SCHEMBL986459

SCHEMBL986459

CCCCc1nc(Cl)c(CO)n1-c1ccc(-c2ccccc2C#N)cc1

nearest known ligand 0.52

Predicted protein targets (top 8)

geneUniProtsupporting neighboursconfidence
AGTR1 P30556 3/20 0.49
AGTR2 P50052 3/20 0.49
ABCC4 O15439 1/20 0.48
ABCB11 O95342 1/20 0.48
PDE3B Q13370 1/20 0.48
PDE3A Q14432 1/20 0.48
APLNR P35414 1/20 0.46
PPARG P37231 1/20 0.45

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
SCHEMBL541 0.84 AGTR1 (0.69) AGTR1AGTR2ABCC4ABCB11PDE3B
SCHEMBL986257 0.84 GP6 (0.48) AGTR1AGTR2APLNRPPARG
SCHEMBL12716746 0.79 PPARG (0.60) AGTR1AGTR2ABCC4ABCB11PDE3B
SCHEMBL10589345 0.78 PPARG (0.59) AGTR1AGTR2ABCC4ABCB11PDE3B
SCHEMBL2927903 0.78 AGTR1 (0.49) AGTR1AGTR2ABCC4ABCB11PDE3B
Hydrochloric Acid SCHEMBL524 0.78 PPARG (0.58) AGTR1AGTR2ABCC4ABCB11PDE3B
SCHEMBL29032842 0.78 PPARG (0.58) AGTR1AGTR2ABCC4ABCB11PDE3B
SCHEMBL559 0.77 AGTR1 (0.43) AGTR1AGTR2
SCHEMBL8229075 0.77 AGTR2 (0.52) AGTR1AGTR2
SCHEMBL9016466 0.76 APLNR (0.44) AGTR1AGTR2APLNRPPARG

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7868180-B2 Process for the preparation of sartan derivatives and intermediates useful in such process KRKA, D.D. NOVO MESTO (SI) 2011-01-11 US disclosed
EP-1589966-B1 PREPARATION OF NEW PHARMACEUTICALLY SUITABLE SALT OF LOSARTAN AND FORMS THEREOF WITH NEW PURIFICATION AND ISOLATION METHODS LEK PHARMACEUTICALS (SI) 2010-11-10 EP 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
WO-2007119246-A2 AN IMPROVED PROCESS FOR THE MANUFACTURE OF LOSARTAN POTASSIUM UNICHEM LABORATORIES LIMITED (IN) 2007-10-25 WO disclosed
US-7271269-B2 Stability, purity, potassium salt of losartan in crystal Form X, as anti-hypertensive agent LEK PHARMACEUTICALS D.D. (SI) 2007-09-18 US disclosed
EP-1764365-A1 A process for the preparation of sartan derivates and intermediates useful in such process KRKA, D.D., Novo Mesto (SI) 2007-03-21 EP disclosed
US-20060004207-A1 Preparation of new pharmaceutically suitable salt of losartan and forms thereof with new purification and isolation methods LEK PHARMACEUTICALS D.D. (SI) 2006-01-05 US disclosed
EP-1589966-A2 PREPARATION OF NEW PHARMACEUTICALLY SUITABLE SALT OF LOSARTAN AND FORMS THEREOF WITH NEW PURIFICATION AND ISOLATION METHODS LEK Pharmaceuticals D.D. (SI) 2005-11-02 EP disclosed
WO-2004066997-A2 PREPARATION OF NEW PHARMACEUTICALLY SUITABLE SALT OF LOSARTAN AND FORMS THEREOF WITH NEW PURIFICATION AND ISOLATION METHODS LEK PHARMACEUTICALS D.D. (SI) 2004-08-12 WO 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-20080312451-A1 Process For the Preparation of Sartan Derivatives and Intermediates Useful in Such Process MC5R, NPY5R, ADRA1D AGTR1 283/4885AGTR2 311/4885ABCC4 1506/4885

“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.