Known targets — ChEMBL curated mechanism
ABL1ACEACHEACVR1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALKAVPR1AAVPR2BCHEBCRCA2CACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCASRCCR5CDK4CDK6CFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNA3CHRNA7CHRNB1CHRNB4CHRNDCHRNECHRNGCOXFA4COXFA4L2CRBNCSF1RCUL4ACYP19A1DDB1DPP4DRD1DRD2DRD3DRD4EDNRAEGFREML4ERBB2ERBB4ESR1ESR2FGFR1FGFR3FLT1FLT3FLT4GAAGABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGHSRGLAGNRHRGPD2GRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BGSTP1HCN4HCRTR1HCRTR2HDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HRH2HRH3HSD11B1HSP90AA1HSP90AB1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IMPDH1IMPDH2ITGA2BITGB3ITKJAK1JAK2KCNA1KCNA10KCNA2KCNA3KCNA4KCNA5KCNA6KCNA7KCNB1KCNB2KCNC1KCNC2KCNC3KCNC4KCND1KCND2KCND3KCNF1KCNG1KCNG2KCNG3KCNG4KCNH1KCNH2KCNH3KCNH4KCNH5KCNH6KCNH7KCNH8KCNJ2KCNJ3KCNJ5KCNK3KCNK9KCNQ1KCNQ2KCNQ3KCNQ4KCNQ5KCNS1KCNS2KCNS3KCNV1KCNV2KDRKITKLKB1LCKMMAOAMAOBMAPK14METMMP1MMP13MMP7MMP8MT-ND1MT-ND2MT-ND3MT-ND4MT-ND4LMT-ND5MT-ND6NDUFA1NDUFA10NDUFA11NDUFA12NDUFA13NDUFA2NDUFA3NDUFA5NDUFA6NDUFA7NDUFA8NDUFA9NDUFAB1NDUFAF1NDUFAF2NDUFAF3NDUFAF4NDUFB1NDUFB10NDUFB11NDUFB2NDUFB3NDUFB4NDUFB5NDUFB6NDUFB7NDUFB8NDUFB9NDUFC1NDUFC2NDUFS1NDUFS2NDUFS3NDUFS4NDUFS5NDUFS6NDUFS7NDUFS8NDUFV1NDUFV2NDUFV3NR3C1NS5ANTRK1NTRK2NTRK3ODC1OPRD1OPRK1OPRM1P2RY12PAHPARP1PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDE5APDE7APDE7BPDE8APDE8BPDGFRAPDGFRBPIK3CAPIK3CDPNPPOLA1POLA2POLD1POLD2POLD3POLD4POLEPOLE2POLE3PPARGPRIM1PRIM2PRKCAPRKCBPRKCDPRKCEPRKCGPRKCHPRKCIPRKCQPRKCZPRKD1PRKD3PTGS1PTGS2RBX1RENRETROCK1ROCK2RPE65RRM1RRM2RRM2BS1PR1S1PR2S1PR3S1PR4S1PR5SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC18A2SLC6A1SLC6A2SLC6A3SLC6A4SLC9A3SRCTACR1TOP1TOP2ATOP2BTTRTYMPdacAdacBdacCembAfolAftsIgyrAgyrBmrcAmrcBmrdAparCparEpolrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO
The experimentally established mechanism targets of Formic Acid. 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 | |
|---|---|---|---|---|
| Formic Acid SCHEMBL29418891 | 1.00 | — | — | |
| Formic Acid SCHEMBL29301 | 1.00 | — | — | |
| Formic Acid SCHEMBL23420519 | 1.00 | — | — | |
| Formic Acid SCHEMBL11389712 | 0.94 | — | — | |
| Formic Acid SCHEMBL9477283 | 0.94 | — | — | |
| Formic Acid SCHEMBL9449497 | 0.94 | — | — | |
| Formic Acid SCHEMBL4678172 | 0.94 | — | — | |
| Formic Acid SCHEMBL5995205 | 0.94 | — | — | |
| Formic Acid SCHEMBL25389190 | 0.94 | — | — | |
| Formic Acid SCHEMBL11557232 | 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 17100 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-119684285-A | Inhibition of cyclic AMP-responsive element binding proteins (CREB) | 福马治疗股份有限公司 | 2025-03-25 | — | — | CN | claimed |
