Known targets — ChEMBL curated mechanism
ABCC8ACEADORA1ADORA2AADORA2BADORA3ALDH5A1ALOX5ALOX5APATP4AATP4BBRAFCA1CA12CA2CA4CYSLTR1DHFRDPEP1EDNRAEDNRBESR2F10FDPSFGF1GABBR1GABBR2GABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGARTGNRHRGSC1HMGCRIMPDH1IMPDH2KCNJ11LY96NOD2NR3C1NS3NS4ANS5bP2RY1P2RY12P2RY2P2RY4P2RY6PBP2XPDE3APDE3BPDE4APDE4BPDE4CPDE4DPDK1PDK2PDK3PDK4PPARGPPATPTGIRPTGS1PTGS2RAF1RYR1RYR3SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASERPINC1SLC12A1SLC12A3SYKTHRATHRBTLR3TLR4TLR9TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TYMSVKORC1XDHblablaIMP-1blaOXA-33blaOXA-58blaT-3blaT-4blaT-5blaT-6dacAdacBdacCfolAfolPfolP1ftsIfusAgaggyrAgyrBmecAmrcAmrcBmrdApbp1apbp1bpbp2pbp2apbp2bpbp3pbp4pbpApbpBpbpCpbpFpolponBrplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpoArpoBrpoCrpoZrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO
The experimentally established mechanism targets of Tert-Butyl Hydroperoxide. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.
Predicted protein targets (top 1)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | ALDH1A1 | P00352 | 1/20 | 0.56 |
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 | |
|---|---|---|---|---|
| Tert-Butyl Hydroperoxide SCHEMBL18421283 | 1.00 | ALDH1A1 (0.56) | ALDH1A1 | |
| Tert-Butyl Hydroperoxide SCHEMBL2874259 | 0.97 | ALDH1A1 (0.53) | ALDH1A1 | |
| Tert-Butyl Hydroperoxide SCHEMBL29031648 | 0.94 | ALDH1A1 (0.50) | ALDH1A1 | |
| Tert-Butyl Hydroperoxide SCHEMBL28130538 | 0.91 | ALDH1A1 (0.53) | ALDH1A1 | |
| Tert-Butyl Hydroperoxide SCHEMBL28340455 | 0.91 | ALDH1A1 (0.53) | ALDH1A1 | |
| Tert-Butyl Hydroperoxide SCHEMBL29902458 | 0.86 | ALDH1A1 (0.47) | ALDH1A1 | |
| Tert-Butyl Hydroperoxide SCHEMBL539430 | 0.84 | ALDH1A1 (0.45) | ALDH1A1 | |
| Metasulfurous Acid SCHEMBL9466790 | 0.82 | ALDH1A1 (0.43) | ALDH1A1 | |
| Tert-Butyl Hydroperoxide SCHEMBL1767577 | 0.80 | ALDH1A1 (0.64) | ALDH1A1 | |
| Tert-Butyl Hydroperoxide SCHEMBL29046154 | 0.78 | ALDH1A1 (0.60) | ALDH1A1 |
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 71 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-109401693-B | Alkyd resin modified polymer electrolyte and preparation method and application thereof | 清华大学深圳研究生院 | 2020-06-26 | — | — | CN | claimed |
| CN-106009004-A | Multiple composite crosslinked acrylic resin emulsion and preparation method thereof | 广东盛方化工有限公司 | 2016-10-12 | — | — | CN | claimed |
| US-11739167-B2 | Process for producing aqueous polyacrylamide solutions | BASF SE (DE) | 2023-08-29 | — | — | US | disclosed |
| US-11643491-B2 | Process for producing an aqueous polyacrylamide concentrate | BASF SE (DE) | 2023-05-09 | — | — | US | disclosed |
| US-20230128528-A1 | PROCESS AND PLANT FOR MANUFACTURING AQUEOUS POLYACRYLAMIDE GELS | BASF SE (DE) | 2023-04-27 | — | — | US | disclosed |
| US-11634516-B2 | Process for producing aqueous polyacrylamide solutions | BASF SE (DE) | 2023-04-25 | — | — | US | disclosed |
| US-11629205-B2 | Process for producing aqueous polyacrylamide solutions | BASF SE (DE) | 2023-04-18 | — | — | US | disclosed |
| US-11608468-B2 | Process of fracturing subterranean formations | BASF SE (DE) | 2023-03-21 | — | — | US | disclosed |
| CN-112940698-B | Ultrahigh-temperature-resistant degradable temporary plugging agent for hot dry rock fracturing and preparation method and application thereof | 中国地质调查局水文地质环境地质调查中心 | 2023-02-17 | — | — | CN | disclosed |
| US-11384177-B2 | Process for producing aqueous polyacrylamide solutions | BASF SE (DE) | 2022-07-12 | — | — | US | disclosed |
| US-20210388256-A1 | PROCESS OF FRACTURING SUBTERRANEAN FORMATIONS | BASF SE (DE) | 2021-12-16 | — | — | US | disclosed |
| CN-1212832-C | Soft capsule containing vinyl ester and poly ether polymer, its use and producing method | BASF AG (DE) | 2005-08-03 | — | — | CN | disclosed |
| CN-1602182-A | Cosmetic agent containing at least one copolymer having N-vinyllactam units | BASF AG (DE) | 2005-03-30 | — | — | CN | disclosed |
| US-6737049-B1 | WATER SOLUBLE OR DISPERSIBLE POLYMERS OBTAINED BY FREE RADICAL POLYMERIZATION OF SPECIFIED MONOMERS; HAIR TREATMENT COMPOSITIONS WHICH HAVE GOOD SETTING PROPERTIES AND HIGH PROPELLANT COMPATIBILITY AND ARE ESSENTIALLY NONFLAKING | BASF AKTIENGESELLSCHAFT (DE) | 2004-05-18 | — | — | US | disclosed |
| CN-1116865-C | Use of crosslinked cation polymer in skin cosmetics and skin disease preparations | BASF AG (DE) | 2003-08-06 | — | — | CN | disclosed |
| US-6355231-B1 | Use of cationic copolymers of unsaturated acids and N-vinylimidazolium salts in cosmetic hair formulations | BASF AKTIENGESELLSCHAFT (DE) | 2002-03-12 | — | — | US | disclosed |
| CN-1326732-A | Soft capsule containing vinyl ester and poly ether polymer, its use and producing method | BASF AG (DE) | 2001-12-19 | — | — | CN | disclosed |
| CN-1282571-A | Use of crosslinked cation polymer in skin cosmetics and skin disease preparations | BASF AG (DE) | 2001-02-07 | — | — | CN | disclosed |
| CN-1209991-A | High molecular mass cationic copolymers | BASF AG (DE) | 1999-03-10 | — | — | CN | disclosed |
| CN-1196232-A | Adnesives for dental prostheses | BASF AG (DE) | 1998-10-21 | — | — | CN | disclosed |