SCHEMBL264785

SCHEMBL264785

CC1(CN)C=CC=CC1

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
SCHEMBL2216251 1.00
SCHEMBL1335734 1.00
Bromide SCHEMBL8413149 0.98
Butyl Alcohol SCHEMBL28205382 0.84 ALDH1A1 (0.37)
SCHEMBL3746748 0.82
SCHEMBL27280308 0.82
SCHEMBL11300457 0.82
SCHEMBL1706136 0.81
SCHEMBL11162704 0.79
SCHEMBL31281425 0.78

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-113527022-B Asymmetric polysulfide compound and its synthesis method and use 华东师范大学 2022-12-06 CN claimed
CN-114409716-A Sugar-modified metal helix complex, preparation method thereof and application of complex as amyloid degradation device 中国科学院长春应用化学研究所 2022-04-29 CN claimed
CN-113527022-A Asymmetric polysulfide compound and its synthesis method and use 华东师范大学 2021-10-22 CN claimed
WO-2020203248-A1 METHOD FOR PRODUCING 4-HALOGENOBENZYLAMINE DERIVATIVE 株式会社トクヤマ 2020-10-08 WO claimed
WO-2012114347-A1 SYNTHESIS OF CHIRAL SUBSTITUTED BENZENES AND RELATED AROMATIC COMPOUNDS CONTAINING 1,2 DIOLS PROTECTED AS DIACETAL GROUPS AVRA LABORATORIES PVT. LTD. (IN) 2012-08-30 WO claimed
US-7105559-B2 Substituted 5-membered polycyclic compounds useful for selective inhibition of the coagulation cascade PHARMACIA CORPORATION (US) 2006-09-12 US claimed
US-20050239860-A1 Substituted 5-membered polycyclic compounds useful for selective inhibition of the coagulation cascade PHARMACIA CORPORATION (US) 2005-10-27 US claimed
EP-1482940-A2 PRODRUGS OF SUBSTITUTED POLYCYCLIC COMPOUNDS USEFUL FOR SELECTIVE INHIBITION OF THE COAGULATION CASCADE Pharmacia Corporation (US) 2004-12-08 EP claimed
EP-1432687-A2 SUBSTITUTED 5-MEMBERED POLYCYCLIC COMPOUNDS USEFUL FOR SELECTIVE INHIBITION OF THE COAGULATION CASCADE Pharmacia Corporation (US) 2004-06-30 EP claimed
US-20040082585-A1 Prodrugs of substituted polycyclic compounds useful for selective inhibition of the coagulation cascade PHARMACIA CORPORATION 2004-04-29 US claimed
WO-2003093242-A2 SUBSTITUTED 5-MEMBERED POLYCYCLIC COMPOUNDS USEFUL FOR SELECTIVE INHIBITION OF THE COAGULATION CASCADE PHARMACIA CORPORATION (US) 2003-11-13 WO claimed
US-20030162776-A1 Substituted 5-membered polycyclic compounds useful for selective inhibition of the coagulation cascade PHARMACIA CORPORATION 2003-08-28 US claimed
WO-2003028729-A2 PRODRUGS OF SUBSTITUTED POLYCYCLIC COMPOUNDS USEFUL FOR SELECTIVE INHIBITION OF THE COAGULATION CASCADE PHARMACIA CORPORATION (US) 2003-04-10 WO claimed
US-6479671-B1 Process for producing optically active chromene derivative SHIONOGI & CO., LTD. (JP) 2002-11-12 US claimed
EP-1057824-A1 PROCESS FOR PRODUCING OPTICALLY ACTIVE CHROMENE DERIVATIVE SHIONOGI & CO., LTD. (JP) 2000-12-06 EP claimed
CN-114409716-B Sugar-modified metal helix complex, preparation method thereof and application thereof as amyloid degradation device 中国科学院长春应用化学研究所 2023-10-20 CN disclosed
US-11702385-B2 Urea group containing anti-sagging rheology control agents BYK-CHEMIE GMBH (DE) 2023-07-18 US disclosed
CN-1035827-A The 4-oxo of opticity-1-chromene-2-carboxylic acid derivative and intermediates preparation thereof SANWA KAGAKU KENKYUSHO K K (JP) 1989-09-27 CN disclosed
EP-0331078-A2 Process for the preparation of optically active 4-oxo-1-benzopyran-2-carboxylic acid derivatives and intermediates thereof SANWA KAGAKU KENKYUSHO CO., LTD. (JP) 1989-09-06 EP disclosed
US-4650795-A Amine salts of clavulanic acid as antibacterial agents BEECHAM GROUP P.L.C. (GB) 1987-03-17 US disclosed