SCHEMBL1471767

SCHEMBL1471767

CC(C)=CC1CC(C)=CCO1

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
SCHEMBL17187646 1.00
SCHEMBL13404928 0.77
SCHEMBL13438774 0.76
SCHEMBL13438963 0.74
SCHEMBL11399543 0.74
SCHEMBL11399537 0.74
SCHEMBL13405018 0.73
SCHEMBL3608344 0.73
SCHEMBL14068302 0.70
SCHEMBL13593153 0.69

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4257663-A1 FOOD CONTACT SURFACE SANITIZING LIQUID The Procter & Gamble Company (US) 2023-10-11 EP claimed
EP-3416729-B1 PRO-FRAGRANCE COMPOSITION AQDOT LTD (GB) 2023-09-20 EP claimed
CN-108601958-B Pro-fragrance compositions 爱客多有限公司 2022-06-17 CN claimed
EP-3416729-A1 PRO-FRAGRANCE COMPOSITION Aqdot Limited (GB) 2018-12-26 EP claimed
WO-2017141030-A1 PRO-FRAGRANCE COMPOSITION AQDOT LIMITED (GB) 2017-08-24 WO claimed
CN-122010886-A Method for synthesizing nerol by 4-methyl-4- [ (3-methylbut-3-en-1-yl) oxy ] -2- (2-methylprop-1-en-1-yl) oxy-cyclohexane 江苏宏邦化工科技有限公司 2026-05-12 CN disclosed
US-20260027136-A1 CANNABIS BASED THERAPEUTIC AND METHOD OF USE YUZU LV LLC (US) 2026-01-29 US disclosed
US-12458653-B2 Cannabis based therapeutic and method of use YUZU LV LLC (US) 2025-11-04 US disclosed
US-12303488-B2 Cannabis based therapeutic and method of use YUZU LV LLC (US) 2025-05-20 US disclosed
CN-119391494-A Essence light stabilizer and liquid detergent composition applied by same 广州立白科技集团有限公司 2025-02-07 CN disclosed
US-12121025-B2 Antimicrobial composition THE PROCTER & GAMBLE COMPANY (US) 2024-10-22 US disclosed
CN-118048210-B Detergent composition 广州立白企业集团有限公司 2024-08-30 CN disclosed
US-7166728-B2 Process for preparation of nerol oxide COUNCIL OF SCIENTIFIC AND INDUSTRIAL RESEARCH (IN) 2007-01-23 US disclosed
US-7166728-B2 Process for preparation of nerol oxide COUNCIL OF SCIENTIFIC AND INDUSTRIAL RESEARCH (IN) 2007-01-23 US disclosed
US-20060207037-A1 Malodor covering perfumery GIVAUDAN FRAGRANCES CORPORATION 2006-09-21 US disclosed
WO-2006070383-A1 PROCESS FOR THE PREPARATION OF NEROL OXIDE COUNCIL OF SCIENTIFIC AND INDUSTRIAL RESEARCH (IN) 2006-07-06 WO disclosed
WO-2006070383-A1 PROCESS FOR THE PREPARATION OF NEROL OXIDE COUNCIL OF SCIENTIFIC AND INDUSTRIAL RESEARCH (IN) 2006-07-06 WO disclosed
US-20060142450-A1 By haloalkoxylating nerol to produce a 7-alkoxy-3,7-dimethyl-6-halo-2-octenol, dehydrohalogenating the product to produce a 7-alkoxy-3,7-dimethyl-octa-2,5-dien-1-ol, which is cyclized, especially using dilute mineral acid, lewis acid or an acidic resin to produce racemic nerol oxide COUNCIL OF SCIENTIFIC AND INDUSTRIAL RESEARCH (IN) 2006-06-29 US disclosed
US-20060142450-A1 By haloalkoxylating nerol to produce a 7-alkoxy-3,7-dimethyl-6-halo-2-octenol, dehydrohalogenating the product to produce a 7-alkoxy-3,7-dimethyl-octa-2,5-dien-1-ol, which is cyclized, especially using dilute mineral acid, lewis acid or an acidic resin to produce racemic nerol oxide COUNCIL OF SCIENTIFIC AND INDUSTRIAL RESEARCH (IN) 2006-06-29 US disclosed
US-6479456-B1 PERFUMED PRODUCTS (SUCH AS BODY CARE PRODUCTS, DETERGENTS ETC.) NOT ONLY GIVES OFF PLEASANT ODOR, BUT INCREASES, SYNERGISTICALLY, THE ANTIMICROBIAL ACTVITY; GRAPEFRUIT-PIT EXTRACT, FUMITORY EXTRACT, FUMARIC ACID, OR IT'S ESTER FIRMENICH SA (CH) 2002-11-12 US disclosed