Orbofiban

Orbofiban

SCHEMBL7417473

CC(=O)O.CCOC(=O)CCNC(=O)N[C@H]1CCN(c2ccc(C(=N)N)cc2)C1=O

nearest known ligand 0.95

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADRA2AADRA2BADRA2CADRB2AGTR1AVPR1AAVPR1BAVPR2BDKRB2CALCRCHRNA3CHRNB4ESR1ESR2GHSRGNRHRGSC1HSPA8MALT1MC1RMC4RNOS1NOS2NOS3OPRK1OXTRRAMP1RAMP2RAMP3SCN5ASSTR1SSTR2SSTR3SSTR4SSTR5dacAdacBdacCfolPftsImrcAmrcBmrdArplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

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

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
ITGB3 P05106 18/20 0.95
ITGA2B P08514 18/20 0.95
PRSS1 P07477 9/20 0.47
PRSS2 P07478 9/20 0.47
PRSS3 P35030 9/20 0.47
F10 P00742 5/20 0.45
PLG P00747 1/20 0.40
ST14 Q9Y5Y6 1/20 0.40
FPR1 P21462 1/20 0.39
FPR2 P25090 1/20 0.39

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
Orbofiban SCHEMBL871101 0.99 ITGB3 (0.93) ITGB3ITGA2BPRSS1PRSS2PRSS3
Orbofiban SCHEMBL7854981 0.97 ITGB3 (1.00) ITGB3ITGA2BPRSS1PRSS2PRSS3
Orbofiban SCHEMBL7415135 0.97 ITGB3 (1.00) ITGB3ITGA2BPRSS1PRSS2PRSS3
Orbofiban SCHEMBL7411884 0.93 ITGB3 (0.88) ITGB3ITGA2BPRSS1PRSS2PRSS3
SCHEMBL7444902 0.90 ITGB3 (0.86) ITGB3ITGA2BPRSS1PRSS2PRSS3
Acetic Acid SCHEMBL7418342 0.89 ITGB3 (0.75) ITGB3ITGA2BPRSS1PRSS2PRSS3
SCHEMBL7451885 0.89 ITGB3 (0.84) ITGB3ITGA2BFPR1FPR2
Acetic Acid SCHEMBL8109437 0.89 ITGB3 (0.75) ITGB3ITGA2BPRSS1PRSS2PRSS3
SCHEMBL7448694 0.89 ITGB3 (0.83) ITGB3ITGA2BPRSS1PRSS2PRSS3
SCHEMBL7446820 0.89 ITGB3 (0.80) ITGB3ITGA2BPRSS1PRSS2PRSS3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2025049453-A2 METHODS OF TREATING MUSCULOSKELETAL INJURIES UNIVERSITY OF PITTSBURGH - OF THE COMMONWEALTH SYSTEM OF HIGHER EDUCATION (US) 2025-03-06 WO disclosed
EP-3728570-B1 GLYCOENGINEERING MASSACHUSETTS GEN HOSPITAL (US) 2025-02-12 EP disclosed
US-20240174988-A1 GLYCOENGINEERING THE GENERAL HOSPITAL CORPORATION 2024-05-30 US disclosed
US-11674125-B2 Glycoengineering THE GENERAL HOSPITAL CORPORATION (US) 2023-06-13 US disclosed
EP-1068183-A2 PROCESS FOR THE PREPARATION OF A 2-OXOPYRROLIDINE COMPOUND G.D. SEARLE & CO. (US) 2001-01-17 EP disclosed
EP-0796245-B1 PROCESS FOR THE PREPARATION OF AMIDINO PHENYL PYRROLIDINE BETA-ALANINE UREA ANALOGS SEARLE & CO (US) 2000-07-26 EP disclosed
US-6025358-A Double prodrugs of potent GP IIb/IIIa antagonists G. D. SEARLE & CO. (US) 2000-02-15 US disclosed
WO-1999064397-A1 DOUBLE PRODRUGS OF POTENT GPIIb/IIIa ANTAGONISTS G.D. SEARLE & CO. (US) 1999-12-16 WO disclosed
US-5986107-A Process for the preparation of a 2-oxopyrrolidine compound G. D. SEARLE & CO. (US) 1999-11-16 US disclosed
WO-1999051573-A2 PROCESS FOR THE PREPARATION OF A 2-OXOPYRROLIDINE COMPOUND G.D. SEARLE & CO. (US) 1999-10-14 WO disclosed
US-5659063-A AMINE-BLOCKED METHIONINE ANALOG CYCLIZABLE TO A LACTAM IN NONVOLATILE OR NONTOXIC REAGENTS; ANTITHROMBOTIC AGENTS G. D. SEARLE & CO. (US) 1997-08-19 US disclosed
US-5610296-A CHEMICAL INTERMEDIATES OF ANTITHROMBOTICS G. D. SEARLE & CO. (US) 1997-03-11 US disclosed
US-5576447-A Process for the preparation of amidino phenyl pyrrolidine β-alanine urea analogs G. D. SEARLE & CO. (US) 1996-11-19 US disclosed
WO-1996017827-A1 PROCESS FOR THE PREPARATION OF AMIDINO PHENYL PYRROLIDINE β-ALANINE UREA ANALOGS G.D. SEARLE & CO. (US) 1996-06-13 WO disclosed
US-5484946-A CYCLIZATION AND DEHYDRATION A METHIONINE DERIVATIVE G. D. SEARLE & CO. (US) 1996-01-16 US disclosed