Known targets — ChEMBL curated mechanism
ABL1ACEACHEACVR1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALKAVPR1AAVPR2BCHEBCRCA2CACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCASRCCR5CDK4CDK6CFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNA3CHRNA7CHRNB1CHRNB4CHRNDCHRNECHRNGCOXFA4COXFA4L2CRBNCSF1RCUL4ACYP19A1DDB1DPP4DRD1DRD2DRD3DRD4EDNRAEGFREML4ERBB2ERBB4ESR1ESR2FGFR1FGFR3FLT1FLT3FLT4GAAGABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGHSRGLAGNRHRGPD2GRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BGSTP1HCN4HCRTR1HCRTR2HDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HRH2HRH3HSD11B1HSP90AA1HSP90AB1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IMPDH1IMPDH2ITGA2BITGB3ITKJAK1JAK2KCNA1KCNA10KCNA2KCNA3KCNA4KCNA5KCNA6KCNA7KCNB1KCNB2KCNC1KCNC2KCNC3KCNC4KCND1KCND2KCND3KCNF1KCNG1KCNG2KCNG3KCNG4KCNH1KCNH2KCNH3KCNH4KCNH5KCNH6KCNH7KCNH8KCNJ2KCNJ3KCNJ5KCNK3KCNK9KCNQ1KCNQ2KCNQ3KCNQ4KCNQ5KCNS1KCNS2KCNS3KCNV1KCNV2KDRKITKLKB1LCKMMAOAMAOBMAPK14METMMP1MMP13MMP7MMP8MT-ND1MT-ND2MT-ND3MT-ND4MT-ND4LMT-ND5MT-ND6NDUFA1NDUFA10NDUFA11NDUFA12NDUFA13NDUFA2NDUFA3NDUFA5NDUFA6NDUFA7NDUFA8NDUFA9NDUFAB1NDUFAF1NDUFAF2NDUFAF3NDUFAF4NDUFB1NDUFB10NDUFB11NDUFB2NDUFB3NDUFB4NDUFB5NDUFB6NDUFB7NDUFB8NDUFB9NDUFC1NDUFC2NDUFS1NDUFS2NDUFS3NDUFS4NDUFS5NDUFS6NDUFS7NDUFS8NDUFV1NDUFV2NDUFV3NR3C1NS5ANTRK1NTRK2NTRK3ODC1OPRD1OPRK1OPRM1P2RY12PAHPARP1PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDE5APDE7APDE7BPDE8APDE8BPDGFRAPDGFRBPIK3CAPIK3CDPNPPOLA1POLA2POLD1POLD2POLD3POLD4POLEPOLE2POLE3PPARGPRIM1PRIM2PRKCAPRKCBPRKCDPRKCEPRKCGPRKCHPRKCIPRKCQPRKCZPRKD1PRKD3PTGS1PTGS2RBX1RENRETROCK1ROCK2RPE65RRM1RRM2RRM2BS1PR1S1PR2S1PR3S1PR4S1PR5SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC18A2SLC6A1SLC6A2SLC6A3SLC6A4SLC9A3SRCTACR1TOP1TOP2ATOP2BTTRTYMPdacAdacBdacCembAfolAftsIgyrAgyrBmrcAmrcBmrdAparCparEpolrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO
The experimentally established mechanism targets of Propanol. 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 | |
|---|---|---|---|---|
| Propanol SCHEMBL4269564 | 1.00 | — | — | |
| Propanol SCHEMBL6098189 | 1.00 | — | — | |
| Propanol SCHEMBL4778557 | 1.00 | — | — | |
| Propanol SCHEMBL27472513 | 1.00 | — | — | |
| Propanol SCHEMBL28853258 | 0.95 | — | — | |
| Propanol SCHEMBL28968828 | 0.95 | — | — | |
| Propanol SCHEMBL8369005 | 0.95 | ALDH1A1 (0.50) | — | |
| Propanol SCHEMBL28381868 | 0.95 | — | — | |
| Propanol SCHEMBL3488334 | 0.95 | — | — | |
| Propanol SCHEMBL17310395 | 0.95 | — | — |
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 216 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| WO-2025125058-A1 | METHOD FOR THE ORGANIC PREPARATION OF A CATALYST IN THE PRESENCE OF A HYDROGEN HALIDE ADDITIVE | IFP Energies Nouvelles (FR) | 2025-06-19 | — | — | WO | claimed |
