SCHEMBL1658878

SCHEMBL1658878

CC/C=C/CC(C)O

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
SCHEMBL1784155 1.00
SCHEMBL14220615 1.00
SCHEMBL6472293 1.00 TSHR (0.42)
SCHEMBL1658879 1.00
SCHEMBL6472297 1.00 TSHR (0.42)
SCHEMBL31391971 0.92 ALDH1A1 (0.40)
SCHEMBL17586680 0.92 ALDH1A1 (0.40)
SCHEMBL3399729 0.87 TSHR (0.44)
SCHEMBL3399731 0.87 TSHR (0.44)
SCHEMBL17943047 0.82 FFAR1 (0.38)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111051483-B Esters and ethers of 2, 4-tetramethyl cyclobutane-1, 3-diol as fragrance chemicals 巴斯夫欧洲公司 2025-01-24 CN claimed
US-12187978-B2 Use of (3-acetoxy-2,2-dimethyl-propyl) acetate in combination with (3-hydroxy-2,2-dimethyl-propyl) acetate as an aroma chemical BASF SE (DE) 2025-01-07 US claimed
US-12630783-B2 Muguet type fragrance compounds SYMRISE AG (DE) 2026-05-19 US disclosed
US-12630781-B2 Fragrance or flavour mixture SYMRISE AG (DE) 2026-05-19 US disclosed
US-12625123-B2 Device and method for the analytical and sensory determination of the release of an active substance from a release system SYMRISE AG (DE) 2026-05-12 US disclosed
EP-4728447-A1 ENVIRONMENTAL ATTRIBUTES FOR AROMA CHEMICAL BASF SE (DE) 2026-04-22 EP disclosed
EP-4724434-A1 AMBERGRIS ISOMERS AND MIXTURES THEREOF Symrise AG (DE) 2026-04-15 EP disclosed
EP-4077299-B1 SUBSTITUTED 4-METHYLENE-TETRAHYDROPYRANS, 4-METHYL-DIHYDROPYRANS AND 4-METHYL-TETRAHYDROPYRANS AND USE THEREOF AS AROMA CHEMICALS BASF SE (DE) 2026-04-01 EP disclosed
EP-4716732-A1 USE OF ALKYL 4-ALKOXYPENTANOATES AS AROMA CHEMICALS BASF SE (DE) 2026-04-01 EP disclosed
US-12590265-B2 1-norbornan-2-ylpropan-2-one as a fragrance SYMRISE AG (DE) 2026-03-31 US disclosed
US-12583833-B2 Enrichment of a diastereomer in Magnolan SYMRISE AG (DE) 2026-03-24 US disclosed
US-20080146491-A1 USE OF CALCITONIN AND CALCITONIN-LIKE PEPTIDES TO TREAT AND PREVENT MULTIPLE SCLEROSIS DELUCA HECTOR F 2008-06-19 US disclosed
US-7247697-B2 Coating compositions for use in golf balls ACUSHNET COMPANY (US) 2007-07-24 US disclosed
EP-1771407-A1 4-HEPTEN-2-YL SALICYLATE AND ITS USE AS A FRAGRANCE INGREDIENT Givaudan SA (CH) 2007-04-11 EP disclosed
US-20060089419-A1 Coating compositions for use in golf balls JPMORGAN CHASE BANK, N.A., AS SUCCESSOR ADMINISTRATIVE AGENT 2006-04-27 US disclosed
WO-2006007755-A1 4-HEPTEN-2-YL SALICYLATE AND ITS USE AS FRAGRANCE INGREDIENT GIVAUDAN SA (CH) 2006-01-26 WO disclosed
US-4178297-A FLAVORS, PERFUMES FROM 1-ALKENYLALUMINUM DIALKYL COMPOUNDS TEXAS ALKYLS, INC. (US) 1979-12-11 US disclosed
US-4133815-A ACETYLENE REACTION WITH TRIALKYLALUMINUM TEXAS ALKYLS, INC. (US) 1979-01-09 US disclosed
US-4110357-A ALKENYL-ALUMINUM COORDINATION COMPLEXES TEXAS ALKYLS, INC. (US) 1978-08-29 US disclosed
US-4069260-A FROM CIS-1-ALKENYLALUMINUM DIALKYL COMPOUND AND EPOXIDE FOLLOWED BY HYDROLYSIS TEXAS ALKYLS, INC. (US) 1978-01-17 US disclosed