SCHEMBL1289638

SCHEMBL1289638

COc1ccc(NC(=O)CCl)cc1

nearest known ligand 0.69

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ L3MBTL1 Q9Y468 2/20 0.69
▸ ALDH1A1 P00352 4/20 0.65
▸ HTT P42858 1/20 0.65
▸ RNF4 P78317 1/20 0.65
▸ SMN1; SMN2 Q16637 4/20 0.63
▸ RAB9A P51151 3/20 0.63
▸ NPC1 O15118 2/20 0.63
▸ MEN1 O00255 3/20 0.62
▸ KMT2A Q03164 3/20 0.62
▸ LMNA P02545 2/20 0.62
▸ MAPT P10636 4/20 0.61
▸ HDAC3 O15379 2/20 0.61
▸ HDAC4 P56524 2/20 0.61
▸ HDAC1 Q13547 2/20 0.61
▸ HDAC7 Q8WUI4 2/20 0.61
▸ HDAC2 Q92769 2/20 0.61
▸ HDAC10 Q969S8 2/20 0.61
▸ HDAC11 Q96DB2 2/20 0.61
▸ HDAC8 Q9BY41 2/20 0.61
▸ HDAC6 Q9UBN7 2/20 0.61

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
SCHEMBL22931143 0.95 L3MBTL1 (0.63) L3MBTL1ALDH1A1HTTRNF4SMN1; SMN2
SCHEMBL23748676 0.95 RNF4 (0.73) L3MBTL1ALDH1A1HTTRNF4SMN1; SMN2
SCHEMBL14704205 0.91 L3MBTL1 (0.58) L3MBTL1ALDH1A1HTTRNF4SMN1; SMN2
SCHEMBL6411466 0.88 L3MBTL1 (0.63) L3MBTL1ALDH1A1HTTSMN1; SMN2RAB9A
SCHEMBL9313874 0.86 L3MBTL1 (0.76) L3MBTL1ALDH1A1HTTSMN1; SMN2RAB9A
SCHEMBL4381948 0.86 L3MBTL1 (0.75) L3MBTL1ALDH1A1HTTSMN1; SMN2RAB9A
SCHEMBL11806908 0.85 RNF4 (0.86) L3MBTL1ALDH1A1HTTRNF4SMN1; SMN2
SCHEMBL9081388 0.84 NPC1 (0.76) L3MBTL1ALDH1A1HTTRNF4SMN1; SMN2
SCHEMBL18778782 0.84 L3MBTL1 (0.67) L3MBTL1ALDH1A1HTTSMN1; SMN2RAB9A
SCHEMBL14702222 0.83 SMN1; SMN2 (0.54) L3MBTL1ALDH1A1HTTRNF4SMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-109912516-B Green preparation method of 1,2,3, 4-tetrahydropyrimidinone compound with SOD activity promoting function 深圳王者天下生物科技有限公司 2022-05-03 — — CN claimed
US-12162820-B2 Peripheral alkyl and alkenyl chains extended benzene derivatives and pharmaceutical composition including the same TAIWANJ PHARMACEUTICALS CO., LTD. (TW) 2024-12-10 — — US disclosed
CN-113660932-B Phenyl derivatives having pendant alkyl and alkenyl extensions and pharmaceutical compositions comprising the same 景凯生物科技股份有限公司 2024-07-12 — — CN disclosed
EP-3426246-B1 THIAZOLIDINONE COMPOUNDS AND USE THEREOF NATIONAL HEALTH RES INST (TW) 2024-05-01 — — EP disclosed
CN-117658932-A Amino dithioester derivative containing amide structural unit, and preparation method and application thereof 郑州大学 2024-03-08 — — CN disclosed
EP-4326721-A1 SPIROCYCLIC IMIDAZOLIDINONES AND IMIDAZOLIDINEDIONES FOR TREATMENT OF LIGHT CHAIN AMYLOIDOSIS Protego Biopharma, Inc. (US) 2024-02-28 — — EP disclosed
US-20240051960-A1 SPIROCYCLIC IMIDAZOLIDINONES AND IMIDAZOLIDINEDIONES FOR TREATMENT OF LIGHT CHAIN AMYLOIDOSIS PROTEGO BIOPHARMA, INC. 2024-02-15 — — US disclosed