| CN-118834124-B | Synthesis method of trans-2-octenal | 济南悟通生物科技有限公司 | 2024-11-26 | — | — | CN | claimed |
| CN-118834124-A | Synthesis method of trans-2-octenal | 济南悟通生物科技有限公司 | 2024-10-25 | — | — | CN | claimed |
| WO-2024150812-A1 | COMPOSITION FOR ELECTRODE FORMATION, ADDITIVE, AND GELATION INHIBITOR | 日産化学株式会社 | 2024-07-18 | — | — | WO | claimed |
| WO-2024150813-A1 | COMPOSITION FOR ELECTRODE FORMATION AND ADDITIVE | 日産化学株式会社 | 2024-07-18 | — | — | WO | claimed |
| WO-2024150450-A1 | COMPOSITION FOR ELECTRODE FORMATION, ADDITIVE, AND GELATION INHIBITOR | 日産化学株式会社 | 2024-07-18 | — | — | WO | claimed |
| WO-2024150446-A1 | COMPOSITION FOR ELECTRODE FORMATION | 日産化学株式会社 | 2024-07-18 | — | — | WO | claimed |
| WO-2024150479-A1 | COMPOSITION FOR ELECTRODE FORMATION, ADDITIVE, AND GELATION INHIBITOR | 日産化学株式会社 | 2024-07-18 | — | — | WO | claimed |
| US-12030774-B2 | Surface-modified inorganic nitride, composition, thermally conductive material, and device with thermally conductive layer | FUJIFILM CORPORATION (JP) | 2024-07-09 | — | — | US | claimed |
| WO-2024142035-A1 | PROCESS FOR THE PREPARATION OF BIGUANIDINES AND TRIAZINES | ADAMA AGAN LTD. (IL) | 2024-07-04 | — | — | WO | claimed |
| US-4104300-A | MOLYBDENUM CATALYST, COMPLEXING AGENT | DYNAMIT NOBEL AKTIENGESELLSCHAFT (DE) | 1978-08-01 | — | — | US | claimed |
| US-4080378-A | REACTING A CARBOXYLIC ACID ESTER WITH A TRICHLOROMETHYL SUBSTITUTED AROMATIC COMPOUND IN THE PRESENCE OF A MOLYBDENUM CATALYST | DYNAMIT NOBEL AKTIENGESELLSCHAFT (DT) | 1978-03-21 | — | — | US | claimed |
| US-4080377-A | Production of cyclic five-membered ring unsaturated phosphine dichlorides | BAYER AKTIENGESELLSCHAFT (DT) | 1978-03-21 | — | — | US | claimed |
| US-4069257-A | THERMAL DECOMPOSITION OF 2-METHYL-3-HYDROXYMETHYLPENT-1-ENE-4-ONE OR ESTER THEROF | BAYER AKTIENGESELLSCHAFT (DT) | 1978-01-17 | — | — | US | claimed |
| US-4058646-A | HIGH SURFACE HARDNESS | BASF AKTIENGESELLSCHAFT (DT) | 1977-11-15 | — | — | US | claimed |
| US-4048166-A | MICROBIOCIDES | THE DOW CHEMICAL COMPANY (US) | 1977-09-13 | — | — | US | claimed |
| US-4036877-A | Process for the production of aldehydes | BUDAPESTI MUSZAKI EGYETEM (HU) | 1977-07-19 | — | — | US | claimed |
| US-3962326-A | CARBOXYLIC ACID OR ANHYDRIDE, PHOSGENE, TRISUBSTITUTED PHOSPHINE OXIDE OR SULFIDE | HOECHST AKTIENGESELLSCHAFT (DT) | 1976-06-08 | — | — | US | claimed |
| US-3962344-A | Process for making 1,3-diene hydrocarbons | GIVAUDAN CORPORATION (US) | 1976-06-08 | — | — | US | claimed |
| US-3957815-A | 3-[3',4'-Dichloro-6'-alkyl-phenyl]-Δ2 -pyrazoline derivatives and their use as optical brighteners | HOECHST AKTIENGESELLSCHAFT (DT) | 1976-05-18 | — | — | US | claimed |