1-Methylimidazole

1-Methylimidazole

SCHEMBL1889707

Cc1ccc(S(=O)(=O)O)cc1.Cn1ccnc1

nearest known ligand 0.48

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABL1BMXBRAFBTKCHRNA4CHRNB2CSNK1EEGFRERBB2F10FLT1FLT3FLT4IGF1RINSRITKJAK3KDRKITOPRM1PARP1PARP2PDGFRBPIK3CDRAF1RETSLC18A2TECTXKdacAdacBdacCftsImrcAmrcBmrdArplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

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 20)

geneUniProtsupporting neighboursconfidence
NFKB1 P19838 1/20 0.48
QPCT Q16769 1/20 0.48
HSD17B10 Q99714 1/20 0.48
QPCTL Q9NXS2 1/20 0.48
ALDH1A1 P00352 4/20 0.48
SMN1; SMN2 Q16637 2/20 0.48
KDM4E B2RXH2 2/20 0.48
MAPT P10636 2/20 0.48
TDP1 Q9NUW8 2/20 0.48
LMNA P02545 1/20 0.48
HTT P42858 1/20 0.48
L3MBTL1 Q9Y468 1/20 0.48
CYP2D6 P10635 2/20 0.43
SNCA P37840 1/20 0.42
TSHR P16473 1/20 0.41
CYP19A1 P11511 3/20 0.40
NR4A1 P22736 1/20 0.40
CYP11B1 P15538 1/20 0.39
CYP11B2 P19099 1/20 0.39
CA1 P00915 1/20 0.39

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 SCHEMBL28157375 0.87 ALDH1A1 (0.44) NFKB1QPCTHSD17B10QPCTLALDH1A1
1-Methylimidazole SCHEMBL17961221 0.85 TSHR (0.53) NFKB1QPCTHSD17B10QPCTLALDH1A1
SCHEMBL9309177 0.83 ALDH1A1 (0.47) ALDH1A1SMN1; SMN2KDM4EMAPTTDP1
SCHEMBL4952812 0.81 ALDH1A1 (0.57) QPCTALDH1A1SMN1; SMN2KDM4EMAPT
SCHEMBL2455924 0.80 ALDH1A1 (0.53) QPCTALDH1A1SMN1; SMN2KDM4EMAPT
1-Methylimidazole SCHEMBL4955404 0.78 NFKB1 (0.71) NFKB1QPCTHSD17B10QPCTLALDH1A1
1-Methylimidazole SCHEMBL27681653 0.78 NFKB1 (0.71) NFKB1QPCTHSD17B10QPCTLALDH1A1
1-Methylimidazole SCHEMBL693786 0.78 NFKB1 (0.71) NFKB1QPCTHSD17B10QPCTLALDH1A1
Fluoride SCHEMBL6570833 0.78 GAA (0.59) ALDH1A1SMN1; SMN2KDM4EMAPTTDP1
SCHEMBL135343 0.77 LMNA (0.57) HSD17B10ALDH1A1SMN1; SMN2KDM4EMAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119912350-A Preparation method of isooctyl p-aminobenzoate 江苏尚莱特医药化工材料有限公司 2025-05-02 CN claimed
CN-118994043-A Preparation method of difluoro pyrazole acid 湖南斯派克科技股份有限公司 2024-11-22 CN claimed
CN-118973288-A Perovskite battery and preparation method thereof 青海黄河上游水电开发有限责任公司西宁太阳能电力分公司 2024-11-15 CN claimed
CN-118546265-A Cellulose aldehyde and preparation method and application thereof 新疆农业大学 2024-08-27 CN claimed
CN-118390128-A Copper/tin composite material with three-dimensional microstructure and preparation and application thereof 上海大学 2024-07-26 CN claimed
CN-117923690-A Apparatus and method for recovering acetonitrile mobile phase waste liquid generated by liquid chromatography 中国石油化工股份有限公司 2024-04-26 CN claimed
CN-113416136-B Application of acidic ionic liquid in catalyzing reaction of cinnamic acid and benzyl alcohol to prepare benzyl cinnamate and method for preparing benzyl cinnamate 河南工业大学 2023-12-22 CN claimed
CN-113429345-B Preparation method of acridone 遂成药业股份有限公司 2023-12-01 CN claimed
CN-115710735-A Electrotinning solution and preparation method and application thereof 广东光华科技股份有限公司 2023-02-24 CN claimed
CN-114316823-A Full-biological carbon dioxide-based biodegradable polyurethane pressure-sensitive adhesive tape and preparation method thereof 中国科学院长春应用化学研究所 2022-04-12 CN 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
US-20070034513-A1 Electrochemical deblocking solution for electrochemical oligomer synthesis on an electrode array COMBIMATRIX CORPORATION 2007-02-15 US claimed
WO-2006105037-A2 ELECTROCHEMICAL DEBLOCKING SOLUTION FOR ELECTROCHEMICAL OLIGOMER SYNTHESIS ON AN ELECTRODE ARRAY COMBIMATRIX CORPORATION (US) 2006-10-05 WO claimed
EP-1663921-A2 METHOD FOR PRODUCING HALOALKANES FROM ALCOHOLS BASF AKTIENGESELLSCHAFT (DE) 2006-06-07 EP claimed
WO-2006029788-A1 METHOD FOR SEPARATING HYDROGEN CHLORIDE AND PHOSGENE BASF AKTIENGESELLSCHAFT (DE) 2006-03-23 WO claimed
WO-2006031814-A2 ELECTROCHEMICAL DEBLOCKING USING A HYDRAZINE DERIVATIVE COMBIMATRIX CORPORATION (US) 2006-03-23 WO claimed
US-20060054511-A1 Electrochemical deblocking using a hydrazine derivative CUSTOMARRAY, INC. 2006-03-16 US claimed
WO-2005026089-A2 METHOD FOR PRODUCING HALOALKANES FROM ALCOHOLS BASF AKTIENGESELLSCHAFT (DE) 2005-03-24 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 (1 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-20070055084-A1 Method for producing haloalkanes from alcohols ADH1C, HDHD5, ADH5 NFKB1 2976/4885QPCT 510/4885HSD17B10 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.