Known targets — ChEMBL curated mechanism
ABCC9ABL1ACEACHEACVR1ADORA1ADORA2AADORA2BADORA3ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALOX5ATP4AATP4BBCRBTKCACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNB1CHRNDCHRNECHRNGCRBNCUL4ACXCR1CXCR2DDB1DDCDHFRDPP4DRD2DRD3DRD4EGFRERBB2ERBB4ESR1ESR2FDPSFKBP1AFLT1FLT3FLT4GARTGHSRGRIA1GRIA2GRIA3GRIA4GRIK1GRIK2GRIK3GRIK4GRIK5GRIN2AGSK3AGSK3BHDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IDH1IDH2IMPA1ITGA2BITGB3JAK1JAK2JAK3KCNJ11KCNK3KCNK9KDRKITMEN1METMMP1MMP13MMP7MMP8NANOD2NS5bODC1OPG057OPRD1OPRK1OPRM1PPARP1PARP2PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDGFRBPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PKLRPPARDPPATPTGS1PTGS2RBX1ROCK1ROCK2RRM1RRM2RRM2BSCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC10A2SLC5A2SLC6A2SLC6A3SLC6A4SLC9A3SYKTACR1THRATHRBTOP1TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TYK2TYMSVDRampCblablaT-3blaT-4blaT-5blaT-6blaUOE-1dacAdacBdacCfolAfolPftsIgyrAgyrBileSmecAmrcAmrcBmrdAparCparEpbp2pbp4pbpApbpFrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUthyAykgMykgO
The experimentally established mechanism targets of Propene. 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 | |
|---|---|---|---|---|
| Propene SCHEMBL27447062 | 1.00 | — | — | |
| Propene SCHEMBL768893 | 1.00 | — | — | |
| Propene SCHEMBL28086077 | 0.94 | — | — | |
| Propene SCHEMBL14765283 | 0.94 | — | — | |
| Propene SCHEMBL28310360 | 0.94 | — | — | |
| Propene SCHEMBL11195626 | 0.94 | — | — | |
| Propene SCHEMBL14786292 | 0.94 | — | — | |
| Propene SCHEMBL10948784 | 0.94 | ALDH1A1 (0.31) | — | |
| Propene SCHEMBL22660951 | 0.94 | ALDH1A1 (0.31) | — | |
| Propene SCHEMBL28126328 | 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
Claimed or disclosed in 48 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-105418892-A | UV-curing halogen-free flame-retardant low-shrinkage epoxy resin composition and preparation method thereof | UNIV SOUTH CHINA TECH | 2016-03-23 | — | — | CN | claimed |
| CN-101622277-B | Conjugated diene-based polymer, method for producing same, and conjugated diene polymer composition | SUMITOMO CO LTD | 2012-06-20 | — | — | CN | claimed |
| EP-1311578-A1 | SPANDEX HAVING LOW SET AT LOW TEMPERATURES | DU PONT-TORAY COMPANY, LTD. (JP) | 2003-05-21 | — | — | EP | claimed |
| EP-1285022-A1 | COMPOSITIONS CONTAINING ELASTOMERIC ETHYLENE OR (METH)ACRYLIC ESTER COPOLYMERS | E.I. DUPONT DE NEMOURS AND COMPANY (US) | 2003-02-26 | — | — | EP | claimed |
| WO-2001088020-A1 | COMPOSITIONS CONTAINING ELASTOMERIC ETHYLENE OR (METH)ACRYLIC ESTER COPOLYMERS | E.I. DUPONT DE NEMOURS AND COMPANY (US) | 2001-11-22 | — | — | WO | claimed |
| EP-0912479-B1 | PROCESS FOR THE MANUFACTURE OF ALPHA-HYDROXYCARBONYL COMPOUNDS | EXXONMOBIL CHEM PATENTS INC (US) | 2001-07-25 | — | — | EP | claimed |
| WO-2001040345-A1 | SPANDEX HAVING LOW SET AT LOW TEMPERATURES | DU PONT-TORAY COMPANY, LTD. (JP) | 2001-06-07 | — | — | WO | claimed |
| US-6191308-B1 | ALPHA-HYDROXYCARBONYL COMPOUNDS ARE OBTAINED FROM ALDEHYDES OR KETONES BY FORMING AN ACETAL OR KETAL WHICH IS DECOMPOSED TO A VINYL ETHER, WHICH IS SELECTIVELY OXIDIZED YIELDING AN ALPHA-HYDROXY-ALDEHYDE OR KETONE | EXXON CHEMICAL PATENTS INC. | 2001-02-20 | — | — | US | claimed |
| EP-0912479-A1 | PROCESS FOR THE MANUFACTURE OF OXYGENATES | EXXON CHEMICAL PATENTS INC. (US) | 1999-05-06 | — | — | EP | claimed |
| WO-1997041086-A1 | PROCESS FOR THE MANUFACTURE OF OXYGENATES | EXXON CHEMICAL PATENTS INC. (US) | 1997-11-06 | — | — | WO | claimed |
| CN-109476573-A | The method for being used to prepare the solvent derived from the chloro- 3,3,3- trifluoro propene (1233zd) of 1- | 霍尼韦尔国际公司 | 2019-03-15 | — | — | CN | disclosed |
| CN-107406396-A | CATIONIC LIPID | 日油株式会社 | 2017-11-28 | — | — | CN | disclosed |
| CN-104546544-B | Nail enamel composition | 施乐公司 | 2017-10-03 | — | — | CN | disclosed |
| CN-105418892-A | UV-curing halogen-free flame-retardant low-shrinkage epoxy resin composition and preparation method thereof | UNIV SOUTH CHINA TECH | 2016-03-23 | — | — | CN | disclosed |
| CN-104546544-A | NAIL POLISH COMPOSITIONS | XEROX CORP | 2015-04-29 | — | — | CN | disclosed |
| EP-0900186-A1 | PROCESS FOR THE MANUFACTURE OF HYDROXYCARBONYL COMPOUNDS | EXXON CHEMICAL PATENTS, INC. (US) | 1999-03-10 | — | — | EP | disclosed |
| WO-1997041086-A1 | PROCESS FOR THE MANUFACTURE OF OXYGENATES | EXXON CHEMICAL PATENTS INC. (US) | 1997-11-06 | — | — | WO | disclosed |
| WO-1997041087-A1 | PROCESS FOR THE MANUFACTURE OF HYDROXYCARBONYL COMPOUNDS | EXXON CHEMICAL PATENTS INC. (US) | 1997-11-06 | — | — | WO | disclosed |
| WO-1997041087-A1 | PROCESS FOR THE MANUFACTURE OF HYDROXYCARBONYL COMPOUNDS | EXXON CHEMICAL PATENTS INC. (US) | 1997-11-06 | — | — | WO | disclosed |
| US-4239879-A | USED AS DECORATIVE AND PROTECTIVE COATINGS, IN FOOTWEAR AND AUTOMOBILES | THE GENERAL TIRE & RUBBER COMPANY (US) | 1980-12-16 | — | — | US | disclosed |