SCHEMBL186161

SCHEMBL186161

O=C(O)c1cncc(O)c1

nearest known ligand 0.59

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 9/20 0.59
ALDH1A1 P00352 7/20 0.59
HCAR2 Q8TDS4 6/20 0.59
POLB P06746 3/20 0.59
MEN1 O00255 2/20 0.59
KMT2A Q03164 2/20 0.59
LMNA P02545 1/20 0.59
DDO Q99489 1/20 0.59
CA12 O43570 2/20 0.54
CA1 P00915 2/20 0.54
CA2 P00918 2/20 0.54
CA9 Q16790 2/20 0.54
CA7 P43166 1/20 0.54
CA14 Q9ULX7 1/20 0.54
GAA P10253 2/20 0.52
HPGD P15428 3/20 0.50
RAF1 P04049 1/20 0.49
ATM Q13315 1/20 0.49
CYP2C9 P11712 1/20 0.48
CYP2C19 P33261 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
SCHEMBL29954688 1.00 KDM4E (0.59) KDM4EALDH1A1HCAR2POLBMEN1
Hydrochloric Acid SCHEMBL5227513 0.98 KDM4E (0.57) KDM4EALDH1A1HCAR2POLBMEN1
SCHEMBL51830 0.85 HCAR2 (0.70) KDM4EALDH1A1HCAR2POLBMEN1
SCHEMBL26680771 0.82 NPC1 (0.51) KDM4EALDH1A1HCAR2POLBMEN1
Hydrochloric Acid SCHEMBL7661020 0.82 HCAR2 (0.67) KDM4EALDH1A1HCAR2POLBMEN1
Fluoride SCHEMBL21331909 0.82 HCAR2 (0.67) KDM4EALDH1A1HCAR2POLBMEN1
SCHEMBL19987838 0.82 HCAR2 (0.67) KDM4EALDH1A1HCAR2POLBMEN1
Bromide SCHEMBL21332093 0.82 HCAR2 (0.67) KDM4EALDH1A1HCAR2POLBMEN1
Hydrochloric Acid SCHEMBL7124062 0.82 HCAR2 (0.67) KDM4EALDH1A1HCAR2POLBMEN1
Hydrochloric Acid SCHEMBL1117746 0.82 HCAR2 (0.67) KDM4EALDH1A1HCAR2POLBMEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115974758-B Carboxymethyl ketone compound and preparation method thereof 生物岛实验室 2025-06-10 CN claimed
CN-120004634-A Low-dielectric-constant aluminum nitride ceramic substrate and preparation method thereof 军瓷电子材料河北有限公司 2025-05-16 CN claimed
CN-119158012-B Antigen targeting peptide nano micelle and application thereof 浙江省肿瘤医院 2025-03-18 CN claimed
CN-119158012-A Antigen targeting peptide nano micelle and application thereof 浙江省肿瘤医院 2024-12-20 CN claimed
US-12077680-B2 Polishing composition, production method of the same, polishing method and a manufacturing method of a semiconductor substrate FUJIMI INCORPORATED (JP) 2024-09-03 US claimed
CN-115974758-A Carboxymethyl ketone compound and preparation method thereof 生物岛实验室 2023-04-18 CN claimed
US-20210301174-A1 POLISHING COMPOSITION, PRODUCTION METHOD OF THE SAME, POLISHING METHOD AND A MANUFACTURING METHOD OF A SEMICONDUCTOR SUBSTRATE FUJIMI INCORPORATED (JP) 2021-09-30 US claimed
CN-113046734-A Bivalent palladium complex solution and preparation method and application thereof 上海天承化学有限公司 2021-06-29 CN claimed
CN-105646552-A Zn(II) complex based on 5-hydroxynictinic acid and preparation method and application thereof 天津师范大学 2016-06-08 CN claimed
US-20030125328-A1 Substituted polycyclic aryl and heteroaryl tertiary-heteroalkylamines useful for inhibiting cholesteryl ester transfer protein activity G.D. SEARLE & CO. (US) 2003-07-03 US claimed
US-20030096818-A1 Substituted polycyclic aryl and heteroaryl tertiary-heteroalkylamines useful for inhibiting cholesteryl ester transfer protein activity G.D. SEARLE & CO. (US) 2003-05-22 US claimed
US-20030087905-A1 Substituted polycyclic aryl and heteroaryl tertiary-heteroalkylamines useful for inhibiting cholesteryl ester transfer protein activity G.D. SEARLE & CO. 2003-05-08 US claimed
US-20030083331-A1 Substituted polycyclic aryl and heteroaryl tertiary-heteroalkylamines useful for inhibiting cholesteryl ester transfer protein activity G.D. SEARLE & CO. (US) 2003-05-01 US claimed
US-20030032644-A1 Substituted polycyclic aryl and heteroaryl tertiary-heteroalkylamines useful for inhibiting cholesteryl ester transfer protein activity G.D. SEARLE & CO. 2003-02-13 US claimed
US-20020165232-A1 Substituted N, N-disubstituted cycloalkyl aminoalcohol compounds useful for inhibiting cholesteryl ester transfer protein activity SIKORSKI JAMES A (US) 2002-11-07 US claimed
US-20020165231-A1 Substituted N-heteroaryl-N-phenyl aminoalcohol compounds useful for inhibiting cholesteryl ester transfer protein activity SIKORSKI JAMES A (US) 2002-11-07 US claimed
EP-1115693-A1 SUBSTITUTED POLYCYCLIC ARYL AND HETEROARYL $i(TERTIARY)-HETEROALKYLAMINES USEFUL FOR INHIBITING CHOLESTERYL ESTER TRANSFER PROTEIN ACTIVITY Monsanto Company (US) 2001-07-18 EP claimed
WO-2000018721-A1 SUBSTITUTED POLYCYCLIC ARYL AND HETEROARYL TERTIARY-HETEROALKYLAMINES USEFUL FOR INHIBITING CHOLESTERYL ESTER TRANSFER PROTEIN ACTIVITY MONSANTO COMPANY (US) 2000-04-06 WO claimed
US-5430049-A Treating hyperproliferative disorders GAUT ZANE N (US) 1995-07-04 US claimed
EP-0003663-A2 Amino-substituted phenyl and heteroaryl compounds, process for their preparation and pharmaceutical compositions containing them AMERICAN CYANAMID COMPANY (US) 1979-08-22 EP claimed

