Known targets — ChEMBL curated mechanism
ABL1ACEACHEACVR1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALKAVPR1AAVPR2BCHEBCRCA2CACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCASRCCR5CDK4CDK6CFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNA3CHRNA7CHRNB1CHRNB4CHRNDCHRNECHRNGCOXFA4COXFA4L2CRBNCSF1RCUL4ACYP19A1DDB1DPP4DRD1DRD2DRD3DRD4EDNRAEGFREML4ERBB2ERBB4ESR1ESR2FGFR1FGFR3FLT1FLT3FLT4GAAGABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGHSRGLAGNRHRGPD2GRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BGSTP1HCN4HCRTR1HCRTR2HDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HRH2HRH3HSD11B1HSP90AA1HSP90AB1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IMPDH1IMPDH2ITGA2BITGB3ITKJAK1JAK2KCNA1KCNA10KCNA2KCNA3KCNA4KCNA5KCNA6KCNA7KCNB1KCNB2KCNC1KCNC2KCNC3KCNC4KCND1KCND2KCND3KCNF1KCNG1KCNG2KCNG3KCNG4KCNH1KCNH2KCNH3KCNH4KCNH5KCNH6KCNH7KCNH8KCNJ2KCNJ3KCNJ5KCNK3KCNK9KCNQ1KCNQ2KCNQ3KCNQ4KCNQ5KCNS1KCNS2KCNS3KCNV1KCNV2KDRKITKLKB1LCKMMAOAMAOBMAPK14METMMP1MMP13MMP7MMP8MT-ND1MT-ND2MT-ND3MT-ND4MT-ND4LMT-ND5MT-ND6NDUFA1NDUFA10NDUFA11NDUFA12NDUFA13NDUFA2NDUFA3NDUFA5NDUFA6NDUFA7NDUFA8NDUFA9NDUFAB1NDUFAF1NDUFAF2NDUFAF3NDUFAF4NDUFB1NDUFB10NDUFB11NDUFB2NDUFB3NDUFB4NDUFB5NDUFB6NDUFB7NDUFB8NDUFB9NDUFC1NDUFC2NDUFS1NDUFS2NDUFS3NDUFS4NDUFS5NDUFS6NDUFS7NDUFS8NDUFV1NDUFV2NDUFV3NR3C1NS5ANTRK1NTRK2NTRK3ODC1OPRD1OPRK1OPRM1P2RY12PAHPARP1PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDE5APDE7APDE7BPDE8APDE8BPDGFRAPDGFRBPIK3CAPIK3CDPNPPOLA1POLA2POLD1POLD2POLD3POLD4POLEPOLE2POLE3PPARGPRIM1PRIM2PRKCAPRKCBPRKCDPRKCEPRKCGPRKCHPRKCIPRKCQPRKCZPRKD1PRKD3PTGS1PTGS2RBX1RENRETROCK1ROCK2RPE65RRM1RRM2RRM2BS1PR1S1PR2S1PR3S1PR4S1PR5SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC18A2SLC6A1SLC6A2SLC6A3SLC6A4SLC9A3SRCTACR1TOP1TOP2ATOP2BTTRTYMPdacAdacBdacCembAfolAftsIgyrAgyrBmrcAmrcBmrdAparCparEpolrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO
The experimentally established mechanism targets of Isopropyl 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 | |
|---|---|---|---|---|
| Isopropyl Alcohol SCHEMBL11574606 | 1.00 | — | — | |
| Isopropyl Alcohol SCHEMBL7647344 | 1.00 | — | — | |
| Isopropyl Alcohol SCHEMBL9070218 | 1.00 | ALDH1A1 (0.86) | — | |
| Isopropyl Alcohol SCHEMBL5181862 | 1.00 | ALDH1A1 (0.86) | — | |
| Isopropyl Alcohol SCHEMBL11574602 | 1.00 | ALDH1A1 (0.86) | — | |
| Isopropyl Alcohol SCHEMBL4332196 | 1.00 | — | — | |
| Isopropyl Alcohol SCHEMBL542797 | 0.94 | — | — | |
| Isopropyl Alcohol SCHEMBL11043172 | 0.94 | — | — | |
| Isopropyl Alcohol SCHEMBL9338163 | 0.94 | — | — | |
| Isopropyl Alcohol SCHEMBL14062189 | 0.94 | — | — |
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
Appears in 2594 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-122079890-A | Ruimei gem Process for the preparation of intermediates | — | 2026-05-26 | — | — | CN | claimed |
