Known targets — ChEMBL curated mechanism
ABCC9ABL1ACEACHEACVR1ADORA1ADORA2AADORA2BADORA3ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALOX5ATP4AATP4BBCRBTKCACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNB1CHRNDCHRNECHRNGCRBNCUL4ACXCR1CXCR2DDB1DDCDHFRDPP4DRD2DRD3DRD4EGFRERBB2ERBB4ESR1ESR2FDPSFKBP1AFLT1FLT3FLT4GARTGHSRGRIA1GRIA2GRIA3GRIA4GRIK1GRIK2GRIK3GRIK4GRIK5GRIN2AGSK3AGSK3BHDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IDH1IDH2IMPA1ITGA2BITGB3JAK1JAK2JAK3KCNJ11KCNK3KCNK9KDRKITMEN1METMMP1MMP13MMP7MMP8NANOD2NS5bODC1OPG057OPRD1OPRK1OPRM1PPARP1PARP2PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDGFRBPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PKLRPPARDPPATPTGS1PTGS2RBX1ROCK1ROCK2RRM1RRM2RRM2BSCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC10A2SLC5A2SLC6A2SLC6A3SLC6A4SLC9A3SYKTACR1THRATHRBTOP1TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TYK2TYMSVDRampCblablaT-3blaT-4blaT-5blaT-6blaUOE-1dacAdacBdacCfolAfolPftsIgyrAgyrBileSmecAmrcAmrcBmrdAparCparEpbp2pbp4pbpApbpFrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUthyAykgMykgO
The experimentally established mechanism targets of Methyl Alcohol. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.
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.
| Compound | similarity | top predicted | shared targets | |
|---|---|---|---|---|
| Methyl Alcohol SCHEMBL44614 | 1.00 | — | — | |
| Methyl Alcohol SCHEMBL9526155 | 1.00 | TSHR (0.75) | — | |
| Methyl Alcohol SCHEMBL9526147 | 1.00 | TSHR (0.75) | — | |
| Methyl Alcohol SCHEMBL449684 | 1.00 | — | — | |
| Methyl Alcohol SCHEMBL15348234 | 1.00 | — | — | |
| Methyl Alcohol SCHEMBL44615 | 1.00 | — | — | |
| Methyl Alcohol SCHEMBL11649435 | 1.00 | — | — | |
| Methyl Alcohol SCHEMBL449756 | 1.00 | — | — | |
| Methyl Alcohol SCHEMBL321255 | 1.00 | TSHR (0.75) | — | |
| Methyl Alcohol SCHEMBL7862958 | 1.00 | TSHR (0.75) | — |
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 1752 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-119899110-A | Callicarpa nudiflora leaf extract, labdane diterpenoid compound, and preparation method and application thereof | 海南师范大学 | 2025-04-29 | — | — | CN | claimed |
| CN-119119161-A | Gynostemma pentaphylla extract, preparation method and application thereof, dammarane type triterpene saponin, preparation method and application thereof and gynostemma pentaphylla plant source bactericide | 烟台先进材料与绿色制造山东省实验室 | 2024-12-13 | — | — | CN | claimed |
| WO-2024131981-A1 | MONOMER COMPOUND IN EFFECTIVE PARTS OF PTERIS CRETICA VAR. LAETA, PREPARATION METHOD, USE AND DRUG | 大连医科大学 | 2024-06-27 | — | — | WO | claimed |
| CN-118236960-A | Three-kettle serial continuous DMM esterification reaction device and method | 河北彩客新材料科技股份有限公司 | 2024-06-25 | — | — | CN | claimed |
| CN-116217428-B | Methanol hydrate crystal of D-calcium pantothenate and process for producing D-calcium pantothenate | 黑龙江新和成生物科技有限公司 | 2024-04-02 | — | — | CN | claimed |
| CN-113629194-B | Two-dimensional molecular crystal-graphene oxide heterojunction, preparation method and application | 南京工业大学 | 2023-12-22 | — | — | CN | claimed |
| US-20230310532-A1 | FOOD EXTRACTS, METHODS OF EXTRACTION AND COMPOSITIONS THEREOF | NATIONAL UNIVERSITY OF SINGAPORE (SG) | 2023-10-05 | — | — | US | claimed |
| EP-3558869-B1 | PROCESS TO CONVERT SYNTHESIS GAS TO OLEFINS USING A BIFUNCTIONAL CHROMIUM / ZINC OXIDE-SAPO-34 CATALYST | DOW GLOBAL TECHNOLOGIES LLC (US) | 2023-08-09 | — | — | EP | claimed |
| EP-3290341-B1 | ELECTRICALLY CONDUCTIVE MATERIALS FOR HEATING AND DEICING AIRFOILS | BOEING CO (US) | 2023-07-26 | — | — | EP | claimed |
| WO-2023134240-A1 | LIGNAN COMPOUNDS FROM EUCOMMIAE FOLIUM, PREPARATION METHOD THEREFOR AND USE IN NEUROPROTECTION | 西北农林科技大学 | 2023-07-20 | — | — | WO | claimed |
| WO-1999007464-A1 | STRATIFICATION RESISTANT EMULSIONS | APACE RESEARCH LIMITED (AU) | 1999-02-18 | — | — | WO | claimed |
| US-4839465-A | SUBSTANCE P ANTAGONIST, HYPOTENSIVE AGENT, ANALGESICS | STERLING DRUG INC. (US) | 1989-06-13 | — | — | US | claimed |
| EP-0155973-B1 | HYDROCARBYLOXY ALKANALS, ORGANOLEPTIC USES THEREOF AND PROCESSORS FOR PREPARING SAME | INTERNATIONAL FLAVORS & FRAGRANCES INC. (US) | 1988-12-14 | — | — | EP | claimed |
| US-4620041-A | Ether carbinols | INTERNATIONAL FLAVORS & FRAGRANCES INC. (US) | 1986-10-28 | — | — | US | claimed |
| US-4619780-A | Ether carbinols, process for preparing same, products produced according to said processes containing said ether carbinols, organoleptic uses thereof, ether carboxaldehydes and organoleptic uses thereof | INTERNATIONAL FLAVORS & FRAGRANCES INC. (US) | 1986-10-28 | — | — | US | claimed |
| US-4556746-A | ORGANOLEPTIC | INTERNATIONAL FLAVORS & FRAGRANCES INC. (US) | 1985-12-03 | — | — | US | claimed |
| EP-0155973-A1 | Hydrocarbyloxy alkanals, organoleptic uses thereof and processors for preparing same | INTERNATIONAL FLAVORS & FRAGRANCES INC. (US) | 1985-10-02 | — | — | EP | claimed |
| US-4544775-A | Ether carbinols, process for preparing same, products produced according to said processes containing said ether carbinols, organoleptic uses thereof, ether carboxaldehydes and organoleptic uses thereof | INTERNATIONAL FLAVORS & FRAGRANCES INC. (US) | 1985-10-01 | — | — | US | claimed |
| US-4521634-A | Ether carbinols and process for preparing same | INTERNATIONAL FLAVORS & FRAGRANCES INC. (US) | 1985-06-04 | — | — | US | claimed |
| US-4253847-A | DISSOLVING A SAMPLE CONTAINING METALS SELECTED FROM MOLYBDENUM, TUNGSTEN, TITANIUM, VANADIUM AND URANIUM ALCOHOL-HYDROGEN CHLORIDE | ENVIRONMENTAL SCIENCES ASSOCIATES, INC. (US) | 1981-03-03 | — | — | US | claimed |