Heptanoate

Heptanoate

SCHEMBL267659

CCCCCCC(=O)[O-].CCCCCCC(=O)[O-].[Mg+2]

nearest known ligand 0.90

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ATP4AATP4BGABBR1GABBR2HMGCR

The experimentally established mechanism targets of Heptanoate. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
▸ FABP3 P05413 7/20 0.72
▸ CA1 P00915 1/20 0.71
▸ CES2 O00748 4/20 0.67
▸ CES1 P23141 4/20 0.67
▸ FFAR3 O14843 1/20 0.57
▸ HDAC3 O15379 1/20 0.57
▸ HDAC1 Q13547 1/20 0.57
▸ HDAC2 Q92769 1/20 0.57
▸ HDAC8 Q9BY41 1/20 0.57
▸ NFKB1 P19838 1/20 0.57

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

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
Nonanoate SCHEMBL9296766 1.00 FABP3 (0.72) FABP3CA1CES2CES1FFAR3
Undecanoate SCHEMBL5857955 1.00 FABP3 (0.72) FABP3CA1CES2CES1FFAR3
Stearic Acid SCHEMBL935 1.00 FABP3 (0.72) FABP3CA1CES2CES1FFAR3
Stearic Acid SCHEMBL1543060 1.00 FABP3 (0.72) FABP3CA1CES2CES1FFAR3
Pentadecanoic Acid SCHEMBL18429968 1.00 FABP3 (0.72) FABP3CA1CES2CES1FFAR3
Myristic Acid SCHEMBL8003084 1.00 FABP3 (0.72) FABP3CA1CES2CES1FFAR3
Arachidic Acid SCHEMBL11867584 1.00 FABP3 (0.72) FABP3CA1CES2CES1FFAR3
Stearic Acid SCHEMBL5694020 1.00 FABP3 (0.72) FABP3CA1CES2CES1FFAR3
Stearic Acid SCHEMBL4655901 1.00 FABP3 (0.72) FABP3CA1CES2CES1FFAR3
Palmitic Acid SCHEMBL103017 1.00 FABP3 (0.72) FABP3CA1CES2CES1FFAR3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2025060941-A1 METHOD FOR PRODUCING POLYHYDROXYALKANOATE 清华大学 2025-03-27 — — WO claimed
CN-116970659-B Method for producing polyhydroxyalkanoate 清华大学 2024-02-09 — — CN claimed
WO-2025060941-A1 METHOD FOR PRODUCING POLYHYDROXYALKANOATE 清华大学 2025-03-27 — — WO disclosed
CN-116970659-B Method for producing polyhydroxyalkanoate 清华大学 2024-02-09 — — CN disclosed
CN-116970659-A Method for producing polyhydroxyalkanoate 清华大学 2023-10-31 — — CN disclosed
EP-3486082-B1 INTERLAYER FOR LAMINATED GLASS, AND LAMINATED GLASS SEKISUI CHEMICAL CO LTD (JP) 2021-11-10 — — EP disclosed
CN-108291016-B Polycarbonate resin, method for producing same, and film 帝人株式会社 2021-08-17 — — CN disclosed
CN-106471061-B Polylactic acid composition, molded body obtained from polylactic acid composition, and method for producing polylactic acid composition 帝人株式会社 2021-06-08 — — CN disclosed
US-11001707-B2 Polylactic acid composition, formed article obtained from polylactic acid composition, and method for producing polylactic acid composition TEIJIN LIMITED (JP) 2021-05-11 — — US disclosed
US-10954356-B2 Interlayer for laminated glass, and laminated glass SEKISUI CHEMICAL CO., LTD. (JP) 2021-03-23 — — US disclosed
US-10800879-B2 Polycarbonate resin, and production method and film thereof TEIJIN LIMITED (JP) 2020-10-13 — — US disclosed
EP-1022261-A1 INTERLAYER FOR LAMINATED GLASS AND LAMINATED GLASS SEKISUI CHEMICAL CO., LTD. (JP) 2000-07-26 — — EP disclosed
US-5330949-A Catalyst supports, silicon dioxide modified with a chlorosilane, an alcohol and a magnesium alkoxide, reduced catalyst residue IDEMITSU PETROCHEMICAL COMPANY, LTD. (JP) 1994-07-19 — — US disclosed
EP-0041384-B2 POLYVINYLBUTYRAL SHEETING E.I. DU PONT DE NEMOURS AND COMPANY (US) 1992-04-29 — — EP disclosed
EP-0206172-B1 METHOD FOR PRODUCING POLYOLEFINS IDEMITSU PETROCHEMICAL CO. LTD. (JP) 1991-07-24 — — EP disclosed
EP-0206172-A1 Method for producing polyolefins IDEMITSU PETROCHEMICAL CO. LTD. (JP) 1986-12-30 — — EP disclosed
US-4569975-A COORDINATION COMPOUND CONTAINING ORGANOMAGNESIUM COMPOUND, CARBON DIOXIDE, HALOGEN COMPOUND, AND TRANSITION METAL COMPOUND THE DOW CHEMICAL COMPANY (US) 1986-02-11 — — US disclosed
EP-0041384-B1 POLYVINYLBUTYRAL SHEETING E.I. DU PONT DE NEMOURS AND COMPANY (US) 1984-10-17 — — EP disclosed
EP-0041384-A1 Polyvinylbutyral sheeting E.I. DU PONT DE NEMOURS AND COMPANY (US) 1981-12-09 — — EP disclosed
US-4290959-A Preparation of propylene oxide HALCON RESEARCH AND DEVELOPMENT CORP. (US) 1981-09-22 — — US disclosed
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