SCHEMBL8971074

SCHEMBL8971074

C=CCCCC(O)CCCC=C

nearest known ligand 0.43

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
USP2 O75604 4/20 0.43
ALDH1A1 P00352 4/20 0.43
MAPT P10636 3/20 0.43
CYP3A4 P08684 2/20 0.43
SMN1; SMN2 Q16637 2/20 0.43
HPGD P15428 1/20 0.43
TSHR P16473 3/20 0.41
ABCC4 O15439 1/20 0.37
LMNA P02545 2/20 0.32
RECQL P46063 1/20 0.32
LPAR3 Q9UBY5 2/20 0.32
LPAR2 Q9HBW0 1/20 0.32
TRPA1 O75762 3/20 0.32

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
SCHEMBL10081314 0.92 USP2 (0.50) USP2ALDH1A1MAPTCYP3A4SMN1; SMN2
SCHEMBL5868467 0.90 USP2 (0.42) USP2ALDH1A1MAPTCYP3A4SMN1; SMN2
SCHEMBL31540500 0.89 USP2 (0.53) USP2ALDH1A1MAPTCYP3A4SMN1; SMN2
SCHEMBL517696 0.89 USP2 (0.53) USP2ALDH1A1MAPTCYP3A4SMN1; SMN2
SCHEMBL31438712 0.89 USP2 (0.53) USP2ALDH1A1MAPTCYP3A4SMN1; SMN2
SCHEMBL10081536 0.89 USP2 (0.53) USP2ALDH1A1MAPTCYP3A4SMN1; SMN2
SCHEMBL15027430 0.89 USP2 (0.53) USP2ALDH1A1MAPTCYP3A4SMN1; SMN2
SCHEMBL4012822 0.89 USP2 (0.53) USP2ALDH1A1MAPTCYP3A4SMN1; SMN2
SCHEMBL27039953 0.89 USP2 (0.53) USP2ALDH1A1MAPTCYP3A4SMN1; SMN2
SCHEMBL3120232 0.88 TSHR (0.56) USP2ALDH1A1MAPTCYP3A4SMN1; SMN2

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 14 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4734981-A1 IONIZABLE LIPIDS AND LIPID NANOPARTICLE COMPOSITIONS FOR DELIVERY OF NUCLEIC ACIDS RVAC Medicines (us) , Inc. (US) 2026-05-06 EP disclosed
CN-121930094-A Preparation method of bevacizidine acid and novel intermediate thereof 南京工业大学 2026-04-28 CN disclosed
WO-2025038864-A1 IONIZABLE LIPIDS WITH LINEAR HEAD GROUPS BEAM THERAPEUTICS INC. (US) 2025-02-20 WO disclosed
CN-118324715-A Compounds, compositions, and methods of use thereof 艾勒维生技公司 2024-07-12 CN disclosed
CN-117750962-A Compounds, compositions, and methods of use thereof 艾勒维生技公司 2024-03-22 CN disclosed
EP-0493601-B1 LIQUID-CRYSTAL COPOLYMER, PRODUCTION THEREOF, DIENE COMPOUND USED IN SAID PRODUCTION, AND PRODUCTION OF SAID COMPOUND IDEMITSU KOSAN CO (JP) 1996-03-20 EP disclosed
US-5437816-A Compatible with low molecular weight liquid crystals to form uniform mixtures IDEMITSU KOSAN CO., LTD. (JP) 1995-08-01 US disclosed
US-5425897-A Electrooptics IDEMITSU KOSAN CO., LTD. (JP) 1995-06-20 US disclosed
US-5380915-A Copolymers of polydimethylsiloxane with diene ethers IDEMITSU KOSAN CO., LTD. (JP) 1995-01-10 US disclosed
US-5336435-A High polymer and ferroelectric liquid crystal composition utilizing same IDEMITSU KOSAN CO., LTD. (JP) 1994-08-09 US disclosed
US-5281685-A Polyether pendant groups, polysiloxane repeating units IDEMITSU KOSAN CO., LTD. (JP) 1994-01-25 US disclosed
US-5264517-A A-C copoly IDEMITSU KOSAN CO., LTD. (JP) 1993-11-23 US disclosed
EP-0548808-A2 High polymer and ferroelectric liquid crystal composition utilizing same IDEMITSU KOSAN COMPANY LIMITED (JP) 1993-06-30 EP disclosed
EP-0493601-A1 LIQUID-CRYSTAL COPOLYMER, PRODUCTION THEREOF, DIENE COMPOUND USED IN SAID PRODUCTION, AND PRODUCTION OF SAID COMPOUND IDEMITSU KOSAN COMPANY LIMITED (JP) 1992-07-08 EP disclosed