Clopidogrel

Clopidogrel

SCHEMBL1031641

COC(=O)[C@@H](c1ccccc1Cl)N1CCc2sccc2C1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

P2RY12

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

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
P2RY12 known ✓ Q9H244 2/20 1.00
ABCB11 O95342 4/20 1.00
OPRM1 P35372 3/20 1.00
ADRA2A P08913 2/20 1.00
CYP2B6 P20813 2/20 1.00
DRD1 P21728 2/20 1.00
CYP2C19 P33261 2/20 1.00
OPRK1 P41145 2/20 1.00
HTR2B P41595 2/20 1.00
KCNH2 Q12809 2/20 1.00
CHRM2 P08172 2/20 1.00
THRB P10828 1/20 1.00
NR1I2 O75469 1/20 1.00
HTR2A P28223 1/20 1.00
SLC6A4 P31645 1/20 1.00
CYP2C8 P10632 1/20 0.64
CES1 P23141 1/20 0.64
ADORA3 P0DMS8 2/20 0.43
ALDH1A1 P00352 2/20 0.43
LMNA P02545 2/20 0.43

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
Clopidogrel SCHEMBL754557 1.00 ABCB11 (1.00) ABCB11OPRM1ADRA2ACYP2B6DRD1
Clopidogrel SCHEMBL30388817 1.00 ABCB11 (1.00) ABCB11OPRM1ADRA2ACYP2B6DRD1
Clopidogrel SCHEMBL19148648 1.00 ABCB11 (1.00) ABCB11OPRM1ADRA2ACYP2B6DRD1
Clopidogrel SCHEMBL14009483 1.00 ABCB11 (1.00) ABCB11OPRM1ADRA2ACYP2B6DRD1
Clopidogrel SCHEMBL1031319 1.00 ABCB11 (1.00) ABCB11OPRM1ADRA2ACYP2B6DRD1
Clopidogrel SCHEMBL29793709 1.00 ABCB11 (1.00) ABCB11OPRM1ADRA2ACYP2B6DRD1
Clopidogrel SCHEMBL5567933 1.00 ABCB11 (1.00) ABCB11OPRM1ADRA2ACYP2B6DRD1
Clopidogrel SCHEMBL4769 1.00 ABCB11 (1.00) ABCB11OPRM1ADRA2ACYP2B6DRD1
Clopidogrel SCHEMBL1130036 0.99 ABCB11 (0.98) ABCB11OPRM1ADRA2ACYP2B6DRD1
Clopidogrel SCHEMBL1402209 0.99 ABCB11 (0.98) ABCB11OPRM1ADRA2ACYP2B6DRD1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250302880-A1 PLATELET DERIVATIVE COMPOSITIONS IN THE FORM OF A POWDER CELLPHIRE, INC. (US) 2025-10-02 US disclosed
US-12419914-B2 Thrombosomes as an antiplatelet agent reversal agent CELLPHIRE, INC. (US) 2025-09-23 US disclosed
US-12370219-B2 Platelet derivative compositions, and pluralities of containers containing same CELLPHIRE, INC. (US) 2025-07-29 US disclosed
US-20250205284-A1 PLATELET DERIVATIVE COMPOSITIONS, AND PLURALITIES OF CONTAINERS CONTAINING SAME CELLPHIRE, INC. (US) 2025-06-26 US disclosed
US-20250177450-A1 METHODS FOR ADMINISTERING FREEZE-DRIED PLATELET DERIVATIVE COMPOSITIONS TO SUBJECTS TREATED WITH A FACTOR XI INHIBITOR CELLPHIRE, INC. (US) 2025-06-05 US disclosed
US-12295972-B2 Methods using freeze-dried platelet derivative compositions for restoring hemostasis in a subject CELLPHIRE, INC. (US) 2025-05-13 US disclosed
CN-119798022-A Method for splitting clopidogrel and camphorsulfonic acid 惠州信立泰药业有限公司 2025-04-11 CN disclosed
US-12208122-B2 Methods of treating bleeding in a subject treated with an antiplatelet agent CELLPHIRE, INC (US) 2025-01-28 US disclosed
