-08 US claimed
CN-1849281-A Method for producing haloalkanes from alcohols BASF AG (DE) 2006-10-18 CN claimed
WO-2006029788-A1 METHOD FOR SEPARATING HYDROGEN CHLORIDE AND PHOSGENE BASF AKTIENGESELLSCHAFT (DE) 2006-03-23 WO claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (2 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-20070293707-A1 Method for Separating Hydrogen Chloride and Phosgene PSPH, SLC9B2, HVCN1 QPCT 1147/4885NFKB1 4377/4885HSD17B10 142/4885
US-20070055084-A1 Method for producing haloalkanes from alcohols ADH1C, HDHD5, ADH5 QPCT 510/4885NFKB1 2976/4885HSD17B10 56/4885

“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.