SCHEMBL2368898

SCHEMBL2368898

CO[C@H]1CC[C@@H](O)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
SCHEMBL2369051 1.00
SCHEMBL473550 1.00
Hydrogen Peroxide SCHEMBL28037399 0.97 TSHR (0.35)
SCHEMBL10876165 0.92 TSHR (0.32)
SCHEMBL6132259 0.92 TSHR (0.32)
SCHEMBL14720917 0.89 TSHR (0.43)
SCHEMBL21420110 0.83
SCHEMBL9393516 0.83 EPHX2 (0.33)
SCHEMBL4456910 0.83 EPHX2 (0.33)
SCHEMBL29700 0.83

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240368173-A1 TRICYCLIC GPR65 MODULATORS Pathios Therapeutics Limited (GB) 2024-11-07 US disclosed
WO-2024218296-A1 COMBINATION TREATMENTS COMPRISING ADMINISTRATION OF LEUCINE-RICH REPEAT KINASE 2 (LRRK2) INHIBITORS H. LUNDBECK A/S (DK) 2024-10-24 WO disclosed
EP-4422750-A1 LRRK2 INHIBITORS H. Lundbeck A/S (DK) 2024-09-04 EP disclosed
CN-118251397-A LRRK2 inhibitors H.隆德贝克有限公司 2024-06-25 CN disclosed
US-11993612-B2 LRRK2 inhibitors H. LUNDBECK A/S (DK) 2024-05-28 US disclosed
US-20230416272-A1 LRRK2 INHIBITORS H. LUNDBECK A/S (DK) 2023-12-28 US disclosed
US-11780851-B2 LRRK2 inhibitors H. LUNDBECK A/S (DK) 2023-10-10 US disclosed
US-11780851-B2 LRRK2 inhibitors H. LUNDBECK A/S (DK) 2023-10-10 US disclosed
US-11780851-B2 LRRK2 inhibitors H. LUNDBECK A/S (DK) 2023-10-10 US disclosed
WO-2023073013-A9 LRRK2 INHIBITORS H. LUNDBECK A/S (DK) 2023-08-17 WO disclosed
WO-2011104338-A1 HALOGEN OR CYANO SUBSTITUTED THIENO [2,3-D]PYRIMIDINES HAVING MNK1/MNK2 INHIBITING ACTIVITY FOR PHARMACEUTICAL COMPOSITIONS BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2011-09-01 WO disclosed
WO-2011104338-A1 HALOGEN OR CYANO SUBSTITUTED THIENO [2,3-D]PYRIMIDINES HAVING MNK1/MNK2 INHIBITING ACTIVITY FOR PHARMACEUTICAL COMPOSITIONS BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2011-09-01 WO disclosed
US-20110201608-A1 SUBSTITUTED NAPHTHYRIDINES AND USE THEREOF AS MEDICINES BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2011-08-18 US disclosed
WO-2010130423-A1 7-ARYL-1,2,4-TRIAZOLO[4,3-A]PYRIDINE DERIVATIVES AND THEIR USE AS POSITIVE ALLOSTERIC MODULATORS OF MGLUR2 RECEPTORS ORTHO-MCNEIL-JANSSEN PHARMACEUTICALS, INC (US) 2010-11-18 WO disclosed
EP-0219257-B1 Esters of dihydrolysergic acid LILLY CO ELI (US) 1994-03-09 EP disclosed
US-4968802-A ESTERIFICATION WITH ALKOXYCYCLOALKYL SULFONATE ELI LILLY AND COMPANY (US) 1990-11-06 US disclosed
US-4914100-A TREATING THROMBOSIS ELI LILLY AND COMPANY (US) 1990-04-03 US disclosed
US-4847261-A ANALGESICS, HYPOTENSIVES ELI LILLY AND COMPANY (US) 1989-07-11 US disclosed
US-4714704-A Alkoxy cycloalkanol esters of dihydrolysergic acid useful as 5HT receptor antagonists ELI LILLY AND COMPANY (US) 1987-12-22 US disclosed
EP-0219257-A2 Esters of dihydrolysergic acid ELI LILLY AND COMPANY (US) 1987-04-22 EP disclosed