SCHEMBL1040476

SCHEMBL1040476

COCOc1cccc(C(F)(F)F)c1

nearest known ligand 0.55

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
L3MBTL1 Q9Y468 2/20 0.55
KDM4E B2RXH2 3/20 0.51
MAOB P27338 2/20 0.50
AOC3 Q16853 1/20 0.50
MRGPRX4 Q96LA9 1/20 0.48
LMNA P02545 1/20 0.48
PKM P14618 1/20 0.48
HSD17B10 Q99714 1/20 0.48
ALDH1A1 P00352 3/20 0.45
KMT2A Q03164 1/20 0.45
ATM Q13315 1/20 0.45
NR4A2 P43354 1/20 0.44
POLB P06746 1/20 0.44
SMN1; SMN2 Q16637 1/20 0.44
GAA P10253 1/20 0.44

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
SCHEMBL12409058 0.84 L3MBTL1 (0.66) L3MBTL1KDM4EMAOBAOC3MRGPRX4
SCHEMBL3197958 0.84 SOD1 (0.51) L3MBTL1LMNANR4A2POLB
SCHEMBL12072717 0.83 L3MBTL1 (0.60) L3MBTL1KDM4EMAOBAOC3MRGPRX4
SCHEMBL5953372 0.81 L3MBTL1 (0.71) L3MBTL1KDM4EMAOBAOC3MRGPRX4
SCHEMBL30628214 0.81 MRGPRX4 (0.45) KDM4EMAOBMRGPRX4LMNAPKM
SCHEMBL17420544 0.81 MRGPRX4 (0.45) KDM4EMAOBMRGPRX4LMNAPKM
SCHEMBL1607526 0.80 MAOB (0.48) KDM4EMAOBLMNAALDH1A1SMN1; SMN2
SCHEMBL16024758 0.80 L3MBTL1 (0.50) L3MBTL1KDM4EMAOBAOC3MRGPRX4
SCHEMBL30167649 0.79 L3MBTL1 (0.55) L3MBTL1KDM4EMAOBAOC3MRGPRX4
SCHEMBL167016 0.79 L3MBTL1 (0.58) L3MBTL1KDM4EMAOBLMNAALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-102020647-B Preparation method of 1-(2,2-difluoroethoxy)-6-trifluoromethyl-N-([1,2,4]triazolezol[1,5-C] pyrimidine-2-)benzsulfamide SUN ZHIHUA 2013-09-11 CN claimed
CN-102020647-A Preparation method of 1-(2,2-difluoroethoxy)-6-trifluoromethyl-N-([1,2,4]triazolezol[1,5-C] pyrimidine-2-)benzsulfamide ZHIHUA SUN 2011-04-20 CN claimed
EP-4112599-A1 KEY INTERMEDIATE FOR SYNTHESIZING PROSTAGLANDIN COMPOUNDS AND PREPARATION METHOD THEREFOR SHENZHEN CATALYS TECHNOLOGY CO., LTD. (CN) 2023-01-04 EP disclosed
CN-110590623-B Method for preparing 6-substituted-2-trifluoromethyl phenyl sulfide in continuous flow microchannel reactor 江苏好收成韦恩农化股份有限公司 2022-04-19 CN disclosed
CN-110590623-A Method for preparing 6-substituted-2-trifluoromethyl phenyl sulfide in continuous flow microchannel reactor 江苏好收成韦恩农化股份有限公司 2019-12-20 CN disclosed
EP-2697213-B1 INHIBITORS OF VIRAL REPLICATION, THEIR PROCESS OF PREPARATION AND THEIR THERAPEUTICAL USES HIVIH (FR) 2018-12-12 EP disclosed
US-9604900-B2 Inhibitors of viral replication, their process of preparation and their therapeutical uses LABORATOIRE BIODIM (FR) 2017-03-28 US disclosed
US-9604900-B2 Inhibitors of viral replication, their process of preparation and their therapeutical uses LABORATOIRE BIODIM (FR) 2017-03-28 US disclosed
US-9604900-B2 Inhibitors of viral replication, their process of preparation and their therapeutical uses LABORATOIRE BIODIM (FR) 2017-03-28 US disclosed
EP-2697213-A1 INHIBITORS OF VIRAL REPLICATION, THEIR PROCESS OF PREPARATION AND THEIR THERAPEUTICAL USES LABORATOIRE BIODIM (FR) 2014-02-19 EP disclosed
US-20140031338-A1 INHIBITORS OF VIRAL REPLICATION, THEIR PROCESS OF PREPARATION AND THEIR THERAPEUTICAL USES LABORATOIRE BIODIM (FR) 2014-01-30 US disclosed
US-20050277631-A1 Vanilloid receptor ligands and their use in treatments AMGEN INC. 2005-12-15 US disclosed
US-20050272777-A1 Vanilloid receptor ligands and their use in treatments AMGEN INC. 2005-12-08 US disclosed
CN-1694873-A Vanilloid receptor ligands and their use in treatments AMGEN INC (US) 2005-11-09 CN disclosed
EP-1546116-A1 VANILLOID RECEPTOR LIGANDS AND THEIR USE IN TREATMENTS Amgen Inc. (US) 2005-06-29 EP disclosed
EP-1290001-B1 PROCESS FOR THE SELECTIVE DEPROTONATION AND FUNCTIONALIZATION OF 3-SUBSTITUTED BENZOTRIFLUORIDES DOW AGROSCIENCES LLC (US) 2004-11-03 EP disclosed
US-20040082780-A1 Vanilloid receptor ligands and their use in treatments AMGEN, INC. 2004-04-29 US disclosed
WO-2004014871-A1 VANILLOID RECEPTOR LIGANDS AND THEIR USE IN TREATMENTS AMGEN INC. (US) 2004-02-19 WO disclosed
US-6462240-B2 FROMING 2-LITHIOBENZOTRIFLORIDE FROM BENZOTRIFLUORIDE AND ALKYLLITHIUM DOW AGROSCIENCES LLC 2002-10-08 US disclosed
US-20020010375-A1 Process for the selective deprotonation and functionalization of 3-substituted benzotrifluorides CORTEVA AGRISCIENCE LLC 2002-01-24 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 (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-20140031338-A1 INHIBITORS OF VIRAL REPLICATION, THEIR PROCESS OF PREPARATION AND THEIR THERAPEUTICAL USES POLRMT, MAVS, EIF2AK2 L3MBTL1 1958/4885KDM4E 1408/4885MAOB 2144/4885
US-20050272777-A1 Vanilloid receptor ligands and their use in treatments TRPV1, TRPV2, TRPV3 L3MBTL1 4532/4885KDM4E 4218/4885MAOB 1213/4885
US-20020010375-A1 Process for the selective deprotonation and functionalization of 3-substituted benzotrifluorides BPTF, FGFR2, FGFR4 L3MBTL1 1258/4885KDM4E 1239/4885MAOB 920/4885
US-20050277631-A1 Vanilloid receptor ligands and their use in treatments TRPV1, TRPV2, TRPV3 L3MBTL1 4532/4885KDM4E 4218/4885MAOB 1213/4885
US-20040082780-A1 Vanilloid receptor ligands and their use in treatments TRPV1, TRPV2, TRPV3 L3MBTL1 4422/4885KDM4E 4111/4885MAOB 1137/4885

“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.