| CN-122054799-A | Vertical orientation 1D/3D perovskite film based on double-layer interface treatment, solar cell and preparation method | 杭州电子科技大学 | 2026-05-15 | — | — | CN | claimed |
| 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 |
| CN-120004890-A | Geagliptin hydrochloride microcrystal and preparation method and application thereof | 安徽峆一药业股份有限公司 | 2025-05-16 | — | — | CN | claimed |
| CN-119161284-A | Pleuromutilin derivative with side chain of natural amino acid amidophenyl derivative, and preparation method and application thereof | 华南农业大学 | 2024-12-20 | — | — | CN | claimed |
| CN-119101183-A | Biological flame retardant based on alginic acid and preparation method and application thereof | 华北科技学院(中国煤矿安全技术培训中心) | 2024-12-10 | — | — | CN | claimed |
| CN-118930441-A | Preparation method of deuterated drug impurity O-desmethylvenlafaxine-d 10 | 江阴积木新材料科技有限公司 | 2024-11-12 | — | — | CN | claimed |
| CN-115850107-B | Industrial synthesis method of hydrochloric acid Luo Xianan | 苏州诚和医药化学有限公司 | 2024-11-12 | — | — | CN | claimed |
| US-20240343738-A1 | Method for preparing pranoprofen and composition comprising pranoprofen and impurity | SHENYANG XINGQI PHARMACEUTICAL CO., LTD. (CN) | 2024-10-17 | — | — | US | claimed |
| CN-118754867-A | Synthesis method of landiolol hydrochloride | 伊诺药物研究(南京)有限公司 | 2024-10-11 | — | — | CN | claimed |
| WO-2008004110-A2 | PROCESS FOR THE PREPARATION OF THE ANGIOTENSIN II ANTAGONIST VALSARTAN | AUROBINDO PHARMA LIMITED (IN) | 2008-01-10 | — | — | WO | claimed |
| EP-1765828-B1 | AN IMPROVED PROCESS FOR THE PREPARATION OF 5,6 -DIHYDRO -4H-4(S)-ETHYLAMINO-6(S)-METHYLTHIENO[2,3-b] THIOPYRAN-2-SULFONAMIDE- 7,7 -DIOXIDE AND ITS SALT | FDC LTD (IN) | 2007-12-05 | — | — | EP | claimed |
| WO-2007077580-A2 | IMPROVED PROCESS FOR PURE DULOXETINE HYDROCHLORIDE | MSN LABORATORIES LIMITED (IN) | 2007-07-12 | — | — | WO | claimed |
| WO-2007026371-A2 | PROCESS FOR PREPARING TRANDOLAPRIL AND INTERMEDIATES THEREOF | WOCKHARDT LIMITED (IN) | 2007-03-08 | — | — | WO | claimed |
| CN-1906200-A | Novel compounds | ASTRAZENECA AB (SE) | 2007-01-31 | — | — | CN | claimed |
| WO-2005047269-A1 | A METHOD FOR THE SEPARATION OF THE LETROZOLE PRECURSOR 4-‘1-(1,2,4-TRIAZOLYL) METHYL!BENZONITRILE FROM ITS 1,3,4-TRIAZOLYL ISOMER | NATCO PHARMA LIMITED (IN) | 2005-05-26 | — | — | WO | claimed |
| CN-1323088-A | Closed electric compressor | SANYO ELECTRIC CO (JP) | 2001-11-21 | — | — | CN | claimed |
| EP-1027609-A2 | METHOD FOR DETERMINATION OF DRUGS OF ABUSE IN BIOLOGICAL SAMPLES | Varian, Inc. (US) | 2000-08-16 | — | — | EP | claimed |
| WO-1999022244-A2 | METHOD FOR DETERMINATION OF DRUGS OF ABUSE IN BIOLOGICAL SAMPLES | VARIAN, INC. (US) | 1999-05-06 | — | — | WO | claimed |
| CN-1131236-A | Sealed electric compressor | SANYO ELECTRIC CO (JP) | 1996-09-18 | — | — | CN | claimed |