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

For each of this compound's patents that has machine-readable text (7 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-20030125328-A1 Substituted polycyclic aryl and heteroaryl tertiary-heteroalkylamines useful for inhibiting cholesteryl ester transfer protein activity CETP, MTTP, LCAT KDM4E 2831/4885ALDH1A1 2277/4885HCAR2 1015/4885
US-20030096818-A1 Substituted polycyclic aryl and heteroaryl tertiary-heteroalkylamines useful for inhibiting cholesteryl ester transfer protein activity CETP, MTTP, LCAT KDM4E 2831/4885ALDH1A1 2277/4885HCAR2 1015/4885
US-20020165231-A1 Substituted N-heteroaryl-N-phenyl aminoalcohol compounds useful for inhibiting cholesteryl ester transfer protein activity CETP, LCAT, MTTP KDM4E 3107/4885ALDH1A1 2079/4885HCAR2 1151/4885
US-20030087905-A1 Substituted polycyclic aryl and heteroaryl tertiary-heteroalkylamines useful for inhibiting cholesteryl ester transfer protein activity CETP, MTTP, LCAT KDM4E 2831/4885ALDH1A1 2277/4885HCAR2 1015/4885
US-20030083331-A1 Substituted polycyclic aryl and heteroaryl tertiary-heteroalkylamines useful for inhibiting cholesteryl ester transfer protein activity CETP, MTTP, LCAT KDM4E 2831/4885ALDH1A1 2277/4885HCAR2 1015/4885
US-20030032644-A1 Substituted polycyclic aryl and heteroaryl tertiary-heteroalkylamines useful for inhibiting cholesteryl ester transfer protein activity CETP, MTTP, PCTP KDM4E 1432/4885ALDH1A1 2611/4885HCAR2 822/4885
US-20020165232-A1 Substituted N, N-disubstituted cycloalkyl aminoalcohol compounds useful for inhibiting cholesteryl ester transfer protein activity CETP, DBI, PLTP KDM4E 3603/4885ALDH1A1 2588/4885HCAR2 1388/4885

“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.