SCHEMBL869314

SCHEMBL869314

ClCn1cccn1

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
Hydrochloric Acid SCHEMBL2186150 0.97
Hydrochloric Acid SCHEMBL2185623 0.97
SCHEMBL464768 0.79
SCHEMBL5713341 0.77 DAO (0.50)
SCHEMBL1651954 0.77 FDPS (0.45)
SCHEMBL1426071 0.75
SCHEMBL10680 0.74
Hydrochloric Acid SCHEMBL3789712 0.74 GAA (0.40)
Bromide SCHEMBL714157 0.72
SCHEMBL5384 0.72

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119859155-A Tri-fused ring derivative inhibitor, preparation method and application thereof 江苏豪森药业集团有限公司 2025-04-22 CN disclosed
EP-4389754-A1 METAL-ORGANIC COORDINATION COMPOUND AND METHOD FOR PRODUCING THE SAME beeOLED GmbH (DE) 2024-06-26 EP disclosed
CN-110536884-B Synthesis of MCL-1 inhibitors 阿斯利康(瑞典)有限公司 2023-05-02 CN disclosed
EP-3131897-B1 FACTOR IXA INHIBITORS MERCK SHARP & DOHME (US) 2022-06-15 EP disclosed
EP-3601230-B1 SYNTHESIS OF MCL-1 INHIBITOR ASTRAZENECA AB (SE) 2022-01-26 EP disclosed
US-11149024-B2 Synthesis of Mcl-1 inhibitor ASTRAZENECA AB (SE) 2021-10-19 US disclosed
US-20210122735-A1 SYNTHESIS OF MCL-1 INHIBITOR ASTRAZENECA AB (SE) 2021-04-29 US disclosed
EP-3601230-A1 SYNTHESIS OF MCL-1 INHIBITOR Astrazeneca AB (SE) 2020-02-05 EP disclosed
CN-106255689-B Heteroaryl SYK Inhibitors 勃林格殷格翰国际有限公司 2019-09-17 CN disclosed
CN-110183440-A Heteroaryl SYK inhibitor 勃林格殷格翰国际有限公司 2019-08-30 CN disclosed
US-4663462-A CHEMICAL INTERMEDIATES FOR HYPOTENSIVES AND ADRENERGIC BLOCK AGENTS HOFFMANN-LA ROCHE INC. (US) 1987-05-05 US disclosed
US-4657579-A HERBICIDE SANDOZ LTD. (CH) 1987-04-14 US disclosed
US-4577030-A Azolyl-substituted phenoxy-aminopropanol derivatives HOFFMANN-LA ROCHE INC. (US) 1986-03-18 US disclosed
EP-0034831-B1 SUBSTITUTED PHENOXY-AMINOPROPANOL DERIVATIVES, INTERMEDIATES AND PROCESS FOR THEIR PREPARATION AND MEDICAMENT CONTAINING THEM F. HOFFMANN-LA ROCHE & CO. Aktiengesellschaft (CH) 1984-12-12 EP disclosed
US-4387100-A AROMATIC N-HETEROCYCLES, ADRENERGIC BLOCKING AGENTS, HYPOTENSIVE AGENTS HOFFMANN-LA ROCHE INC. (US) 1983-06-07 US disclosed
EP-0069848-A2 Substituted phenoxyphenyl-azolylalkyl ethers, process for their preparation and their application as herbicides and as plant growth regulators BAYER AG (DE) 1983-01-19 EP disclosed
EP-0069881-A1 S-azolyl-methyl-di(tri)-thiophosphoric-acid esters, process for their preparation and their use as pesticides BAYER AG (DE) 1983-01-19 EP disclosed
US-4325962-A ANTIINFLAMMATORY AGENTS, ANALGESICS, ANTIDYRETICS BYK-GULDEN LOMBERG CHEMISCHE FABRIK GMBH (DE) 1982-04-20 US disclosed
EP-0034831-A2 Substituted phenoxy-aminopropanol derivatives, intermediates and process for their preparation and medicament containing them F. HOFFMANN-LA ROCHE & CO. Aktiengesellschaft (CH) 1981-09-02 EP disclosed
US-4146721-A ANALGESICS, ANTIINFLAMMATORY AGENTS AND ANTIPYRETICS BYK GULDEN LOMBERG CHEMISCHE FABRIK GMBH (DE) 1979-03-27 US disclosed