| US-11834425-B2 | Full continuous-flow preparation method of vitamin B1 | FUDAN UNIVERSITY (CN) | 2023-12-05 | — | — | US | claimed |
| US-20230183196-A1 | FULL CONTINUOUS-FLOW PREPARATION METHOD OF VITAMIN B1 | FUDAN UNIVERSITY (CN) | 2023-06-15 | — | — | US | claimed |
| CN-116064165-A | Agent for treating coking and blocking of hydrogenation unit and its application | 中国石油化工股份有限公司 | 2023-05-05 | — | — | CN | claimed |
| CN-113563007-A | High-strength composite fiber expansion anti-cracking agent and preparation process thereof | 南京晶磊兴建材有限公司 | 2021-10-29 | — | — | CN | claimed |
| CN-113336467-A | Low-alkali waterproof anti-cracking expanding agent | 南京晶磊兴建材有限公司 | 2021-09-03 | — | — | CN | claimed |
| CN-107417663-B | A kind of preparation method of high-purity (S) -3- methylamino -1- (thiophene -2- base) propyl alcohol | 台州职业技术学院 | 2019-05-28 | — | — | CN | claimed |
| CN-107417663-A | A kind of preparation method of high-purity (S) 3 methylamino 1 (base of thiophene 2) propyl alcohol | 台州职业技术学院 | 2017-12-01 | — | — | CN | claimed |
| CN-106632131-A | Hexythiazox and preparation method thereof | 温州大学 | 2017-05-10 | — | — | CN | claimed |
| CN-105669699-A | Preparation method of prasugrel hydrochloride | 山东罗欣药业集团股份有限公司 | 2016-06-15 | — | — | CN | claimed |
| CN-104370851-A | Synthesis method of 2-aminomethyl-thiazole hydrochloride | KEJIE BIO SUZHOU PHARMACEUTICALS CO LTD | 2015-02-25 | — | — | CN | claimed |
| CN-103570645-A | Method for preparing N-(2,6-dimethyl phenyl)-2-(1-piperazine)acetamide | SHANGHAI DESANO CHEMICAL PHARM | 2014-02-12 | — | — | CN | claimed |
| CN-103420920-A | Rilpivrine hydrochloride alcoholate polymorphs and preparation methods thereof | SHANGHAI DESANO PHARMACEUTICAL CO LTD | 2013-12-04 | — | — | CN | claimed |
| EP-0629625-B1 | Loracarbef hydrochloride C1-C3 alcohol solvates and uses thereof | LILLY CO ELI (US) | 2002-10-09 | — | — | EP | claimed |
| CN-1053446-C | Novel thiomarinol derivatives, and processes for their preparation | SANKYO CO (JP) | 2000-06-14 | — | — | CN | claimed |
| US-5578720-A | ETHANOL, METHANOL AND PROPANOL SOLVATES; ANTIBIOTICS | ELI LILLY AND COMPANY (US) | 1996-11-26 | — | — | US | claimed |
| EP-0629625-A1 | Loracarbef hydrochloride C1-C3 alcohol solvates and uses thereof | ELI LILLY AND COMPANY (US) | 1994-12-21 | — | — | EP | claimed |
| CN-1092811-A | New thiomarinol derivative and preparation method thereof | SANKYO CO (JP) | 1994-09-28 | — | — | CN | claimed |
| US-12398140-B2 | Substituted pyrrolo [2,3-d]pyrimidines for treating familial dysautonomia | PTC THERAPEUTICS, INC. (US) | 2025-08-26 | — | — | US | disclosed |
| US-3937832-A | ADMINISTERING | SOCIETE ANONYME DITE: HEXACHIMIE (FR) | 1976-02-10 | — | — | US | disclosed |