SCHEMBL10050997

SCHEMBL10050997

CCCNC(=O)CI

nearest known ligand 0.00

⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.

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
SCHEMBL6040899 0.85
SCHEMBL14231351 0.83 CASP2 (0.63)
SCHEMBL134099 0.83 ALDH1A1 (0.39)
SCHEMBL18519236 0.82 MEN1 (0.61)
SCHEMBL8973921 0.81 CASP2 (0.67)
SCHEMBL933644 0.81 CASP2 (0.67)
SCHEMBL28806490 0.81 CASP2 (0.67)
SCHEMBL935157 0.81 CASP2 (0.67)
SCHEMBL934477 0.81 CASP2 (0.67)
SCHEMBL5501338 0.81 CASP2 (0.67)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12472166-B2 Inhibition of mycobacterial type VII secretion STICHTING VUMC (NL) 2025-11-18 US disclosed
EP-4021898-B1 INHIBITION OF MYCOBACTERIAL TYPE VII SECRETION Stichting Amsterdam UMC (NL) 2024-05-29 EP disclosed
US-20230321267-A1 Method And Molecules THE REGENTS OF THE UNIVERSITY OF CALIFORNIA 2023-10-12 US disclosed
US-11759526-B2 Method and molecules MEDIMMUNE, LLC (US) 2023-09-19 US disclosed
US-20220280487-A1 INHIBITION OF MYCOBACTERIAL TYPE VII SECRETION STICHTING VU (NL) 2022-09-08 US disclosed
EP-4021898-A1 INHIBITION OF MYCOBACTERIAL TYPE VII SECRETION Stichting VUmc (NL) 2022-07-06 EP disclosed
WO-2021040519-A1 INHIBITION OF MYCOBACTERIAL TYPE VII SECRETION STICHTING VUMC (NL) 2021-03-04 WO disclosed
US-9885035-B2 Method for the synthesis of a bifunctional complex NUEVOLUTION A/S (DK) 2018-02-06 US disclosed
US-20170218085-A1 SITE-SPECIFIC LABELING METHODS AND MOLECULES PRODUCED THEREBY NOVARTIS AG (CH) 2017-08-03 US disclosed
US-20170198283-A1 TEMPLATED MOLECULES AND METHODS FOR USING SUCH MOLECULES NUEVOLUTION A/S (DK) 2017-07-13 US disclosed
US-20150011434-A1 METHOD FOR THE SYNTHESIS OF A BIFUNCTIONAL COMPLEX NUEVOLUTION A/S (DK) 2015-01-08 US disclosed
EP-2515928-B1 OXYNTOMODULIN PEPTIDE ANALOGUE LILLY CO ELI (US) 2014-06-18 EP disclosed
US-20140065171-A1 Site-Specific Labeling Methods and Molecules Produced Thereby NOVARTIS INTERNATIONAL PHARMACEUTICAL LTD. (BM) 2014-03-06 US disclosed
US-20130040823-A1 METHOD FOR THE SYNTHESIS OF A BIFUNCTIONAL COMPLEX NUEVOLUTION A/S (DK) 2013-02-14 US disclosed
US-20130040823-A1 METHOD FOR THE SYNTHESIS OF A BIFUNCTIONAL COMPLEX NUEVOLUTION A/S (DK) 2013-02-14 US disclosed
US-20120225089-A1 NOVEL CONJUGATES, PREPARATION THEREOF, AND THERAPEUTIC USE THEREOF SANOFI (FR) 2012-09-06 US disclosed
US-8206901-B2 Method for the synthesis of a bifunctional complex NUEVOLUTION A/S (DK) 2012-06-26 US disclosed
US-8206901-B2 Method for the synthesis of a bifunctional complex NUEVOLUTION A/S (DK) 2012-06-26 US disclosed
US-20110150820-A1 METHODS FOR COVALENTLY ATTACHING A POLYMER TO A METHIONINE RESIDUE IN PROTEINS AND PEPTIDES INSIGHT BIOPHARMACEUTICALS LTD. (IL) 2011-06-23 US disclosed
US-20080161537-A1 SELECTIVE RADIOLABELING OF BIOMOLECULES GENERAL ELECTRIC COMPANY (US) 2008-07-03 US disclosed