SCHEMBL4853924

SCHEMBL4853924

Cc1cc(O)c(Cl)cc1Cl

nearest known ligand 0.60

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ HSD17B10 Q99714 7/20 0.60
▸ TSHR P16473 6/20 0.60
▸ HPGD P15428 5/20 0.60
▸ LMNA P02545 2/20 0.58
▸ ALDH1A1 P00352 5/20 0.47
▸ GAA P10253 3/20 0.47
▸ KDM4E B2RXH2 2/20 0.47
▸ SMN1; SMN2 Q16637 1/20 0.47
▸ CD44 P16070 1/20 0.46
▸ MCL1 Q07820 1/20 0.42
▸ CYP3A4 P08684 5/20 0.42
▸ ALOX15 P16050 2/20 0.42
▸ MAPT P10636 2/20 0.42
▸ MAPK1 P28482 2/20 0.42
▸ CYP1A2 P05177 1/20 0.42
▸ CYP2D6 P10635 1/20 0.42
▸ G6PD P11413 1/20 0.42
▸ CYP2C9 P11712 1/20 0.42
▸ PKM P14618 1/20 0.42
▸ ALOX12 P18054 1/20 0.42

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
SCHEMBL8459523 0.89 TSHR (0.60) HSD17B10TSHRHPGDLMNAALDH1A1
SCHEMBL2662863 0.86 LMNA (0.60) HSD17B10TSHRHPGDLMNAALDH1A1
SCHEMBL738726 0.86 HSD17B10 (0.55) HSD17B10TSHRHPGDLMNAALDH1A1
SCHEMBL6853371 0.83 HSD17B10 (0.60) HSD17B10TSHRHPGDLMNAALDH1A1
SCHEMBL4062679 0.83 LMNA (0.58) HSD17B10TSHRHPGDLMNAALDH1A1
SCHEMBL69259 0.78 HSD17B10 (0.80) HSD17B10TSHRHPGDALDH1A1CYP3A4
SCHEMBL8261003 0.78 CD44 (0.58) HSD17B10TSHRHPGDLMNAALDH1A1
SCHEMBL6841859 0.78 LMNA (0.52) HSD17B10TSHRHPGDLMNAALDH1A1
SCHEMBL13855825 0.78 HSD17B10 (0.52) HSD17B10TSHRHPGDLMNAALDH1A1
SCHEMBL16250473 0.77 HSD17B10 (0.46) HSD17B10TSHRHPGDLMNAALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-4429168-A PREFERENTIAL COMPLEXING WITH A METAL HALIDE SALT KOPPERS COMPANY, INC. (US) 1984-01-31 — — US claimed
EP-4085059-B1 HETEROARYL COMPOUNDS AS INHIBITORS OF PROGRAMMED NECROSIS PATHWAY, COMPOSITION AND METHOD USING THE SAME ACCRO BIOSCIENCE HK LTD (HK) 2024-03-20 — — EP disclosed
US-20230121233-A1 Heteroaryl compounds as inhibitors of programmed necrosis pathway, composition and method using the same ACCRO BIOSCIENCE (HK) LIMITED (HK) 2023-04-20 — — US disclosed
US-11555012-B2 ACLY inhibitors and uses thereof Nimbus Artemis, Inc. (US) 2023-01-17 — — US disclosed
EP-4001269-A1 BENZOISOTHIAZOLE, ISOTHIAZOLO[3,4-B]PYRIDINE, QUINAZOLINE, PHTHALAZINE, PYRIDO[2,3-D]PYRIDAZINE AND PYRIDO[2,3-D]PYRIMIDINE DERIVATIVES AS KRAS G12C INHIBITORS FOR TREATING LUNG, PANCREATIC OR COLORECTAL CANCER Amgen Inc. (US) 2022-05-25 — — EP disclosed
WO-2021138694-A1 HETEROARYL COMPOUNDS AS INHIBITORS OF PROGRAMMED NECROSIS PATHWAY, COMPOSITION AND METHOD USING THE SAME ACCRO BIOSCIENCE INC. (KY) 2021-07-08 — — WO disclosed
US-20200148634-A1 ACLY INHIBITORS AND USES THEREOF Nimbus Artemis, Inc. 2020-05-14 — — US disclosed
US-20200148634-A1 ACLY INHIBITORS AND USES THEREOF Nimbus Artemis, Inc. 2020-05-14 — — US disclosed
US-20200055845-A1 KRAS G12C INHIBITORS AND METHODS OF USING THE SAME AMGEN INC. 2020-02-20 — — US disclosed
US-10383331-B2 Liquid antimicrobial comprising a water-soluble polymer and a water-soluble antimicrobial agent FANTEX LIMITED (GB) 2019-08-20 — — US disclosed
US-7399890-B2 Method for the hydrodehalogenation of halogenated meta-cresols LANXESS DEUTSCHLAND GMBH (DE) 2008-07-15 — — US disclosed
WO-2007104944-A1 PYRROLOPYRIMIDINE DERIVATIVES USED AS HSP90 INHIBITORS VERNALIS (R & D) LTD. (GB) 2007-09-20 — — WO disclosed
US-20070149829-A1 Method for the hydrodehalogenation of halogenated meta-cresols LANXESS DEUTSCHLAND GMBH (DE) 2007-06-28 — — US disclosed
EP-0443533-B1 Positive photoresist composition FUJI PHOTO FILM CO LTD (JP) 1998-09-30 — — EP disclosed
EP-0443533-A2 Positive photoresist composition FUJI PHOTO FILM CO., LTD. (JP) 1991-08-28 — — EP disclosed
US-4588835-A Process for preparing alkoxyphenols OTSUKA KAGAKU YAKUHIN KABUSHIKI KAISHA (JP) 1986-05-13 — — US disclosed
US-4489210-A PREVENTION OF THE FORMATION OF BUBBLES BAYER AKTIENGESELLSCHAFT (DE) 1984-12-18 — — US disclosed
US-4469900-A PREFERENTIAL COMPLEXING WITH CALCIUM BROMIDE KOPPERS COMPANY, INC. (US) 1984-09-04 — — US disclosed
US-4429168-A PREFERENTIAL COMPLEXING WITH A METAL HALIDE SALT KOPPERS COMPANY, INC. (US) 1984-01-31 — — US disclosed
US-4219547-A Phosphoroimidophenyl insecticides STAUFFER CHEMICAL COMPANY (US) 1980-08-26 — — 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-20070149829-A1 Method for the hydrodehalogenation of halogenated meta-cresols C5, C9, C1S HSD17B10 626/4885TSHR 853/4885HPGD 1413/4885
US-20230121233-A1 Heteroaryl compounds as inhibitors of programmed necrosis pathway, composition and method using the same BAX, PDCD1, PDCD4 HSD17B10 948/4885TSHR 3786/4885HPGD 176/4885
US-20200148634-A1 ACLY INHIBITORS AND USES THEREOF ACLY, ATP5ME, ATP5MG HSD17B10 392/4885TSHR 4803/4885HPGD 1212/4885
US-11555012-B2 ACLY inhibitors and uses thereof ACLY, ATP5ME, ATP5MG HSD17B10 392/4885TSHR 4803/4885HPGD 1212/4885
US-20200055845-A1 KRAS G12C INHIBITORS AND METHODS OF USING THE SAME KRAS, NRAS, HRAS HSD17B10 3891/4885TSHR 4206/4885HPGD 1878/4885

“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.

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