SCHEMBL120255

SCHEMBL120255

CCC[C@H](NC(=O)OCC1c2ccccc2-c2ccccc21)C(=O)O

nearest known ligand 0.60

Predicted protein targets (top 6)

geneUniProtsupporting neighboursconfidence
TLR2 O60603 2/20 0.59
MDM4 O15151 2/20 0.58
TP53 P04637 2/20 0.58
MDM2 Q00987 5/20 0.56
CASP3 P42574 2/20 0.55
TNF P01375 1/20 0.50

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
SCHEMBL29398908 1.00 TLR2 (0.59) TLR2MDM4TP53MDM2CASP3
SCHEMBL119530 1.00 TLR2 (0.59) TLR2MDM4TP53MDM2CASP3
SCHEMBL7532853 1.00 TLR2 (0.59) TLR2MDM4TP53MDM2CASP3
SCHEMBL29400620 1.00 TLR2 (0.59) TLR2MDM4TP53MDM2CASP3
SCHEMBL30291728 1.00 TLR2 (0.59) TLR2MDM4TP53MDM2CASP3
SCHEMBL29867802 1.00 TLR2 (0.59) TLR2MDM4TP53MDM2CASP3
SCHEMBL1044856 0.93 TLR2 (0.62) TLR2MDM4TP53MDM2CASP3
SCHEMBL7420121 0.93 TLR2 (0.62) TLR2MDM4TP53MDM2CASP3
SCHEMBL29382791 0.93 TLR2 (0.62) TLR2MDM4TP53MDM2CASP3
SCHEMBL1000115 0.93 TLR2 (0.62) TLR2MDM4TP53MDM2CASP3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1212348-A2 PURIFICATION AND ANALYSIS OF CYCLIC PEPTIDE LIBRARIES, AND COMPOSITIONS THEREOF Consensus Pharmaceuticals, Inc. (US) 2002-06-12 EP claimed
US-20020019061-A1 PURIFICATION AND ANALYSIS OF CYCLIC PEPTIDE LIBRARIES, AND COMPOSITIONS THEREOF IWA, LLC 2002-02-14 US claimed
WO-2001016160-A2 PURIFICATION AND ANALYSIS OF CYCLIC PEPTIDE LIBRARIES, AND COMPOSITIONS THEREOF CONSENSUS PHARMACEUTICALS, INC. (US) 2001-03-08 WO claimed
CN-117377759-A Self-purified nucleic acid-encoded libraries 约尔格·谢尔曼 2024-01-09 CN disclosed
US-20230257343-A1 NOVEL AMINO ACID DERIVATIVES PEPTIDREAM INC (JP) 2023-08-17 US disclosed
US-11702452-B2 Process for making arylomycin ring analogs GENENTECH, INC. (US) 2023-07-18 US disclosed
US-11685714-B2 Prodrugs of cytotoxic active agents having enzymatically cleavable groups BAYER PHARMA AKTIENGESELLSCHAFT (DE) 2023-06-27 US disclosed
US-20230151060-A1 CYCLIC PEPTIDE COMPOUND HAVING KRAS INHIBITORY ACTION CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2023-05-18 US disclosed
US-20230151060-A1 CYCLIC PEPTIDE COMPOUND HAVING KRAS INHIBITORY ACTION CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2023-05-18 US disclosed
US-20220218664-A1 DRUG AND METHOD FOR TREATING OR PREVENTING COMPLICATIONS FROM DIABETES, USING SAID DRUG SHOWA UNIVERSITY (JP) 2022-07-14 US disclosed
US-20210322381-A1 DRUG FOR TREATMENT OR PREVENTION OF BLOOD CEREBRAL HEMORRHAGE, AND METHOD FOR TREATING OR PREVENTING CEREBRAL HEMORRHAGE USING THE DRUG CORXEL PHARMACEUTICALS HONG KONG LIMITED (CN) 2021-10-21 US disclosed
WO-2006127948-A2 N-TERMINALLY MODIFIED GLP-1 RECEPTOR MODULATORS BRISTOL-MYERS SQUIBB COMPANY (US) 2006-11-30 WO disclosed
EP-1656390-A2 COMPOSITIONS OF LIPOPEPTIDE ANTIBIOTIC DERIVATIVES AND METHODS OF USE THEREOF MIGENIX INC. (CA) 2006-05-17 EP disclosed
WO-2006014287-A1 HUMAN GLUCAGON-LIKE-PEPTIDE-1 MODULATORS AND THEIR USE IN THE TREATMENT OF DIABETES AND RELATED CONDITIONS BRISTOL-MYERS SQUIBB COMPANY (US) 2006-02-09 WO disclosed
US-20050153876-A1 Compositions of lipopeptide antibiotic derivatives and methods of use thereof MIGENIX INC. (CA) 2005-07-14 US disclosed
WO-2005000878-A2 COMPOSITIONS OF LIPOPEPTIDE ANTIBIOTIC DERIVATIVES AND METHODS OF USE THEREOF MIGENIX INC. (CA) 2005-01-06 WO disclosed
EP-1212348-A2 PURIFICATION AND ANALYSIS OF CYCLIC PEPTIDE LIBRARIES, AND COMPOSITIONS THEREOF Consensus Pharmaceuticals, Inc. (US) 2002-06-12 EP disclosed
US-20020019061-A1 PURIFICATION AND ANALYSIS OF CYCLIC PEPTIDE LIBRARIES, AND COMPOSITIONS THEREOF IWA, LLC 2002-02-14 US disclosed
WO-2001016160-A2 PURIFICATION AND ANALYSIS OF CYCLIC PEPTIDE LIBRARIES, AND COMPOSITIONS THEREOF CONSENSUS PHARMACEUTICALS, INC. (US) 2001-03-08 WO disclosed
US-5872146-A Mercapto alkyl peptidyl compounds having MMP and TNF inhibitory activity CHIROSCIENCE LIMITED (GB) 1999-02-16 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 (7 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-20210322381-A1 DRUG FOR TREATMENT OR PREVENTION OF BLOOD CEREBRAL HEMORRHAGE, AND METHOD FOR TREATING OR PREVENTING CEREBRAL HEMORRHAGE USING THE DRUG PROC, FABP7, TIMP3 TLR2 4456/4885MDM4 4844/4885TP53 3440/4885
US-20230151060-A1 CYCLIC PEPTIDE COMPOUND HAVING KRAS INHIBITORY ACTION KRAS, NRAS, HRAS TLR2 3821/4885MDM4 441/4885TP53 34/4885
US-11685714-B2 Prodrugs of cytotoxic active agents having enzymatically cleavable groups BUB1B, KIF5B, TK1 TLR2 4530/4885MDM4 2123/4885TP53 85/4885
US-20220218664-A1 DRUG AND METHOD FOR TREATING OR PREVENTING COMPLICATIONS FROM DIABETES, USING SAID DRUG SLC5A2, SLC5A1, IAPP TLR2 3406/4885MDM4 4652/4885TP53 4749/4885
US-11702452-B2 Process for making arylomycin ring analogs RRS1, GLRA1, MRPL21 TLR2 1136/4885MDM4 3039/4885TP53 2740/4885
US-20050153876-A1 Compositions of lipopeptide antibiotic derivatives and methods of use thereof NRDC, NOD2, NGLY1 TLR2 20/4885MDM4 2087/4885TP53 2126/4885
US-20230257343-A1 NOVEL AMINO ACID DERIVATIVES DNPEP, BCAT1, ANPEP TLR2 3866/4885MDM4 1648/4885TP53 614/4885

“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.