SCHEMBL986792

SCHEMBL986792

CCCc1nc(C(C)(C)O)c(C(=O)OCC)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1

nearest known ligand 0.76

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
AGTR1 P30556 8/20 0.62
AGTR2 P50052 8/20 0.62
ABCC3 O15438 1/20 0.61
ABCC4 O15439 1/20 0.61
ABCB11 O95342 1/20 0.61
CYP3A4 P08684 1/20 0.61
PDE4D Q08499 1/20 0.61
PDE3A Q14432 1/20 0.61
SLCO1B3 Q9NPD5 1/20 0.61
TDP1 Q9NUW8 1/20 0.61
SLCO1B1 Q9Y6L6 1/20 0.61

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
Hydrochloric Acid SCHEMBL7305266 0.99 AGTR1 (0.62) AGTR1AGTR2ABCC3ABCC4ABCB11
SCHEMBL683727 0.95 AGTR1 (0.58) AGTR1AGTR2ABCC3ABCC4ABCB11
SCHEMBL668336 0.94 AGTR1 (0.57) AGTR1AGTR2ABCC3ABCC4ABCB11
SCHEMBL7886344 0.94 AGTR1 (0.53) AGTR1AGTR2ABCC3ABCC4ABCB11
SCHEMBL7308359 0.94 AGTR1 (0.53) AGTR1AGTR2ABCC3ABCC4ABCB11
SCHEMBL16327937 0.93 AGTR1 (0.61) AGTR1AGTR2ABCC3ABCC4ABCB11
SCHEMBL6598015 0.92 AGTR1 (0.54) AGTR1AGTR2ABCC3ABCC4ABCB11
SCHEMBL669267 0.92 AGTR1 (0.58) AGTR1AGTR2ABCC3ABCC4ABCB11
SCHEMBL329001 0.92 AGTR1 (0.62) AGTR1AGTR2ABCC3ABCC4ABCB11
SCHEMBL7887632 0.91 AGTR1 (0.53) AGTR1AGTR2ABCC3ABCC4ABCB11

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2902385-B1 DEPROTECTION METHOD FOR TETRAZOLE COMPOUND API CORP (JP) 2019-01-09 EP disclosed
US-9624181-B2 Method for producing biaryl compound API CORPORATION (JP) 2017-04-18 US disclosed
US-9527821-B2 Deprotection method for tetrazole compound API CORPORATION (JP) 2016-12-27 US disclosed
US-20150239853-A1 METHOD FOR PRODUCING BIARYL COMPOUND API CORPORATION (JP) 2015-08-27 US disclosed
US-20150239854-A1 DEPROTECTION METHOD FOR TETRAZOLE COMPOUND API CORPORATION (JP) 2015-08-27 US disclosed
EP-2902385-A1 DEPROTECTION METHOD FOR TETRAZOLE COMPOUND API Corporation (JP) 2015-08-05 EP disclosed
EP-2298763-B1 METHOD FOR PRODUCING 1-BIPHENYLMETHYLIMIDAZOLE COMPOUND DAIICHI SANKYO CO LTD (JP) 2015-03-25 EP disclosed
EP-2298763-B1 METHOD FOR PRODUCING 1-BIPHENYLMETHYLIMIDAZOLE COMPOUND DAIICHI SANKYO CO LTD (JP) 2015-03-25 EP disclosed
US-8735598-B2 Method for producing 1-biphenylmethylimidazole compound DAIICHI SANKYO COMPANY, LIMITED (JP) 2014-05-27 US disclosed
US-8735598-B2 Method for producing 1-biphenylmethylimidazole compound DAIICHI SANKYO COMPANY, LIMITED (JP) 2014-05-27 US disclosed
US-20080312451-A1 Process For the Preparation of Sartan Derivatives and Intermediates Useful in Such Process KRKA, D.D. NOVO MESTO (SK) 2008-12-18 US disclosed
EP-1931655-A2 A PROCESS FOR THE PREPARATION OF SARTAN DERIVATIVES AND INTERMEDIATES USEFUL IN SUCH PROCESS KRKA, D.D., Novo Mesto (SI) 2008-06-18 EP disclosed
WO-2007048361-A1 A METHOD OF REMOVING THE TRIPHENYLMETHANE PROTECTING GROUP FROM PRECURSORS OF ANTIHYPERTENSIVE DRUGS ZENTIVA, A.S. (CZ) 2007-05-03 WO disclosed
WO-2007039117-A2 A PROCESS FOR THE PREPARATION OF SARTAN DERIVATIVES AND INTERMEDIATES USEFUL IN SUCH PROCESS KRKA, D.D., NOVO, MESTO (SI) 2007-04-12 WO disclosed
US-20070054948-A1 Purification of olmesartan medoxomil TEVA PHARMACEUTICALS USA, INC. 2007-03-08 US disclosed
US-20070054948-A1 Purification of olmesartan medoxomil TEVA PHARMACEUTICALS USA, INC. 2007-03-08 US disclosed
EP-0503785-B1 1-Biphenylimidazole derivatives, their preparation and their therapeutic use SANKYO CO (JP) 2001-04-25 EP disclosed
US-5646171-A HYPOTENSIVE AGENTS SANKYO COMPANY, LIMITED (JP) 1997-07-08 US disclosed
US-5616599-A HYPOTENSIVE AGENTS FOR CARDIOVASCULAR DISORDER SANKYO COMPANY, LIMITED (JP) 1997-04-01 US disclosed
EP-0503785-A1 1-Biphenylimidazole derivatives, their preparation and their therapeutic use Sankyo Company Limited (JP) 1992-09-16 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 (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-20150239853-A1 METHOD FOR PRODUCING BIARYL COMPOUND MLX, BMX, BRIX1 AGTR1 1993/4885AGTR2 954/4885ABCC3 1950/4885
US-20070054948-A1 Purification of olmesartan medoxomil AGTR2, AGTR1, REN AGTR1 2/4885AGTR2 1/4885ABCC3 3660/4885
US-20150239854-A1 DEPROTECTION METHOD FOR TETRAZOLE COMPOUND AGTR2, AGTR1, REN AGTR1 2/4885AGTR2 1/4885ABCC3 2863/4885
US-20080312451-A1 Process For the Preparation of Sartan Derivatives and Intermediates Useful in Such Process MC5R, NPY5R, ADRA1D AGTR1 283/4885AGTR2 311/4885ABCC3 2256/4885

“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.