Known targets — ChEMBL curated mechanism
ABCC9ABL1ACEACHEACVR1ADORA1ADORA2AADORA2BADORA3ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALOX5ATP4AATP4BBCRBTKCACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNB1CHRNDCHRNECHRNGCRBNCUL4ACXCR1CXCR2DDB1DDCDHFRDPP4DRD2DRD3DRD4EGFRERBB2ERBB4ESR1ESR2FDPSFKBP1AFLT1FLT3FLT4GARTGHSRGRIA1GRIA2GRIA3GRIA4GRIK1GRIK2GRIK3GRIK4GRIK5GRIN2AGSK3AGSK3BHDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IDH1IDH2IMPA1ITGA2BITGB3JAK1JAK2JAK3KCNJ11KCNK3KCNK9KDRKITMEN1METMMP1MMP13MMP7MMP8NANOD2NS5bODC1OPG057OPRD1OPRK1OPRM1PPARP1PARP2PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDGFRBPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PKLRPPARDPPATPTGS1PTGS2RBX1ROCK1ROCK2RRM1RRM2RRM2BSCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC10A2SLC5A2SLC6A2SLC6A3SLC6A4SLC9A3SYKTACR1THRATHRBTOP1TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TYK2TYMSVDRampCblablaT-3blaT-4blaT-5blaT-6blaUOE-1dacAdacBdacCfolAfolPftsIgyrAgyrBileSmecAmrcAmrcBmrdAparCparEpbp2pbp4pbpApbpFrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUthyAykgMykgO
The experimentally established mechanism targets of Allylamine. 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 | |
|---|---|---|---|---|
| Allylamine SCHEMBL8858077 | 1.00 | ALDH1A1 (0.90) | — | |
| Allylamine SCHEMBL8858079 | 1.00 | ALDH1A1 (0.90) | — | |
| Allylamine SCHEMBL1115529 | 1.00 | — | — | |
| Allylamine SCHEMBL28169112 | 0.95 | — | — | |
| Allylamine SCHEMBL28859167 | 0.95 | — | — | |
| Allylamine SCHEMBL27403991 | 0.95 | — | — | |
| Allylamine SCHEMBL6032547 | 0.95 | — | — | |
| Allylamine SCHEMBL15197 | 0.95 | — | — | |
| Allylamine SCHEMBL11373125 | 0.90 | — | — | |
| Allylamine SCHEMBL5891273 | 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
Appears in 2864 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 |
|---|---|---|---|---|---|---|---|
| US-12044974-B2 | Compositions for removing photoresists and methods of manufacturing semiconductor devices and semiconductor packages using the compositions | SAMSUNG ELECTRONICS CO., LTD. (KR) | 2024-07-23 | — | — | US | claimed |
| CN-118315595-A | Wide-temperature nickel-hydrogen battery negative electrode material and preparation method thereof | 深圳市量能科技有限公司 | 2024-07-09 | — | — | CN | claimed |
| US-12023657-B2 | Desilicated ZSM-5 catalysts for xylene isomerization | INEOS US CHEMICALS COMPANY (US) | 2024-07-02 | — | — | US | claimed |
| CN-115709077-B | Method for preparing 5-methyl-N-substituted pyrrolidone compound | 中国科学院广州能源研究所 | 2024-06-28 | — | — | CN | claimed |
| CN-118165301-A | Cellulose mild dissolution method, fiber solution and application thereof | 华南理工大学 | 2024-06-11 | — | — | CN | claimed |
| EP-4377294-A1 | PROCESS FOR PREPARING (2,2,2-TRIFLUOROETHYL)SULFANYLANILINE DERIVATIVES | Bayer Aktiengesellschaft (DE) | 2024-06-05 | — | — | EP | claimed |
| CN-118139607-A | Silane hydrolysates and methods of making and using the same | 陶氏环球技术有限责任公司 | 2024-06-04 | — | — | CN | claimed |
| CN-115106122-B | Preparation method and application of molecular sieve catalyst | 中国科学院大连化学物理研究所 | 2024-06-04 | — | — | CN | claimed |
| CN-118064127-A | Quantum dot, preparation method thereof and light-emitting device | 广东聚华新型显示研究院 | 2024-05-24 | — | — | CN | claimed |
| CN-113165885-B | Aqueous silica dispersion with long pot life for refractory glass | 赢创运营有限公司 | 2024-05-14 | — | — | CN | claimed |
| EP-0184787-A2 | Cyanide-free hemoglobin reagent | TECHNICON INSTRUMENTS CORPORATION(a Delaware corporation) (US) | 1986-06-18 | — | — | EP | claimed |
| EP-0077202-B1 | PROCESS FOR HYDROXYLATING OLEFINS USING OSMIUM-HALOGEN COMPOUND CATALYSTS | EXXON RESEARCH AND ENGINEERING COMPANY (US) | 1986-04-09 | — | — | EP | claimed |
| US-4578286-A | Electrically conductive coating composition of a chlorosulfonated polyethylene | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 1986-03-25 | — | — | US | claimed |
| EP-0174725-A1 | Chlorosulfonated ethylene vinyl acetate polymer coating composition | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 1986-03-19 | — | — | EP | claimed |
| US-4572870-A | INCLUDING AN EPOXIDE, POLYAMINE AND AMIDINE; PRIMERS AND PROTECTIVE COATINGS FOR LARGE METAL SUBSTRATES | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 1986-02-25 | — | — | US | claimed |
| EP-0161736-A1 | Chlorosulfonated polyethylene coating composition | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 1985-11-21 | — | — | EP | claimed |
| EP-0022113-B1 | PROCESS FOR ELECTROFORMING OBJECTS STARTING FROM A BATH CONTAINING SUSPENDED PARTICLES | ANDROMAQUE S.A. (LU) | 1984-07-25 | — | — | EP | claimed |
| US-4338230-A | POLISHES, SIZING, FRUIT COATINGS | EASTMAN KODAK COMPANY (US) | 1982-07-06 | — | — | US | claimed |
| US-4159287-A | GRAFT POLYMER WITH POLYPIVALOLACTONE | EASTMAN KODAK COMPANY (US) | 1979-06-26 | — | — | US | claimed |
| US-4039371-A | TETRAALKYL AMMONIUM HYDROXIDE, ACETIC, TARTARIC AND OXALIC ACIDS N | INTERNATIONAL BUSINESS MACHINES CORPORATION (US) | 1977-08-02 | — | — | US | claimed |