Known targets — ChEMBL curated mechanism
ABCC9ABL1ACEACHEACVR1ADORA1ADORA2AADORA2BADORA3ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALOX5ATP4AATP4BBCRBTKCACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNB1CHRNDCHRNECHRNGCRBNCUL4ACXCR1CXCR2DDB1DDCDHFRDPP4DRD2DRD3DRD4EGFRERBB2ERBB4ESR1ESR2FDPSFKBP1AFLT1FLT3FLT4GARTGHSRGRIA1GRIA2GRIA3GRIA4GRIK1GRIK2GRIK3GRIK4GRIK5GRIN2AGSK3AGSK3BHDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IDH1IDH2IMPA1ITGA2BITGB3JAK1JAK2JAK3KCNJ11KCNK3KCNK9KDRKITMEN1METMMP1MMP13MMP7MMP8NANOD2NS5bODC1OPG057OPRD1OPRK1OPRM1PPARP1PARP2PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDGFRBPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PKLRPPARDPPATPTGS1PTGS2RBX1ROCK1ROCK2RRM1RRM2RRM2BSCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC10A2SLC5A2SLC6A2SLC6A3SLC6A4SLC9A3SYKTACR1THRATHRBTOP1TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TYK2TYMSVDRampCblablaT-3blaT-4blaT-5blaT-6blaUOE-1dacAdacBdacCfolAfolPftsIgyrAgyrBileSmecAmrcAmrcBmrdAparCparEpbp2pbp4pbpApbpFrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUthyAykgMykgO
The experimentally established mechanism targets of Propionic 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 | |
|---|---|---|---|---|
| Propionic Acid SCHEMBL2355573 | 1.00 | FFAR3 (0.91) | — | |
| Propionic Acid SCHEMBL29270980 | 1.00 | FFAR3 (0.91) | — | |
| Propionic Acid SCHEMBL906440 | 1.00 | — | — | |
| Propionic Acid SCHEMBL27762967 | 1.00 | FFAR3 (0.91) | — | |
| Propionic Acid SCHEMBL2232000 | 1.00 | FFAR3 (0.91) | — | |
| Propionic Acid SCHEMBL1533412 | 1.00 | — | — | |
| Propionic Acid SCHEMBL27968417 | 1.00 | — | — | |
| Propionic Acid SCHEMBL8037205 | 0.96 | — | — | |
| Propionic Acid SCHEMBL15428841 | 0.96 | FFAR3 (0.83) | — | |
| Propionic Acid SCHEMBL6466570 | 0.96 | — | — |
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 12 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-10596259-B2 | Tumor radiosensitization with monomethyl auristatin E (MMAE) and derivatives thereof | THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) | 2020-03-24 | — | — | US | disclosed |
| US-20180140703-A1 | TUMOR RADIOSENSITIZATION WITH ANTIBODY CONJUGATES | THE REGENTS OF THE UNIVERSITY OF CALIFORNIA | 2018-05-24 | — | — | US | disclosed |
| WO-2014120837-A9 | PRETARGETED ACTIVATABLE CELL PENETRATING PEPTIDE WITH INTRACELLULARY RELEASEABLE PRODRUG | THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) | 2015-03-26 | — | — | WO | disclosed |
| WO-2014120837-A2 | PRETARGETED ACTIVATABLE CELL PENETRATING PEPTIDE WITH INTRACELLULARY RELEASEABLE PRODRUG | THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) | 2014-08-07 | — | — | WO | disclosed |
| EP-1674444-B9 | METHOD FOR PRODUCING ESTER CONDENSED PRODUCT | JAPAN SCIENCE & TECH AGENCY (JP) | 2013-11-20 | — | — | EP | disclosed |
| EP-1674444-B1 | METHOD FOR PRODUCING ESTER CONDENSED PRODUCT | JAPAN SCIENCE & TECH AGENCY (JP) | 2013-07-17 | — | — | EP | disclosed |
| US-7973193-B2 | Method for producing ester condensed product | JAPAN SCIENCE AND TECHNOLOGY AGENCY (JP) | 2011-07-05 | — | — | US | disclosed |
| US-20090187042-A1 | METHOD FOR PRODUCING ESTER CONDENSED PRODUCT | JAPAN SCIENCE AND TECHNOLOGY AGENCY (JP) | 2009-07-23 | — | — | US | disclosed |
| US-20070004936-A1 | Method for producing ester condensed product | JAPAN SCIENCE AND TECHNOLOGY AGENCY (JP) | 2007-01-04 | — | — | US | disclosed |
| EP-1674444-A1 | METHOD FOR PRODUCING ESTER CONDENSED PRODUCT | Japan Science and Technology Agency (JP) | 2006-06-28 | — | — | EP | disclosed |
| US-4831060-A | MOLYBDENUM, IRON, FISCHER-TROPSCH PROMOTER, SULFIDED | THE DOW CHEMICAL COMPANY (US) | 1989-05-16 | — | — | US | disclosed |
| US-4752623-A | USING MOLEBDENUM OR TUNGSTEN CATALYST COBALT OR NICKEL COCATALYST AND A PROMOTER | THE DOW CHEMICAL COMPANY (US) | 1988-06-21 | — | — | US | disclosed |