SCHEMBL1198044

SCHEMBL1198044

CCOC(=O)c1cccc(CCl)c1

nearest known ligand 0.66

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
CYP4F2 P78329 1/20 0.66
CYP4A11 Q02928 1/20 0.66
MEP1B Q16820 1/20 0.57
NPC1 O15118 3/20 0.54
RAB9A P51151 3/20 0.54
ALDH1A1 P00352 3/20 0.54
SMN1; SMN2 Q16637 3/20 0.54
MAPT P10636 2/20 0.54
CA2 P00918 2/20 0.53
CA12 O43570 1/20 0.51
CA1 P00915 1/20 0.51
CA7 P43166 1/20 0.51
CA9 Q16790 1/20 0.51
CA14 Q9ULX7 1/20 0.51
TSHR P16473 1/20 0.50
KMT2A Q03164 1/20 0.50
LMNA P02545 1/20 0.49
KDM4E B2RXH2 1/20 0.49

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
SCHEMBL129801 0.88 CYP4F2 (0.71) CYP4F2CYP4A11MEP1BNPC1RAB9A
SCHEMBL321524 0.87 CYP4F2 (0.71) CYP4F2CYP4A11MEP1BNPC1RAB9A
SCHEMBL6527211 0.87 LMNA (0.60) CYP4F2CYP4A11MEP1BRAB9AALDH1A1
SCHEMBL3118174 0.86 TDP1 (0.50) CYP4F2CYP4A11MEP1BNPC1RAB9A
SCHEMBL2089661 0.85 CYP4F2 (0.68) CYP4F2CYP4A11MEP1BNPC1RAB9A
SCHEMBL128387 0.85 CYP4F2 (0.72) CYP4F2CYP4A11MEP1BNPC1RAB9A
SCHEMBL27537771 0.84 TSHR (0.54) CYP4F2CYP4A11NPC1RAB9AALDH1A1
SCHEMBL110276 0.84 CYP4F2 (0.65) CYP4F2CYP4A11NPC1RAB9AALDH1A1
SCHEMBL318600 0.83 TDP1 (0.71) NPC1RAB9AALDH1A1SMN1; SMN2MAPT
SCHEMBL129800 0.83 CYP4F2 (0.66) CYP4F2CYP4A11MEP1BNPC1RAB9A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119684287-A 4- (3- (Piperidin-4-yl) -1H-pyrazol-5-yl) -1H-pyrrole [2,3-b ] pyridine derivative, and preparation method and application thereof 烟台新药创制山东省实验室 2025-03-25 CN disclosed
US-20230011131-A1 NOVEL COMPOUND FOR INHIBITING HISTONE ACETYLTRANSFERASE P300 AND ANTI-FIBROSIS COMPOSITION COMPRISING SAME REFURE LIFE SCIENCE, INC. (KR) 2023-01-12 US disclosed
US-20220194911-A1 NOVEL COMPOUND FOR INHIBITING HISTONE ACETYLTRANSFERASE P300 AND ANTIFIBROTIC COMPOSITION COMPRISING SAME REFURE LIFE SCIENCE, INC. (KR) 2022-06-23 US disclosed
EP-4011862-A1 NOVEL COMPOUND FOR INHIBITING HISTONE ACETYLTRANSFERASE P300 AND ANTI-FIBROSIS COMPOSITION COMPRISING SAME Refure Life Science Inc. (KR) 2022-06-15 EP disclosed
CN-110452168-B N-phenyl-N-quinoline carboxylic acid compound and preparation method and pharmaceutical application thereof 中国医学科学院药物研究所 2022-03-15 CN disclosed
WO-2021025448-A1 NOVEL COMPOUND FOR INHIBITING HISTONE ACETYLTRANSFERASE P300 AND ANTIFIBROTIC COMPOSITION COMPRISING SAME 리퓨어생명과학 주식회사 2021-02-11 WO disclosed
WO-2021025447-A1 NOVEL COMPOUND FOR INHIBITING HISTONE ACETYLTRANSFERASE P300 AND ANTI-FIBROSIS COMPOSITION COMPRISING SAME 리퓨어생명과학 주식회사 2021-02-11 WO disclosed
US-10807959-B2 WDR5-MLL1 inhibitors and modulators VANDERBILT UNIVERSITY (US) 2020-10-20 US disclosed
US-20200055824-A1 WDR5-MLL1 INHIBITORS AND MODULATORS VANDERBILT UNIVERSITY 2020-02-20 US disclosed
CN-110452168-A N- phenyl-N- quinoline carboxylic acid compound and its preparation method and medicinal usage INST MATERIA MEDICA CAMS 2019-11-15 CN disclosed
US-5587504-A Sulfonyloxy-biphenylcarboxylic ester derivatives which are intermediates EISAI CO., LTD. (JP) 1996-12-24 US disclosed
US-5583229-A Process for the preparation of imidazopyridine derivatives EISAI CO., LTD. (JP) 1996-12-10 US disclosed
US-5563158-A CARDIOVASCULAR DISORDERS THE DUPONT MERCK PHARMACEUTICAL COMPANY (US) 1996-10-08 US disclosed
US-5559236-A Intermediates for substituted biphenylmethylmidazopyridine angiotensin II antagonists EISAI CO., LTD. (JP) 1996-09-24 US disclosed
US-5557002-A Process for the preparation of biphenyl containing intermediates useful in making angiotensin II receptor antagonists EISAI CO., LTD. (JP) 1996-09-17 US disclosed
US-5554757-A Process for the preparation of imidazopyridine derivatives, and intermediates therefore EISAI CO., LTD. (JP) 1996-09-10 US disclosed
EP-0315399-B1 Quinoline derivatives, their use in the treatment of hypersensitive ailments and a pharmaceutical composition containing the same RHONE POULENC RORER INT (US) 1996-01-10 EP disclosed
EP-0627433-A1 PROCESS FOR PRODUCING IMIDAZOPYRIDINE DERIVATIVE AND INTERMEDIATE Eisai Co., Ltd. (JP) 1994-12-07 EP disclosed
US-5059610-A QUINOLINE DERIVATIVES AND THEIR USE AS ANTAGONISTS OF LEUKOTRIENE D4 RHONE-POULENC RORER PHARMACEUTICALS INC. (US) 1991-10-22 US disclosed
US-4920132-A Quinoline derivatives and use thereof as antagonists of leukotriene D4 RORER PHARMACEUTICAL CORP. (US) 1990-04-24 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 (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-20230011131-A1 NOVEL COMPOUND FOR INHIBITING HISTONE ACETYLTRANSFERASE P300 AND ANTI-FIBROSIS COMPOSITION COMPRISING SAME EP300, HDAC1, KAT2A CYP4F2 4713/4885CYP4A11 4465/4885MEP1B 1308/4885
US-20220194911-A1 NOVEL COMPOUND FOR INHIBITING HISTONE ACETYLTRANSFERASE P300 AND ANTIFIBROTIC COMPOSITION COMPRISING SAME EP300, HDAC1, HDAC11 CYP4F2 4659/4885CYP4A11 4413/4885MEP1B 1028/4885
US-10807959-B2 WDR5-MLL1 inhibitors and modulators WDR5, WDR1, WDR3 CYP4F2 4403/4885CYP4A11 4429/4885MEP1B 1708/4885
US-20200055824-A1 WDR5-MLL1 INHIBITORS AND MODULATORS WDR5, WDR1, WDR3 CYP4F2 4403/4885CYP4A11 4429/4885MEP1B 1708/4885

“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.