SCHEMBL1479915

SCHEMBL1479915

O=C(Cc1ccc(Cl)cc1)Cc1ccc(Cl)cc1

nearest known ligand 0.67

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
NPC1 O15118 4/20 0.55
RAB9A P51151 4/20 0.55
CTBP2 P56545 1/20 0.55
L3MBTL1 Q9Y468 4/20 0.53
LMNA P02545 2/20 0.53
MEN1 O00255 4/20 0.52
KMT2A Q03164 4/20 0.52
MAPT P10636 2/20 0.52
PIK3CA P42336 2/20 0.52
CNR2 P34972 1/20 0.52
CYP3A4 P08684 1/20 0.52
HPGD P15428 1/20 0.52
MAPK1 P28482 1/20 0.52
ALDH1A1 P00352 2/20 0.50
TDP1 Q9NUW8 1/20 0.50
EGFR P00533 1/20 0.50
ERBB2 P04626 1/20 0.50
POLB P06746 1/20 0.48
HTT P42858 1/20 0.48
SMN1; SMN2 Q16637 1/20 0.48

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
SCHEMBL8406795 0.91 L3MBTL1 (0.66) CTBP2L3MBTL1MEN1KMT2AMAPT
SCHEMBL4632976 0.88 NPC1 (0.50) NPC1RAB9ACTBP2L3MBTL1LMNA
SCHEMBL2251562 0.88 RAB9A (0.50) NPC1RAB9ACTBP2L3MBTL1LMNA
SCHEMBL28837741 0.87 NPC1 (0.62) NPC1RAB9ACTBP2L3MBTL1LMNA
SCHEMBL622333 0.86 GSK3B (0.52) NPC1RAB9ACTBP2L3MBTL1LMNA
SCHEMBL1512094 0.86 NPC1 (0.48) NPC1RAB9ACTBP2L3MBTL1LMNA
SCHEMBL3070923 0.86 L3MBTL1 (0.52) NPC1RAB9ACTBP2L3MBTL1LMNA
SCHEMBL4327956 0.84 CTBP2 (0.52) NPC1RAB9ACTBP2L3MBTL1LMNA
SCHEMBL11221142 0.84 L3MBTL1 (0.58) NPC1RAB9ACTBP2L3MBTL1LMNA
Hydrochloric Acid SCHEMBL1151043 0.84 NPC1 (0.47) NPC1RAB9ACTBP2L3MBTL1LMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115141146-A Synthesis method of hypoglycemic active compound 1,2, 3-trimethyl-4- (p-chlorophenyl) -pyrazolium salt 东力(南通)化工有限公司 2022-10-04 CN claimed
CN-117486682-A Preparation method of functionalized beta-naphthalenyl ether compound 中国海洋石油集团有限公司 2024-02-02 CN disclosed
CN-117486681-A Preparation method of 3-aryl/alkyl-beta-anisole compound 中国海洋石油集团有限公司 2024-02-02 CN disclosed
WO-2023185149-A1 SULFONATED BENZENE POLYPHENYL IONOMER AND METHOD FOR PREPARING SAME, AND PROTON EXCHANGE MEMBRANE 中国科学院深圳先进技术研究院 2023-10-05 WO disclosed
CN-115141146-A Synthesis method of hypoglycemic active compound 1,2, 3-trimethyl-4- (p-chlorophenyl) -pyrazolium salt 东力(南通)化工有限公司 2022-10-04 CN disclosed
US-11384055-B2 Glycolate oxidase inhibitors for the treatment of disease BIOMARIN PHARMACEUTICAL INC. (US) 2022-07-12 US disclosed
US-20210171474-A1 GLYCOLATE OXIDASE INHIBITORS FOR THE TREATMENT OF DISEASE BIOMARIN PHARMACEUTICAL INC. (US) 2021-06-10 US disclosed
WO-2020257487-A1 GLYCOLATE OXIDASE INHIBITORS FOR THE TREATMENT OF DISEASE BIOMARIN PHARMACEUTICAL INC. (US) 2020-12-24 WO disclosed
US-20160280819-A1 CATALYST FOR OLEFIN POLYMERIZATION, METHOD FOR PRODUCING OLEFIN POLYMER, METHOD FOR PRODUCING PROPYLENE-BASED COPOLYMER, PROPYLENE POLYMER, PROPYLENE-BASED POLYMER COMPOSITION, AND USE OF THOSE MITSUI CHEMICALS, INC. (JP) 2016-09-29 US disclosed
EP-1900758-B9 METHOD FOR PRODUCING OLEFIN POLYMER MITSUI CHEMICALS INC (JP) 2016-07-13 EP disclosed
US-5200561-A PROCESS FOR PRODUCING OPTICALLY ACTIVE AMINES SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1993-04-06 US disclosed
EP-0485069-A1 Process for producing optically active amines SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1992-05-13 EP disclosed
EP-0187659-B1 PROCESS FOR GRAFTING UNSATURATED MONOMERS ON OLEFINIC POLYMERS Montedison S.p.A. (IT) 1989-12-27 EP disclosed
US-4624992-A Process for grafting unsaturated monomers on olefinic polymers AUSIMONT S.P.A. (IT) 1986-11-25 US disclosed
EP-0187659-A2 Process for grafting unsaturated monomers on olefinic polymers Montedison S.p.A. (IT) 1986-07-16 EP disclosed
US-4568490-A REDUCTIVE CONDENSATION WITH A CARBONYL COMPOUND ZAIDAN HOJIN BISEIBUTSU KAGAKU KENKYU KAI (JP) 1986-02-04 US disclosed
US-4537880-A Aminopropylaminobleomycin derivatives and process for preparation thereof ZAIDAN HOJIN BISEIBUTSU KAGAKU KENKYU KAI (JP) 1985-08-27 US disclosed
US-4340756-A Polyamine compounds as antibacterial agents MERCK & CO., INC. (US) 1982-07-20 US disclosed
US-4169951-A PROCESS FOR THE PRODUCTION OF SUBSTITUTED PYRIDINE (B) DEUTSCHE GOLD- UND SILBER-SCHEIDEANSTALT VORMALS ROESSLER (DE) 1979-10-02 US disclosed
US-4028481-A ACTIVATED TITANIUM TRICHLORIDE AND AN ORGANOALUMINUM COMPOUND MITSUI TOATSU CHEMICALS, INCORPORATED (JA) 1977-06-07 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 (2 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-11384055-B2 Glycolate oxidase inhibitors for the treatment of disease XDH, PNPO, AGXT NPC1 1158/4885RAB9A 3923/4885CTBP2 4861/4885
US-20210171474-A1 GLYCOLATE OXIDASE INHIBITORS FOR THE TREATMENT OF DISEASE XDH, PNPO, AGXT NPC1 1158/4885RAB9A 3923/4885CTBP2 4861/4885

“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.