SCHEMBL48543

SCHEMBL48543

O=C(O)CC[PH](c1ccccc1)(c1ccccc1)c1ccccc1

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KEAP1 Q14145 1/20 0.46
NR4A2 P43354 1/20 0.45
FFAR1 O14842 3/20 0.43
HDAC3 O15379 2/20 0.43
HDAC4 P56524 2/20 0.43
HDAC1 Q13547 2/20 0.43
HDAC7 Q8WUI4 2/20 0.43
HDAC2 Q92769 2/20 0.43
HDAC10 Q969S8 2/20 0.43
HDAC11 Q96DB2 2/20 0.43
HDAC8 Q9BY41 2/20 0.43
HDAC6 Q9UBN7 2/20 0.43
HDAC9 Q9UKV0 2/20 0.43
HDAC5 Q9UQL6 2/20 0.43
SMN1; SMN2 Q16637 2/20 0.43
MAPK1 P28482 1/20 0.43
ADRA1A P35348 1/20 0.43
SLC6A3 Q01959 1/20 0.43
ALDH1A1 P00352 3/20 0.42
CYP2C19 P33261 3/20 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
Hydrochloric Acid SCHEMBL5359414 0.98 KEAP1 (0.45) KEAP1NR4A2FFAR1HDAC3HDAC4
Bromide SCHEMBL25379769 0.98 KEAP1 (0.45) KEAP1NR4A2FFAR1HDAC3HDAC4
Bromide SCHEMBL12497329 0.98 KEAP1 (0.45) KEAP1NR4A2FFAR1HDAC3HDAC4
Hydrochloric Acid SCHEMBL28832277 0.98 KEAP1 (0.45) KEAP1NR4A2FFAR1HDAC3HDAC4
Bromide SCHEMBL28027686 0.96 KEAP1 (0.43) KEAP1NR4A2FFAR1HDAC3HDAC4
SCHEMBL838217 0.87 HDAC3 (0.50) KEAP1NR4A2FFAR1HDAC3HDAC4
SCHEMBL7524058 0.86 GAA (0.41) KEAP1NR4A2FFAR1HDAC3HDAC4
Bromide SCHEMBL8104984 0.85 HDAC3 (0.48) KEAP1NR4A2FFAR1HDAC3HDAC4
SCHEMBL1838985 0.85 HDAC3 (0.50) KEAP1NR4A2HDAC3HDAC4HDAC1
SCHEMBL15132444 0.84 HDAC3 (0.53) KEAP1HDAC3HDAC4HDAC1HDAC7

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115594713-A Small molecule probe for extracting and purifying mitochondria and preparation method and application thereof 西北工业大学(CN) 2023-01-13 CN claimed
WO-2026100367-A1 RESIST MATERIAL AND PATTERN FORMATION METHOD 東京応化工業株式会社 2026-05-15 WO disclosed
WO-2025094826-A1 HETEROPOLYOXOMETALATE HAVING MODIFIED LACUNARY SITE, OR MIXTURE THEREOF 東京応化工業株式会社 2025-05-08 WO disclosed
WO-2025094854-A1 METHOD FOR PRODUCING POLYACID SALTS OR MIXTURES THEREOF, AND METHOD FOR REMOVING IMPURITIES 東京応化工業株式会社 2025-05-08 WO disclosed
CN-119948603-A Dry etching residue removing liquid 株式会社德山 2025-05-06 CN disclosed
CN-119601113-A Method for comprehensively identifying and comprehensively evaluating risk of phosphorus-containing organic compounds in environment 中国科学院生态环境研究中心 2025-03-11 CN disclosed
CN-118974895-A Filter lubricant containing onium ion 株式会社德山 2024-11-15 CN disclosed
CN-118613472-A Nicotinamide ester and nicotinamide riboside-based compounds and derivatives thereof 新前沿生物公司 2024-09-06 CN disclosed
US-20240216516-A1 GLUTARIMIDE-CONTAINING KRAS-MUTANT DEGRADER COMPOUNDS AND USES THEREOF TIGER BIOTHERAPEUTICS INC. 2024-07-04 US disclosed
WO-2024143473-A1 DECOMPOSITION INHIBITOR FOR TRANSITION METAL OXIDANTS 株式会社トクヤマ 2024-07-04 WO disclosed
US-4766128-A Optionally 11- to 13-substituted ergoline compounds useful as medicinal agents SCHERING AKTIENGESELLSCHAFT (DE) 1988-08-23 US disclosed
EP-0056358-B1 NOVEL (2-HALOERGOLINYL)-N'-N'-DIETHYLUREA DERIVATIVES, PROCESS FOR THE PREPARATION THEREOF, AND USE THEREOF AS MEDICINAL AGENTS SCHERING AKTIENGESELLSCHAFT (DE) 1987-04-22 EP disclosed
US-4639464-A Antihypertensive substituted imidazole derivatives FARMOS GROUP, LTD. (FI) 1987-01-27 US disclosed
EP-0201071-A2 2-Substituted-1-naphthols as 5-lipoxygenase inhibitors THE DU PONT MERCK PHARMACEUTICAL COMPANY (US) 1986-11-12 EP disclosed
EP-0072615-B1 SUBSTITUTED IMIDAZOLE DERIVATIVES AND THEIR PREPARATION AND USE Farmos Group Ltd. (FI) 1985-12-27 EP disclosed
US-4544664-A Antihypertensive substituted imidazole derivatives FARMOS GROUP, LTD. (FI) 1985-10-01 US disclosed
US-4492797-A DIURETICS HOFFMANN-LA ROCHE INC. (US) 1985-01-08 US disclosed
EP-0072615-A1 Substituted imidazole derivatives and their preparation and use Farmos Group Ltd. (FI) 1983-02-23 EP disclosed
EP-0056358-A1 Novel (2-haloergolinyl)-N'-N'-diethylurea derivatives, process for the preparation thereof, and use thereof as medicinal agents SCHERING AKTIENGESELLSCHAFT (DE) 1982-07-21 EP disclosed
US-4255436-A 2-Oxo-3 thiazoline-oximes as pesticides HOFFMANN-LA ROCHE INC. (US) 1981-03-10 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 (1 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-20240216516-A1 GLUTARIMIDE-CONTAINING KRAS-MUTANT DEGRADER COMPOUNDS AND USES THEREOF KRAS, VHL, HRAS KEAP1 46/4885NR4A2 3520/4885FFAR1 3201/4885

“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.