SCHEMBL2029005

SCHEMBL2029005

N[C@H](CCc1ccccc1)CC(=O)O

nearest known ligand 0.64

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
S1PR2 O95136 2/20 0.64
S1PR1 P21453 2/20 0.64
DPP4 P27487 2/20 0.55
ANPEP P15144 2/20 0.53
ERAP1 Q9NZ08 2/20 0.53
ERAP2 Q6P179 1/20 0.53
MMP12 P39900 2/20 0.53
MMP2 P08253 1/20 0.53
MMP9 P14780 1/20 0.53
MMP13 P45452 1/20 0.53
MMP14 P50281 1/20 0.53
KEAP1 Q14145 1/20 0.50
CPA1 P15085 2/20 0.47
CPB1 P15086 1/20 0.47
CPA3 P15088 1/20 0.47
CPB2 Q96IY4 1/20 0.47
HDAC3 O15379 1/20 0.47
MAPK1 P28482 1/20 0.47
ADRA1A P35348 1/20 0.47
HDAC4 P56524 1/20 0.47

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
SCHEMBL45498 1.00 S1PR2 (0.64) S1PR2S1PR1DPP4ANPEPERAP1
SCHEMBL288680 1.00 S1PR2 (0.64) S1PR2S1PR1DPP4ANPEPERAP1
Hydrochloric Acid SCHEMBL1927328 0.98 S1PR2 (0.62) S1PR2S1PR1DPP4ANPEPERAP1
SCHEMBL27453353 0.89 S1PR2 (0.60) S1PR2S1PR1ANPEPERAP1ERAP2
SCHEMBL1669596 0.89 S1PR2 (0.60) S1PR2S1PR1ANPEPERAP1ERAP2
SCHEMBL6049800 0.87 S1PR2 (0.63) S1PR2S1PR1DPP4MMP12MMP2
SCHEMBL1105478 0.85 ALDH1A1 (0.53) S1PR2S1PR1DPP4ANPEPERAP1
SCHEMBL27999568 0.85 S1PR2 (0.65) S1PR2S1PR1DPP4ANPEPERAP1
SCHEMBL289093 0.85 S1PR2 (0.65) S1PR2S1PR1DPP4ANPEPERAP1
SCHEMBL6467442 0.84 S1PR2 (0.63) S1PR2S1PR1DPP4MMP12MMP2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250367300-A1 Nanomaterial and Methods of Use Thereof UNIVERSITY OF CONNECTICUT (US) 2025-12-04 US disclosed
US-20250302971-A1 Therapeutic Nanomaterials UNIV CONNECTICUT (US) 2025-10-02 US disclosed
US-20250229081-A1 NANOMATERIAL COATED ELECTRODE AND METHODS OF USE THEREOF UNIVERSITY OF CONNECTICUT 2025-07-17 US disclosed
EP-4578868-A1 CYCLIC PEPTIDE OR SALT THEREOF, AND MDMX INHIBITOR FUJIFILM Corporation (JP) 2025-07-02 EP disclosed
EP-4578867-A1 CYCLIC PEPTIDE OR SALT THEREOF AND MDMX INHIBITOR FUJIFILM Corporation (JP) 2025-07-02 EP disclosed
CN-120202010-A Ligand-oligonucleotide conjugates and linkers for use therewith 上海京新生物医药有限公司 2025-06-24 CN disclosed
US-20250179120-A1 CYCLIC PEPTIDE OR SALT THEREOF, AND MDMX INHIBITOR FUJIFILM CORPORATION (JP) 2025-06-05 US disclosed
US-20250179119-A1 CYCLIC PEPTIDE OR SALT THEREOF, AND MDMX INHIBITOR FUJIFILM CORPORATION (JP) 2025-06-05 US disclosed
US-20250084410-A1 INCORPORATION OF UNNATURAL NUCLEOTIDES AND METHODS THEREOF Synthorx, Inc. (US) 2025-03-13 US disclosed
EP-4504732-A2 NANOMATERIAL DELIVERY VEHICLE AND METHOD OF USE THEREOF University of Connecticut (US) 2025-02-12 EP disclosed
WO-2008151434-A1 SMALL CATIONIC ANTIMICROBIAL PEPTIDES THE UNIVERSITY OF BRITISH COLUMBIA (CA) 2008-12-18 WO disclosed
WO-2008022444-A1 SMALL CATIONIC ANTIMICROBIAL PEPTIDES THE UNIVERSITY OF BRITISH COLUMBIA (CA) 2008-02-28 WO disclosed
EP-1646718-A2 METHODS FOR THE STEREOSELECTIVE SYNTHESIS AND ENANTIOMERIC ENRICHMENT OF B-AMINO ACIDS Pharmacia Corporation (US) 2006-04-19 EP disclosed
WO-2005005633-A2 METHODS FOR THE STEREOSELECTIVE SYNTHESIS AND ENANTIOMERIC ENRICHMENT OF B-AMINO ACIDS PHARMACIA CORPORATION (US) 2005-01-20 WO disclosed
US-20050009151-A1 Methods for the stereospecific and enantiomeric enrichment of beta-amino acids PHARMACIA CORPORATION 2005-01-13 US disclosed
EP-1082302-B1 A VLA-4 INHIBITOR: OMEPUPA-V BIOGEN INC (US) 2003-12-17 EP disclosed
US-6495525-B1 N-((4-(((2-METHYLPHENYLAMINO)CARBONYL)AMINO)PHENYL)ACETYL)-L -PROLYL-3-METHYL)-BETA-ALANINE; VERY LATE ANTIGEN-4 CELL ADHESION INHIBITOR; INFLAMMATION AND IMMUNE REACTIONS BIOGEN, INC. 2002-12-17 US disclosed
EP-1082302-A1 A VLA-4 INHIBITOR: OMEPUPA-V BIOGEN, INC. (US) 2001-03-14 EP disclosed
WO-1999061421-A1 A NOVEL VLA-4 INHIBITOR: oMePUPA-V BIOGEN, INC. (US) 1999-12-02 WO disclosed
US-5952306-A INHIBITING THE BINDING OF FIBRINOGEN TO BLOOD PLATELETS AND INHIBITING THE AGGREGATION OF BLOOD PLATELETS; INHIBITING OSTEOCLAST CELLULAR ADHESION TO BONE SURFACES MERCK & CO., INC. (US) 1999-09-14 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 (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-20250302971-A1 Therapeutic Nanomaterials TIE1, TEKT1, POLRMT S1PR2 2052/4885S1PR1 1863/4885DPP4 1357/4885
US-20250179119-A1 CYCLIC PEPTIDE OR SALT THEREOF, AND MDMX INHIBITOR MLX, BMX, ADM2 S1PR2 3371/4885S1PR1 3841/4885DPP4 1217/4885
US-20250367300-A1 Nanomaterial and Methods of Use Thereof EPCAM, CD47, JAK2 S1PR2 2844/4885S1PR1 2366/4885DPP4 1271/4885
US-20250179120-A1 CYCLIC PEPTIDE OR SALT THEREOF, AND MDMX INHIBITOR MDN1, MLX, BMX S1PR2 2613/4885S1PR1 3182/4885DPP4 1374/4885
US-20250084410-A1 INCORPORATION OF UNNATURAL NUCLEOTIDES AND METHODS THEREOF RNGTT, TRMT1, OSGEP S1PR2 4799/4885S1PR1 4776/4885DPP4 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.