Known targets — ChEMBL curated mechanism
ABCC8ACEADORA1ADORA2AADORA2BADORA3ALDH5A1ALOX5ALOX5APATP4AATP4BBRAFCA1CA12CA2CA4CYSLTR1DHFRDPEP1EDNRAEDNRBESR2F10FDPSFGF1GABBR1GABBR2GABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGARTGNRHRGSC1HMGCRIMPDH1IMPDH2KCNJ11LY96NOD2NR3C1NS3NS4ANS5bP2RY1P2RY12P2RY2P2RY4P2RY6PBP2XPDE3APDE3BPDE4APDE4BPDE4CPDE4DPDK1PDK2PDK3PDK4PPARGPPATPTGIRPTGS1PTGS2RAF1RYR1RYR3SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASERPINC1SLC12A1SLC12A3SYKTHRATHRBTLR3TLR4TLR9TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TYMSVKORC1XDHblablaIMP-1blaOXA-33blaOXA-58blaT-3blaT-4blaT-5blaT-6dacAdacBdacCfolAfolPfolP1ftsIfusAgaggyrAgyrBmecAmrcAmrcBmrdApbp1apbp1bpbp2pbp2apbp2bpbp3pbp4pbpApbpBpbpCpbpFpolponBrplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpoArpoBrpoCrpoZrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO
The experimentally established mechanism targets of T-Butylacetic Acid. 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 | |
|---|---|---|---|---|
| T-Butylacetic Acid SCHEMBL973429 | 0.94 | — | — | |
| T-Butylacetic Acid SCHEMBL18258678 | 0.94 | CA4 (0.43) | — | |
| T-Butylacetic Acid SCHEMBL11218671 | 0.94 | — | — | |
| T-Butylacetic Acid SCHEMBL4319302 | 0.94 | — | — | |
| T-Butylacetic Acid SCHEMBL28123305 | 0.91 | CA4 (0.42) | — | |
| T-Butylacetic Acid SCHEMBL3159252 | 0.91 | CA4 (0.42) | — | |
| T-Butylacetic Acid SCHEMBL6098037 | 0.91 | CA4 (0.42) | — | |
| T-Butylacetic Acid SCHEMBL7859363 | 0.88 | CA4 (0.40) | — | |
| T-Butylacetic Acid SCHEMBL28494927 | 0.88 | CA4 (0.40) | — | |
| T-Butylacetic Acid SCHEMBL6567111 | 0.84 | CA4 (0.42) | — |
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 13 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-114469965-A | Inhibitor of core fucosyltransferase and application thereof | 大连医科大学 | 2022-05-13 | — | — | CN | disclosed |
| CN-107406389-B | Electrochromic compounds with improved color stability in the free radical state | 金泰克斯公司 | 2021-05-11 | — | — | CN | disclosed |
| US-10464900-B2 | Electrochromic compounds with improved color stability in their radical states | GENTEX CORPORATION (US) | 2019-11-05 | — | — | US | disclosed |
| US-20180346421-A1 | ELECTROCHROMIC COMPOUNDS WITH IMPROVED COLOR STABILITY IN THEIR RADICAL STATES | GENTEX CORPORATION | 2018-12-06 | — | — | US | disclosed |
| US-10040763-B2 | Electrochromic compounds with improved color stability in their radical states | GENTEX CORPORATION (US) | 2018-08-07 | — | — | US | disclosed |
| EP-3256544-A2 | ELECTROCHROMIC COMPOUNDS WITH IMPROVED COLOR STABILITY IN THEIR RADICAL STATES | Gentex Corporation (US) | 2017-12-20 | — | — | EP | disclosed |
| WO-2016130712-A2 | ELECTROCHROMIC COMPOUNDS WITH IMPROVED COLOR STABILITY IN THEIR RADICAL STATES | GENTEX CORPORATION (US) | 2016-08-18 | — | — | WO | disclosed |
| US-20160229803-A1 | ELECTROCHROMIC COMPOUNDS WITH IMPROVED COLOR STABILITY IN THEIR RADICAL STATES | GENTEX CORPORATION | 2016-08-11 | — | — | US | disclosed |
| US-6908996-B2 | Compounds and method for preparing 3-methylcephams | IMPERIAL COLLEGE OF LONDON (GB) | 2005-06-21 | — | — | US | disclosed |
| US-6683176-B2 | FOR USE IN PRODUCING AMINO ACID DERIVATIVE ANTIBIOTICS | COOPER CONSULTING | 2004-01-27 | — | — | US | disclosed |
| EP-1183262-A4 | INTERMEDIATES FOR AND SYNTHESIS OF 3-METHYLENE CEPHAMS | COOPER CONSULTING INC (US) | 2003-04-09 | — | — | EP | disclosed |
| EP-1183262-A1 | INTERMEDIATES FOR AND SYNTHESIS OF 3-METHYLENE CEPHAMS | Cooper Consulting Inc. (US) | 2002-03-06 | — | — | EP | disclosed |
| WO-2001060828-A1 | INTERMEDIATES FOR AND SYNTHESIS OF 3-METHYLENE CEPHAMS | COOPER CONSULTING INC. (US) | 2001-08-23 | — | — | WO | disclosed |