SCHEMBL1626324

SCHEMBL1626324

Cc1cc(Cl)c([N+](=O)[O-])cc1Cl

nearest known ligand 0.50

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
TSHR P16473 3/20 0.50
MAPK1 P28482 1/20 0.50
CYP3A4 P08684 3/20 0.48
ALDH1A1 P00352 2/20 0.48
VCAM1 P19320 6/20 0.44
PPIA P62937 1/20 0.44
PGK1 P00558 1/20 0.44
HSD17B10 Q99714 1/20 0.43
CYP1A2 P05177 1/20 0.42
RECQL P46063 1/20 0.42
GPR35 Q9HC97 1/20 0.42
TDP1 Q9NUW8 1/20 0.42

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
SCHEMBL864500 0.91 TSHR (0.50) TSHRMAPK1CYP3A4ALDH1A1VCAM1
SCHEMBL29721556 0.91 TSHR (0.50) TSHRMAPK1CYP3A4ALDH1A1VCAM1
SCHEMBL3633645 0.89 TSHR (0.52) TSHRMAPK1CYP3A4ALDH1A1VCAM1
SCHEMBL31592017 0.89 TSHR (0.52) TSHRMAPK1CYP3A4ALDH1A1VCAM1
SCHEMBL772624 0.89 CYP1A2 (0.48) TSHRMAPK1CYP3A4ALDH1A1PPIA
SCHEMBL5068830 0.87 PPIA (0.47) TSHRMAPK1CYP3A4ALDH1A1PPIA
SCHEMBL29586844 0.87 PPIA (0.47) TSHRMAPK1CYP3A4ALDH1A1PPIA
SCHEMBL80032 0.87 PPIA (0.47) TSHRMAPK1CYP3A4ALDH1A1PPIA
SCHEMBL358890 0.87 TSHR (0.50) TSHRMAPK1CYP3A4ALDH1A1VCAM1
SCHEMBL16013560 0.87 TSHR (0.50) TSHRMAPK1CYP3A4ALDH1A1VCAM1

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 54 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-112851493-B Preparation method of 2,4, 5-trifluoro phenylacetic acid 台州臻挚生物科技有限公司 2022-09-06 CN claimed
WO-2022099439-A1 PREPARATION METHOD FOR 2,4,5-TRIFLUOROPHENYLACETIC ACID 杭州臻挚生物科技有限公司 2022-05-19 WO claimed
CN-112851493-A Preparation method of 2,4, 5-trifluorophenylacetic acid 杭州臻挚生物科技有限公司 2021-05-28 CN claimed
US-12391663-B2 Isoindolinone compounds MONTE ROSA THERAPEUTICS AG (CH) 2025-08-19 US disclosed
US-20240261274-A1 TREATMENT OF MYC-DRIVEN CANCERS WITH GSPT1 DEGRADERS MONTE ROSA THERAPEUTICS AG (CH) 2024-08-08 US disclosed
CN-117820076-A Method for preparing 2, 6-dichlorotoluene by micro-channel reactor 盐城师范学院 2024-04-05 CN disclosed
US-20240083869-A1 ISOINDOLINONE COMPOUNDS MONTE ROSA THERAPEUTICS AG (CH) 2024-03-14 US disclosed
US-11912682-B2 Isoindolinone compounds MONTE ROSA THERAPEUTICS, INC. (US) 2024-02-27 US disclosed
CN-117242060-A Isoindolinone compounds 蒙特罗萨医疗公司 2023-12-15 CN disclosed
EP-4278014-A1 TREATMENT OF MYC-DRIVEN CANCERS WITH GSPT1 DEGRADERS Monte Rosa Therapeutics, Inc. (US) 2023-11-22 EP disclosed
EP-4277901-A1 ISOINDOLINONE COMPOUNDS Monte Rosa Therapeutics, Inc. (US) 2023-11-22 EP disclosed
WO-2002032422-A2 EP4 RECEPTOR INHIBITORS TO TREAT RHEUMATOID ARTHRITIS PFIZER PHARMACEUTICALS INC. (JP) 2002-04-25 WO disclosed
EP-0706524-A1 PROCESSES AND INTERMEDIATES FOR THE PREPARATION OF 5- 2-(4-(BENZOISOTHIAZOL-3-YL)-PIPERAZIN-1-YL)ETHYL]-6-CHLORO-1,3-DIHYDRO-INDOL-2-ONE PFIZER INC. (US) 1996-04-17 EP disclosed
WO-1995000510-A1 PROCESSES AND INTERMEDIATES FOR THE PREPARATION OF 5-[2-(4-(BENZOISOTHIAZOL-3-YL)-PIPERAZIN-1-YL)ETHYL]-6-CHLORO-1,3-DIHYDRO-INDOL-2-ONE PFIZER INC. (US) 1995-01-05 WO disclosed
US-5359068-A Processes and intermediates for the preparation of 5-[2-(4-(benzoisothiazol-3-yl)-piperazin-1-yl)ethyl]-6-chloro-1,3-dihydro-indol-2-one PFIZER INC. (US) 1994-10-25 US disclosed
US-4532350-A Process for the selective preparation of meta-chloroanilines RHONE-POULENC AGROCHIMIE (FR) 1985-07-30 US disclosed
US-4418213-A HYDRODEHALOGENATION LEWIS ACID AND NOBLE METAL CATALYSTS RHONE-POULENC AGROCHIMIE (FR) 1983-11-29 US disclosed
US-4351959-A Process for preparation of anilines substituted by chlorine in the meta-position RHONE-POULENC AGROCHIMIE (FR) 1982-09-28 US disclosed
US-4340759-A Process for the preparation of anilines substituted by chlorine in the meta-position RHONE-POULENC AGROCHIMIE (FR) 1982-07-20 US disclosed
US-4324914-A Process for preparation of anilines substituted by chlorine in the meta-position RHONE-POULENC AGROCHIMIE (FR) 1982-04-13 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (4 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-12391663-B2 Isoindolinone compounds CYP4F2, AOC2, AOC3 TSHR 1114/4885MAPK1 3281/4885CYP3A4 684/4885
US-20240083869-A1 ISOINDOLINONE COMPOUNDS CYP4F2, AOC2, AOC3 TSHR 1114/4885MAPK1 3281/4885CYP3A4 684/4885
US-11912682-B2 Isoindolinone compounds CYP4F2, AOC2, AOC3 TSHR 1114/4885MAPK1 3281/4885CYP3A4 684/4885
US-20240261274-A1 TREATMENT OF MYC-DRIVEN CANCERS WITH GSPT1 DEGRADERS MYC, MYCBP, GSPT1 TSHR 2333/4885MAPK1 2937/4885CYP3A4 4304/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.