SCHEMBL950964

SCHEMBL950964

CC1(C)SCN[C@@H]1C(=O)O

nearest known ligand 0.35

Predicted protein targets (top 4)

geneUniProtsupporting neighboursconfidence
HTT P42858 1/20 0.35
APLNR P35414 1/20 0.33
ARG1 P05089 1/20 0.33
KMT2A Q03164 1/20 0.32

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
SCHEMBL190446 1.00 HTT (0.35) HTTAPLNRARG1KMT2A
SCHEMBL951739 1.00 HTT (0.35) HTTAPLNRARG1KMT2A
Allylamine SCHEMBL27651104 0.85 ARG1 (0.30) ARG1
Allylamine SCHEMBL27651106 0.85 ARG1 (0.30) ARG1
SCHEMBL13534665 0.84
Valine SCHEMBL16004731 0.83 SLC7A5 (0.46)
Gamma-Aminobutyric Acid SCHEMBL1828323 0.82 LMNA (0.44) ARG1KMT2A
SCHEMBL5694169 0.81 HTT (0.31) HTT
SCHEMBL1770442 0.79 ARG1 (0.38) HTTAPLNRARG1KMT2A
SCHEMBL6290400 0.79 ARG1 (0.38) HTTAPLNRARG1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250296971-A1 GASTRIC INHIBITORY PEPTIDE RECEPTOR LIGANDS 3B PHARMACEUTICALS GMBH (DE) 2025-09-25 US disclosed
EP-4455159-A1 GASTRIC INHIBITORY PEPTIDE RECEPTOR LIGANDS WITH BIO-DISTRIBUTION MODIFIER 3B Pharmaceuticals GmbH (DE) 2024-10-30 EP disclosed
EP-4043076-B1 CYCLIC PEPTIDE HAVING CTLA-4 INHIBITORY ACTIVITY AND USE THEREOF GENEFRONTIER CORP (JP) 2024-06-26 EP disclosed
US-20240092836-A1 CYCLIC PEPTIDE HAVING CTLA-4 INHIBITORY ACTIVITY AND USE THEREOF GENEFRONTIER CORPORATION (JP) 2024-03-21 US disclosed
WO-2023176487-A1 METHOD FOR PRODUCING L-PENICILLAMINE 株式会社カネカ 2023-09-21 WO disclosed
EP-4216946-A1 PHARMACEUTICAL COMPOUNDS FOR THE TREATMENT OF COMPLEMENT MEDIATED DISORDERS Achillion Pharmaceuticals, Inc. (US) 2023-08-02 EP disclosed
CN-116437913-A Pharmaceutical compounds for treating complement-mediated disorders 艾其林医药公司 2023-07-14 CN disclosed
WO-2023072971-A2 GASTRIC INHIBITORY PEPTIDE RECEPTOR LIGANDS 3B PHARMACEUTICALS GMBH (DE) 2023-05-04 WO disclosed
EP-4170347-A1 GASTRIC INHIBITORY PEPTIDE RECEPTOR LIGANDS 3B Pharmaceuticals GmbH (DE) 2023-04-26 EP disclosed
CN-115925790-A Methods for synthesizing alpha 4 beta 7 peptide antagonists 领导医疗有限公司 2023-04-07 CN disclosed
US-20030032150-A1 Process for producing optically active (4r)-1,3-tiazolidine-4-carboxylic acid MITSUBISHI GAS CHEMICAL CO., INC. (JP) 2003-02-13 US disclosed
WO-2002100845-A1 HV PROTEASE INHIBITORS, COMPOSITIONS CONTAINING THE SAME, THEIR PHARMACEUTICAL USES AND MATERIALS FOR THEIR SYNTHESIS AGOURON PHARMACEUTICALS, INC. (US) 2002-12-19 WO disclosed
JP-2002234881-A METHOD FOR PRODUCING OPTICALLY ACTIVE 5,5-DIMETHYL-1,3- THIAZOLIDINE-4-CRABOXYLIC ACID DERIVATIVE NAGASE & CO LTD 2002-08-23 JP disclosed
US-6291432-B1 (R)-N-(2-METHYLBENZYL)-3-((2S, 3S)-3-(N-(2-CHROMONECARBONYL)-L-ASPARAGINYL)AMINO-2-HYDROXY-4-PHENYLBUTANO YL)-5,5-DIMETHYL-1,3-THIAZOLIDINE-4-CARBOXAMIDE CAN BE GIVEN AS A TYPICAL EXAMPLE OF THIS COMPOUND. JAPAN ENERGY CORPORATION (JP) 2001-09-18 US disclosed
US-6222043-B1 COUPLING 2-AMIDO-THIAZOLE DERIVATIVE WITH 2-PHENYL4-(PROTECTED)AMINO-BUTYRIC ACID; DEPROTECTING AMINO PROTECTING GROUP; ACYLATING PRODUCT WITH CARBOXYLIC ACID CONTAINING CARBOCYCLIC OR HETEROCYCLIC GROUP; DEPROTECTING JAPAN ENERGY CORPORATION (JP) 2001-04-24 US disclosed
US-6022885-A Pyrrolidine and thiazole derivatives with antibacterial and . metallo-.beta-lactamase inhibitory properties SMITHKLINE BEECHAM P.L.C. (GB) 2000-02-08 US disclosed
US-5962640-A MAKING A DIPEPTIDE COMPOUND OF GIVEN FORMULA COMPRISING A ALPHA-AMINOCARBOXAMIDE INCLUDING CYCLIC GROUP LINKED TO 3-AMINO-2-HYDROXY-4-PHENYLBUTANOYL RESIDUE; HIV PROTEASE INHIBITION AND EXCELLENT BIOAVAILABILITY FROM DIGESTIVE TRACT JAPAN ENERGY CORPORATION (JP) 1999-10-05 US disclosed
US-5932550-A PROTEASE INHIBITOR; AIDS THERAPY JAPAN ENERGY CORPORATION (JP) 1999-08-03 US disclosed
EP-0900566-A1 NOVEL TRIPEPTIDE COMPOUNDS AND ANTI-AIDS DRUGS JAPAN ENERGY CORPORATION (JP) 1999-03-10 EP disclosed
EP-0751145-A2 HIV-protease inhibitors Japan Energy Corporation (JP) 1997-01-02 EP 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 (2 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-20250296971-A1 GASTRIC INHIBITORY PEPTIDE RECEPTOR LIGANDS GIPR, VIP, GRPR HTT 4550/4885APLNR 23/4885ARG1 617/4885
US-20240092836-A1 CYCLIC PEPTIDE HAVING CTLA-4 INHIBITORY ACTIVITY AND USE THEREOF CXCL10, CXCR3, CXCR6 HTT 3771/4885APLNR 1731/4885ARG1 209/4885

“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.