Known targets — ChEMBL curated mechanism
ABL1ACEACHEACVR1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALKAVPR1AAVPR2BCHEBCRCA2CACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCASRCCR5CDK4CDK6CFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNA3CHRNA7CHRNB1CHRNB4CHRNDCHRNECHRNGCOXFA4COXFA4L2CRBNCSF1RCUL4ACYP19A1DDB1DPP4DRD1DRD2DRD3DRD4EDNRAEGFREML4ERBB2ERBB4ESR1ESR2FGFR1FGFR3FLT1FLT3FLT4GAAGABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGHSRGLAGNRHRGPD2GRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BGSTP1HCN4HCRTR1HCRTR2HDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HRH2HRH3HSD11B1HSP90AA1HSP90AB1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IMPDH1IMPDH2ITGA2BITGB3ITKJAK1JAK2KCNA1KCNA10KCNA2KCNA3KCNA4KCNA5KCNA6KCNA7KCNB1KCNB2KCNC1KCNC2KCNC3KCNC4KCND1KCND2KCND3KCNF1KCNG1KCNG2KCNG3KCNG4KCNH1KCNH2KCNH3KCNH4KCNH5KCNH6KCNH7KCNH8KCNJ2KCNJ3KCNJ5KCNK3KCNK9KCNQ1KCNQ2KCNQ3KCNQ4KCNQ5KCNS1KCNS2KCNS3KCNV1KCNV2KDRKITKLKB1LCKMMAOAMAOBMAPK14METMMP1MMP13MMP7MMP8MT-ND1MT-ND2MT-ND3MT-ND4MT-ND4LMT-ND5MT-ND6NDUFA1NDUFA10NDUFA11NDUFA12NDUFA13NDUFA2NDUFA3NDUFA5NDUFA6NDUFA7NDUFA8NDUFA9NDUFAB1NDUFAF1NDUFAF2NDUFAF3NDUFAF4NDUFB1NDUFB10NDUFB11NDUFB2NDUFB3NDUFB4NDUFB5NDUFB6NDUFB7NDUFB8NDUFB9NDUFC1NDUFC2NDUFS1NDUFS2NDUFS3NDUFS4NDUFS5NDUFS6NDUFS7NDUFS8NDUFV1NDUFV2NDUFV3NR3C1NS5ANTRK1NTRK2NTRK3ODC1OPRD1OPRK1OPRM1P2RY12PAHPARP1PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDE5APDE7APDE7BPDE8APDE8BPDGFRAPDGFRBPIK3CAPIK3CDPNPPOLA1POLA2POLD1POLD2POLD3POLD4POLEPOLE2POLE3PPARGPRIM1PRIM2PRKCAPRKCBPRKCDPRKCEPRKCGPRKCHPRKCIPRKCQPRKCZPRKD1PRKD3PTGS1PTGS2RBX1RENRETROCK1ROCK2RPE65RRM1RRM2RRM2BS1PR1S1PR2S1PR3S1PR4S1PR5SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC18A2SLC6A1SLC6A2SLC6A3SLC6A4SLC9A3SRCTACR1TOP1TOP2ATOP2BTTRTYMPdacAdacBdacCembAfolAftsIgyrAgyrBmrcAmrcBmrdAparCparEpolrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO
The experimentally established mechanism targets of Allyl 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 | |
|---|---|---|---|---|
| Allyl Alcohol SCHEMBL4940557 | 0.95 | — | — | |
| Allyl Alcohol SCHEMBL3782 | 0.95 | — | — | |
| Allyl Alcohol SCHEMBL1331425 | 0.95 | — | — | |
| Allyl Alcohol SCHEMBL1332489 | 0.95 | — | — | |
| Allyl Alcohol SCHEMBL5382706 | 0.90 | — | — | |
| Allyl Alcohol SCHEMBL565195 | 0.90 | — | — | |
| Allyl Alcohol SCHEMBL4654133 | 0.90 | — | — | |
| Allyl Alcohol SCHEMBL9845385 | 0.90 | — | — | |
| Allyl Alcohol SCHEMBL4665160 | 0.90 | — | — | |
| Allyl Alcohol SCHEMBL4729230 | 0.90 | — | — |
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 48 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-104087283-A | Fracturing thickening agent for fast dispersing and tackifying under acidic condition and preparation method thereof | KUNSHAN JINGKUN OILFIELD CHEMICAL TECHNOLOGY DEV COMPANY | 2014-10-08 | — | — | CN | claimed |
