SCHEMBL429475

SCHEMBL429475

CCCCC(NC)C(=O)O

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CA2 P00918 4/20 0.50
MAPK1 P28482 1/20 0.50
NOD1 Q9Y239 3/20 0.49
GPR84 Q9NQS5 3/20 0.43
FFAR1 O14842 1/20 0.43
SLC1A3 P43003 1/20 0.42
SLC1A2 P43004 1/20 0.42
SLC1A1 P43005 1/20 0.42
HDAC2 Q92769 2/20 0.42
MAPT P10636 1/20 0.42
LCK P06239 1/20 0.42
PPARD Q03181 1/20 0.42
ZDHHC20 Q5W0Z9 1/20 0.42
ZDHHC2 Q9UIJ5 1/20 0.42
MME P08473 1/20 0.41
CHRM1 P11229 1/20 0.41
AKR1A1 P14550 1/20 0.41
CHRM3 P20309 1/20 0.41
HTR2A P28223 1/20 0.41
HTR2C P28335 1/20 0.41

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
SCHEMBL201058 1.00 CA2 (0.50) CA2MAPK1NOD1GPR84FFAR1
SCHEMBL288045 1.00 CA2 (0.50) CA2MAPK1NOD1GPR84FFAR1
Hydrochloric Acid SCHEMBL4908040 0.98 CA2 (0.48) CA2MAPK1NOD1GPR84FFAR1
Hydrochloric Acid SCHEMBL20361641 0.98 CA2 (0.48) CA2MAPK1NOD1GPR84FFAR1
SCHEMBL24709075 0.93 GPR84 (0.52) CA2MAPK1NOD1GPR84FFAR1
SCHEMBL21102191 0.93 GPR84 (0.52) CA2MAPK1NOD1GPR84FFAR1
SCHEMBL15451410 0.93 GPR84 (0.52) CA2MAPK1NOD1GPR84FFAR1
SCHEMBL20366017 0.91 GPR84 (0.55) NOD1GPR84FFAR1MAPTLCK
SCHEMBL25208251 0.91 GPR84 (0.55) NOD1GPR84FFAR1MAPTLCK
SCHEMBL3896154 0.91 GPR84 (0.55) NOD1GPR84FFAR1MAPTLCK

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 1433 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250161408-A1 PEPTIDIC INHIBITORS OF AMYLOID SELF- AND CROSS-ASSEMBLY LUDWIG-MAXIMILIANS-UNIVERSITÄT MÜNCHEN (DE) 2025-05-22 US claimed
WO-2025100520-A1 PEPTIDE, PEPTIDE COMPLEX, PHARMACEUTICAL COMPOSITION, COMPOSITION FOR CELL CULTURE, AND COMPOSITION FOR MEDICAL USE, DIAGNOSTIC USE, OR RESEARCH USE ペプチドリーム株式会社 2025-05-15 WO claimed
CN-118632867-A GLP-1/GIP receptor co-agonist prodrugs and uses thereof 诺和诺德股份有限公司 2024-09-10 CN claimed
US-20240083965-A1 PRODRUGS AND USES THEREOF NOVO NORDISK AS (DK) 2024-03-14 US claimed
EP-4230645-A1 PEPTIDIC INHIBITORS OF AMYLOID SELF- AND CROSS-ASSEMBLY Technische Universität München (DE) 2023-08-23 EP claimed
WO-2023139187-A1 GLP-1/GIP RECEPTOR CO-AGONIST PRODRUGS AND USES THEREOF NOVO NORDISK A/S (DK) 2023-07-27 WO claimed
US-20230227521-A1 PRODRUGS AND USES THEREOF NOVO NORDISK A/S (DK) 2023-07-20 US claimed
US-20220241377-A1 RECEPTOR-TARGETING PEPTIDE-DRUG CONJUGATES Molgenie GmbH (DE) 2022-08-04 US claimed
EP-4003403-A1 RECEPTOR-TARGETING PEPTIDE-DRUG CONJUGATES Molgenie GmbH (DE) 2022-06-01 EP claimed
CN-114450299-A Receptor-targeting peptide-drug conjugates 莫尔吉尼有限责任公司 2022-05-06 CN claimed
EP-1506221-A2 FAP-ACTIVATED ANTI-TUMOR PRODRUGS Boehringer Ingelheim Pharma GmbH & Co.KG (DE) 2005-02-16 EP claimed
EP-1472277-A1 FAP-ACTIVATED ANTI-TUMOR COMPOUNDS Boehringer Ingelheim Pharma GmbH & Co.KG (DE) 2004-11-03 EP claimed
EP-1442050-A2 LINEAR BASIC COMPOUNDS HAVING NK-2 ANTAGONIST ACTIVITY AND FORMULATIONS THEREOF MALESCI ISTITUTO FARMACOBIOLOGICO S.p.A. (IT) 2004-08-04 EP claimed
US-20040033957-A1 FAP-activated anti-tumor prodrugs BOEHRINGER INGELHEIM PHARMA GMBH & CO. KG (DE) 2004-02-19 US claimed
WO-2003094972-A2 FAP-ACTIVATED ANTI-TUMOR PRODRUGS BOEHRINGER INGELHEIM PHARMA GMBH & CO KG (DE) 2003-11-20 WO claimed
US-20030211979-A1 FAP-activated anti-tumor compounds BOEHRINGER INGELHEIM PHARMA GMBH & CO. KG (DE) 2003-11-13 US claimed
WO-2003064454-A1 FAP-ACTIVATED ANTI-TUMOR COMPOUNDS BOEHRINGER INGELHEIM PHARMA GMBH & CO KG (DE) 2003-08-07 WO claimed
EP-1333033-A1 FAP-activated anti-tumor compounds Boehringer Ingelheim Pharma GmbH & Co.KG (DE) 2003-08-06 EP claimed
WO-2003037916-A2 LINEAR BASIC COMPOUNDS HAVING NK-2 ANTAGONIST ACTIVITY AND FORMULATIONS THEREOF MALESCI ISTITUTO FARMACOBIOLOGICO S.P.A. (IT) 2003-05-08 WO claimed
WO-1993000359-A1 MODIFIED PEPTIDES TRANSPORTABLE INTO THE CENTRAL NERVOUS SYSTEM THE DU PONT MERCK PHARMACEUTICAL COMPANY (US) 1993-01-07 WO claimed

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-20230227521-A1 PRODRUGS AND USES THEREOF GIPR, GLP1R, GRPR CA2 2144/4885MAPK1 2486/4885NOD1 687/4885
US-20220241377-A1 RECEPTOR-TARGETING PEPTIDE-DRUG CONJUGATES NPY1R, NPY2R, NPY5R CA2 3512/4885MAPK1 2263/4885NOD1 4078/4885
US-20040033957-A1 FAP-activated anti-tumor prodrugs FAP, DNPEP, PAICS CA2 444/4885MAPK1 3876/4885NOD1 691/4885
US-20030211979-A1 FAP-activated anti-tumor compounds FAP, FIBP, APC CA2 737/4885MAPK1 2494/4885NOD1 2007/4885
US-20240083965-A1 PRODRUGS AND USES THEREOF GIPR, GLP1R, GRPR CA2 2144/4885MAPK1 2486/4885NOD1 687/4885

“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.