SCHEMBL1402272

SCHEMBL1402272

Oc1ccc(OC2CCCCC2)cc1

nearest known ligand 0.54

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
PARP10 Q53GL7 1/20 0.52
ALDH1A1 P00352 2/20 0.49
TSHR P16473 1/20 0.49
EPHX2 P34913 3/20 0.45
HPGD P15428 1/20 0.45
FURIN P09958 2/20 0.44
NAAA Q02083 1/20 0.43
HRH3 Q9Y5N1 1/20 0.42
MEN1 O00255 1/20 0.42
KMT2A Q03164 1/20 0.42
ESR1 P03372 1/20 0.42
ESR2 Q92731 1/20 0.42
FFAR1 O14842 1/20 0.42
ALOX12 P18054 1/20 0.42
S1PR1 P21453 1/20 0.41

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
SCHEMBL1836444 1.00 PARP10 (0.52) PARP10ALDH1A1TSHREPHX2HPGD
SCHEMBL1834840 1.00 PARP10 (0.52) PARP10ALDH1A1TSHREPHX2HPGD
SCHEMBL1837838 0.98 PARP10 (0.53) PARP10ALDH1A1TSHREPHX2HPGD
SCHEMBL10858201 0.93 PARP10 (0.58) PARP10ALDH1A1TSHREPHX2HPGD
SCHEMBL20455794 0.89 MEN1 (0.48) PARP10ALDH1A1TSHREPHX2HPGD
SCHEMBL16902836 0.89 MEN1 (0.48) PARP10ALDH1A1TSHREPHX2HPGD
SCHEMBL2242868 0.89 PARP10 (0.55) PARP10ALDH1A1TSHREPHX2HPGD
SCHEMBL24578025 0.88 PARP10 (0.58) PARP10ALDH1A1EPHX2HPGDFURIN
SCHEMBL16561483 0.88 PARP10 (0.58) PARP10ALDH1A1EPHX2HPGDFURIN
Phenol SCHEMBL28176906 0.86 HRH1 (0.53) PARP10ALDH1A1TSHREPHX2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
JP-3206059-A None JP disclosed
US-20260035394-A1 1`-CYANO NUCLEOSIDE ANALOGS AND USES THEREOF GILEAD SCIENCES INC (US) 2026-02-05 US disclosed
US-12404289-B2 1′-cyano nucleoside analogs and uses thereof GILEAD SCIENCES, INC. (US) 2025-09-02 US disclosed
US-20240425448-A1 METHOD FOR PRODUCING ISOCYANATE COMPOUND, METHOD FOR PRODUCING CARBAMATE COMPOUND, METHOD FOR RECOVERING AMINE COMPOUND, AND ISOCYANATE COMPOSITION ASAHI KASEI KABUSHIKI KAISHA (JP) 2024-12-26 US disclosed
EP-4431490-A1 METHOD FOR PRODUCING ISOCYANATE COMPOUNDS, METHOD FOR PRODUCING CARBAMATE COMPOUNDS, METHOD FOR RECOVERING AMINE COMPOUNDS, AND ISOCYANATE COMPOSITION Asahi Kasei Kabushiki Kaisha (JP) 2024-09-18 EP disclosed
US-20240287109-A1 1'-CYANO NUCLEOSIDE ANALOGS AND USES THEREOF GILEAD SCIENCES, INC. 2024-08-29 US disclosed
CN-118215651-A Method for producing isocyanate compound, method for producing urethane compound, method for recovering amine compound, and isocyanate composition 旭化成株式会社 2024-06-18 CN disclosed
US-11939347-B2 1′-cyano nucleoside analogs and uses thereof GILEAD SCIENCES, INC. (US) 2024-03-26 US disclosed
US-11873288-B2 Inhibitors for soluble epoxide hydrolase (sEH) and fatty acid amide hydrolase (FAAH) THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2024-01-16 US disclosed
WO-2023238925-A1 RADICAL POLYMERIZABLE COMPOSITION AND POLYMERIZED PRODUCT THEREOF 株式会社日本触媒 2023-12-14 WO disclosed
US-5210330-A Alkylating hydroquinone with cyclohexane in presence of acidic heterogeneous alkylation catalyst and solvent of biphenyl, diphenyl ether and/or methylnaphthalene; cooling; separating precipitated hydroquinone; catalytically dehydrogenating EASTMAN KODAK COMPANY (US) 1993-05-11 US disclosed
WO-1993004027-A1 PROCESS FOR THE PREPARATION OF PHENYLHYDROQUINONE EASTMAN KODAK COMPANY (US) 1993-03-04 WO disclosed
JP-H03206059-A ALKYLATION OF HYDROQUINONE ASAHI CHEM IND CO LTD 1991-09-09 JP disclosed
US-4847429-A ALKYLATION, ACID CATALYSTS, DEHYDROGENATION EASTMAN KODAK COMPANY (US) 1989-07-11 US disclosed
US-4631252-A PHOTOGRAPHIC STABILIZERS CIBA-GEIGY AG (CH) 1986-12-23 US disclosed
US-4616082-A PHOTOGRAPHIC STABILIZERS CIBA-GEIGY AG (CH) 1986-10-07 US disclosed
US-4549015-A PHOTOHRAPHIC STABILIZERS CIBA-GEIGY AG (CH) 1985-10-22 US disclosed
US-4256672-A REACTING PHOSPHORUS OXYCHLORIDE OR PHOSPHORUS THIOCHLORIDE WITH AN AMINO-SUBSTUTUTED PHENOL COMPOUND MITSUI TOATSU CHEMICALS, INC. (JP) 1981-03-17 US disclosed
US-4123556-A Insecticidal composition CIBA-GEIGY CORPORATION (US) 1978-10-31 US disclosed
US-4061683-A INSECTICIDE, MITICIDE CIBA-GEIGY CORPORATION (US) 1977-12-06 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 (6 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-11873288-B2 Inhibitors for soluble epoxide hydrolase (sEH) and fatty acid amide hydrolase (FAAH) FAAH, FAAH2, EPHX2 PARP10 3365/4885ALDH1A1 261/4885TSHR 2275/4885
US-20240287109-A1 1'-CYANO NUCLEOSIDE ANALOGS AND USES THEREOF TYMP, PNP, DUT PARP10 1383/4885ALDH1A1 1269/4885TSHR 4786/4885
US-12404289-B2 1′-cyano nucleoside analogs and uses thereof TYMP, PNP, DUT PARP10 1225/4885ALDH1A1 1324/4885TSHR 4765/4885
US-20240425448-A1 METHOD FOR PRODUCING ISOCYANATE COMPOUND, METHOD FOR PRODUCING CARBAMATE COMPOUND, METHOD FOR RECOVERING AMINE COMPOUND, AND ISOCYANATE COMPOSITION IDH3A, CA7, C9 PARP10 2417/4885ALDH1A1 630/4885TSHR 4594/4885
US-11939347-B2 1′-cyano nucleoside analogs and uses thereof TYMP, PNP, DUT PARP10 1225/4885ALDH1A1 1324/4885TSHR 4765/4885
US-20260035394-A1 1`-CYANO NUCLEOSIDE ANALOGS AND USES THEREOF PNP, SLC28A1, SLC29A1 PARP10 4720/4885ALDH1A1 2839/4885TSHR 4134/4885

“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.