US-20240408141-A1 FREEZE-DRIED PLATELET DERIVATIVE COMPOSITIONS FOR TREATING A SUBJECT TAKING AN ANTI-PLATELET AGENT CELLPHIRE, INC. (US) 2024-12-12 US disclosed
US-20240277771-A1 METHODS OF TREATING BLEEDING IN A SUBJECT TREATED WITH AN ANTIPLATELET AGENT CELLPHIRE, INC. (US) 2024-08-22 US disclosed
US-7470707-B2 Crystalline monohydrate clopidogrel naphthalenedisulfonate and process of preparation HANMI PHARM. CO., LTD (KR) 2008-12-30 US disclosed
US-20080249311-A1 Using halogen phenyl acetonitrile as starting material; tetrahydrothienopyridine (acetate or acetonitrile) as chemical intermediates; kinetic resolution; anticoagulant ZHEJIANG HUAHAI PHARMACEUTICAL CO., LTD. (CN) 2008-10-09 US disclosed
US-20080249311-A1 Using halogen phenyl acetonitrile as starting material; tetrahydrothienopyridine (acetate or acetonitrile) as chemical intermediates; kinetic resolution; anticoagulant ZHEJIANG HUAHAI PHARMACEUTICAL CO., LTD. (CN) 2008-10-09 US disclosed
US-20080182869-A1 Method of Racemization of the R(-) Isomer of the (2-Chlorophenyl)-6,7-Dihydrothieno[3,2-C]Pyridine-5(4H)-Acetic Acid Methyl Ester ZENTIVA K.S. (CZ) 2008-07-31 US disclosed
US-20080182869-A1 Method of Racemization of the R(-) Isomer of the (2-Chlorophenyl)-6,7-Dihydrothieno[3,2-C]Pyridine-5(4H)-Acetic Acid Methyl Ester ZENTIVA K.S. (CZ) 2008-07-31 US disclosed
WO-2008081473-A2 PROCESS FOR PREPARING CLOPIDOGREL CADILA HEALTHCARE LIMITED (IN) 2008-07-10 WO disclosed
WO-2008062421-A1 A PROCESS FOR PREPARING (S)-(+)-CLOPIDOGREL BASE AND ITS SALTS CADILA HEALTHCARE LIMITED (IN) 2008-05-29 WO disclosed
US-20070225320-A1 PROCESS FOR PREPARING CLOPIDOGREL DR. REDDY'S LABORATORIES, INC. 2007-09-27 US disclosed
EP-1606231-A1 PROCESS FOR PREPARATION OF CLOPIDOGREL, ITS SALTS AND PHARMACEUTICAL COMPOSITIONS Nadkarni, Sunil Sadanand (IN) 2005-12-21 EP disclosed
WO-2004074215-A1 PROCESS FOR PREPARATION OF CLOPIDOGREL, ITS SALTS AND PHARMACEUTICAL COMPOSITIONS NADKARNI SUNIL SADANAND (IN) 2004-09-02 WO 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 (3 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-20080182869-A1 Method of Racemization of the R(-) Isomer of the (2-Chlorophenyl)-6,7-Dihydrothieno[3,2-C]Pyridine-5(4H)-Acetic Acid Methyl Ester HRH2, HTR3E, ADRA2C P2RY12 168/4885ABCB11 867/4885OPRM1 49/4885
US-20070225320-A1 PROCESS FOR PREPARING CLOPIDOGREL PFKP, SELP, P2RY13 P2RY12 7/4885ABCB11 200/4885OPRM1 3881/4885
US-20080249311-A1 Using halogen phenyl acetonitrile as starting material; tetrahydrothienopyridine (acetate or acetonitrile) as chemical intermediates; kinetic resolution; anticoagulant TFPI, F2, CYP2C19 P2RY12 20/4885ABCB11 539/4885OPRM1 278/4885

“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.