SCHEMBL2089458

SCHEMBL2089458

O=COc1ccc(Cl)c(Cl)c1Cl

nearest known ligand 0.36

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
CYP3A4 P08684 1/20 0.36
MAPK1 P28482 1/20 0.36
FABP3 P05413 1/20 0.35
MRGPRX4 Q96LA9 1/20 0.35
TDP1 Q9NUW8 2/20 0.34
ALDH1A1 P00352 2/20 0.32
GPR84 Q9NQS5 1/20 0.32
AHR P35869 2/20 0.31
MEN1 O00255 1/20 0.30
KMT2A Q03164 1/20 0.30

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
SCHEMBL2095443 0.80 ALDH1A1 (0.43) CYP3A4MRGPRX4TDP1ALDH1A1MEN1
SCHEMBL15475846 0.77 CYP3A4 (0.36) CYP3A4MAPK1FABP3MRGPRX4TDP1
SCHEMBL28202875 0.77 CYP3A4 (0.43) CYP3A4MAPK1ALDH1A1AHR
SCHEMBL11703762 0.74 ALDH1A1 (0.33) CYP3A4MAPK1TDP1ALDH1A1MEN1
SCHEMBL9486392 0.72 HTR2A (0.33) CYP3A4MAPK1MRGPRX4GPR84
SCHEMBL11283671 0.72 CYP3A4 (0.43) CYP3A4MAPK1FABP3MRGPRX4TDP1
SCHEMBL27278573 0.72 CYP3A4 (0.48) CYP3A4MAPK1TDP1ALDH1A1AHR
SCHEMBL8665449 0.71 TDP1 (0.43) CYP3A4MRGPRX4TDP1ALDH1A1
SCHEMBL4593314 0.71 TTR (0.49) TDP1KMT2A
SCHEMBL54889 0.70 LMNA (0.47) TDP1ALDH1A1MEN1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119059981-A Preparation method of Olaparib 山东新时代药业有限公司 2024-12-03 CN disclosed
CN-118812361-A Method for preparing carboxylic acid aryl ester by internal olefin migration hydrogen esterification reaction 常州大学 2024-10-22 CN disclosed
CN-117417253-A Method for preparing phenyl alkyl acid ester by alkyl olefin 常州大学 2024-01-19 CN disclosed
US-11591225-B2 Method for producing carbon monoxide COMMISSARIAT A L'ENERGIE ATOMIQUE ET AUX ENERGIES ALTERNATIVES (FR) 2023-02-28 US disclosed
US-20210188650-A1 METHOD FOR PRODUCING CARBON MONOXIDE COMMISSARIAT A L'ENERGIE ATOMIQUE ET AUX ENERGIES ALTERNATIVES (FR) 2021-06-24 US disclosed
WO-2021065893-A1 TETRALIN DERIVATIVE OR PHARMACEUTICALLY ACCEPTABLE ACID ADDITION SALT THEREOF 国立大学法人 筑波大学 2021-04-08 WO disclosed
EP-3740465-A1 METHOD FOR PRODUCING CARBON MONOXIDE Commissariat à l'énergie atomique et aux énergies alternatives (CEA) (FR) 2020-11-25 EP disclosed
EP-3699167-A1 PROCESS FOR PREPARING METHYL 1-BENZOSUBERONE-7-CARBOXYLATE Sanofi (FR) 2020-08-26 EP disclosed
WO-2019141634-A1 METHOD FOR PRODUCING CARBON MONOXIDE COMMISSARIAT A L'ENERGIE ATOMIQUE ET AUX ENERGIES ALTERNATIVES (FR) 2019-07-25 WO disclosed
US-8883777-B2 Compositions controlling pH range of release and/or release rate MITSUBISHI TANABE PHARMA CORPORATION (JP) 2014-11-11 US disclosed
EP-1678185-B1 2,3-DIHYDRO-6-NITROIMIDAZO [2,1-B] OXAZOLE COMPOUNDS FOR THE TREATMENT OF TUBERCULOSIS OTSUKA PHARMA CO LTD (JP) 2008-10-08 EP disclosed
US-20080119478-A1 2,3-Dihydro-6-Nitroimidazo (2,1-b) Oxazole Compounds for the Treatment of Tuberculosis OTSUKA PHAMACEUTICAL CO., LTD. (JP) 2008-05-22 US disclosed
US-7262212-B2 2,3-dihydro-6-nitroimidazo[2,1-b]oxazoles OTSUKA PHARMACEUTICAL CO., LTD. (JP) 2007-08-28 US disclosed
EP-1678185-A1 2,3-DIHYDRO-6-NITROIMIDAZO [2,1-B] OXAZOLE COMPOUNDS FOR THE TREATMENT OF TUBERCULOSIS OTSUKA PHARMACEUTICAL CO., LTD. (JP) 2006-07-12 EP disclosed
US-20060094767-A1 2,3-Dihydro-6-nitroimidazo[2,1-b]oxazoles OTSUKA PHARMACEUTICAL CO., LTD. (JP) 2006-05-04 US disclosed
EP-1555267-A1 2,3-DIHYDRO-6-NITROIMIDAZO 2,1-b OXAZOLES OTSUKA PHARMACEUTICAL CO., LTD. (JP) 2005-07-20 EP disclosed
WO-2005042542-A1 2,3-DIHYDRO-6-NITROIMIDAZO (2,1-B) OXAZOLE COMPOUNDS FOR THE TREATMENT OF TUBERCULOSIS OTSUKA PHARMACEUTICAL CO., LTD. (JP) 2005-05-12 WO disclosed
EP-1351992-A2 HYBRID PEPTIDES FOR TREATMENT OF BACTEREMIA AND SEPTICEMIA Ramot at Tel Aviv University Ltd. (IL) 2003-10-15 EP disclosed
US-20030130268-A1 Mixture containing water soluble polymer and surfactant; antiinflammatory agents, antiulcer agents, Crohn's disease MITSUBISHI TANABE PHARMA CORPORATION (JP) 2003-07-10 US disclosed
WO-2002055543-A2 HYBRID PEPTIDES FOR TREATMENT OF BACTEREMIA AND SEPTICEMIA UNIV RAMOT (IL) 2002-07-18 WO 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 (5 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-11591225-B2 Method for producing carbon monoxide ALDOA, CYP4A11, ADH1A CYP3A4 18/4885MAPK1 2148/4885FABP3 988/4885
US-20210188650-A1 METHOD FOR PRODUCING CARBON MONOXIDE ALDOA, CYP4A11, ADH1A CYP3A4 18/4885MAPK1 2148/4885FABP3 988/4885
US-20060094767-A1 2,3-Dihydro-6-nitroimidazo[2,1-b]oxazoles NR2C2, NR4A3, NR4A2 CYP3A4 1683/4885MAPK1 1392/4885FABP3 349/4885
US-20030130268-A1 Mixture containing water soluble polymer and surfactant; antiinflammatory agents, antiulcer agents, Crohn's disease SI, ABCB11, NOD2 CYP3A4 1477/4885MAPK1 1584/4885FABP3 4150/4885
US-20080119478-A1 2,3-Dihydro-6-Nitroimidazo (2,1-b) Oxazole Compounds for the Treatment of Tuberculosis NR2C2, NR0B2, NR4A2 CYP3A4 1734/4885MAPK1 2105/4885FABP3 1722/4885

“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.