Known targets — ChEMBL curated mechanism
ABCC9ABL1ACEACHEACVR1ADORA1ADORA2AADORA2BADORA3ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALOX5ATP4AATP4BBCRBTKCACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNB1CHRNDCHRNECHRNGCRBNCUL4ACXCR1CXCR2DDB1DDCDHFRDPP4DRD2DRD3DRD4EGFRERBB2ERBB4ESR1ESR2FDPSFKBP1AFLT1FLT3FLT4GARTGHSRGRIA1GRIA2GRIA3GRIA4GRIK1GRIK2GRIK3GRIK4GRIK5GRIN2AGSK3AGSK3BHDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IDH1IDH2IMPA1ITGA2BITGB3JAK1JAK2JAK3KCNJ11KCNK3KCNK9KDRKITMEN1METMMP1MMP13MMP7MMP8NANOD2NS5bODC1OPG057OPRD1OPRK1OPRM1PPARP1PARP2PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDGFRBPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PKLRPPARDPPATPTGS1PTGS2RBX1ROCK1ROCK2RRM1RRM2RRM2BSCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC10A2SLC5A2SLC6A2SLC6A3SLC6A4SLC9A3SYKTACR1THRATHRBTOP1TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TYK2TYMSVDRampCblablaT-3blaT-4blaT-5blaT-6blaUOE-1dacAdacBdacCfolAfolPftsIgyrAgyrBileSmecAmrcAmrcBmrdAparCparEpbp2pbp4pbpApbpFrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUthyAykgMykgO
The experimentally established mechanism targets of Water. 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 | |
|---|---|---|---|---|
| Water SCHEMBL1542414 | 1.00 | CHRNA7 (0.32) | — | |
| SCHEMBL18960 | 0.96 | — | — | |
| SCHEMBL538360 | 0.92 | — | — | |
| Hydrochloric Acid SCHEMBL353996 | 0.92 | — | — | |
| Fluoride SCHEMBL8813655 | 0.92 | — | — | |
| Fluoride SCHEMBL2112417 | 0.92 | CHRNA7 (0.32) | — | |
| Iodide SCHEMBL3277614 | 0.92 | — | — | |
| SCHEMBL9232705 | 0.92 | — | — | |
| Charcoal, Activated SCHEMBL230089 | 0.92 | — | — | |
| SCHEMBL6735678 | 0.92 | — | — |
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 40 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-4559918-A2 | GLUCOSYLCERAMIDE SYNTHASE INHIBITORS | Genzyme Corporation (US) | 2025-05-28 | — | — | EP | disclosed |
| EP-3673906-B1 | GLUCOSYLCERAMIDE SYNTHASE INHIBITORS | GENZYME CORP (US) | 2025-05-14 | — | — | EP | disclosed |
| CN-117679415-A | Glucoamide synthase inhibitors | 建新公司 | 2024-03-12 | — | — | CN | disclosed |
| US-20220409595-A1 | GLUCOSYLCERAMIDE SYNTHASE INHIBITORS | GENZYME CORPORATION | 2022-12-29 | — | — | US | disclosed |
| CN-108290747-B | Synthesis of molecular sieve SSZ-105 | 雪佛龙美国公司 | 2021-06-11 | — | — | CN | disclosed |
| EP-3079695-B1 | GLUCOSYLCERAMIDE SYNTHASE INHIBITORS | GENZYME CORP (US) | 2021-03-17 | — | — | EP | disclosed |
| CN-107080747-B | Glucosylceramide synthase inhibitors | 建新公司 | 2021-02-26 | — | — | CN | disclosed |
| EP-3673906-A1 | GLUCOSYLCERAMIDE SYNTHASE INHIBITORS | Genzyme Corporation (US) | 2020-07-01 | — | — | EP | disclosed |
| EP-3386918-B1 | SYNTHESIS OF MOLECULAR SIEVE SSZ-105 | CHEVRON USA INC (US) | 2020-03-11 | — | — | EP | disclosed |
| US-20200048266-A1 | GLUCOSYLCERAMIDE SYNTHASE INHIBITORS | GENZYME CORP (US) | 2020-02-13 | — | — | US | disclosed |
| WO-2014007874-A1 | METHOD FOR PREPARING HIGH-SILICA LEV-TYPE ZEOLITES | CHEVRON U.S.A. INC. (US) | 2014-01-09 | — | — | WO | disclosed |
| CN-102928527-A | Method for measuring optical purity of R-3-quinuclidine alcohol | DISHA PHARMACEUTICAL GROUP CO | 2013-02-13 | — | — | CN | disclosed |
| WO-2012129084-A2 | GLUCOSYLCERAMIDE SYNTHASE INHIBITORS | GENZYME CORPORATION (US) | 2012-09-27 | — | — | WO | disclosed |
| US-7208137-B2 | Maintaining reaction mixture comprising zeolite which is an active source of aluminum oxide, active source of alkali metal oxide, an active source of an oxide of a tetravalent element, and an organic template under condition to form crystals | CHEVRON U.S.A. INC. (US) | 2007-04-24 | — | — | US | disclosed |
| US-20050135999-A1 | Aluminum-containing zeolite with IFR structure | CHEVRON U.S.A. INC. | 2005-06-23 | — | — | US | disclosed |
| US-6821502-B2 | MAINTAINING REACTION MIXTURE COMPRISING ZEOLITE WHICH IS AN ACTIVE SOURCE OF ALUMINUM OXIDE, ACTIVE SOURCE OF ALKALI METAL OXIDE, AN ACTIVE SOURCE OF AN OXIDE OF A TETRAVALENT ELEMENT, AND AN ORGANIC TEMPLATE UNDER CONDITION TO FORM CRYSTALS | CHEVRON U.S.A. INC. | 2004-11-23 | — | — | US | disclosed |
| WO-2004041722-A2 | METHOD OF MAKING ALUMINUM-CONTAINING ZEOLITE WITH IFR STRUCTURE | CHEVRON U.S.A. INC. (US) | 2004-05-21 | — | — | WO | disclosed |
| US-20030232007-A1 | Method of making aluminum-containing zeolite with IFR structure | CHEVRON U.S.A., INC. | 2003-12-18 | — | — | US | disclosed |
| EP-0345330-A1 | PROCESSES FOR THE PRODUCTION OF AMINES | UNION CARBIDE CORPORATION (US) | 1989-12-13 | — | — | EP | disclosed |
| WO-1989005810-A1 | PROCESSES FOR THE PRODUCTION OF AMINES | UNION CARBIDE CORPORATION (US) | 1989-06-29 | — | — | WO | disclosed |