SCHEMBL1304705

SCHEMBL1304705

S=C1NCCCS1

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
SCHEMBL30331251 0.92
SCHEMBL1628000 0.82
SCHEMBL17102937 0.82
SCHEMBL34680 0.82
SCHEMBL13599846 0.71 SMN1; SMN2 (0.32)
SCHEMBL4651720 0.71 FKBP5 (0.33)
SCHEMBL6053394 0.71 FKBP5 (0.33)
SCHEMBL9577017 0.69 FKBP5 (0.32)
SCHEMBL13513149 0.67
SCHEMBL5918490 0.67 FKBP5 (0.31)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-4643997-A PROTECTIVE COATINGS; SUNSCREEN AGENTS WELLA AKTIENGESELLSCHAFT (DE) 1987-02-17 US claimed
EP-4720058-A2 BIFUNCTIONAL DEGRADERS AND USES THEREOF Casma Therapeutics, Inc. (US) 2026-04-08 EP disclosed
WO-2024249291-A2 BIFUNCTIONAL DEGRADERS AND USES THEREOF CASMA THERAPEUTICS, INC. (US) 2024-12-05 WO disclosed
US-20230365556-A1 N-ACYL AMINO ACID COMPOUNDS AND METHODS OF USE PLIANT THERAPEUTICS, INC. (US) 2023-11-16 US disclosed
US-20230365556-A1 N-ACYL AMINO ACID COMPOUNDS AND METHODS OF USE PLIANT THERAPEUTICS, INC. (US) 2023-11-16 US disclosed
US-11673887-B2 N-acyl amino acid compounds and methods of use PLIANT THERAPEUTICS, INC. (US) 2023-06-13 US disclosed
US-11673887-B2 N-acyl amino acid compounds and methods of use PLIANT THERAPEUTICS, INC. (US) 2023-06-13 US disclosed
CN-112142586-B Ketone or oxime compounds and herbicides 日产化学株式会社 2023-05-09 CN disclosed
EP-4053097-A1 KETONE COMPOUND AS HERBICIDE Corteva Agriscience LLC (US) 2022-09-07 EP disclosed
EP-3235799-B1 OXIME COMPOUND AND HERBICIDE NISSAN CHEMICAL CORP (JP) 2022-02-23 EP disclosed
US-4665172-A Process for producing heterocyclic compound having nitromethylene group as the side chain group UBE INDUSTRIES, LTD. (JP) 1987-05-12 US disclosed
US-4643997-A PROTECTIVE COATINGS; SUNSCREEN AGENTS WELLA AKTIENGESELLSCHAFT (DE) 1987-02-17 US disclosed
US-4625025-A Process for producing a 2H-1,3-thiazolidine, 2H-tetrahydro-1,3-thiazine, or 2H-hexahydro-1,3-thiazepine derivative substituted at the 2 position by a nitromethylene group derivative UBE INDUSTRIES, LTD. (JP) 1986-11-25 US disclosed
EP-0189972-A1 Preparation of thiazine derivatives FINE ORGANICS LIMITED (GB) 1986-08-06 EP disclosed
US-4532322-A Preparation of thiazine derivatives FINE ORGANICS LIMITED (GB) 1985-07-30 US disclosed
EP-0135803-A2 Process for producing heterocyclic compounds having nitromethylene group as the side chain group UBE INDUSTRIES, LTD. (JP) 1985-04-03 EP disclosed
EP-0127413-A2 Preparation of thiazine derivatives FINE ORGANICS LIMITED (GB) 1984-12-05 EP disclosed
EP-0115323-A2 Process for producing heterocyclic compound having nitromethylene group as the side chain group UBE INDUSTRIES, LTD. (JP) 1984-08-08 EP disclosed
US-4031228-A 5(6)-Benzene ring substituted benzimidazole-2-carbamate derivatives having anti-protozoal activity SYNTEX (U.S.A.) INC. (US) 1977-06-21 US disclosed
US-3962437-A 5(6)-Benzene ring substituted benzimidazole-2-carbamate derivatives having anthelmintic activity SYNTEX (U.S.A.) INC. (US) 1976-06-08 US disclosed