SCHEMBL222302

SCHEMBL222302

CCCC[n+]1ccccc1.O=[Al]Cl

nearest known ligand 0.63

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ACHE P22303 4/20 0.63
CHRM2 P08172 2/20 0.63
ADRA2A P08913 2/20 0.63
ADORA3 P0DMS8 2/20 0.63
CHRM1 P11229 2/20 0.63
SLC6A2 P23975 2/20 0.63
SLC6A4 P31645 2/20 0.63
SLC6A3 Q01959 2/20 0.63
ABCB11 O95342 1/20 0.63
ESR1 P03372 1/20 0.63
PGR P06401 1/20 0.63
HTR1A P08908 1/20 0.63
DRD1 P21728 1/20 0.63
TBXA2R P21731 1/20 0.63
PTGS1 P23219 1/20 0.63
PDE4A P27815 1/20 0.63
ADRA1A P35348 1/20 0.63
OPRM1 P35372 1/20 0.63
DRD3 P35462 1/20 0.63
KCNH2 Q12809 1/20 0.63

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
SCHEMBL34882 0.87 ACHE (0.81) ACHECHRM2ADRA2AADORA3CHRM1
Formaldehyde SCHEMBL28001350 0.85 ACHE (0.71) ACHECHRM2ADRA2AADORA3CHRM1
SCHEMBL3188166 0.85 ACHE (0.71) ACHECHRM2ADRA2AADORA3CHRM1
SCHEMBL3188172 0.85 ACHE (0.71) ACHECHRM2ADRA2AADORA3CHRM1
Fluoride Ion SCHEMBL1502795 0.84 ACHE (0.77) ACHECHRM2ADRA2AADORA3CHRM1
Iodide SCHEMBL1502803 0.84 CHRM2 (0.77) ACHECHRM2ADRA2AADORA3CHRM1
SCHEMBL28843829 0.84 ACHE (0.77) ACHECHRM2ADRA2AADORA3CHRM1
Hydrochloric Acid SCHEMBL2696916 0.84 ACHE (0.77) ACHECHRM2ADRA2AADORA3CHRM1
Bromide SCHEMBL382846 0.84 ACHE (0.82) ACHECHRM2ADRA2AADORA3CHRM1
Bromide SCHEMBL18062500 0.84 ACHE (0.82) ACHECHRM2ADRA2AADORA3CHRM1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3337876-B1 METHOD FOR MAKING POLYALPHAOLEFINS USING IONIC LIQUID CATALYZED OLIGOMERIZATION OF OLEFINS CHEVRON PHILLIPS CHEMICAL CO LP (US) 2024-06-12 EP claimed
CN-117209638-B Amphoteric ion rare earth element alkyl catalyst and preparation method and application thereof 传化智联股份有限公司 2024-02-13 CN claimed
CN-113966319-B Synthesis of base oils by ion catalyst oligomerization and anhydrous separation of oligomerization catalysts 雪佛龙美国公司 2023-12-19 CN claimed
CN-117209638-A Amphoteric ion rare earth element alkyl catalyst and preparation method and application thereof 传化智联股份有限公司 2023-12-12 CN claimed
US-11753355-B2 Base oil synthesis via ionic catalyst oligomerization and waterless separation of the oligomerization catalyst CHEVRON U.S.A. INC. (US) 2023-09-12 US claimed
EP-3962883-A1 BASE OIL SYNTHESIS VIA IONIC CATALYST OLIGOMERIZATION AND WATERLESS SEPARATION OF THE OLIGOMERIZATION CATALYST Chevron U.S.A. Inc. (US) 2022-03-09 EP claimed
US-20220041526-A1 BASE OIL SYNTHESIS VIA IONIC CATALYST OLIGOMERIZATION AND WATERLESS SEPARATION OF THE OLIGOMERIZATION CATALYST CHEVRON U.S.A. INC. 2022-02-10 US claimed
CN-111909193-A Phenyl trimethylsilane and preparation method thereof 江西星火狮达科技有限公司 2020-11-10 CN claimed
WO-2020222168-A1 Base Oil Synthesis via Ionic Catalyst Oligomerization and Waterless Separation of the Oligomerization Catalyst CHEVRON U.S.A. INC. (US) 2020-11-05 WO claimed
EP-1836285-B1 INTEGRATED ALKYLATION PROCESS USING IONIC LIQUID CATALYSTS CHEVRON USA INC (US) 2019-11-20 EP claimed
US-20080146858-A1 ISOMERIZATION OF BUTENE IN THE IONIC LIQUID-CATALYZED ALKYLATION OF LIGHT ISOPARAFFINS AND OLEFINS CHEVRON U.S.A. INC. 2008-06-19 US claimed
US-20080142413-A1 ALKYLATION PROCESS USING AN ALKYL HALIDE PROMOTED IONIC LIQUID CATALYST CHEVRON U.S.A. INC. 2008-06-19 US claimed
CN-100374410-C Method of preparing amide from ketoximes by Beckmann rearrangement LANZHOU CHEM PHYS INST (CN) 2008-03-12 CN claimed
US-20070225538-A1 Alkylation process using an alkyl halide promoted ionic liquid catalyst CHEVRON U.S.A. INC. 2007-09-27 US claimed
EP-1836285-A2 INTEGRATED ALKYLATION PROCESS USING IONIC LIQUID CATALYSTS Chevron U.S.A. Inc. (US) 2007-09-26 EP claimed
CN-1919833-A Method of preparing amide from ketoximes by Beckmann rearrangement LANZHOU CHEM PHYS INST (CN) 2007-02-28 CN claimed
WO-2006073749-A2 INTEGRATED ALKYLATION PROCESS USING IONIC LIQUID CATALYSTS CHEVRON U.S.A., INC. (US) 2006-07-13 WO claimed
WO-2006068983-A2 ALKYLATION PROCESS USING CHLOROALUMINATE IONIC LIQUID CATALYSTS CHEVRON U.S.A. INC. (US) 2006-06-29 WO claimed
US-20060131209-A1 Integrated alkylation process using ionic liquid catalysts CHEVRON U.S.A., INC. 2006-06-22 US claimed
US-20060135839-A1 Alkylation process using chloroaluminate ionic liquid catalysts CHEVERON U.S.A., INC. 2006-06-22 US 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 (4 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-20080146858-A1 ISOMERIZATION OF BUTENE IN THE IONIC LIQUID-CATALYZED ALKYLATION OF LIGHT ISOPARAFFINS AND OLEFINS INF2, MACF1, ILF2 ACHE 2234/4885CHRM2 1220/4885ADRA2A 2117/4885
US-20070225538-A1 Alkylation process using an alkyl halide promoted ionic liquid catalyst ALKBH3, ALK, L3MBTL3 ACHE 2245/4885CHRM2 117/4885ADRA2A 2613/4885
US-20060131209-A1 Integrated alkylation process using ionic liquid catalysts ELL, ALKBH3, INTS9 ACHE 324/4885CHRM2 427/4885ADRA2A 3773/4885
US-20060135839-A1 Alkylation process using chloroaluminate ionic liquid catalysts ELOB, INTS6, RTF1 ACHE 1612/4885CHRM2 182/4885ADRA2A 3539/4885

“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.