SCHEMBL1203540

SCHEMBL1203540

Cc1ccc(S(=O)(=O)N[C@H](Cc2ccccc2)C(=O)O)cc1

nearest known ligand 0.79

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
▸ MMP2 P08253 11/20 0.79
▸ MMP9 P14780 10/20 0.79
▸ ADAMTS4 O75173 1/20 0.79
▸ TDP1 Q9NUW8 1/20 0.78
▸ ALDH1A1 P00352 1/20 0.74
▸ MAPT P10636 1/20 0.74
▸ POLB P06746 1/20 0.74
▸ MMP3 P08254 2/20 0.70
▸ MMP13 P45452 2/20 0.70
▸ ADAMTS5 Q9UNA0 1/20 0.70
▸ MMP1 P03956 1/20 0.70
▸ MMP7 P09237 1/20 0.70
▸ CTSL P07711 1/20 0.61
▸ CA2 P00918 1/20 0.61
▸ CA7 P43166 1/20 0.61

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
SCHEMBL697477 1.00 MMP2 (0.79) MMP2MMP9ADAMTS4TDP1ALDH1A1
SCHEMBL697476 1.00 MMP2 (0.79) MMP2MMP9ADAMTS4TDP1ALDH1A1
Hydrochloric Acid SCHEMBL3839410 0.99 MMP2 (0.77) MMP2MMP9ADAMTS4TDP1ALDH1A1
Hydrochloric Acid SCHEMBL11133046 0.99 MMP2 (0.77) MMP2MMP9ADAMTS4TDP1ALDH1A1
Hydrochloric Acid SCHEMBL28872216 0.97 MMP2 (0.75) MMP2MMP9ADAMTS4TDP1ALDH1A1
Chloromethane SCHEMBL7649372 0.97 MMP2 (0.75) MMP2MMP9ADAMTS4TDP1ALDH1A1
SCHEMBL3856155 0.96 MMP2 (0.73) MMP2MMP9ADAMTS4TDP1ALDH1A1
SCHEMBL561565 0.95 MMP2 (0.71) MMP2MMP9ADAMTS4TDP1ALDH1A1
SCHEMBL433897 0.95 MMP2 (0.71) MMP2MMP9ADAMTS4TDP1ALDH1A1
SCHEMBL8063645 0.94 TDP1 (0.78) MMP2MMP9ADAMTS4TDP1ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9115058-B2 Process of preparation of optically active αaminoacetals WEYLCHEM LAMOTTE S.A.S. (FR) 2015-08-25 — — US claimed
EP-2245000-B1 PROCESS OF PREPARATION OF OPTICALLY ACTIVE ALPHA AMINOACETALS CLARIANT SPECIALTY FINE CHEM F (FR) 2013-01-02 — — EP claimed
US-20110034726-A1 Process Of Preparation Of Optically Active Alpha Aminoacetals CLARIANT SPECIALTY FINE CHEMICALS (FRANCE) (FR) 2011-02-10 — — US claimed
EP-2245000-A1 PROCESS OF PREPARATION OF OPTICALLY ACTIVE ALPHA AMINOACETALS Clariant Specialty Fine Chemicals (France) (FR) 2010-11-03 — — EP claimed
WO-2009106386-A1 PROCESS OF PREPARATION OF OPTICALLY ACTIVE ALPHA AMINOACETALS CLARIANT SPECIALTY FINE CHEMICALS (FRANCE) (FR) 2009-09-03 — — WO claimed
US-9115058-B2 Process of preparation of optically active αaminoacetals WEYLCHEM LAMOTTE S.A.S. (FR) 2015-08-25 — — US disclosed
EP-2245000-B1 PROCESS OF PREPARATION OF OPTICALLY ACTIVE ALPHA AMINOACETALS CLARIANT SPECIALTY FINE CHEM F (FR) 2013-01-02 — — EP disclosed
US-20110034726-A1 Process Of Preparation Of Optically Active Alpha Aminoacetals CLARIANT SPECIALTY FINE CHEMICALS (FRANCE) (FR) 2011-02-10 — — US disclosed
EP-1513814-B1 NOVEL PIPERIDINE COMPOUND MITSUBISHI TANABE PHARMA CORP (JP) 2010-03-17 — — EP disclosed
US-7619092-B2 Piperidine compounds MITSUBISHI TANABE PHARMA CORPORATION (JP) 2009-11-17 — — US disclosed
US-20090198052-A1 METHOD FOR PREPARING OPTICALLY ACTIVE PIPERIDINE COMPOUNDS MITSUBISHI TANABE PHARMA CORPORATION (JP) 2009-08-06 — — US disclosed
EP-2022782-A1 PROCESS FOR PRODUCTION OF OPTICALLY ACTIVE PIPERIDINE COMPOUND Mitsubishi Tanabe Pharma Corporation (JP) 2009-02-11 — — EP disclosed
US-20030195159-A1 HIV protease inhibitors based on amino acid derivatives TAIMED BIOLOGICS, INC. (TW) 2003-10-16 — — US disclosed
US-6610689-B2 Viricides PHARMACOR INC. (CA) 2003-08-26 — — US disclosed
US-6608100-B1 N-epsilon-amino acid substituted L-lysine sulfonamide derivatives possessing aspartyl protease inhibitory properties PHARMACOR INC. (CA) 2003-08-19 — — US disclosed
US-20030144265-A1 HIV protease inhibitors based on amino acid derivatives TAIMED BIOLOGICS, INC. (TW) 2003-07-31 — — US disclosed
US-20030119803-A1 HIV protease inhibitors based on amino acid derivatives TAIMED BIOLOGICS, INC. (TW) 2003-06-26 — — US disclosed
US-6506786-B2 Such as N-isobutyl-N-(4-methylbenzene-sulfonyl)-N-(N-(4-methylbenzenesulfonyl)-L -phenylalanyl)-L-lysine PHARMACOR INC. (CA) 2003-01-14 — — US disclosed
US-20020151546-A1 HIV protease inhibitors based on amino acid derivatives TAIMED BIOLOGICS, INC. (TW) 2002-10-17 — — US disclosed
WO-2002064551-A1 HIV PROTEASE INHIBITORS BASED ON AMINO ACID DERIVATIVES PHARMACOR INC. (CA) 2002-08-22 — — 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 (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-20030144265-A1 HIV protease inhibitors based on amino acid derivatives ANPEP, PEPD, XPNPEP1 MMP2 845/4885MMP9 732/4885ADAMTS4 4020/4885
US-20020151546-A1 HIV protease inhibitors based on amino acid derivatives ANPEP, PEPD, XPNPEP1 MMP2 845/4885MMP9 732/4885ADAMTS4 4020/4885
US-20030195159-A1 HIV protease inhibitors based on amino acid derivatives ANPEP, PEPD, XPNPEP1 MMP2 845/4885MMP9 732/4885ADAMTS4 4020/4885
US-20090198052-A1 METHOD FOR PREPARING OPTICALLY ACTIVE PIPERIDINE COMPOUNDS SNCA, SYNJ1, KCNH2 MMP2 2580/4885MMP9 2726/4885ADAMTS4 4696/4885
US-20110034726-A1 Process Of Preparation Of Optically Active Alpha Aminoacetals ALDH7A1, AADAT, ALAD MMP2 3032/4885MMP9 3391/4885ADAMTS4 4377/4885
US-20030119803-A1 HIV protease inhibitors based on amino acid derivatives ANPEP, PEPD, XPNPEP1 MMP2 845/4885MMP9 732/4885ADAMTS4 4020/4885

“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.

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