SCHEMBL3896575

SCHEMBL3896575

COCCCOc1ccnc(COC(C)=O)c1C

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 4/20 0.46
KMT2A Q03164 3/20 0.46
CYP2C9 P11712 2/20 0.46
WDR5 P61964 2/20 0.46
DDAH1 O94760 1/20 0.46
LMNA P02545 1/20 0.46
HTR1A P08908 1/20 0.46
ADORA3 P0DMS8 1/20 0.46
MAPT P10636 1/20 0.46
IDE P14735 1/20 0.46
HPGD P15428 1/20 0.46
ADRA2B P18089 1/20 0.46
TBXA2R P21731 1/20 0.46
ACHE P22303 1/20 0.46
PTGS1 P23219 1/20 0.46
SLC6A2 P23975 1/20 0.46
NPY1R P25929 1/20 0.46
ADORA1 P30542 1/20 0.46
ADRA1A P35348 1/20 0.46
OPRM1 P35372 1/20 0.46

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
SCHEMBL29752552 1.00 ALDH1A1 (0.46) ALDH1A1KMT2ACYP2C9WDR5DDAH1
SCHEMBL8081113 0.88 ALDH1A1 (0.38) ALDH1A1KMT2ACYP2C9WDR5DDAH1
SCHEMBL2994158 0.88 ALDH1A1 (0.42) ALDH1A1KMT2ACYP2C9WDR5DDAH1
SCHEMBL8503271 0.87 ALDH1A1 (0.40) ALDH1A1KMT2ACYP2C9WDR5DDAH1
SCHEMBL2992903 0.86 LMNA (0.39) ALDH1A1KMT2ACYP2C9LMNAMAPT
SCHEMBL31515431 0.86 ALDH1A1 (0.41) ALDH1A1KMT2ACYP2C9WDR5DDAH1
SCHEMBL2991805 0.86 IKBKB (0.40) ALDH1A1KMT2ACYP2C9WDR5DDAH1
SCHEMBL1735008 0.85 ALDH1A1 (0.36) ALDH1A1KMT2ACYP2C9WDR5DDAH1
SCHEMBL1733369 0.85 ALDH1A1 (0.36) ALDH1A1KMT2ACYP2C9WDR5DDAH1
SCHEMBL1734018 0.85 ALDH1A1 (0.36) ALDH1A1KMT2ACYP2C9WDR5DDAH1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111704573-B Preparation method of rabeprazole chloride and intermediate thereof 珠海润都制药股份有限公司 2022-07-08 CN claimed
CN-111704573-A Preparation method of rabeprazole chloride and intermediate thereof 珠海润都制药股份有限公司 2020-09-25 CN claimed
US-20240238264-A1 INHIBITORS OF SARM1 NADASE ACTIVITY AND USES THEREOF DISARM THERAPEUTICS, INC. 2024-07-18 US disclosed
CN-111704573-B Preparation method of rabeprazole chloride and intermediate thereof 珠海润都制药股份有限公司 2022-07-08 CN disclosed
US-11253503-B2 Inhibitors of SARM1 NADase activity and uses thereof WASHINGTON UNIVERSITY (US) 2022-02-22 US disclosed
CN-111704573-A Preparation method of rabeprazole chloride and intermediate thereof 珠海润都制药股份有限公司 2020-09-25 CN disclosed
US-20200129493-A1 INHIBITORS OF SARM1 NADASE ACTIVITY AND USES THEREOF WASHINGTON UNIVERSITY (US) 2020-04-30 US disclosed
WO-2018057989-A1 INHIBITORS OF SARM1 NADase ACTIVITY AND USES THEREOF WASHINGTON UNIVERSITY (US) 2018-03-29 WO disclosed
WO-2009116072-A2 PROCESS FOR PREPARATION OF PYRIDINYLMETHYLSULPHINYL BENZIMIDAZOLE COMPOUNDS AND PYRIDINE INTERMEDIATES IPCA LABORATORIES LIMITED (IN) 2009-09-24 WO disclosed
EP-2022789-A1 Process for the preparation of a gastric acid secretion inhibitor Farmaprojects, S.A. (ES) 2009-02-11 EP disclosed
WO-2001004109-A1 PROCESS FOR THE PRODUCTION OF 2-(2-PYRIDINYLMETHYLSULPHINYL)-1H-BENZIMIDAZOLES QUIMICA SINTETICA, S.A. (ES) 2001-01-18 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 (3 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-20200129493-A1 INHIBITORS OF SARM1 NADASE ACTIVITY AND USES THEREOF SARM1, NADK, NNMT ALDH1A1 1659/4885KMT2A 2098/4885CYP2C9 4424/4885
US-20240238264-A1 INHIBITORS OF SARM1 NADASE ACTIVITY AND USES THEREOF SARM1, NADK, NNMT ALDH1A1 1659/4885KMT2A 2098/4885CYP2C9 4424/4885
US-11253503-B2 Inhibitors of SARM1 NADase activity and uses thereof SARM1, NADK, NNMT ALDH1A1 1659/4885KMT2A 2098/4885CYP2C9 4424/4885

“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.