Known targets — ChEMBL curated mechanism
ABCC8ACEADORA1ADORA2AADORA2BADORA3ALDH5A1ALOX5ALOX5APATP4AATP4BBRAFCA1CA12CA2CA4CYSLTR1DHFRDPEP1EDNRAEDNRBESR2F10FDPSFGF1GABBR1GABBR2GABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGARTGNRHRGSC1HMGCRIMPDH1IMPDH2KCNJ11LY96NOD2NR3C1NS3NS4ANS5bP2RY1P2RY12P2RY2P2RY4P2RY6PBP2XPDE3APDE3BPDE4APDE4BPDE4CPDE4DPDK1PDK2PDK3PDK4PPARGPPATPTGIRPTGS1PTGS2RAF1RYR1RYR3SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASERPINC1SLC12A1SLC12A3SYKTHRATHRBTLR3TLR4TLR9TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TYMSVKORC1XDHblablaIMP-1blaOXA-33blaOXA-58blaT-3blaT-4blaT-5blaT-6dacAdacBdacCfolAfolPfolP1ftsIfusAgaggyrAgyrBmecAmrcAmrcBmrdApbp1apbp1bpbp2pbp2apbp2bpbp3pbp4pbpApbpBpbpCpbpFpolponBrplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpoArpoBrpoCrpoZrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO
The experimentally established mechanism targets of None. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.
Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | P2RY2 known ✓ | P41231 | 1/20 | 0.36 |
| ▸ | ALDH1A1 | P00352 | 4/20 | 0.53 |
| ▸ | HSD17B10 | Q99714 | 3/20 | 0.53 |
| ▸ | CASP6 | P55212 | 2/20 | 0.53 |
| ▸ | CYP2C9 | P11712 | 1/20 | 0.53 |
| ▸ | CYP2C19 | P33261 | 1/20 | 0.53 |
| ▸ | NT5E | P21589 | 4/20 | 0.43 |
| ▸ | SNCA | P37840 | 2/20 | 0.43 |
| ▸ | DUSP5 | Q16690 | 1/20 | 0.41 |
| ▸ | TSHR | P16473 | 2/20 | 0.40 |
| ▸ | SUMO2 | P61956 | 2/20 | 0.40 |
| ▸ | SUMO1 | P63165 | 2/20 | 0.40 |
| ▸ | SENP7 | Q9BQF6 | 2/20 | 0.40 |
| ▸ | SENP2 | Q9HC62 | 2/20 | 0.40 |
| ▸ | APEX1 | P27695 | 2/20 | 0.40 |
| ▸ | NSD2 | O96028 | 1/20 | 0.40 |
| ▸ | DUSP3 | P51452 | 1/20 | 0.40 |
| ▸ | PTPN5 | P54829 | 1/20 | 0.40 |
| ▸ | PTPN11 | Q06124 | 1/20 | 0.40 |
| ▸ | TDP1 | Q9NUW8 | 1/20 | 0.40 |
Click a target to see other patent compounds predicted against it — the reverse direction, in place.
