SCHEMBL2169427

SCHEMBL2169427

COC(=O)[C@H](OS(=O)(=O)c1ccccc1)c1ccccc1Cl

nearest known ligand 0.41

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ ABCB11 O95342 2/20 0.39
▸ KMT2A Q03164 3/20 0.39
▸ MEN1 O00255 2/20 0.39
▸ THRB P10828 1/20 0.37
▸ NR1I2 O75469 1/20 0.37
▸ CHRM2 P08172 1/20 0.37
▸ ADRA2A P08913 1/20 0.37
▸ CYP2B6 P20813 1/20 0.37
▸ DRD1 P21728 1/20 0.37
▸ HTR2A P28223 1/20 0.37
▸ SLC6A4 P31645 1/20 0.37
▸ CYP2C19 P33261 1/20 0.37
▸ OPRM1 P35372 1/20 0.37
▸ OPRK1 P41145 1/20 0.37
▸ HTR2B P41595 1/20 0.37
▸ KCNH2 Q12809 1/20 0.37
▸ P2RY12 Q9H244 1/20 0.37
▸ CASP1 P29466 1/20 0.37
▸ ALDH1A1 P00352 3/20 0.37
▸ LMNA P02545 2/20 0.37

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
SCHEMBL28560399 1.00 ABCB11 (0.39) ABCB11KMT2AMEN1THRBNR1I2
SCHEMBL26301826 1.00 ABCB11 (0.39) ABCB11KMT2AMEN1THRBNR1I2
SCHEMBL6139230 0.92 PSEN1 (0.43) ABCB11KMT2AMEN1ALDH1A1LMNA
SCHEMBL28824902 0.92 PSEN1 (0.43) ABCB11KMT2AMEN1ALDH1A1LMNA
SCHEMBL28555501 0.91 LMNA (0.42) ABCB11KMT2AMEN1CASP1ALDH1A1
SCHEMBL28566525 0.90 GCKR (0.44) KMT2AALDH1A1LMNASMN1; SMN2POLB
SCHEMBL29993001 0.86 KMT2A (0.44) KMT2AMEN1ALDH1A1LMNAMAPT
SCHEMBL23524 0.86 KMT2A (0.44) KMT2AMEN1ALDH1A1LMNAMAPT
SCHEMBL14141639 0.86 KMT2A (0.44) KMT2AMEN1ALDH1A1LMNAMAPT
SCHEMBL5672285 0.85 TDP1 (0.40) KMT2AMEN1CYP2C19CASP1ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6894186-B2 Hydroxyacetic ester derivatives, preparation method and use as synthesis intermediates SANOFI-SYNTHELABO (FR) 2005-05-17 — — US claimed
US-11834413-B2 Antiplatelet drugs and uses thereof SHANGHAI CUREGENE PHARMACEUTICAL CO LTD. (CN) 2023-12-05 — — US disclosed
US-11834413-B2 Antiplatelet drugs and uses thereof SHANGHAI CUREGENE PHARMACEUTICAL CO LTD. (CN) 2023-12-05 — — US disclosed
US-20230295089-A1 ANTIPLATELET DRUGS AND USES THEREOF SHANGHAI CUREGENE PHARMACEUTICAL CO., LTD. (CN) 2023-09-21 — — US disclosed
CN-106928251-B Preparation method of high-purity clopidogrel 江苏天士力帝益药业有限公司 2021-05-04 — — CN disclosed
CN-105153192-A Substituted tetrahydrothienopyridine derivative and application thereof NANJING MAJOR BIOTECHNOLOGY CO LTD 2015-12-16 — — CN disclosed
US-20110190502-A1 PROCESS FOR THE PREPARATION OF S-CLOPIDOGREL SANDOZ AG (CH) 2011-08-04 — — US disclosed
EP-2346879-A1 A PROCESS FOR THE PREPARATION OF S-CLOPIDOGREL Sandoz AG (CH) 2011-07-27 — — EP disclosed
WO-2010046476-A1 A PROCESS FOR THE PREPARATION OF S-CLOPIDOGREL SANDOZ AG (CH) 2010-04-29 — — WO disclosed
EP-2168969-A2 Racemization and Enantiomer Separation of Clopidogrel TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2010-03-31 — — EP disclosed
US-7259261-B2 Racemization and enantiomer separation of clopidogrel TEVA Gyógyszergyár Zártkörűen Működő Részvénytársaság (HU) 2007-08-21 — — US disclosed
EP-1802280-A2 CLOPIDOGREL COMPOSITIONS Dr. Reddy's Laboratories Ltd. (IN) 2007-07-04 — — EP disclosed
WO-2006044548-A2 CLOPIDOGREL COMPOSITIONS DR. REDDY'S LABORATORIES LTD. (IN) 2006-04-27 — — WO disclosed
US-20050049275-A1 Racemization and enantiomer separation of clopidogrel ENTIRE INTEREST 2005-03-03 — — US disclosed
EP-1483269-A1 RACEMIZATION AND ENANTIOMER SEPARATION OF CLOPIDOGREL Teva Pharmaceutical Industries Limited (IL) 2004-12-08 — — EP disclosed
US-6800759-B2 REACTING MIXTURE OF (R) AND (S) CLOPIDOGREL FREE BASE WITH LEVOROTATORY CAMPHORSULFONIC ACID IN C5 TO C12 HYDROCARBON TO PRECIPITATE (S) CLOPIDOGREL CAMPHORSULFONATE, CONVERTING TO FREE BASE, PRECIPITATING CLOPIDOGREL BISULFATE IN SOLVENT TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2004-10-05 — — US disclosed
US-6737411-B2 CRYSTALLIZING AS CAMPHOR SULFONATE SALT; CONVERTING PURIFIED MATERIAL BACK TO FREE BASE FORM TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2004-05-18 — — US disclosed
WO-2004013147-A1 RACEMIZATION AND ENANTIOMER SEPARATION OF CLOPIDOGREL TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2004-02-12 — — WO disclosed
US-20040024012-A1 Racemization and enantiomer separation of clopidogrel TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2004-02-05 — — US disclosed
US-20040024011-A1 RACEMIZATION AND ENANTIOMER SEPARATION OF CLOPIDOGREL TEVA PHARMACEUTICALS USA, INC. 2004-02-05 — — US 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 (6 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-20040024012-A1 Racemization and enantiomer separation of clopidogrel SRR, TBXA2R, PTGIR ABCB11 763/4885KMT2A 3811/4885MEN1 3570/4885
US-20110190502-A1 PROCESS FOR THE PREPARATION OF S-CLOPIDOGREL SRR, P2RY13, P2RY11 ABCB11 740/4885KMT2A 3925/4885MEN1 3419/4885
US-20040024011-A1 RACEMIZATION AND ENANTIOMER SEPARATION OF CLOPIDOGREL SRR, TBXA2R, PTGIR ABCB11 763/4885KMT2A 3811/4885MEN1 3570/4885
US-11834413-B2 Antiplatelet drugs and uses thereof PFKP, GP6, PF4 ABCB11 847/4885KMT2A 4857/4885MEN1 2835/4885
US-20050049275-A1 Racemization and enantiomer separation of clopidogrel SRR, TBXA2R, PTGIR ABCB11 763/4885KMT2A 3811/4885MEN1 3570/4885
US-20230295089-A1 ANTIPLATELET DRUGS AND USES THEREOF PFKP, GP6, PF4 ABCB11 847/4885KMT2A 4857/4885MEN1 2835/4885

“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.

Send feedback