| CN-103242483-A | Preparation method of instant polyacrylamide | ANHUI TIANRUN CHEMICALS CO LTD | 2013-08-14 | — | — | CN | claimed |
| CN-1065670-A | EMULSIVE WATER-PROOF COATINGS MAKING METHOD FROM WASTE RESIN | CHINA MINERAL UNIV (CN) | 1992-10-28 | — | — | CN | claimed |
| JP-62026243-A | — | — | None | — | — | JP | disclosed |
| CN-121755230-A | Solid-borne BF3Catalyst, preparation method thereof and synthesis method of allyl glycidyl ether | 中国石油化工股份有限公司 | 2026-03-31 | — | — | CN | disclosed |
| WO-2024037904-A1 | COMPOSITION FOR REDUCING CRYSTALLIZATION OF PARAFFIN CRYSTALS IN FUELS | BASF SE (DE) | 2024-02-22 | — | — | WO | disclosed |
| US-20230340012-A1 | NATURAL AND SYNTHETIC COMPOUNDS FOR TREATING CANCER AND OTHER DISEASES | PACIFIC ARROW LTD (CN) | 2023-10-26 | — | — | US | disclosed |
| US-20230159436-A1 | APPLICATIONS OF AMIDE ANALOGS OF TRITERPENES IN CURES OF CANCER AND OTHER DISEASES | PACIFIC ARROW LTD (CN) | 2023-05-25 | — | — | US | disclosed |
| EP-4095217-A1 | COPOLYMER AND ITS USE IN REDUCING THE CRYSTALLIZATION OF PARAFFIN CRYSTALS IN FUELS | BASF SE (DE) | 2022-11-30 | — | — | EP | disclosed |
| US-11485755-B2 | Natural and synthetic compounds for treating cancer and other diseases | PACIFIC ARROW LTD (CN) | 2022-11-01 | — | — | US | disclosed |
| CN-114702464-A | Closed cycle production method for preparing epichlorohydrin by adopting allyl alcohol method | 宁波环洋新材料股份有限公司 | 2022-07-05 | — | — | CN | disclosed |
| CN-1007976-B | PROCESS FOR THE PREPARATION OF MODIFIED SUCCINIMIDS | CHEVRON RES (US) | 1990-05-16 | — | — | CN | disclosed |
| JP-S6226243-A | PRODUCTION OF 2,3-DICHLORO-1-PROPANOL | OSAKA SODA CO LTD | 1987-02-04 | — | — | JP | disclosed |
| CN-85107639-A | The preparation method of modified succinimides | — | 1986-10-08 | — | — | CN | disclosed |
| US-4138421-A | Process for the polymerization of allyl halides to produce poly(allylsilicoformate) polymers | BLOUNT DAVID H | 1979-02-06 | — | — | US | disclosed |
| US-4125694-A | Process for the polymerization of allyl halides to form polyallyl alcohol | BLOUNT DAVID H | 1978-11-14 | — | — | US | disclosed |
| US-4115635-A | Process for the production of poly (allyl halide allyl alcohol) polymer | BLOUNT DAVID H | 1978-09-19 | — | — | US | disclosed |
| US-4104456-A | Process for the production of poly(allylhalide-allyl alcohol) | BLOUNT DAVID H | 1978-08-01 | — | — | US | disclosed |
| US-4069391-A | Process for the production of poly(allyl silicofurmate) | BLOUNT DAVID H | 1978-01-17 | — | — | US | disclosed |
| US-4020259-A | Process for the polymerization of allyl halides | BLOUNT DAVID H | 1977-04-26 | — | — | US | disclosed |