Known targets — ChEMBL curated mechanism
ABL1ACEACHEACVR1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALKAVPR1AAVPR2BCHEBCRCA2CACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCASRCCR5CDK4CDK6CFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNA3CHRNA7CHRNB1CHRNB4CHRNDCHRNECHRNGCOXFA4COXFA4L2CRBNCSF1RCUL4ACYP19A1DDB1DPP4DRD1DRD2DRD3DRD4EDNRAEGFREML4ERBB2ERBB4ESR1ESR2FGFR1FGFR3FLT1FLT3FLT4GAAGABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGHSRGLAGNRHRGPD2GRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BGSTP1HCN4HCRTR1HCRTR2HDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HRH2HRH3HSD11B1HSP90AA1HSP90AB1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IMPDH1IMPDH2ITGA2BITGB3ITKJAK1JAK2KCNA1KCNA10KCNA2KCNA3KCNA4KCNA5KCNA6KCNA7KCNB1KCNB2KCNC1KCNC2KCNC3KCNC4KCND1KCND2KCND3KCNF1KCNG1KCNG2KCNG3KCNG4KCNH1KCNH2KCNH3KCNH4KCNH5KCNH6KCNH7KCNH8KCNJ2KCNJ3KCNJ5KCNK3KCNK9KCNQ1KCNQ2KCNQ3KCNQ4KCNQ5KCNS1KCNS2KCNS3KCNV1KCNV2KDRKITKLKB1LCKMMAOAMAOBMAPK14METMMP1MMP13MMP7MMP8MT-ND1MT-ND2MT-ND3MT-ND4MT-ND4LMT-ND5MT-ND6NDUFA1NDUFA10NDUFA11NDUFA12NDUFA13NDUFA2NDUFA3NDUFA5NDUFA6NDUFA7NDUFA8NDUFA9NDUFAB1NDUFAF1NDUFAF2NDUFAF3NDUFAF4NDUFB1NDUFB10NDUFB11NDUFB2NDUFB3NDUFB4NDUFB5NDUFB6NDUFB7NDUFB8NDUFB9NDUFC1NDUFC2NDUFS1NDUFS2NDUFS3NDUFS4NDUFS5NDUFS6NDUFS7NDUFS8NDUFV1NDUFV2NDUFV3NR3C1NS5ANTRK1NTRK2NTRK3ODC1OPRD1OPRK1OPRM1P2RY12PAHPARP1PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDE5APDE7APDE7BPDE8APDE8BPDGFRAPDGFRBPIK3CAPIK3CDPNPPOLA1POLA2POLD1POLD2POLD3POLD4POLEPOLE2POLE3PPARGPRIM1PRIM2PRKCAPRKCBPRKCDPRKCEPRKCGPRKCHPRKCIPRKCQPRKCZPRKD1PRKD3PTGS1PTGS2RBX1RENRETROCK1ROCK2RPE65RRM1RRM2RRM2BS1PR1S1PR2S1PR3S1PR4S1PR5SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC18A2SLC6A1SLC6A2SLC6A3SLC6A4SLC9A3SRCTACR1TOP1TOP2ATOP2BTTRTYMPdacAdacBdacCembAfolAftsIgyrAgyrBmrcAmrcBmrdAparCparEpolrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO
The experimentally established mechanism targets of Dimethylformamide. 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 | |
|---|---|---|---|---|
| Dimethylformamide SCHEMBL11184345 | 1.00 | — | — | |
| Dimethylformamide SCHEMBL11184302 | 1.00 | TSHR (0.90) | — | |
| Dimethylformamide SCHEMBL27600017 | 0.95 | — | — | |
| Dimethylformamide SCHEMBL29206894 | 0.95 | — | — | |
| Dimethylformamide SCHEMBL28205862 | 0.95 | — | — | |
| Dimethylformamide SCHEMBL28645765 | 0.95 | — | — | |
| Dimethylformamide SCHEMBL10423096 | 0.95 | — | — | |
| Dimethylformamide SCHEMBL28292810 | 0.95 | — | — | |
| Dimethylformamide SCHEMBL28257570 | 0.95 | — | — | |
| Dimethylformamide SCHEMBL2280000 | 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 188 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-108570041-B | Preparation method of isoxazoline-containing uracil compound | 沈阳中化农药化工研发有限公司 | 2024-02-09 | — | — | CN | claimed |
| US-11014028-B2 | Method for preparation and activation of super-hydrophobic electret fiber material for cleaning PM2.5 | SOUTH CHINA UNIVERSITY OF TECHNOLOGY | 2021-05-25 | — | — | US | claimed |