US-20240018135-A1 COMPOUND HAVING INHIBITORY ACTIVITY AGAINST O-GLUSACASE AND USE THEREOF MEDIFRON DBT INC. (KR) 2024-01-18 — — US disclosed
US-20240018135-A1 COMPOUND HAVING INHIBITORY ACTIVITY AGAINST O-GLUSACASE AND USE THEREOF MEDIFRON DBT INC. (KR) 2024-01-18 — — US disclosed
US-20240018135-A1 COMPOUND HAVING INHIBITORY ACTIVITY AGAINST O-GLUSACASE AND USE THEREOF MEDIFRON DBT INC. (KR) 2024-01-18 — — US disclosed
WO-1999001454-A1 IMIDAZOPYRIMIDINES AND IMIDAZOPYRIDINES FOR THE TREATMENT OF NEUROLOGICAL DISORDERS DU PONT PHARMACEUTICALS COMPANY (US) 1999-01-14 — — WO disclosed
US-5631403-A HYDROLYSIS OF HALOCARBOXANILIDE IN SOLVENT HOECHST AG (DE) 1997-05-20 — — US disclosed
EP-0283310-B1 N-BENZHYDRYL-SUBSTITUTED HETEROCYCLIC DERIVATIVES, THEIR PREPARATION AND THEIR USE Sankyo Company Limited (JP) 1993-05-26 — — EP disclosed
US-5028610-A Calcium Channel Blockers SANKYO COMPANY LIMITED (JP) 1991-07-02 — — US disclosed
US-4567264-A ADRENERGIC BLOCKING AGENTS SYNTEX (U.S.A.) INC. (US) 1986-01-28 — — US disclosed
US-4558129-A Benzodioxanyl-hydroxyethylene-piperazinyl acetanilides which effect calcium entry and β-blockade SYNTEX (U.S.A.) INC. (US) 1985-12-10 — — US disclosed
US-4530931-A 8-Quinoline carbanilates for the inhibition of lipolysis USV PHARMACEUTICAL CORP. (US) 1985-07-23 — — US disclosed
US-4499100-A CARDIOUVASCULAR DISORDERS SYNTEX (U.S.A.) INC. (US) 1985-02-12 — — US disclosed
EP-0126449-A1 Cardioselective aryloxy- and arylthio-hydroxypropyl piperazinyl acetanilides wich affect calcium entry SYNTEX (U.S.A.) INC. (US) 1984-11-28 — — EP disclosed
US-4102924-A REACTING ACYLAMINO-ARYLS WITH HALO-ARYLS BAYER AKTIENGESELLSCHAFT (DE) 1978-07-25 — — 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 (3 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-20240051960-A1 SPIROCYCLIC IMIDAZOLIDINONES AND IMIDAZOLIDINEDIONES FOR TREATMENT OF LIGHT CHAIN AMYLOIDOSIS IGLV6-57, TTR, MAP1LC3C L3MBTL1 4416/4885ALDH1A1 458/4885HTT 154/4885
US-20240018135-A1 COMPOUND HAVING INHIBITORY ACTIVITY AGAINST O-GLUSACASE AND USE THEREOF OGA, OGT, ENGASE L3MBTL1 1625/4885ALDH1A1 1141/4885HTT 3292/4885
US-12162820-B2 Peripheral alkyl and alkenyl chains extended benzene derivatives and pharmaceutical composition including the same AADAC, ENPP2, ATXN10 L3MBTL1 3270/4885ALDH1A1 1691/4885HTT 8/4885

“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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