SCHEMBL1658183

SCHEMBL1658183

CCCCCCCC(C)CCO

nearest known ligand 0.57

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ACE2 Q9BYF1 1/20 0.57
LMNA P02545 5/20 0.52
ALDH1A1 P00352 2/20 0.50
OPRM1 P35372 1/20 0.50
HSD17B10 Q99714 1/20 0.50
MEN1 O00255 1/20 0.50
KMT2A Q03164 1/20 0.50
TSHR P16473 1/20 0.50
PRKD3 O94806 1/20 0.49
PRKCG P05129 1/20 0.49
PRKCB P05771 1/20 0.49
PRKCA P17252 1/20 0.49
PRKCH P24723 1/20 0.49
PRKCI P41743 1/20 0.49
PRKCE Q02156 1/20 0.49
PRKCQ Q04759 1/20 0.49
PRKCZ Q05513 1/20 0.49
PRKCD Q05655 1/20 0.49
PRKD1 Q15139 1/20 0.49
SPHK1 Q9NYA1 2/20 0.46

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
SCHEMBL27498134 1.00 ACE2 (0.57) ACE2LMNAALDH1A1OPRM1HSD17B10
SCHEMBL28744285 1.00 ACE2 (0.57) ACE2LMNAALDH1A1OPRM1HSD17B10
SCHEMBL236012 1.00 ACE2 (0.57) ACE2LMNAALDH1A1OPRM1HSD17B10
SCHEMBL7209007 1.00 ACE2 (0.57) ACE2LMNAALDH1A1OPRM1HSD17B10
SCHEMBL3367737 1.00 ACE2 (0.57) ACE2LMNAALDH1A1OPRM1HSD17B10
SCHEMBL22986838 1.00 ACE2 (0.57) ACE2LMNAALDH1A1OPRM1HSD17B10
SCHEMBL1556084 1.00 ACE2 (0.57) ACE2LMNAALDH1A1OPRM1HSD17B10
SCHEMBL3367475 1.00 ACE2 (0.57) ACE2LMNAALDH1A1OPRM1HSD17B10
SCHEMBL20055710 1.00 ACE2 (0.57) ACE2LMNAALDH1A1OPRM1HSD17B10
SCHEMBL5684486 1.00 ACE2 (0.57) ACE2LMNAALDH1A1OPRM1HSD17B10

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119955091-A Polymer, positive-type negative-type photosensitive resin composition, pattern forming method, cured film forming method, interlayer insulating film, surface protective film, and electronic component 信越化学工业株式会社 2025-05-09 CN disclosed
WO-2025094045-A1 PROCESS FOR PREPARATION OF ODOROUS COMPOUNDS S H KELKAR AND COMPANY LIMITED (IN) 2025-05-08 WO disclosed
US-20250000088-A1 ANT CONTROL AGENT AND ANT CONTROL METHOD SHIN-ETSU CHEMICAL CO., LTD. (JP) 2025-01-02 US disclosed
EP-4424164-A1 ANT CONTROL AGENT AND ANT CONTROL METHOD SHIN-ETSU CHEMICAL CO., LTD. (JP) 2024-09-04 EP disclosed
CN-118139527-A Ant control agent and ant control method 信越化学工业株式会社 2024-06-04 CN disclosed
CN-113260603-B Preparation of 5-aryl pentanols 巴斯夫欧洲公司 2023-12-01 CN disclosed
EP-3908566-B1 PREPARATION OF 5-ARYL PENTANOLS BASF SE (DE) 2023-07-26 EP disclosed
WO-2023074396-A1 ANT CONTROL AGENT AND ANT CONTROL METHOD 信越化学工業株式会社 2023-05-04 WO disclosed
US-11365168-B2 Preparation of 5-aryl-pentanols BASF SE (DE) 2022-06-21 US disclosed
CN-113260603-A Preparation of 5-arylpentanols 巴斯夫欧洲公司 2021-08-13 CN disclosed
US-6600079-B2 Effecting hydrogenolysis of a pyran compound of formula (1): catalyst carrying two or more elements selected from noble metals in Group VIII in the periodic table and (b) an acid type palladium-supporting catalyst. KAO CORPORATION (JP) 2003-07-29 US disclosed
EP-1298118-A2 Process for production of 5-arylpentanols Kao Corporation (JP) 2003-04-02 EP disclosed
US-20030060667-A1 Process for production of 5-arylpentanols KAO CORPORATION (JP) 2003-03-27 US disclosed
EP-1201632-A1 FUSED RING COMPOUND DAINIPPON INK AND CHEMICALS, INC. (JP) 2002-05-02 EP disclosed
WO-2002022257-A1 CATALYST PRECURSOR FOR PRODUCING MALEIC ACID ANHYDRIDE BASF AKTIENGESELLSCHAFT (DE) 2002-03-21 WO disclosed
US-4524059-A Fatty acid analogs THE GENERAL HOSPITAL CORPORATION (US) 1985-06-18 US disclosed
EP-0024517-B1 3-METHYL ALDEHYDES, PROCESS FOR THEIR PREPARATION AND THEIR USE AS ODORANTS HAARMANN & REIMER GMBH (DE) 1982-06-09 EP disclosed
US-4263459-A 3-Methyl-aldehydes, processes for their preparation and their use as odorants HAARMANN & REIMER GMBH (DE) 1981-04-21 US disclosed
EP-0024517-A1 3-Methyl aldehydes, process for their preparation and their use as odorants HAARMANN & REIMER GMBH (DE) 1981-03-11 EP disclosed
US-4225444-A Fragrance compositions containing 3-methyl-1-phenyl-pentanol-5 or specific optical isomers thereof and one or more butanoyl cyclohexane derivatives INTERNATIONAL FLAVORS & FRAGRANCES INC. (US) 1980-09-30 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (2 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-11365168-B2 Preparation of 5-aryl-pentanols HPD, CYP3A5, HTR3C ACE2 316/4885LMNA 2222/4885ALDH1A1 127/4885
US-20030060667-A1 Process for production of 5-arylpentanols CYP1A2, CYP11B2, POR ACE2 1257/4885LMNA 4044/4885ALDH1A1 253/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.