SCHEMBL320644

SCHEMBL320644

CC(C)(C)OC(=O)NCCOCC(=O)O

nearest known ligand 0.51

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 1/20 0.51
GAA P10253 1/20 0.51
KMT2A Q03164 1/20 0.51
TDP1 Q9NUW8 1/20 0.50
IDO1 P14902 1/20 0.46
CA12 O43570 7/20 0.45
CA1 P00915 7/20 0.45
CA2 P00918 7/20 0.45
CA9 Q16790 7/20 0.45
MAOA P21397 1/20 0.44
MAOB P27338 1/20 0.44
EPHX1 P07099 1/20 0.42
NPSR1 Q6W5P4 1/20 0.41
ALDH1A1 P00352 2/20 0.40
GFER P55789 1/20 0.40
HTT P42858 1/20 0.38
SUCNR1 Q9BXA5 1/20 0.38

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
SCHEMBL21069640 0.97 MEN1 (0.49) MEN1GAAKMT2ATDP1IDO1
SCHEMBL13699512 0.97 MEN1 (0.49) MEN1GAAKMT2ATDP1IDO1
SCHEMBL25695638 0.97 MEN1 (0.49) MEN1GAAKMT2ATDP1IDO1
SCHEMBL3617073 0.97 MEN1 (0.49) MEN1GAAKMT2ATDP1IDO1
SCHEMBL21071644 0.97 MEN1 (0.49) MEN1GAAKMT2ATDP1IDO1
SCHEMBL23728812 0.97 MEN1 (0.49) MEN1GAAKMT2ATDP1IDO1
SCHEMBL1261192 0.97 MEN1 (0.49) MEN1GAAKMT2ATDP1IDO1
SCHEMBL29230312 0.94 MEN1 (0.50) MEN1GAAKMT2ATDP1IDO1
SCHEMBL25194819 0.92 MEN1 (0.49) MEN1GAAKMT2ATDP1IDO1
SCHEMBL14958594 0.92 TDP1 (0.51) MEN1GAAKMT2ATDP1IDO1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-113512035-B Dihydropyrimidine-pomalidomide conjugate, and preparation method and application thereof 山东大学 2023-11-24 CN claimed
CN-113512035-A Dihydropyrimidine-pomalidomide conjugate and preparation method and application thereof 山东大学 2021-10-19 CN claimed
US-20260116923-A1 CYCLIC PEPTIDE IL-1BETA TRAP FOR THE TREATMENT OF ATHEROSCLEROSIS AND INFLAMMATORY DISORDERS MERCK SHARP & DOHME LLC (US) 2026-04-30 US disclosed
CN-121574171-A Difunctional protein degradation agent of direct targeting proteasome, preparation method and application thereof 浙大城市学院 2026-02-27 CN disclosed
EP-4695237-A1 NOVEL COMPOUNDS FOR THE TREATMENT OF BACTERIAL INFECTIONS F. Hoffmann-La Roche AG (CH) 2026-02-18 EP disclosed
EP-4043447-B1 HALOGENATED TETRACYCLIC TRITERPENE DERIVATIVE, PREPARATION AND APPLICATION THEREOF SHANGHAI QINGDONG BIOTECHNOLOGY CO LTD (CN) 2026-01-21 EP disclosed
US-20260008778-A1 COMPOUNDS AND USES THEREOF FOGHORN THERAPEUTICS INC (US) 2026-01-08 US disclosed
US-12479840-B2 HMG-CoA reductase degradation inducing compound UPPTHERA INC. (KR) 2025-11-25 US disclosed
EP-4053126-B1 BRIDGED CYCLOFORMYLPYRIDINE DERIVATIVE AND USE THEREOF BROADENBIO CO LTD (CN) 2025-11-19 EP disclosed
US-12454524-B2 (r)-n-(4-(chlorodifluoromethoxy)phenyl)-2-(difluoromethyl)-1-(1-hydroxypropan-2-yl)-7-(pyrimidin-5-yl)-1H-benzo[d]imidazole-5-carboxamide, or a pharmaceutically acceptable salt or tautomer thereof, for treating certain leukemias TERNS PHARMACEUTICALS, INC. (US) 2025-10-28 US disclosed
US-20250325673-A1 IRAK DEGRADERS AND USES THEREOF KYMERA THERAPEUTICS INC (US) 2025-10-23 US disclosed
