SCHEMBL13213430

SCHEMBL13213430

CC(C)NC(CO)C(=O)C(C)C

nearest known ligand 0.34

Predicted protein targets (top 4)

geneUniProtsupporting neighboursconfidence
▸ TGFBR1 P36897 3/20 0.34
▸ TDP1 Q9NUW8 1/20 0.32
▸ MME P08473 4/20 0.32
▸ TSHR P16473 1/20 0.30

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
SCHEMBL12766316 1.00 TGFBR1 (0.34) TGFBR1TDP1MMETSHR
SCHEMBL19483467 0.82 — —
SCHEMBL2625030 0.81 ALDH1A1 (0.35) TDP1TSHR
SCHEMBL10166040 0.81 ALDH1A1 (0.35) TDP1TSHR
SCHEMBL23306943 0.80 MMP1 (0.35) TGFBR1TSHR
SCHEMBL21153561 0.80 MME (0.43) MME
SCHEMBL18932853 0.79 ALDH1A1 (0.32) TDP1TSHR
SCHEMBL7602603 0.79 ALDH1A1 (0.44) —
SCHEMBL24494714 0.79 ACE (0.39) TDP1
SCHEMBL19361692 0.79 TDP1 (0.30) TDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240239828-A1 MANNOSE 6-PHOSPHATE OR ASGPR RECEPTOR BINDING COMPOUNDS FOR THE DEGRADATION OF EXTRACELLULAR PROTEINS AVILAR THERAPEUTICS, INC. (US) 2024-07-18 — — US disclosed
US-20240072809-A1 ASGPR-BINDING COMPOUNDS FOR THE DEGRADATION OF EXTRACELLULAR PROTEINS AVILAR THERAPEUTICS, INC. (US) 2024-02-29 — — US disclosed
US-11819551-B2 ASGPR-binding compounds for the degradation of extracellular proteins AVILAR THERAPEUTICS, INC. (US) 2023-11-21 — — US disclosed
WO-2023217744-A1 PRODRUGS OF GLP-1 POLYPEPTIDE AND USES THEREOF NOVO NORDISK A/S (DK) 2023-11-16 — — WO disclosed
US-20230233689-A1 Bifunctional Small Molecules to Target the Selective Degradation of Circulating Proteins UNIV YALE (US) 2023-07-27 — — US disclosed
WO-2023028338-A2 MANNOSE 6-PHOSPHATE OR ASGPR RECEPTOR BINDING COMPOUNDS FOR THE DEGRADATION OF EXTRACELLULAR PROTEINS AVILAR THERAPEUTICS, INC. (US) 2023-03-02 — — WO disclosed
US-11572398-B2 GLP-1 derivatives and uses thereof NOVO NORDISK A/S (DK) 2023-02-07 — — US disclosed
WO-2022235699-A2 POTENT ASGPR-BINDING COMPOUNDS FOR THE DEGRADATION OF IMMUNOGLOBULINS AND OTHER PROTEINS AVILAR THERAPEUTICS, INC. (US) 2022-11-10 — — WO disclosed
US-11358985-B2 Tripeptide compound, preparation method therefor, and application thereof NORTHWEST UNIVERSITY (CN) 2022-06-14 — — US disclosed
WO-2022096636-A1 GLP-1 PRODRUGS AND USES HEREOF NOVO NORDISK A/S (DK) 2022-05-12 — — WO disclosed
US-20170320927-A1 GLP-1 Derivatives and Uses Thereof NOVO NORDISK A/S (DK) 2017-11-09 — — US disclosed
US-20170320927-A1 GLP-1 Derivatives and Uses Thereof NOVO NORDISK A/S (DK) 2017-11-09 — — US disclosed
US-20170267718-A1 TRIPEPTIDE COMPOUND, PREPARATION METHOD THEREFOR, AND APPLICATION THEREOF NORTHWEST UNIVERSITY (CN) 2017-09-21 — — US disclosed
US-20170267718-A1 TRIPEPTIDE COMPOUND, PREPARATION METHOD THEREFOR, AND APPLICATION THEREOF NORTHWEST UNIVERSITY (CN) 2017-09-21 — — US disclosed
US-9725483-B2 Compounds for the treatment and/or care of the skin and/or mucous membranes and their use in cosmetic or pharmaceutical compositions LIPOTEC, S.A. (ES) 2017-08-08 — — US disclosed
US-20170144998-A1 ELASTASE INHIBITORS THE CALIFORNIA INSTITUTE FOR BIOMEDICAL RESEARCH 2017-05-25 — — US disclosed
US-9656972-B2 Compounds for treatment of cystic fibrosis THE CALIFORNIA INSTITUTE FOR BIOMEDICAL RESEARCH (US) 2017-05-23 — — US disclosed
US-20160159754-A1 COMPOUNDS FOR TREATMENT OF CYSTIC FIBROSIS THE CALIFORNIA INSTITUTE FOR BIOMEDICAL RESEARCH 2016-06-09 — — US disclosed
US-8653278-B2 Isoform selective HDAC inhibitors GEORGETOWN UNIVERSITY (US) 2014-02-18 — — US disclosed
US-20100196502-A1 Isoform Selective HDAC Inhibitors GEORGETOWN UNIVERSITY (US) 2010-08-05 — — 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 (10 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-11819551-B2 ASGPR-binding compounds for the degradation of extracellular proteins ASGR1, ENGASE, FCGR2A TGFBR1 701/4885TDP1 3930/4885MME 158/4885
US-20160159754-A1 COMPOUNDS FOR TREATMENT OF CYSTIC FIBROSIS CFTR, ELANE, OTC TGFBR1 2445/4885TDP1 4703/4885MME 396/4885
US-11358985-B2 Tripeptide compound, preparation method therefor, and application thereof VIP, PREP, ACE TGFBR1 997/4885TDP1 2218/4885MME 85/4885
US-20230233689-A1 Bifunctional Small Molecules to Target the Selective Degradation of Circulating Proteins ASGR1, LDLR, FCGR2A TGFBR1 366/4885TDP1 4559/4885MME 1308/4885
US-11572398-B2 GLP-1 derivatives and uses thereof GLP1R, GIPR, GCG TGFBR1 2005/4885TDP1 3599/4885MME 1401/4885
US-20240239828-A1 MANNOSE 6-PHOSPHATE OR ASGPR RECEPTOR BINDING COMPOUNDS FOR THE DEGRADATION OF EXTRACELLULAR PROTEINS M6PR, ASGR1, IGF2R TGFBR1 506/4885TDP1 3682/4885MME 104/4885
US-20100196502-A1 Isoform Selective HDAC Inhibitors HDAC5, HDAC6, HDAC3 TGFBR1 2340/4885TDP1 1198/4885MME 3166/4885
US-20170320927-A1 GLP-1 Derivatives and Uses Thereof GLP1R, GIPR, GCG TGFBR1 2005/4885TDP1 3599/4885MME 1401/4885
US-20170144998-A1 ELASTASE INHIBITORS SERPINB1, ELANE, CELA1 TGFBR1 3602/4885TDP1 1042/4885MME 53/4885
US-20170267718-A1 TRIPEPTIDE COMPOUND, PREPARATION METHOD THEREFOR, AND APPLICATION THEREOF VIP, PREP, ACE TGFBR1 997/4885TDP1 2218/4885MME 85/4885

“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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