Acotiamide

Acotiamide

SCHEMBL6968566

COc1cc(O)c(C(=O)Nc2nc(C(=O)NCCN(C(C)C)C(C)C)cs2)cc1OC.Cl

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACHE

The experimentally established mechanism targets of Acotiamide. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ACHE known ✓ P22303 2/20 1.00
LMNA P02545 2/20 0.42
NPSR1 Q6W5P4 1/20 0.42
HSD17B10 Q99714 1/20 0.42
TSHR P16473 2/20 0.41
HPGD P15428 1/20 0.41
MEN1 O00255 1/20 0.38
POLB P06746 1/20 0.38
KMT2A Q03164 1/20 0.38
MME P08473 1/20 0.38
KDM4E B2RXH2 2/20 0.37
SMN1; SMN2 Q16637 2/20 0.37
NPC1 O15118 1/20 0.37
MITF O75030 1/20 0.37
RAB9A P51151 1/20 0.37
APP P05067 3/20 0.37
ALDH1A1 P00352 1/20 0.36
PDE5A O76074 1/20 0.36
MAPK1 P28482 2/20 0.36
MAPKAPK2 P49137 1/20 0.36

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
Acotiamide SCHEMBL29362154 0.99 ACHE (0.98) ACHELMNANPSR1HSD17B10TSHR
Acotiamide SCHEMBL27938245 0.99 ACHE (0.98) ACHELMNANPSR1HSD17B10TSHR
Acotiamide SCHEMBL30872102 0.99 ACHE (1.00) ACHELMNANPSR1HSD17B10TSHR
Acotiamide SCHEMBL28293346 0.99 ACHE (1.00) ACHELMNANPSR1HSD17B10TSHR
Acotiamide SCHEMBL1043131 0.99 ACHE (1.00) ACHELMNANPSR1HSD17B10TSHR
Hydrochloric Acid SCHEMBL6973893 0.95 ACHE (0.91) ACHELMNANPSR1HSD17B10TSHR
Hydrochloric Acid SCHEMBL6975742 0.95 ACHE (0.91) ACHELMNANPSR1HSD17B10TSHR
Hydrochloric Acid SCHEMBL27944898 0.94 ACHE (0.88) ACHELMNANPSR1HSD17B10TSHR
Hydrochloric Acid SCHEMBL6963022 0.93 ACHE (0.86) ACHELMNANPSR1HSD17B10TSHR
Hydrochloric Acid SCHEMBL28208032 0.93 ACHE (0.86) ACHELMNANPSR1HSD17B10TSHR

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 12 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111518052-A Preparation method of acotiamide hydrochloride impurity 廊坊市泽康医药科技有限公司 2020-08-11 CN disclosed
CN-111440128-A Preparation method of acotiamide hydrochloride impurity 廊坊市泽康医药科技有限公司 2020-07-24 CN disclosed
EP-2650277-B1 METHOD FOR PRODUCING 2-BROMO-4,5-DIALKOXY BENZOIC ACID ZERIA PHARM CO LTD (JP) 2018-07-11 EP disclosed
US-9096511-B2 Method for producing 2-bromo-4,5-dialkoxy benzoic acid ZERIA PHARMACEUTICAL CO., LTD. (JP) 2015-08-04 US disclosed
EP-2650277-A1 METHOD FOR PRODUCING 2-BROMO-4,5-DIALKOXY BENZOIC ACID Zeria Pharmaceutical Co., Ltd. (JP) 2013-10-16 EP disclosed
US-20130253222-A1 METHOD FOR PRODUCING 2-BROMO-4,5-DIALKOXY BENZOIC ACID ZERIA PHARMACEUTICAL CO., LTD (JP) 2013-09-26 US disclosed
EP-0870765-B1 AMINOTHIAZOLE DERIVATIVES, DRUG CONTAINING THE SAME AND INTERMEDIATE IN THE PRODUCTION OF THE COMPOUNDS ZERIA PHARM CO LTD (JP) 2003-11-19 EP disclosed
EP-0994108-B1 PROCESS FOR PRODUCING 2-HYDROXYBENZAMIDE DERIVATIVES ZERIA PHARM CO LTD (JP) 2003-05-14 EP disclosed
US-6197970-B1 REACTING WITH SECONDARY OR TERTIARY AMINE; DEBLOCKING, DEPROTECTING ZERIA PHARMACEUTICAL CO., LTD. (JP) 2001-03-06 US disclosed
EP-0994108-A1 PROCESS FOR PRODUCING 2-HYDROXYBENZAMIDE DERIVATIVES ZERIA PHARMACEUTICAL CO., LTD. (JP) 2000-04-19 EP disclosed
US-5981557-A HAVING IMPROVING EFFECTS ON THE DYSMOTILITY IN THE GASTROINTESTINAL TRACT ZERIA PHARMACEUTICAL CO., LTD. (JP) 1999-11-09 US disclosed
EP-0870765-A1 AMINOTHIAZOLE DERIVATIVES, DRUG CONTAINING THE SAME AND INTERMEDIATE IN THE PRODUCTION OF THE COMPOUNDS ZERIA PHARMACEUTICAL CO., LTD. (JP) 1998-10-14 EP 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-20130253222-A1 METHOD FOR PRODUCING 2-BROMO-4,5-DIALKOXY BENZOIC ACID HAO2, HAAO, BBOX1 ACHE 3526/4885LMNA 2835/4885NPSR1 1086/4885

“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.