| US-10577535-B2 | Substantially solid acidizing composition for treatment of subterranean formations | HALLIBURTON ENERGY SERVICES, INC. (US) | 2020-03-03 | — | — | US | claimed |
| US-20190143254-A1 | Method for Preparation and Activation of Super-Hydrophobic Electret Fiber Material for Cleaning PM2.5 | SOUTH CHINA UNIVERSITY OF TECHNOLOGY (CN) | 2019-05-16 | — | — | US | claimed |
| CN-109721577-A | A kind of purification process of furans dicarboxylic acids | 中国科学院宁波材料技术与工程研究所 | 2019-05-07 | — | — | CN | claimed |
| CN-105168130-B | A kind of tumour target polymer micella and preparation method thereof | 安徽医科大学 | 2017-10-27 | — | — | CN | claimed |
| US-20160272879-A1 | SUBSTANTIALLY SOLID ACIDIZING COMPOSITION FOR TREATMENT OF SUBTERRANEAN FORMATIONS | HALLIBURTON ENERGY SERVICES, INC. | 2016-09-22 | — | — | US | claimed |
| CN-104140112-B | The ion process for thermosynthesizing of a kind of microspheroidal porous alkali formula magnesium borate and magnesium borate nano-superstructure | QUFU NORMAL UNIVERSITY (CN) | 2016-06-01 | — | — | CN | claimed |
| WO-2015126397-A1 | SUBSTANTIALLY SOLID ACIDIZING COMPOSITION FOR TREATMENT OF SUBTERRANEAN FORMATIONS | HALLIBURTON ENERGY SERVICES, INC. (US) | 2015-08-27 | — | — | WO | claimed |
| EP-1212273-B1 | METHOD FOR PURIFYING ACID CHLORIDES | BASF AG (DE) | 2005-02-02 | — | — | EP | claimed |
| CN-1174954-C | Method for purifying acid chlorides | �����ɷ� | 2004-11-10 | — | — | CN | claimed |
| US-6727384-B1 | PREPARED BY REACTION OF CARBOXYLIC ACID WITH PHOSGENE OR THIONYL CHLORIDE; TREATING WITH CARBOXAMIDE HYDROHALIDE; SEPARATION | BASF AKTIENGESELLSCHAFT (DE) | 2004-04-27 | — | — | US | claimed |
| CN-1373743-A | Method for purifying phosgene | BASF AG (DE) | 2002-10-09 | — | — | CN | claimed |
| WO-2001072704-A1 | AZETIDINONE DERIVATIVES, A PROCESS FOR THEIR PREPARATION AND A METHOD FOR PRODUCING 1-β-ALKYL AZETIDINONE USING THE SAME | DAEWOONG PHARMACEUTICAL CO., LTD. (KR) | 2001-10-04 | — | — | WO | claimed |
| EP-0000609-A1 | Novel 19-nor-pregnahexaenes, process for the preparation thereof, and pharmaceutical compositions containing them | Technobiotic Ltd. (CH) | 1979-02-07 | — | — | EP | claimed |
| US-3948966-A | METAL CHLORIDE-DIMETHYLFORMAMIDE CATALYSTS | KAO SOAP CO., LTD. (JA) | 1976-04-06 | — | — | US | claimed |
| JP-2064129-A | — | — | None | — | — | JP | disclosed |
| EP-4709708-A1 | NOVEL CARBOXAMIDE DERIVATIVES | ANGELINI PHARMA S.P.A. (IT) | 2026-03-18 | — | — | EP | disclosed |
| US-3948966-A | METAL CHLORIDE-DIMETHYLFORMAMIDE CATALYSTS | KAO SOAP CO., LTD. (JA) | 1976-04-06 | — | — | US | disclosed |
| US-3884631-A | PREPARATION OF CELLULOSE N,N-DIMETHYLFORMIMIDATE CHLORIDE IN TEXTILE FORM, AND CONVERSION TO HALOGENODEOXYCELLULOSES AND CELLULOSE FORMATE | US AGRICULTURE | 1975-05-20 | — | — | US | disclosed |