SCHEMBL9697902

SCHEMBL9697902

O=C1OC(O)C2C1=C1CCC2C1

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
SCHEMBL4686297 0.79 CA1 (0.31)
SCHEMBL11327108 0.75
SCHEMBL346877 0.64
SCHEMBL14119779 0.64
SCHEMBL9697898 0.60
SCHEMBL136645 0.59
SCHEMBL12152692 0.58
SCHEMBL2545205 0.57 MAP3K14 (0.39)
SCHEMBL11996425 0.57 MAP3K14 (0.39)
Hydrochloric Acid SCHEMBL15546474 0.55 MAP3K14 (0.36)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5136050-A Process for resolving amino acids using substituted lactones ROUSSEL UCLAF (FR) 1992-08-04 US claimed
EP-0030505-B1 LACTONES SUBSTITUTED BY AN AMINO-ACID RESIDUE, THEIR PREPARATION AND THEIR USE IN THE SEPARATION OF SAID LACTONES OR AMINO ACIDS ROUSSEL-UCLAF (FR) 1985-07-24 EP claimed
EP-0030505-A1 Lactones substituted by an amino-acid residue, their preparation and their use in the separation of said lactones or amino acids ROUSSEL-UCLAF (FR) 1981-06-17 EP claimed
EP-0004493-B1 ETHERS WHOSE ORGANIC MOIETIES HAVE ASYMMETRIC ATOMS, METHODS FOR THEIR PREPARATION AND THEIR USE FOR THE RESOLUTION OF ALCOHOLS, PHENOLS OR CERTAIN COMPOUNDS WITH A LACTONE STRUCTURE ROUSSEL-UCLAF (FR) 1981-05-06 EP claimed
EP-0004493-A1 Ethers whose organic moieties have asymmetric atoms, methods for their preparation and their use for the resolution of alcohols, phenols or certain compounds with a lactone structure ROUSSEL-UCLAF (FR) 1979-10-03 EP claimed
US-5136050-A Process for resolving amino acids using substituted lactones ROUSSEL UCLAF (FR) 1992-08-04 US disclosed
US-4935532-A Hemiacetals ROUSSEL UCLAF (FR) 1990-06-19 US disclosed
US-4788305-A HETEROCYCLIC HEMIACETALS ROUSSEL UCLAF (FR) 1988-11-29 US disclosed
US-4720556-A 3-oxabicyclo-(3,1,0)-hexan-2-ones ROUSSEL UCLAF (FR) 1988-01-19 US disclosed
US-4701542-A Resolution of hemiacetals and alcohols ROUSSEL UCLAF (FR) 1987-10-20 US disclosed
EP-0082049-B1 ETHERS WITH CHIRAL ATOMS IN THE ORGANIC REST GROUPS, THEIR PREPARATION, THEIR USE IN THE RESOLUTION OF ALCOHOLS OR OF CERTAIN HEMIACETALS, AND COMPOUNDS SO RESOLVED ROUSSEL-UCLAF (FR) 1987-07-29 EP disclosed
US-4658043-A Ethers of pantolactone ROUSSEL UCLAF (FR) 1987-04-14 US disclosed
EP-0030505-B1 LACTONES SUBSTITUTED BY AN AMINO-ACID RESIDUE, THEIR PREPARATION AND THEIR USE IN THE SEPARATION OF SAID LACTONES OR AMINO ACIDS ROUSSEL-UCLAF (FR) 1985-07-24 EP disclosed
EP-0082049-A2 Ethers with chiral atoms in the organic rest groups, their preparation, their use in the resolution of alcohols or of certain hemiacetals, and compounds so resolved ROUSSEL-UCLAF (FR) 1983-06-22 EP disclosed
US-4374257-A Novel ethers containing a lactone group and a chiral atom ROUSSEL UCLAF (FR) 1983-02-15 US disclosed
US-4350637-A STEREOISOMERS, RESOLUTION ROUSSEL UCLAF (FR) 1982-09-21 US disclosed
EP-0030505-A1 Lactones substituted by an amino-acid residue, their preparation and their use in the separation of said lactones or amino acids ROUSSEL-UCLAF (FR) 1981-06-17 EP disclosed
EP-0004493-B1 ETHERS WHOSE ORGANIC MOIETIES HAVE ASYMMETRIC ATOMS, METHODS FOR THEIR PREPARATION AND THEIR USE FOR THE RESOLUTION OF ALCOHOLS, PHENOLS OR CERTAIN COMPOUNDS WITH A LACTONE STRUCTURE ROUSSEL-UCLAF (FR) 1981-05-06 EP disclosed
US-4265817-A Novel chiral ethers and their use in resolution of alcohols and phenols ROUSSEL UCLAF (FR) 1981-05-05 US disclosed
EP-0004493-A1 Ethers whose organic moieties have asymmetric atoms, methods for their preparation and their use for the resolution of alcohols, phenols or certain compounds with a lactone structure ROUSSEL-UCLAF (FR) 1979-10-03 EP disclosed