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 | |
|---|---|---|---|---|
| SCHEMBL1755222 | 0.88 | ALDH1A1 (0.62) | ALDH1A1HSD17B10CASP6CYP2C9CYP2C19 | |
| SCHEMBL30389978 | 0.88 | DUSP5 (0.41) | ALDH1A1HSD17B10CASP6CYP2C9CYP2C19 | |
| SCHEMBL29624161 | 0.88 | ALDH1A1 (0.62) | ALDH1A1HSD17B10CASP6CYP2C9CYP2C19 | |
| SCHEMBL17976508 | 0.88 | DUSP5 (0.41) | ALDH1A1HSD17B10CASP6CYP2C9CYP2C19 | |
| SCHEMBL1146228 | 0.88 | ALDH1A1 (0.62) | ALDH1A1HSD17B10CASP6CYP2C9CYP2C19 | |
| SCHEMBL30639252 | 0.88 | ALDH1A1 (0.62) | ALDH1A1HSD17B10CASP6CYP2C9CYP2C19 | |
| SCHEMBL7651109 | 0.88 | ALDH1A1 (0.62) | ALDH1A1HSD17B10CASP6CYP2C9CYP2C19 | |
| SCHEMBL11598411 | 0.87 | ALDH1A1 (0.60) | ALDH1A1HSD17B10CASP6CYP2C9CYP2C19 | |
| SCHEMBL28071057 | 0.87 | ALDH1A1 (0.60) | ALDH1A1HSD17B10CASP6CYP2C9CYP2C19 | |
| SCHEMBL7692151 | 0.84 | ALDH1A1 (0.65) | ALDH1A1HSD17B10CASP6CYP2C9CYP2C19 |
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 17 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-116903874-A | Preparation method of cucurbituril rare earth supermolecule hydrogel | 南京信息工程大学 | 2023-10-20 | — | — | CN | claimed |
| CN-115738767-A | Chiral separation membrane with spiral pore channel | 天津工业大学 | 2023-03-07 | — | — | CN | claimed |
| US-5500668-A | INK JET PRINTING | XEROX CORPORATION (US) | 1996-03-19 | — | — | US | claimed |
| CN-116903874-A | Preparation method of cucurbituril rare earth supermolecule hydrogel | 南京信息工程大学 | 2023-10-20 | — | — | CN | disclosed |
| CN-116903874-A | Preparation method of cucurbituril rare earth supermolecule hydrogel | 南京信息工程大学 | 2023-10-20 | — | — | CN | disclosed |
| WO-2023190598-A1 | COMPOSITION | アース製薬株式会社 | 2023-10-05 | — | — | WO | disclosed |
| CN-116322332-A | Antipathogenic agent, antibacterial agent, antiviral agent, pathogen treatment device, method for producing antipathogenic agent, antibacterial method, virus inactivation method, and pathogen treatment method | 株式会社ACENET | 2023-06-23 | — | — | CN | disclosed |
| CN-115738767-A | Chiral separation membrane with spiral pore channel | 天津工业大学 | 2023-03-07 | — | — | CN | disclosed |
| CN-114501996-A | Chemical, method for producing chemical, and method for purifying water | 株式会社ACENET | 2022-05-13 | — | — | CN | disclosed |
| WO-2022075451-A1 | ANTIPATHOGENIC DRUG, ANTIBACTERIAL AGENT, ANTIVIRAL AGENT, PATHOGEN PROCESSING DEVICE, METHOD FOR PRODUCING ANTIPATHOGENIC DRUG, ANTIBACTERIAL METHOD, VIRUS INACTIVATION METHOD, AND PATHOGEN PROCESSING METHOD | 株式会社エースネット | 2022-04-14 | — | — | WO | disclosed |
| CN-110769931-A | Catalyst for generating free radical, method for producing oxidation reaction product, chemical, and chemical for agricultural and livestock use | 株式会社ACENET | 2020-02-07 | — | — | CN | disclosed |
| US-6350795-B1 | ACOUSTIC PHASE-CHANGE CONDUCTIVE INK CONTAINING LOW MOLECULAR WEIGHT OXYALKYLENE SEGMENTS COMPLEXED WITH UREA DERIVATIVES | XEROX CORPORATION | 2002-02-26 | — | — | US | disclosed |
| US-6096125-A | Ink compositions | XEROX CORPORATION (US) | 2000-08-01 | — | — | US | disclosed |
| EP-0388356-B1 | Ultraviolet absorbing lenses and methods of making the same | CIBA GEIGY AG (CH) | 1998-07-08 | — | — | EP | disclosed |
| US-5500668-A | INK JET PRINTING | XEROX CORPORATION (US) | 1996-03-19 | — | — | US | disclosed |
| EP-0388356-A2 | Ultraviolet absorbing lenses and methods of making the same | CIBA-GEIGY AG (CH) | 1990-09-19 | — | — | EP | disclosed |
| US-4129591-A | INHIBITORS OF THE COMPLEMENT SYSTEM | AMERICAN CYANAMID COMPANY (US) | 1978-12-12 | — | — | US | disclosed |