SCHEMBL2033

SCHEMBL2033

CCCCC(=O)N(Cc1ccc(-c2ccccc2C#N)cc1)[C@H](C(=O)OC)C(C)C

nearest known ligand 0.66

Predicted protein targets (top 7)

geneUniProtsupporting neighboursconfidence
AGTR1 P30556 9/20 0.66
LTB4R2 Q9NPC1 11/20 0.52
ABCB11 O95342 1/20 0.52
GP6 Q9HCN6 1/20 0.52
MME P08473 1/20 0.40
FFAR1 O14842 1/20 0.40
AKR1B1 P15121 1/20 0.40

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
SCHEMBL29561367 1.00 AGTR1 (0.66) AGTR1LTB4R2ABCB11GP6MME
SCHEMBL2032 1.00 AGTR1 (0.66) AGTR1LTB4R2ABCB11GP6MME
SCHEMBL1808771 1.00 AGTR1 (0.66) AGTR1LTB4R2ABCB11GP6MME
SCHEMBL2978 0.93 AGTR1 (0.57) AGTR1LTB4R2ABCB11GP6MME
SCHEMBL2979 0.93 AGTR1 (0.57) AGTR1LTB4R2ABCB11GP6MME
SCHEMBL8487504 0.91 AGTR1 (0.56) AGTR1LTB4R2ABCB11GP6MME
SCHEMBL2629 0.90 LTB4R2 (0.54) AGTR1LTB4R2ABCB11GP6MME
SCHEMBL2628 0.90 LTB4R2 (0.54) AGTR1LTB4R2ABCB11GP6MME
SCHEMBL27791229 0.90 AGTR1 (0.53) AGTR1LTB4R2ABCB11GP6MME
SCHEMBL27791231 0.90 AGTR1 (0.53) AGTR1LTB4R2ABCB11GP6MME

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115215813-A Method for controlling valsartan impurity 江苏新瑞药业有限公司 2022-10-21 CN claimed
CN-110078640-B Synthesis method of valsartan intermediate 浙江美诺华药物化学有限公司 2022-04-05 CN claimed
EP-3939967-A1 A CONTINUOUS PROCESS FOR THE PREPARATION OF (S)-METHYL N-((2'-CYANO-[1,1'-BIPHENYL]-4-YL)METHYL)-N-PENTANOYLVALINATE IN A FLOW REACTOR KRKA, d.d., Novo mesto (SI) 2022-01-19 EP claimed
US-7659406-B2 Process for preparing valsartan DR. REDDY'S LABORATORIES LIMITED (IN) 2010-02-09 US claimed
US-20060149079-A1 Process for preparing valsartan DR. REDDY'S LABORATORIES, INC. 2006-07-06 US claimed
EP-4037679-B1 A PROCESS FOR THE PREPARATION OF HIGHLY PURE VALSARTAN HARMAN FINOCHEM LTD (IN) 2025-08-06 EP disclosed
US-12365654-B2 Process for the preparation of highly pure valsartan HARMAN FINOCHEM LIMITED (IN) 2025-07-22 US disclosed
WO-2023148748-A1 AN IMPROVED SAFE PROCESS FOR THE PREPARATION OF SARTAN DRUGS OF FORMULA I IOL CHEMICALS AND PHARMACEUTICALS LIMITED (IN) 2023-08-10 WO disclosed
WO-2023148748-A1 AN IMPROVED SAFE PROCESS FOR THE PREPARATION OF SARTAN DRUGS OF FORMULA I IOL CHEMICALS AND PHARMACEUTICALS LIMITED (IN) 2023-08-10 WO disclosed
US-11655220-B2 Process for the preparation of angiotensin II receptor blockers HETERO LABS LIMITED (IN) 2023-05-23 US disclosed
US-20230057675-A1 A PROCESS FOR THE PREPARATION OF HIGHLY PURE VALSARTAN HARMAN FINOCHEM LIMITED (IN) 2023-02-23 US disclosed
US-20230057675-A1 A PROCESS FOR THE PREPARATION OF HIGHLY PURE VALSARTAN HARMAN FINOCHEM LIMITED (IN) 2023-02-23 US disclosed
WO-2005049587-A1 PROCESS FOR PREPARATION OF BIPHENYL TETRAZOLE RANBAXY LABORATORIES LIMITED (IN) 2005-06-02 WO disclosed
WO-2004111018-A1 A NOVEL PROCESS FOR PREPARATION OF VALSARTAN HETERO DRUGS LIMITED (IN) 2004-12-23 WO disclosed
WO-2004101534-A1 A METHOD OF PREPARATION OF N-(1-OXOPENTYL)-N-[[2'-(1H-TETRAZOL-5-y1) [1,1'-BIPHENYL] -4-y1]METHYL]-L-VALINE (VALSARTAN) ZENTIVA, A. S. (CZ) 2004-11-25 WO disclosed
US-20040072886-A1 Novel crystalline forms of (S)-N- (1-Carboxy-2-methyl-prop-1-yl) -N-pentanoyl-N- [2' -(1H-tetrazol-5-yl)- biphenyl-4-yl methyl] amine (Valsartan) DR. REDDY'S LABORATORIES LIMITED 2004-04-15 US disclosed
US-5965592-A HYPOTENSIVE AGENTS NOVARTIS CORPORATION (US) 1999-10-12 US disclosed
EP-0443983-B1 Acyl compounds CIBA GEIGY AG (CH) 1996-02-28 EP disclosed
US-5399578-A Hypotensive; valsartan; high blood pressure and cardiac insufficiency CIBA-GEIGY CORP (US) 1995-03-21 US disclosed
EP-0443983-A1 Acyl compounds CIBA-GEIGY AG (CH) 1991-08-28 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 (5 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-20230057675-A1 A PROCESS FOR THE PREPARATION OF HIGHLY PURE VALSARTAN REN, AGT, ACE AGTR1 4/4885LTB4R2 2553/4885ABCB11 1169/4885
US-12365654-B2 Process for the preparation of highly pure valsartan REN, AGT, ACE AGTR1 4/4885LTB4R2 2074/4885ABCB11 1142/4885
US-20040072886-A1 Novel crystalline forms of (S)-N- (1-Carboxy-2-methyl-prop-1-yl) -N-pentanoyl-N- [2' -(1H-tetrazol-5-yl)- biphenyl-4-yl methyl] amine (Valsartan) REN, AGTR1, TTR AGTR1 2/4885LTB4R2 2812/4885ABCB11 3133/4885
US-11655220-B2 Process for the preparation of angiotensin II receptor blockers AGTR2, AGTR1, ADRB1 AGTR1 2/4885LTB4R2 725/4885ABCB11 2292/4885
US-20060149079-A1 Process for preparing valsartan PREP, TMPRSS15, REN AGTR1 14/4885LTB4R2 2490/4885ABCB11 922/4885

“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.