SCHEMBL3905928

SCHEMBL3905928

CC(=O)OCCCCI

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
SCHEMBL5833371 0.98 ALDH1A1 (0.56)
SCHEMBL22352622 0.98 ALDH1A1 (0.56)
SCHEMBL29054777 0.98 ALDH1A1 (0.56)
SCHEMBL1263892 0.98 ALDH1A1 (0.56)
SCHEMBL11408895 0.98 ALDH1A1 (0.56)
SCHEMBL2541950 0.92
SCHEMBL28627801 0.90
SCHEMBL189930 0.87 ALDH1A1 (0.74)
SCHEMBL11492305 0.84 ALDH1A1 (0.70)
SCHEMBL5136503 0.84 ALDH1A1 (0.70)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114853624-B Preparation method of 4-amino-1-butanol and N-protected derivative thereof 青岛贞开生物医药技术有限公司 2024-07-02 CN disclosed
CN-118221724-A Catalyst and application thereof in synthesis of 4-amino-1-butanol 郑州大学 2024-06-21 CN disclosed
WO-2023193789-A1 WEE1 DEGRADING COMPOUNDS BEIJING NEOX BIOTECH LIMITED (CN) 2023-10-12 WO disclosed
CN-114853624-A Preparation method of 4-amino-1-butanol and N-protected derivative thereof 青岛贞开生物医药技术有限公司 2022-08-05 CN disclosed
CN-108707227-B Preparation method of fluorine-containing alkyl copolyether 苏州大学 2020-09-08 CN disclosed
US-10299476-B2 3′-substituted-abscisic acid derivatives VALENT BIOSCIENCES LLC (US) 2019-05-28 US disclosed
US-9869027-B2 Cleaning composition and method of manufacturing metal wiring using the same SAMSUNG DISPLAY CO., LTD. (KR) 2018-01-16 US disclosed
US-20170360037-A1 3′-SUBSTITUTED-ABSCISIC ACID DERIVATIVES VALENT BIOSCIENCES LLC (US) 2017-12-21 US disclosed
US-9781930-B2 3′-substituted-abscisic acid derivatives VALENT BIOSCIENCES LLC (US) 2017-10-10 US disclosed
EP-3166405-A2 3'-SUBSTITUTED-ABSCISIC ACID DERIVATIVES Valent Biosciences Corporation (US) 2017-05-17 EP disclosed
EP-0728757-A1 Process for producing purine derivatives Ajinomoto Co., Inc. (JP) 1996-08-28 EP disclosed
EP-0619803-A1 PROCESS FOR THE MANUFACTURE OF ADIPIC ACID. DU PONT (US) 1994-10-19 EP disclosed
WO-1993012063-A1 PROCESS FOR THE MANUFACTURE OF ADIPIC ACID E.I. DU PONT DE NEMOURS AND COMPANY (US) 1993-06-24 WO disclosed
US-5218144-A Hydrocarboxylation of pentanoic compounds; iridium catalyst, E. I. DU PONT DE NEMOURS AND COMPANY (US) 1993-06-08 US disclosed
US-5166421-A Reaction of butadiene or allylic butenol with carbon monoxide and water in the presence of a rhodium catalyst E. I. DU PONT DE NEMOURS AND COMPANY (US) 1992-11-24 US disclosed
WO-1992016476-A2 PROCESS FOR THE MANUFACTURE OF ADIPIC ACID E.I. DU PONT DE NEMOURS AND COMPANY (US) 1992-10-01 WO disclosed
EP-0111997-B1 VINYL CARBOXYLIC ACID DERIVATIVES, THEIR PRODUCTION AND USE Takeda Chemical Industries, Ltd. (JP) 1991-04-10 EP disclosed
US-4812442-A TREATMENT OF HYPERTENSION, CONCESTIVE HEART FAILURE MERCK & CO., INC. (US) 1989-03-14 US disclosed
US-4518602-A Vinyl carboxylic acid derivatives, their production and use as inhibitors of thromboxane synthetase TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 1985-05-21 US disclosed
EP-0111997-A2 Vinyl carboxylic acid derivatives, their production and use Takeda Chemical Industries, Ltd. (JP) 1984-06-27 EP disclosed