SCHEMBL342262

SCHEMBL342262

O=C(O)c1c(Cl)ccc(Cl)c1O

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
DPP4 P27487 1/20 1.00
ALDH1A1 P00352 6/20 0.52
KDM4E B2RXH2 3/20 0.52
HSD17B10 Q99714 3/20 0.52
TTR P02766 1/20 0.44
TSHR P16473 5/20 0.43
CA12 O43570 1/20 0.42
CA1 P00915 1/20 0.42
CA2 P00918 1/20 0.42
CA7 P43166 1/20 0.42
CA9 Q16790 1/20 0.42
CA14 Q9ULX7 1/20 0.42
TP53 P04637 1/20 0.41
AKR1C2 P52895 2/20 0.40
AKR1C1 Q04828 2/20 0.40
AKR1C4 P17516 1/20 0.40
AKR1C3 P42330 1/20 0.40
MEN1 O00255 2/20 0.39
KMT2A Q03164 2/20 0.39
MAPT P10636 1/20 0.39

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.

Compoundsimilaritytop predictedshared targets
SCHEMBL29375924 1.00 DPP4 (1.00) DPP4ALDH1A1KDM4EHSD17B10TTR
SCHEMBL28078921 0.98 DPP4 (0.95) DPP4ALDH1A1KDM4EHSD17B10TTR
Potassium SCHEMBL16619331 0.98 DPP4 (0.95) DPP4ALDH1A1KDM4EHSD17B10TTR
SCHEMBL17318752 0.98 DPP4 (0.95) DPP4ALDH1A1KDM4EHSD17B10TTR
SCHEMBL16824105 0.98 DPP4 (0.95) DPP4ALDH1A1KDM4EHSD17B10TTR
SCHEMBL16619328 0.98 DPP4 (0.95) DPP4ALDH1A1KDM4EHSD17B10TTR
SCHEMBL29113265 0.98 DPP4 (0.95) DPP4ALDH1A1KDM4EHSD17B10TTR
SCHEMBL5693505 0.86 DPP4 (0.75) DPP4ALDH1A1KDM4EHSD17B10TTR
SCHEMBL1903652 0.86 DPP4 (0.75) DPP4ALDH1A1KDM4EHSD17B10TTR
SCHEMBL28268386 0.84 DPP4 (0.71) DPP4ALDH1A1KDM4EHSD17B10TTR

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

Appears in 6295 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3452439-B1 PROCESS FOR PREPARATION OF 3,6-DICHLORO-2-METHOXYBENZOIC ACID (DICAMBA) GHARDA KEKI HORMUSJI (IN) 2025-06-11 EP claimed
CN-114163325-B Method for synthesizing dicamba by using continuous flow reactor 江苏优嘉植物保护有限公司 2024-06-28 CN claimed
EP-3551601-B1 PROCESSES FOR PURIFICATION, RECOVERY, AND CONVERSION OF CHLOROPHENOL SALTS AND PREPARATION AND RECOVERY OF PRODUCTS PREPARED THEREFROM MONSANTO TECHNOLOGY LLC (US) 2024-06-19 EP claimed
CN-117286161-B Dicamba anaerobic degradation intermediate product 3, 6-dichloro salicylic acid decarboxylase CsaDC and application thereof 南京农业大学三亚研究院 2024-03-19 CN claimed
CN-117286161-A Dicamba anaerobic degradation intermediate product 3, 6-dichloro salicylic acid decarboxylase CsaDC and application thereof 南京农业大学三亚研究院 2023-12-26 CN claimed
CN-117126401-A Polar polyarylene sulfide resin and film, and preparation method and application thereof 新凝合科技(成都)有限公司 2023-11-28 CN claimed
CN-116854579-A Process for purifying, recovering and converting chlorophenolates and for preparing and recovering products made from chlorophenolates 孟山都技术公司 2023-10-10 CN claimed
CN-110248919-B Process for purifying, recovering and converting chlorophenolates and for preparing and recovering products made from chlorophenolates 孟山都技术公司 2023-07-14 CN claimed
US-20230202961-A1 PROCESSES FOR PURIFICATION, RECOVERY, AND CONVERSION OF CHLOROPHENOL SALTS AND PREPARATION AND RECOVERY OF PRODUCTS PREPARED THEREFROM MONSANTO TECHNOLOGY LLC 2023-06-29 US claimed
US-20230157284-A1 HIGH-LOAD SOLUTION CONCENTRATES OF DICAMBA BASF CORPORATION 2023-05-25 US claimed
US-6586624-B1 Preferential hydroxylation of 1,4-dichlorobenzene to form 2,5-dichlorophenol in the presence of metal peroxides, then carboxylating, and methylating the 2-hydroxy-3,6-dichloro-benzoic acid to dicamba SYNGENTA PARTICIPATIONS AG (CH) 2003-07-01 US claimed
US-20030115626-A1 Methods and materials for making and using transgenic dicamba-degrading organisms WEEKS DONALD P (US) 2003-06-19 US claimed
WO-2002068607-A2 METHODS AND MATERIALS FOR MAKING AND USING TRANSGENIC DICAMBA-DEGRADING ORGANISMS BOARD OF REGENTS OF THE UNIVERSITY OF NEBRASKA (US) 2002-09-06 WO claimed
US-6274776-B1 PREPARATION OF 2,5-DICHLOROPHENOL BY SELECTIVELY OXIDIZING 1,4-DICHLOROBENZENE USING A PEROXO-, HYDROPEROXO-, SUPEROXO-OR ALKYLPEROXO-METAL SPECIES IN THE PRESENCE OF AN ALPHA-HYDROXY-, DIBASIC-, TRIBASIC- OR SULFONIC ACID. SYNGENTA PARTICIPATIONS (CH) 2001-08-14 US claimed
EP-1012257-A1 METHODS AND MATERIALS FOR MAKING AND USING TRANSGENIC DICAMBA-DEGRADING ORGANISMS Weeks, Donald P. (US) 2000-06-28 EP claimed
EP-0975569-A1 PROCESS FOR THE HYDROXYLATION OF 1,4-DICHLOROBENZENE Novartis AG (CH) 2000-02-02 EP claimed
WO-1998047843-A1 PROCESS FOR THE HYDROXYLATION OF 1,4-DICHLOROBENZENE NOVARTIS AG (CH) 1998-10-29 WO claimed
WO-1998045424-A1 METHODS AND MATERIALS FOR MAKING AND USING TRANSGENIC DICAMBA-DEGRADING ORGANISMS WEEKS DONALD P (US) 1998-10-15 WO claimed
US-4232172-A Process for the preparation of 3,6-dichloro-salicyclic CELAMERCK GMBH & CO. KG (DE) 1980-11-04 US claimed
US-4161611-A Process for the production of 2-methoxy-3,6-dichlorobenzoic acid Veesicol Chemical Corporation (US) 1979-07-17 US claimed