SCHEMBL969754

SCHEMBL969754

O=C(O)CC(=O)Oc1ccccn1

nearest known ligand 0.42

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
TSHR P16473 1/20 0.42
PSMB5 P28074 1/20 0.42
LMNA P02545 2/20 0.41
NAPRT Q6XQN6 1/20 0.41
P4HTM Q9NXG6 1/20 0.41
L3MBTL1 Q9Y468 1/20 0.41
GAA P10253 3/20 0.41
SMN1; SMN2 Q16637 4/20 0.40
NPC1 O15118 4/20 0.40
RAB9A P51151 4/20 0.40
ALDH1A1 P00352 2/20 0.40
PKM P14618 1/20 0.39
HPGD P15428 1/20 0.39
ALOX15 P16050 1/20 0.39
TDP1 Q9NUW8 1/20 0.39
CES2 O00748 1/20 0.38
CES1 P23141 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
SCHEMBL240908 0.91 TSHR (0.45) TSHRPSMB5LMNANAPRTP4HTM
SCHEMBL38661115 0.84 TSHR (0.45) TSHRPSMB5LMNAGAASMN1; SMN2
SCHEMBL240655 0.84 SMN1; SMN2 (0.46) TSHRLMNAL3MBTL1GAASMN1; SMN2
SCHEMBL27811093 0.81 TSHR (0.41) TSHRPSMB5LMNANAPRTP4HTM
SCHEMBL1177985 0.81 CYP19A1 (0.54) TSHRPSMB5LMNAL3MBTL1GAA
SCHEMBL7414860 0.80 TSHR (0.40) TSHRPSMB5LMNANAPRTP4HTM
SCHEMBL4996914 0.80 ALDH1A1 (0.45) TSHRLMNAGAASMN1; SMN2NPC1
SCHEMBL30571184 0.80 ALDH1A1 (0.45) TSHRLMNAGAASMN1; SMN2NPC1
SCHEMBL6245082 0.80 TSHR (0.40) TSHRPSMB5LMNANAPRTP4HTM
SCHEMBL14501436 0.80 SMN1; SMN2 (0.44) TSHRLMNANAPRTP4HTML3MBTL1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117440945-A Pyrimidine or pyridine derivative, preparation method thereof and application thereof in pharmacy 上海和誉生物医药科技有限公司 2024-01-23 CN disclosed
CN-115867539-A 2, 3-dihydro-1H-pyrrolo [3,2-b ] pyridine derivatives, preparation method and application thereof 上海和誉生物医药科技有限公司 2023-03-28 CN disclosed
CN-115836064-A Triazine derivative with EGFR (epidermal growth factor receptor) inhibitory activity and preparation method and application thereof 上海和誉生物医药科技有限公司 2023-03-21 CN disclosed
US-10954231-B2 Anxiolytic compounds BIONOMICS LIMITED (AU) 2021-03-23 US disclosed
EP-3109227-B1 METHOD FOR CONTINUOUSLY PRODUCING KETOMALONIC ACID COMPOUND USING FLOW REACTOR KUMIAI CHEMICAL INDUSTRY CO (JP) 2020-04-08 EP disclosed
CN-105980345-B Method for continuously producing ketomalonic acid compound using flow reactor 组合化学工业株式会社 2019-12-20 CN disclosed
WO-2019109150-A1 METHODS OF TREATING AGITATION BIONOMICS LIMITED (AU) 2019-06-13 WO disclosed
US-10233181-B2 Anxiolytic compounds BIONOMICS LIMITED (AU) 2019-03-19 US disclosed
EP-3023411-B1 PRODUCTION METHOD OF KETOMALONIC ACID COMPOUND KUMIAI CHEMICAL INDUSTRY CO (JP) 2018-12-05 EP disclosed
US-20180305290-A1 METHOD FOR CONTINUOUSLY PRODUCING KETOMALONIC ACID COMPOUND USING FLOW REACTOR KUMIAI CHEMICAL INDUSTRY CO., LTD. (JP) 2018-10-25 US disclosed
EP-1091953-B1 NOVEL BENZOTHIEPINES HAVING ACTIVITY AS INHIBITORS OF ILEAL BILE ACID TRANSPORT AND TAUROCHOLATE UPTAKE SEARLE & CO (US) 2003-12-10 EP disclosed
WO-2003040127-A1 NOVEL MONO- AND DI-FLUORINATED BENZOTHIEPINE COMPOUNDS AS INHIBITORS OF APICAL SODIUM CO-DEPENDENT BILE ACID TRANSPORT (ASBT) AND TAUROCHOLATE UPTAKE G.D. SEARLE LLC (US) 2003-05-15 WO disclosed
US-6387924-B2 ATHEROSCLEROSIS; ANTICHOLESTEROL AGENTS; ANTILIPIDEMIC AGENTS G.D. SEARLE & CO. 2002-05-14 US disclosed
US-20020013476-A1 Novel benzothiepines having activity as inhibitors of ileal bile acid transport and taurocholate uptake G.D. SEARLE & CO. 2002-01-31 US disclosed
US-6262277-B1 IN MEDICINE FOR PROPHYLAXIS AND THERAPY OF HYPERLIPIDEMIC CONDITIONS SUCH AS THOSE ASSOCIATED WITH ATHEROSCLEROSIS OR HYPERCHOLESTEROLEMIA, IN MAMMALS G.D. SEARLE AND COMPANY 2001-07-17 US disclosed
EP-1091953-A1 NOVEL BENZOTHIEPINES HAVING ACTIVITY AS INHIBITORS OF ILEAL BILE ACID TRANSPORT AND TAUROCHOLATE UPTAKE G.D. Searle & Co. (US) 2001-04-18 EP disclosed
US-6107494-A FOR TREATMENT OF HYPERLIPIDEMIC CONDITIONS SUCH AS THOSE ASSOCIATED WITH ATHEROSCLEROSIS OR HYPERCHOLESTEROLEMIA, IN MAMMALS G.D. SEARLE AND COMPANY (US) 2000-08-22 US disclosed
WO-2000001687-A9 BENZOTHIEPINES HAVING ACTIVITY AS INHIBITORS OF ILEAL BILE ACID TRANSPORT AND TAUROCHOLATE UPTAKE SEARLE & CO (US) 2000-07-20 WO disclosed
WO-2000001687-A1 BENZOTHIEPINES HAVING ACTIVITY AS INHIBITORS OF ILEAL BILE ACID TRANSPORT AND TAUROCHOLATE UPTAKE G.D. SEARLE & CO. (US) 2000-01-13 WO disclosed
US-5994391-A HYPERLIPEMIC AGENTS; ANTICHOLESTEROL AGENTS G.D. SEARLE AND COMPANY (US) 1999-11-30 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 (4 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-20020013476-A1 Novel benzothiepines having activity as inhibitors of ileal bile acid transport and taurocholate uptake SLC10A2, SLC10A1, ABCB11 TSHR 4128/4885PSMB5 2236/4885LMNA 3300/4885
US-20180305290-A1 METHOD FOR CONTINUOUSLY PRODUCING KETOMALONIC ACID COMPOUND USING FLOW REACTOR ME1, ME3, CA6 TSHR 3838/4885PSMB5 2616/4885LMNA 4446/4885
US-10233181-B2 Anxiolytic compounds GABBR1, GABRA6, SLC18A2 TSHR 1298/4885PSMB5 1118/4885LMNA 2761/4885
US-10954231-B2 Anxiolytic compounds GABRA6, GABRA2, GABRA5 TSHR 1279/4885PSMB5 1142/4885LMNA 2879/4885

“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.