Saralasin

Saralasin

SCHEMBL23

CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)C(C)C)C(C)C

nearest known ligand 0.59

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

AGTR1

The experimentally established mechanism targets of Saralasin. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
▸ AGTR1 known ✓ P30556 3/20 0.55
▸ C5AR1 P21730 2/20 0.59
▸ EPHA2 P29317 2/20 0.54
▸ AGTR2 P50052 1/20 0.54
▸ APLNR P35414 1/20 0.53
▸ CTSL P07711 3/20 0.52
▸ CTSS P25774 3/20 0.52
▸ CTSK P43235 3/20 0.52
▸ CTSH P09668 1/20 0.52
▸ NMUR2 Q9GZQ4 1/20 0.50
▸ NMUR1 Q9HB89 1/20 0.50
▸ F2 P00734 2/20 0.49
▸ MC4R P32245 1/20 0.49
▸ RAMP3 O60896 1/20 0.49
▸ CALCR P30988 1/20 0.49

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
Saralasin SCHEMBL18699973 1.00 C5AR1 (0.59) C5AR1AGTR1EPHA2AGTR2APLNR
Saralasin SCHEMBL2199404 0.99 C5AR1 (0.58) C5AR1AGTR1EPHA2AGTR2APLNR
Saralasin SCHEMBL125013 0.99 C5AR1 (0.58) C5AR1AGTR1EPHA2AGTR2APLNR
SCHEMBL19780882 0.98 C5AR1 (0.60) C5AR1AGTR1EPHA2AGTR2APLNR
Saralasin SCHEMBL2200145 0.98 C5AR1 (0.57) C5AR1AGTR1EPHA2AGTR2APLNR
SCHEMBL34470047 0.97 C5AR1 (0.62) C5AR1AGTR1EPHA2AGTR2APLNR
Trv-120027 SCHEMBL11023969 0.97 AGTR1 (0.60) C5AR1AGTR1EPHA2AGTR2APLNR
Trv-120027 SCHEMBL19780884 0.97 AGTR1 (0.60) C5AR1AGTR1EPHA2AGTR2APLNR
Trv-120027 SCHEMBL17274208 0.97 AGTR1 (0.60) C5AR1AGTR1EPHA2AGTR2APLNR
Trv-120027 SCHEMBL11024001 0.97 AGTR1 (0.60) C5AR1AGTR1EPHA2AGTR2APLNR

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

Appears in 3901 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260124148-A1 POLYPEPTIDE FORMULATIONS FOR ORAL DELIVERY BHAMIS RES LABORATORY PVT LTD (IN) 2026-05-07 — — US claimed
US-12605345-B2 Transdermal drug delivery system BioPhysics Pharma, Inc. (US) 2026-04-21 — — US claimed
US-12533321-B2 Polypeptide formulations for oral delivery Bhami's Research Laboratory, Pvt. Ltd. (IN) 2026-01-27 — — US claimed
US-20250268841-A1 Trans-Epithelial Membrane Drug Delivery System Masiz, John J. (US) 2025-08-28 — — US claimed
EP-4601623-A1 POLYPEPTIDE FORMULATIONS FOR ORAL DELIVERY Bhami's Research Laboratory, Pvt. Ltd. (IN) 2025-08-20 — — EP claimed
EP-4601697-A2 A FORMULATION FOR ORAL DELIVERY OF PEPTIDES AND BIOSIMILARS FOR SYSTEMIC ABSORPTION AND METHOD OF MANUFACTURING THE SAME NBI Biosciences Pvt Ltd (IN) 2025-08-20 — — EP claimed
WO-2025111482-A1 COMPLEXING AGENT SALT FORMULATIONS OF PHARMACEUTICAL COMPOUNDS AT LOW STOICHIOMETRIC RATIOS BEXSON BIOMEDICAL, INC. (US) 2025-05-30 — — WO claimed
US-20250120907-A1 Transmucosal Drug Delivery System Masiz, John J. (US) 2025-04-17 — — US claimed
WO-2025050228-A1 PHARMACEUTICAL COMPOSITION COMPRISING A PEPTIDE OR A COMBINATION OF PEPTIDES AGONISTIC TO THE MAS, AT1 AND AT2 RECEPTORS PONTIFICIA UNIVERSIDAD CATÓLICA DE CHILE (CL) 2025-03-13 — — WO claimed
US-12246098-B2 Trans-epithelial membrane drug delivery system BioPhysics Pharma, Inc. (US) 2025-03-11 — — US claimed
WO-1996040256-A1 METHOD TO TREAT CARDIOFIBROSIS WITH A COMBINATION OF AN ANGIOTENSIN II ANTAGONIST AND SPIRONOLACTONE G.D. SEARLE & CO. (US) 1996-12-19 — — WO claimed
WO-1996040258-A2 SPIRONOLACTONE AND ANGIOTENSIN II ANTAGONIST COMBINATION THERAPY FOR TREATMENT OF CONGESTIVE HEART FAILURE G.D. SEARLE & CO. (US) 1996-12-19 — — WO claimed
WO-1995033454-A1 UTERINE FIBROID TREATMENT THE UNIVERSITY OF BIRMINGHAM (GB) 1995-12-14 — — WO claimed
WO-1995022992-A2 METHOD AND COMPOSITIONS FOR INCREASING THE SERUM HALF-LIFE OF PHARMACOLOGICALLY ACTIVE AGENTS CHIRON CORP (US) 1995-08-31 — — WO claimed
WO-1995022992-A1 METHOD AND COMPOSITIONS FOR INCREASING THE SERUM HALF-LIFE OF PHARMACOLOGICALLY ACTIVE AGENTS CHIRON CORPORATION (US) 1995-08-31 — — WO claimed
WO-1992013564-A1 COMBINATION OF AN ANGIOTENSIN II ANTAGONIST OR RENIN INHIBITOR WITH A NEUTRAL ENDOPEPTIDASE INHIBITOR SCHERING CORPORATION (US) 1992-08-20 — — WO claimed
EP-0498361-A2 Combination of an angiotensin II antagonist or renin inhibitor with a neutral endopeptidase inhibitor SCHERING CORPORATION (US) 1992-08-12 — — EP claimed
US-5036048-A Angiotensin II receptor blockers as antiglaucoma agents SCHERING CORPORATION (US) 1991-07-30 — — US claimed
EP-0036145-B1 AN ORALLY ADMINISTERED DRUG FORM COMPRISING A POLAR BIOACTIVE AGENT AND AN ADJUVANT INTERx RESEARCH CORPORATION (US) 1985-05-29 — — EP claimed
US-3932624-A Method for prolonging the inhibitory effect of saralasin on angiotensin II MORTON-NORWICH PRODUCTS, INC. (US) 1976-01-13 — — US claimed
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