SCHEMBL1307697

SCHEMBL1307697

COCCCOc1ccnc(CCl)c1C

nearest known ligand 0.48

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPT P10636 5/20 0.48
ALDH1A1 P00352 5/20 0.48
LMNA P02545 4/20 0.48
HPGD P15428 4/20 0.48
CYP2C9 P11712 3/20 0.48
KMT2A Q03164 3/20 0.48
WDR5 P61964 2/20 0.48
DDAH1 O94760 1/20 0.48
HTR1A P08908 1/20 0.48
ADORA3 P0DMS8 1/20 0.48
IDE P14735 1/20 0.48
ADRA2B P18089 1/20 0.48
TBXA2R P21731 1/20 0.48
ACHE P22303 1/20 0.48
PTGS1 P23219 1/20 0.48
SLC6A2 P23975 1/20 0.48
NPY1R P25929 1/20 0.48
ADORA1 P30542 1/20 0.48
ADRA1A P35348 1/20 0.48
OPRM1 P35372 1/20 0.48

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
SCHEMBL29645275 1.00 MAPT (0.48) MAPTALDH1A1LMNAHPGDCYP2C9
Hydrochloric Acid SCHEMBL28082928 0.98 MAPT (0.47) MAPTALDH1A1LMNAHPGDCYP2C9
Hydrochloric Acid SCHEMBL2781673 0.98 MAPT (0.47) MAPTALDH1A1LMNAHPGDCYP2C9
Water SCHEMBL28093018 0.97 MAPT (0.46) MAPTALDH1A1LMNAHPGDCYP2C9
SCHEMBL8551045 0.92 ALDH1A1 (0.41) MAPTALDH1A1LMNAHPGDCYP2C9
SCHEMBL6872706 0.88 MAPT (0.38) MAPTALDH1A1LMNAHPGDCYP2C9
SCHEMBL27971566 0.85 CYP2C9 (0.40) MAPTALDH1A1LMNAHPGDCYP2C9
Hydrochloric Acid SCHEMBL6865752 0.85 MAPT (0.36) MAPTALDH1A1LMNAHPGDCYP2C9
SCHEMBL24520493 0.85 MAPT (0.49) MAPTALDH1A1LMNAHPGDCYP2C9
SCHEMBL1308045 0.85 KMT2A (0.49) MAPTALDH1A1LMNAHPGDCYP2C9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114609268-B Detection method for related substances in sodium rabeprazole bulk drug 南京海纳医药科技股份有限公司 2024-04-16 CN claimed
CN-114609268-A Method for detecting related substances in dextral rabeprazole sodium bulk drug 南京海纳医药科技股份有限公司 2022-06-10 CN claimed
CN-103965166-B Rabeprazole intermediate impurities 2-{ [4-(3-methoxy propoxy)-3-oxide of mathylpyridine-2-base] methyl sulfur } preparation method of-1H-benzimidazole 东南大学 2016-08-17 CN claimed
CN-103058997-A Synthesis method of thioether nitrogen oxides (2-{[4-(3-methoxy-propoxy)-3-methyl nitrogen-oxygen pyridine-2-group] methylmercapto}-1H-benzimidazole) NEW DRUG DEV COMPANY LTD OF JILIN XIUZHENG PHARMACEUTICAL GROUP 2013-04-24 CN claimed
EP-1851212-B1 NEW PROCESS FOR SYNTHESIS OF PROTON PUMP INHIBITORS CIPLA LTD (IN) 2010-07-07 EP claimed
WO-2025016200-A1 CHELATING RESIN COMPOSITION, PREPARATION METHOD THEREFOR AND USE THEREOF 上海稀固科技有限公司 2025-01-23 WO disclosed
US-20240238264-A1 INHIBITORS OF SARM1 NADASE ACTIVITY AND USES THEREOF DISARM THERAPEUTICS, INC. 2024-07-18 US disclosed
US-20240238264-A1 INHIBITORS OF SARM1 NADASE ACTIVITY AND USES THEREOF DISARM THERAPEUTICS, INC. 2024-07-18 US disclosed
CN-114609268-B Detection method for related substances in sodium rabeprazole bulk drug 南京海纳医药科技股份有限公司 2024-04-16 CN disclosed
CN-115215877-B Preparation method of Annarazole 轩竹(北京)医药科技有限公司 2024-03-15 CN disclosed
CN-115215877-A Preparation method of anaprazole 轩竹(北京)医药科技有限公司 2022-10-21 CN disclosed
WO-2022143610-A1 NOVEL AMIDE PYRROLE COMPOUNDS AND USE THEREOF IN MEDICAMENTS 广东东阳光药业有限公司 2022-07-07 WO disclosed
US-5998445-A PEPTIC ULCERS EISAI CO., LTD. (JP) 1999-12-07 US disclosed
US-5840910-A Pyridine derivatives having anti-ulcerative activity ESAI CO., LTD. (JP) 1998-11-24 US disclosed
EP-0268956-B2 Pyridine derivatives, pharmaceutical compositions comprising the same, the use of the same for the manufacture of medicaments having therapeutic or preventative value, and a process for preparing the same EISAI CO LTD (JP) 1998-04-15 EP disclosed
EP-0786461-A1 Pyridine derivatives, pharmaceutical compositions comprising the same, the use of the same for the manufacture of medicaments having therapeutic or preventative value, and a process for preparing the same Eisai Co., Ltd. (JP) 1997-07-30 EP disclosed
EP-0654471-A1 Pyridine derivatives, pharmaceutical compositions comprising the same, the use of the same for the manufacture of medicaments having therapeutic or preventative value, and process for preparing the same Eisai Co., Ltd. (JP) 1995-05-24 EP disclosed
EP-0475456-A1 Pyridine derivatives, pharmaceutical compositions comprising the same, the use of the same for the manufacture of medicaments having therapeutic or preventative value, and a process for preparing the same Eisai Co., Ltd. (JP) 1992-03-18 EP disclosed
US-5045552-A Pyridine derivatives having anti-ulcerative activity EISAI CO., LTD. (JP) 1991-09-03 US disclosed
EP-0268956-A2 Pyridine derivatives, pharmaceutical compositions comprising the same, the use of the same for the manufacture of medicaments having therapeutic or preventative value, and a process for preparing the same Eisai Co., Ltd. (JP) 1988-06-01 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-20240238264-A1 INHIBITORS OF SARM1 NADASE ACTIVITY AND USES THEREOF SARM1, NADK, NNMT MAPT 242/4885ALDH1A1 1659/4885LMNA 1715/4885

“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.