Eptifibatide

Eptifibatide

SCHEMBL43237

NC(=O)[C@@H]1CSSCCC(=O)N[C@H](CCCCN=C(N)N)C(=O)NCC(=O)N[C@H](CC(=O)O)C(=O)N[C@@H](Cc2c[nH]c3ccccc23)C(=O)N2CCC[C@@H]2C(=O)N1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ITGA2BITGB3

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

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
ITGB3 known ✓ P05106 5/20 1.00
ITGA2B known ✓ P08514 3/20 1.00
ITGAV P06756 5/20 1.00
MC3R P41968 5/20 0.59
MC5R P33032 4/20 0.59
MC4R P32245 3/20 0.59
ITGA5 P08648 4/20 0.57
ITGB1 P05556 2/20 0.57
ITGB5 P18084 2/20 0.57
LDLR P01130 9/20 0.57
PCSK9 Q8NBP7 9/20 0.57
KLK5 Q9Y337 1/20 0.53

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
Eptifibatide SCHEMBL18504808 1.00 ITGB3 (1.00) ITGB3ITGAVITGA2BMC3RMC5R
Eptifibatide SCHEMBL22193879 1.00 ITGB3 (1.00) ITGB3ITGAVITGA2BMC3RMC5R
Eptifibatide SCHEMBL29353236 1.00 ITGB3 (1.00) ITGB3ITGAVITGA2BMC3RMC5R
Eptifibatide SCHEMBL16883987 1.00 ITGB3 (1.00) ITGB3ITGAVITGA2BMC3RMC5R
Eptifibatide SCHEMBL1649793 1.00 ITGB3 (1.00) ITGB3ITGAVITGA2BMC3RMC5R
Eptifibatide SCHEMBL16884017 1.00 ITGB3 (1.00) ITGB3ITGAVITGA2BMC3RMC5R
SCHEMBL29356871 0.98 ITGB3 (0.97) ITGB3ITGAVITGA2BMC3RMC5R
SCHEMBL16883997 0.93 ITGB3 (0.87) ITGB3ITGAVITGA2BLDLRPCSK9
SCHEMBL24433345 0.93 ITGB3 (0.86) ITGB3ITGAVITGA2BMC3RMC5R
SCHEMBL16883930 0.91 ITGB3 (0.84) ITGB3ITGAVITGA2BMC3RMC5R

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 4247 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2026103722-A1 COMPOSITIONS AND METHODS FOR INHIBITING EXPRESSION OF COAGULATION FACTOR XI (FXI) SHANGHAI ARGO BIOPHARMACEUTICAL CO., LTD. (CN) 2026-05-21 WO claimed
EP-4705465-A1 COMPOSITIONS AND METHODS FOR INHIBITING EXPRESSION OF COAGULATION FACTOR XI (FXI) Shanghai Argo Biopharmaceutical Co., Ltd. (CN) 2026-03-11 EP claimed
US-20240390364-A1 Novel Pyridine Compositions and their use in methods for preventing or treating diseases, disorders and conditions REID CHRISTOPHER BRIAN (US) 2024-11-28 US claimed
WO-2024240058-A1 COMPOSITIONS AND METHODS FOR INHIBITING EXPRESSION OF COAGULATION FACTOR XI (FXI) SHANGHAI ARGO BIOPHARMACEUTICAL CO., LTD. (CN) 2024-11-28 WO claimed
US-20240058455-A1 BIOORTHOGONAL LINKERS AND REACTIONS THE GENERAL HOSPITAL CORPORATION 2024-02-22 US claimed
US-20220403036-A1 P-SELECTIN INHIBITOR, COMPOSITIONS THEREOF AND METHODS OF USE THEREOF THE JOHNS HOPKINS UNIVERSITY 2022-12-22 US claimed
WO-2022072949-A2 BIOORTHOGONAL LINKERS AND REACTIONS THE GENERAL HOSPITAL CORPORATION (US) 2022-04-07 WO claimed
US-20210179577-A1 AROMATIC SULFONAMIDE DERIVATIVES FOR THE TREATMENT OF ISCHEMIC STROKE BAYER AKTIENGESELLSCHAFT (DE) 2021-06-17 US claimed
US-20210109110-A1 PATIENT ASSESSMENT METHOD UNIVERSITY OF COPENHAGEN (DK) 2021-04-15 US claimed
EP-3764988-A1 GEL-FORMING POLYPEPTIDES Adepthera LLC (US) 2021-01-20 EP claimed
WO-2002019935-A1 METHOD AND SYSTEM FOR ANTICOAGULANT DOSE REVISION THE RXFILES CORPORATION (US) 2002-03-14 WO claimed
US-6344028-B1 Replenishable stent and delivery system BOSTON SCIENTIFIC CORPORATION 2002-02-05 US claimed
WO-2001092283-A2 COBALAMIN COMPOUNDS USEFUL AS CARDIOVASCULAR AGENTS AND AS IMAGING AGENTS MAYO FOUNDATION FOR MEDICAL EDUCATION AND RESEARCH (US) 2001-12-06 WO claimed
WO-2001049311-A1 PHARMACEUTICAL FORMULATION COMPOSED OF A POLYMER BLEND AND AN ACTIVE COMPOUND FOR TIME-CONTROLLED RELEASE RUTGERS, THE STATE UNIVERSITY (US) 2001-07-12 WO claimed
WO-2001049249-A2 PHARMACEUTICAL FORMULATION FOR REGULATING THE TIMED RELEASE OF BIOLOGICALLY ACTIVE COMPOUNDS BASED ON A POLYMER MATRIX RUTGERS, THE STATE UNIVERSITY (US) 2001-07-12 WO claimed
EP-1090132-A1 METHODS FOR PRODUCTION OF RECOMBINANT POLYPEPTIDES PPL Therapeutics (Scotland) Limited (GB) 2001-04-11 EP claimed
EP-1062229-A1 PHARMACOLOGICALLY ACTIVE PEPTIDE CONJUGATES HAVING A REDUCED TENDENCY TOWARDS ENZYMATIC HYDROLYSIS Zealand Pharmaceuticals A/S (DK) 2000-12-27 EP claimed
WO-2000000625-A1 METHODS FOR PRODUCTION OF RECOMBINANT POLYPEPTIDES PPL THERAPEUTICS (SCOTLAND) LIMITED (GB) 2000-01-06 WO claimed
WO-1999046283-A9 PHARMACOLOGICALLY ACTIVE PEPTIDE CONJUGATES HAVING A REDUCED TENDENCY TOWARDS ENZYMATIC HYDROLYSIS ZEALAND PHARMACEUTICALS A S (DK) 1999-11-18 WO claimed
WO-1999046283-A1 PHARMACOLOGICALLY ACTIVE PEPTIDE CONJUGATES HAVING A REDUCED TENDENCY TOWARDS ENZYMATIC HYDROLYSIS ZEALAND PHARMACEUTICALS A/S (DK) 1999-09-16 WO claimed