SCHEMBL1472569

SCHEMBL1472569

CCCCc1nc(Cl)c(COC(c2ccccc2)(c2ccccc2)c2ccccc2)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1

nearest known ligand 0.57

Predicted protein targets (top 6)

geneUniProtsupporting neighboursconfidence
▸ AGTR1 P30556 5/20 0.51
▸ AGTR2 P50052 4/20 0.51
▸ ABCC4 O15439 1/20 0.51
▸ ABCB11 O95342 1/20 0.51
▸ PDE3B Q13370 1/20 0.51
▸ PDE3A Q14432 1/20 0.51

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
SCHEMBL10053021 0.88 AGTR1 (0.55) AGTR1AGTR2ABCC4ABCB11PDE3B
SCHEMBL3630129 0.88 AGTR1 (0.53) AGTR1AGTR2ABCC4ABCB11PDE3B
SCHEMBL17653793 0.88 AGTR1 (0.54) AGTR1AGTR2ABCC4ABCB11PDE3B
SCHEMBL6891884 0.88 AGTR1 (0.56) AGTR1AGTR2ABCC4ABCB11PDE3B
SCHEMBL13755335 0.86 AGTR1 (0.58) AGTR1AGTR2ABCC4ABCB11PDE3B
SCHEMBL1237602 0.86 AGTR1 (0.57) AGTR1AGTR2
SCHEMBL10021557 0.86 AGTR1 (0.53) AGTR1AGTR2ABCC4ABCB11PDE3B
SCHEMBL8791077 0.85 AGTR1 (0.52) AGTR1AGTR2ABCC4ABCB11PDE3B
Losartan SCHEMBL60 0.85 AGTR1 (0.67) AGTR1AGTR2ABCC4ABCB11PDE3B
Losartan SCHEMBL6092394 0.85 AGTR1 (0.67) AGTR1AGTR2ABCC4ABCB11PDE3B

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-105017226-A Trityl Losartan synthesis method CHEER FINE PHARMACEUTICAL ANHUI CO LTD 2015-11-04 — — CN claimed
CN-103965171-A Preparation method for Allisartan Isoproxil ALLIST PHARMACEUTICALS INC 2014-08-06 — — CN claimed
CN-102711735-A Capsules of active pharmaceutical ingredients and polyunsaturated fatty acid esters for the treatment of cardiovascular diseases GP PHARM SA 2012-10-03 — — CN claimed
US-20090076281-A1 PROCESS FOR THE PREPARATION OF LOSARTAN AND ITS SALTS MEDICHEM, S.A. (ES) 2009-03-19 — — US claimed
US-7345071-B2 Process for the synthesis of Losartan potassium IPCA LABORATORIES LIMITED (IN) 2008-03-18 — — US claimed
EP-1891055-A2 PROCESS FOR THE PREPARATION OF LOSARTAN POTASSIUM Medichem, S.A. (ES) 2008-02-27 — — EP claimed
US-20070249839-A1 Process for the Preparation of Losartan Potassium Form I CADILA PHARMACEUTICALS LTD. (IN) 2007-10-25 — — US claimed
WO-2007020533-A2 PROCESS FOR THE PREPARATION OF LOSARTAN POTASSIUM MEDICHEM, S.A. (US) 2007-02-22 — — WO claimed
US-20060287537-A1 Method of removing the triphenylmethane protecting group ZENTIVA, A.S. (CZ) 2006-12-21 — — US claimed
EP-1709034-A2 AN IMPROVED PROCESS FOR THE SYNTHESIS OF LOSARTAN POTASSIUM IPCA Laboratories Limited (IN) 2006-10-11 — — EP claimed
US-20060020005-A1 Process for preparing losartan DR. REDDY'S LABORATORIES LIMITED (IN) 2006-01-26 — — US claimed
EP-1608641-A1 A PROCESS FOR THE SYNTHESIS OF LOSARTAN POTASSIUM IPCA Laboratories Limited (IN) 2005-12-28 — — EP claimed
WO-2005066158-A2 AN IMPROVED PROCESS FOR THE SYNTHESIS OF LOSARTAN POTASSIUM IPCA LABORATORIES LIMITED (IN) 2005-07-21 — — WO claimed
US-6916935-B2 Losartan potassium synthesis IPCA LABORATORIES (IN) 2005-07-12 — — US claimed
US-20050070586-A1 Process for the synthesis of losartan potassium IPCA LABORATORIES LIMITED (IN) 2005-03-31 — — US claimed
WO-2005023758-A2 PROCESS FOR THE PREPARATION OF LOSARTAN POTASSIUM FORM I KHAMAR BAKULESH MAFATLAL (IN) 2005-03-17 — — WO claimed
WO-2005021535-A2 A METHOD OF REMOVING THE TRIPHENYLMETHANE PROTECTING GROUP ZENTIVA, A.S. (CZ) 2005-03-10 — — WO claimed
US-20040224998-A1 Losartan potassium synthesis IPCA LABORATORIES, LTD. (IN) 2004-11-11 — — US claimed
WO-2004087691-A1 A PROCESS FOR THE SYNTHESIS OF LOSARTAN POTASSIUM IPCA LABORATORIES LIMITED (IN) 2004-10-14 — — WO claimed
US-20040097568-A1 Crystalline form of losartan potassium DR. REDDY'S LABORATORIES LIMITED 2004-05-20 — — US claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (6 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-20040097568-A1 Crystalline form of losartan potassium REN, AGT, AGTR1 AGTR1 3/4885AGTR2 5/4885ABCC4 1987/4885
US-20060287537-A1 Method of removing the triphenylmethane protecting group AGTR1, REN, AGTR2 AGTR1 1/4885AGTR2 3/4885ABCC4 3624/4885
US-20070249839-A1 Process for the Preparation of Losartan Potassium Form I AGTR1, REN, AGT AGTR1 1/4885AGTR2 4/4885ABCC4 2414/4885
US-20050070586-A1 Process for the synthesis of losartan potassium ADH1C, KCNN3, AGTR1 AGTR1 3/4885AGTR2 13/4885ABCC4 3985/4885
US-20060020005-A1 Process for preparing losartan AGTR1, AGT, REN AGTR1 1/4885AGTR2 4/4885ABCC4 3814/4885
US-20040224998-A1 Losartan potassium synthesis ADH1A, AGTR1, ADH1C AGTR1 2/4885AGTR2 12/4885ABCC4 3203/4885

“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.

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