SCHEMBL624930

SCHEMBL624930

COc1ccc(C(=O)CBr)c(OC)c1

nearest known ligand 0.61

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 3/20 0.61
LMNA P02545 1/20 0.61
HTT P42858 1/20 0.61
RAB9A P51151 5/20 0.60
NPC1 O15118 4/20 0.60
PKM P14618 1/20 0.57
MEN1 O00255 1/20 0.56
KMT2A Q03164 1/20 0.56
GSK3B P49841 1/20 0.56
HPGDS O60760 1/20 0.55
MAPT P10636 4/20 0.55
USP2 O75604 1/20 0.55
CASP3 P42574 1/20 0.55
SENP8 Q96LD8 1/20 0.55
SENP7 Q9BQF6 1/20 0.55
SENP6 Q9GZR1 1/20 0.55
L3MBTL1 Q9Y468 1/20 0.55
TP53 P04637 1/20 0.54
ALDH1A1 P00352 3/20 0.53
KDM4E B2RXH2 1/20 0.53

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
SCHEMBL29799615 1.00 SMN1; SMN2 (0.61) SMN1; SMN2LMNAHTTRAB9ANPC1
SCHEMBL5052478 0.89 KDM4E (0.56) SMN1; SMN2LMNAHTTRAB9ANPC1
SCHEMBL30016497 0.86 HTT (0.60) SMN1; SMN2LMNAHTTMEN1KMT2A
SCHEMBL628989 0.86 HTT (0.60) SMN1; SMN2LMNAHTTMEN1KMT2A
SCHEMBL2978070 0.86 SMN1; SMN2 (0.65) SMN1; SMN2LMNAHTTRAB9ANPC1
SCHEMBL7396688 0.85 LMNA (0.51) SMN1; SMN2LMNAHTTRAB9ANPC1
SCHEMBL10756137 0.85 HPGDS (0.48) SMN1; SMN2LMNAHTTRAB9ANPC1
SCHEMBL5051445 0.84 GSK3B (0.58) SMN1; SMN2LMNAHTTRAB9ANPC1
SCHEMBL5914630 0.84 SMN1; SMN2 (0.63) SMN1; SMN2LMNAHTTRAB9ANPC1
SCHEMBL4653380 0.84 SMN1; SMN2 (0.63) SMN1; SMN2LMNAHTTRAB9ANPC1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11958844-B2 1,3,4-oxadiazole derivative compounds as histone deacetylase 6 inhibitor, and pharmaceutical composition comprising the same CHONG KUN DANG PHARMACEUTICAL CORP. (KR) 2024-04-16 US disclosed
EP-3212636-B1 NEW PYRIDINYLOXY- AND PHENYLOXY-PYRAZOLYL COMPOUNDS HOFFMANN LA ROCHE (CH) 2023-11-29 EP disclosed
EP-3827004-B1 4-(1,3,4-OXADIAZOLE-2-YL)PYRIDINE-2(1H)-ONE DERIVATIVES AS HISTONE DEACETYLASE 6 (HDAC6) INHIBITORS FOR THE TREATMENT OF E.G. INFECTIONS CHONG KUN DANG PHARMACEUTICAL CORP (KR) 2023-10-11 EP disclosed
US-11071736-B2 Modulators of HEC1 activity and methods therefor TAIVEX THERAPEUTICS CORPORATION 2021-07-27 US disclosed
US-20210188831-A1 1,3,4-OXADIAZOLE DERIVATIVE COMPOUNDS AS HISTONE DEACETYLASE 6 INHIBITOR, AND PHARMACEUTICAL COMPOSITION COMPRISING THE SAME CHONG KUN DANG PHARMACEUTICAL CORP. (KR) 2021-06-24 US disclosed
EP-3827004-A1 1,3,4-OXADIAZOLE DERIVATIVE COMPOUNDS AS HISTONE DEACETYLASE 6 INHIBITOR, AND PHARMACEUTICAL COMPOSITION COMPRISING THE SAME Chong Kun Dang Pharmaceutical Corp. (KR) 2021-06-02 EP disclosed
CN-112839942-A 1,3, 4-oxadiazole derivative compounds as histone deacetylase 6 inhibitors and pharmaceutical compositions comprising the same 株式会社钟根堂 2021-05-25 CN disclosed
US-20200247800-A1 SUBSTITUTED BICYCLIC HETEROCYCLIC COMPOUNDS AS NADPH OXIDASE INHIBITORS GLENMARK PHARMACEUTICALS S.A. (CH) 2020-08-06 US disclosed
