SCHEMBL614208

SCHEMBL614208

C=CCOC[C@H](NC(=O)OC(C)(C)C)C(=O)O

nearest known ligand 0.53

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
PPARA Q07869 7/20 0.53
PPARG P37231 6/20 0.51
SMN1; SMN2 Q16637 1/20 0.48
CTSS P25774 7/20 0.43
CTSK P43235 6/20 0.43
CTSL P07711 1/20 0.41
CTSB P07858 1/20 0.41
ACE P12821 1/20 0.41
PPARD Q03181 2/20 0.40
MAPT P10636 1/20 0.39
CA1 P00915 1/20 0.39
CA2 P00918 1/20 0.39
CA7 P43166 1/20 0.39
IDO1 P14902 1/20 0.39
ITGB3 P05106 1/20 0.39
ITGA2B P08514 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
SCHEMBL614209 1.00 PPARA (0.53) PPARAPPARGSMN1; SMN2CTSSCTSK
SCHEMBL1430675 1.00 PPARA (0.53) PPARAPPARGSMN1; SMN2CTSSCTSK
Serine SCHEMBL8588277 0.90 PPARA (0.46) PPARAPPARGSMN1; SMN2CTSSCTSK
Serine SCHEMBL8588281 0.90 PPARA (0.46) PPARAPPARGSMN1; SMN2CTSSCTSK
Benzoic Acid SCHEMBL9540832 0.88 PPARA (0.61) PPARAPPARGSMN1; SMN2CTSSCTSK
SCHEMBL1604541 0.87 SMN1; SMN2 (0.50) PPARAPPARGSMN1; SMN2CTSSCTSK
SCHEMBL615910 0.87 SMN1; SMN2 (0.50) PPARAPPARGSMN1; SMN2CTSSCTSK
SCHEMBL615909 0.87 SMN1; SMN2 (0.50) PPARAPPARGSMN1; SMN2CTSSCTSK
SCHEMBL2241213 0.86 SMN1; SMN2 (0.46) PPARAPPARGSMN1; SMN2CTSSCTSK
SCHEMBL25755437 0.86 SMN1; SMN2 (0.46) PPARAPPARGSMN1; SMN2CTSSCTSK

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12540162-B2 Preparation of functional homocysteine residues in polypeptides and peptides THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2026-02-03 US disclosed
US-12404274-B2 Macrocycles as factor xia inhibitors BRISTOL-MYERS SQUIBB COMPANY (US) 2025-09-02 US disclosed
US-12365674-B2 Inhibitors of histone deacetylase useful for the treatment or prevention of HIV infection MERCK SHARP & DOHME LLC (US) 2025-07-22 US disclosed
CN-115335373-B Compounds and uses thereof 福宏治疗公司 2025-05-20 CN disclosed
CN-118256591-A Cyclic peptide compound having high membrane permeability and library comprising same 中外制药株式会社 2024-06-28 CN disclosed
US-20240092833-A1 PREPARATION OF FUNCTIONAL HOMOCYSTEINE RESIDUES IN POLYPEPTIDES AND PEPTIDES THE REGENTS OF THE UNIVERSITY OF CALIFORNIA 2024-03-21 US disclosed
CN-110869544-B Cyclic peptide compound having high membrane permeability and library comprising same 中外制药株式会社 2024-03-08 CN disclosed
US-20230348452-A1 COMPOUNDS AND USES THEREOF FOGHORN THERAPEUTICS INC. 2023-11-02 US disclosed
US-20230348452-A1 COMPOUNDS AND USES THEREOF FOGHORN THERAPEUTICS INC. 2023-11-02 US disclosed
US-20230348452-A1 COMPOUNDS AND USES THEREOF FOGHORN THERAPEUTICS INC. 2023-11-02 US disclosed
US-7592419-B2 Macrocyclic inhibitors of hepatitis C virus NS3-serine protease SCHERING CORPORATION (US) 2009-09-22 US disclosed
US-7592419-B2 Macrocyclic inhibitors of hepatitis C virus NS3-serine protease SCHERING CORPORATION (US) 2009-09-22 US disclosed
WO-2008070733-A2 MACROCYCLIC HEPATITIS C SERINE PROTEASE INHIBITORS AND USES THEREFOR PHENOMIX CORPORATION (US) 2008-06-12 WO disclosed
WO-2008070733-A2 MACROCYCLIC HEPATITIS C SERINE PROTEASE INHIBITORS AND USES THEREFOR PHENOMIX CORPORATION (US) 2008-06-12 WO disclosed
US-7384934-B2 Piperazine substituted aryl benzodiazepines ELI LILLY AND COMPANY (US) 2008-06-10 US disclosed
US-7384934-B2 Piperazine substituted aryl benzodiazepines ELI LILLY AND COMPANY (US) 2008-06-10 US disclosed
EP-1165613-B1 MELANOCORTIN RECEPTOR LIGANDS PROCTER & GAMBLE (US) 2008-04-30 EP disclosed
WO-2005030796-A1 MACROCYCLIC INHIBITORS OF HEPATITIS C VIRUS NS3 SERINE PROTEASE SCHERING CORPORATION (US) 2005-04-07 WO disclosed
US-6221865-B1 INHIBITORS OF PROTEIN FARNESYLTRANSFERASE AND PROTEIN GERANYLGERANYLTRANSFERASE. UNIVERSITY OF PITTSBURGH 2001-04-24 US disclosed
WO-1993005011-A1 NOVEL IMMUNOSUPPRESSANTS SANDOZ LTD. (CH) 1993-03-18 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 (5 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-12404274-B2 Macrocycles as factor xia inhibitors TFPI, TFPI2, F11 PPARA 4860/4885PPARG 4858/4885SMN1; SMN2 3689/4885
US-12365674-B2 Inhibitors of histone deacetylase useful for the treatment or prevention of HIV infection HDAC1, HDAC11, HDAC3 PPARA 3493/4885PPARG 3815/4885SMN1; SMN2 4407/4885
US-12540162-B2 Preparation of functional homocysteine residues in polypeptides and peptides PTMS, AHCY, BHMT2 PPARA 3362/4885PPARG 3024/4885SMN1; SMN2 2229/4885
US-20230348452-A1 COMPOUNDS AND USES THEREOF VHL, CLN6, BRCA1 PPARA 1346/4885PPARG 269/4885SMN1; SMN2 49/4885
US-20240092833-A1 PREPARATION OF FUNCTIONAL HOMOCYSTEINE RESIDUES IN POLYPEPTIDES AND PEPTIDES BHMT2, BHMT, PTMS PPARA 3694/4885PPARG 4068/4885SMN1; SMN2 1927/4885

“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.