WO-2012148550-A1 PRODRUGS OF THERAPEUTIC COMPOUNDS MYREXIS, INC. (US) 2012-11-01 WO disclosed
WO-2012004005-A1 CONJUGATES COMPRISING HYDROXYALKYL STARCH AND A CYTOTOXIC AGENT AND PROCESS FOR THEIR PREPARATION FRESENIUS KABI DEUTSCHLAND GMBH (DE) 2012-01-12 WO disclosed
WO-2012004005-A1 CONJUGATES COMPRISING HYDROXYALKYL STARCH AND A CYTOTOXIC AGENT AND PROCESS FOR THEIR PREPARATION FRESENIUS KABI DEUTSCHLAND GMBH (DE) 2012-01-12 WO disclosed
WO-2012004006-A1 CONJUGATES COMPRISING HYDROXYALKYL STARCH AND A CYTOTOXIC AGENT AND PROCESS FOR THEIR PREPARATION FRESENIUS KABI DEUTSCHLAND GMBH (DE) 2012-01-12 WO disclosed
WO-2012004006-A1 CONJUGATES COMPRISING HYDROXYALKYL STARCH AND A CYTOTOXIC AGENT AND PROCESS FOR THEIR PREPARATION FRESENIUS KABI DEUTSCHLAND GMBH (DE) 2012-01-12 WO disclosed
US-8084643-B2 Nitrogen-containing esters of the secondary alcohol group of florfenicol and of its analogs,including salts; veterinary medicine; nonhydrolyzing as needed to maintain the prodrug in aqueous solution in the subjects system until appropriate; cattle drinking water; bovine respiratory disease INTERVET INC. (US) 2011-12-27 US disclosed
US-20110300174-A1 CONJUGATES FOR THE PREVENTION OR TREATMENT OF NICOTINE ADDICTION PFIZER VACCINES LLC (US) 2011-12-08 US disclosed
WO-2011151807-A1 CONJUGATES FOR THE PREVENTION OR TREATMENT OF NICOTINE ADDICTION PFIZER VACCINES LLC (US) 2011-12-08 WO disclosed
US-20080188556-A1 Water-Soluble Prodrugs of Florfenicol and its Analogs SCHERING-PLOUGH ANIMAL HEALTH CORPORATION 2008-08-07 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 (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-20250325673-A1 IRAK DEGRADERS AND USES THEREOF IRAK2, IRAK3, IRAK1 MEN1 4055/4885GAA 1234/4885KMT2A 445/4885
US-20110300174-A1 CONJUGATES FOR THE PREVENTION OR TREATMENT OF NICOTINE ADDICTION CHRNG, CHRND, CHRNA3 MEN1 1750/4885GAA 1418/4885KMT2A 741/4885
US-20260116923-A1 CYCLIC PEPTIDE IL-1BETA TRAP FOR THE TREATMENT OF ATHEROSCLEROSIS AND INFLAMMATORY DISORDERS IL1A, IL1B, IL1RN MEN1 1933/4885GAA 3941/4885KMT2A 3953/4885
US-20080188556-A1 Water-Soluble Prodrugs of Florfenicol and its Analogs PFAS, ADH5, SI MEN1 2179/4885GAA 1057/4885KMT2A 1864/4885
US-12454524-B2 (r)-n-(4-(chlorodifluoromethoxy)phenyl)-2-(difluoromethyl)-1-(1-hydroxypropan-2-yl)-7-(pyrimidin-5-yl)-1H-benzo[d]imidazole-5-carboxamide, or a pharmaceutically acceptable salt or tautomer thereof, for treating certain leukemias ABL1, ABL2, BCR MEN1 4339/4885GAA 961/4885KMT2A 122/4885
US-12479840-B2 HMG-CoA reductase degradation inducing compound HMGCR, HMGB2, LDLR MEN1 3715/4885GAA 640/4885KMT2A 2204/4885
US-20260008778-A1 COMPOUNDS AND USES THEREOF BRD9, BCL9L, BCL9 MEN1 270/4885GAA 1384/4885KMT2A 1478/4885

“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.