Known targets — ChEMBL curated mechanism
ABCC9ABL1ACEACHEACVR1ADORA1ADORA2AADORA2BADORA3ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALOX5ATP4AATP4BBCRBTKCACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNB1CHRNDCHRNECHRNGCRBNCUL4ACXCR1CXCR2DDB1DDCDHFRDPP4DRD2DRD3DRD4EGFRERBB2ERBB4ESR1ESR2FDPSFKBP1AFLT1FLT3FLT4GARTGHSRGRIA1GRIA2GRIA3GRIA4GRIK1GRIK2GRIK3GRIK4GRIK5GRIN2AGSK3AGSK3BHDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IDH1IDH2IMPA1ITGA2BITGB3JAK1JAK2JAK3KCNJ11KCNK3KCNK9KDRKITMEN1METMMP1MMP13MMP7MMP8NANOD2NS5bODC1OPG057OPRD1OPRK1OPRM1PPARP1PARP2PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDGFRBPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PKLRPPARDPPATPTGS1PTGS2RBX1ROCK1ROCK2RRM1RRM2RRM2BSCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC10A2SLC5A2SLC6A2SLC6A3SLC6A4SLC9A3SYKTACR1THRATHRBTOP1TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TYK2TYMSVDRampCblablaT-3blaT-4blaT-5blaT-6blaUOE-1dacAdacBdacCfolAfolPftsIgyrAgyrBileSmecAmrcAmrcBmrdAparCparEpbp2pbp4pbpApbpFrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUthyAykgMykgO
The experimentally established mechanism targets of 2-Ethoxyethanol. 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 | |
|---|---|---|---|---|
| 2-Ethoxyethanol SCHEMBL28220903 | 0.97 | — | — | |
| 2-Ethoxyethanol SCHEMBL10343650 | 0.97 | ALDH1A1 (0.88) | — | |
| 2-Ethoxyethanol SCHEMBL11024472 | 0.97 | ALDH1A1 (1.00) | — | |
| 2-Ethoxyethanol SCHEMBL9432157 | 0.97 | ALDH1A1 (1.00) | — | |
| 2-Ethoxyethanol SCHEMBL4686 | 0.97 | — | — | |
| 2-Ethoxyethanol SCHEMBL9547497 | 0.97 | ALDH1A1 (1.00) | — | |
| Diethylene Glycol Monoethyl Ether SCHEMBL29378907 | 0.94 | ALDH1A1 (0.82) | — | |
| Diethylene Glycol Monoethyl Ether SCHEMBL5187865 | 0.94 | ALDH1A1 (0.82) | — | |
| Water SCHEMBL31282314 | 0.94 | ALDH1A1 (0.82) | — | |
| 2-Ethoxyethanol SCHEMBL8056895 | 0.93 | ALDH1A1 (0.93) | — |
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 186 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-117486942-A | Near infrared light excited iridium complex, preparation method thereof and application thereof in resisting breast cancer | 中山大学 | 2024-02-02 | — | — | CN | claimed |
| CN-117186159-A | Self-reporting photosensitizer and preparation method and application thereof | 陕西师范大学 | 2023-12-08 | — | — | CN | claimed |
| CN-117186159-B | Self-reporting photosensitizer and preparation method and application thereof | 陕西师范大学 | 2026-01-06 | — | — | CN | disclosed |
| EP-4472386-A2 | ORGANIC ELECTROLUMINESCENT MATERIALS AND DEVICES | Universal Display Corporation (US) | 2024-12-04 | — | — | EP | disclosed |
| US-12059468-B2 | Carbohydrate conjugates as delivery agents for oligonucleotides | ALNYLAM PHARMACEUTICALS, INC. (US) | 2024-08-13 | — | — | US | disclosed |
| EP-3816175-B1 | ORGANIC ELECTROLUMINESCENT MATERIALS AND DEVICES | UNIVERSAL DISPLAY CORP (US) | 2024-07-17 | — | — | EP | disclosed |
| US-11985888-B2 | Organic electroluminescent device | THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) | 2024-05-14 | — | — | US | disclosed |
| EP-4321177-A2 | CARBOHYDRATE CONJUGATES AS DELIVERY AGENTS FOR OLIGONUCLEOTIDES | Alnylam Pharmaceuticals, Inc. (US) | 2024-02-14 | — | — | EP | disclosed |
| CN-117486942-A | Near infrared light excited iridium complex, preparation method thereof and application thereof in resisting breast cancer | 中山大学 | 2024-02-02 | — | — | CN | disclosed |
| CN-117186159-A | Self-reporting photosensitizer and preparation method and application thereof | 陕西师范大学 | 2023-12-08 | — | — | CN | disclosed |
| CN-117186159-A | Self-reporting photosensitizer and preparation method and application thereof | 陕西师范大学 | 2023-12-08 | — | — | CN | disclosed |
| WO-1998029098-A1 | PROCESSES FOR SPRAY DRYING AQUEOUS SUSPENSIONS OF HYDROPHOBIC DRUGS WITH HYDROPHILIC EXCIPIENTS AND COMPOSITIONS PREPARED BY SUCH PROCESSES | INHALE THERAPEUTIC SYSTEMS, INC. (US) | 1998-07-09 | — | — | WO | disclosed |
| WO-1998029140-A1 | PROCESSES AND COMPOSITIONS FOR SPRAY DRYING HYDROPHOBIC DRUGS IN ORGANIC SOLVENT SUSPENSIONS OF HYDROPHILIC EXCIPIENTS | INHALE THERAPEUTIC SYSTEMS (US) | 1998-07-09 | — | — | WO | disclosed |
| EP-0369864-B1 | Process for producing aromatic amines | SUMITOMO CHEMICAL CO (JP) | 1994-03-09 | — | — | EP | disclosed |
| US-5087755-A | Using a carbon monoxide/water system in the presence of a rhodium compound catalyst and an alkali solution | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1992-02-11 | — | — | US | disclosed |
| EP-0216047-B1 | PROCESS FOR PRODUCING ORGANOPHILIC SILICA | THE SHERWIN-WILLIAMS COMPANY (US) | 1990-05-02 | — | — | EP | disclosed |
| US-4530837-A | Containing tryptophan | COMMISSARIAT A L'ENERGIE ATOMIQUE (FR) | 1985-07-23 | — | — | US | disclosed |
| US-4460488-A | DECOLDRING, SHAMPOO | SOCIETE ANONYME DITE: L'OREAL (FR) | 1984-07-17 | — | — | US | disclosed |
| US-4393175-A | CROSSLINKING INHIBITION | DYNAPOL (US) | 1983-07-12 | — | — | US | disclosed |
| US-4358286-A | Cosmetic hair dye composition based on a powder of vegetable origin | L'OREAL (FR) | 1982-11-09 | — | — | US | disclosed |