US-10633377-B2 Imidazole and thiazole compositions for modifying biological signaling OHIO UNIVERSITY (US) 2020-04-28 US disclosed
US-10588909-B2 Modulators of HEC1 activity and methods therefor TAIVEX THERAPEUTICS CORPORATION (TW) 2020-03-17 US disclosed
EP-0052930-A1 Novel group VA salts and process for preparing same GULF RESEARCH & DEVELOPMENT COMPANY (US) 1982-06-02 EP disclosed
EP-0052931-A1 Novel group VA ylides and process for preparing same GULF RESEARCH & DEVELOPMENT COMPANY (US) 1982-06-02 EP disclosed
EP-0046331-A2 Nickel ylides GULF RESEARCH & DEVELOPMENT COMPANY (US) 1982-02-24 EP disclosed
EP-0046329-A1 Process for the oligomerization of ethylene GULF RESEARCH & DEVELOPMENT COMPANY (US) 1982-02-24 EP disclosed
EP-0046328-A1 Process for the oligomerization of ethylene in methanol GULF RESEARCH & DEVELOPMENT COMPANY (US) 1982-02-24 EP disclosed
EP-0046332-A2 Process for the preparation of nickel ylides containing ylide ligands with a sulfonated group V component GULF RESEARCH & DEVELOPMENT COMPANY (US) 1982-02-24 EP disclosed
US-4310716-A NICKEL YLIDE CATALYST GULF RESEARCH & DEVELOPMENT COMPANY (US) 1982-01-12 US disclosed
US-4301318-A OBTAINED BY REACTING ETHYLENE USING A NICKEL YLIDE CATALYST; SOLVENT EXTRACTION OF CATALYST USING AMMONIUM HYDROXIDE GULF RESEARCH & DEVELOPMENT COMPANY (US) 1981-11-17 US disclosed
US-4293727-A CATALYSIS WITH NICKEL YLIDE GULF RESEARCH & DEVELOPMENT COMPANY (US) 1981-10-06 US disclosed
US-4293502-A CATALYST FOR OLIGOMERIZATION OF ETHYLENE GULF RESEARCH & DEVELOPMENT COMPANY (US) 1981-10-06 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 (6 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-20200247800-A1 SUBSTITUTED BICYCLIC HETEROCYCLIC COMPOUNDS AS NADPH OXIDASE INHIBITORS NOX1, CYBB, NOX4 SMN1; SMN2 3077/4885LMNA 3874/4885HTT 3669/4885
US-11958844-B2 1,3,4-oxadiazole derivative compounds as histone deacetylase 6 inhibitor, and pharmaceutical composition comprising the same HDAC6, HDAC1, HDAC3 SMN1; SMN2 1465/4885LMNA 4019/4885HTT 265/4885
US-20210188831-A1 1,3,4-OXADIAZOLE DERIVATIVE COMPOUNDS AS HISTONE DEACETYLASE 6 INHIBITOR, AND PHARMACEUTICAL COMPOSITION COMPRISING THE SAME HDAC6, HDAC1, HDAC3 SMN1; SMN2 1465/4885LMNA 4019/4885HTT 265/4885
US-10588909-B2 Modulators of HEC1 activity and methods therefor WEE1, WEE2, NEK11 SMN1; SMN2 3067/4885LMNA 1837/4885HTT 1314/4885
US-11071736-B2 Modulators of HEC1 activity and methods therefor WEE1, WEE2, NEK11 SMN1; SMN2 3067/4885LMNA 1837/4885HTT 1314/4885
US-10633377-B2 Imidazole and thiazole compositions for modifying biological signaling TYRO3, FGFR1, STAT6 SMN1; SMN2 4866/4885LMNA 3392/4885HTT 3282/4885

“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.