SCHEMBL3040228

SCHEMBL3040228

CC(C)CCCCCOC=O

nearest known ligand 0.39

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
LMNA P02545 1/20 0.39
HIF1A Q16665 3/20 0.36
EPAS1 Q99814 3/20 0.36
RARB P10826 1/20 0.34
ALDH1A1 P00352 1/20 0.33
ADH1B P00325 1/20 0.32
ADH1C P00326 1/20 0.32
ADH1A P07327 1/20 0.32
ADH4 P08319 1/20 0.32
ADH7 P40394 1/20 0.32
KDM4C Q9H3R0 2/20 0.31
KDM4A O75164 1/20 0.31
PHF8 Q9UPP1 1/20 0.31
KDM2A Q9Y2K7 1/20 0.31
MAOA P21397 1/20 0.30
MAOB P27338 1/20 0.30
FUT7 Q11130 1/20 0.30

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
SCHEMBL8813040 1.00 LMNA (0.39) LMNAHIF1AEPAS1RARBALDH1A1
SCHEMBL30909503 1.00 LMNA (0.39) LMNAHIF1AEPAS1RARBALDH1A1
SCHEMBL30052986 1.00 LMNA (0.39) LMNAHIF1AEPAS1RARBALDH1A1
SCHEMBL3030885 1.00 LMNA (0.39) LMNAHIF1AEPAS1RARBALDH1A1
SCHEMBL3031777 1.00 LMNA (0.39) LMNAHIF1AEPAS1RARBALDH1A1
SCHEMBL28390578 1.00 LMNA (0.39) LMNAHIF1AEPAS1RARBALDH1A1
SCHEMBL8811513 1.00 LMNA (0.39) LMNAHIF1AEPAS1RARBALDH1A1
SCHEMBL3041307 0.98 LMNA (0.40) LMNAHIF1AEPAS1RARBALDH1A1
Benzene SCHEMBL28158350 0.94 RARB (0.38) LMNAHIF1AEPAS1RARBALDH1A1
SCHEMBL16174549 0.92 LMNA (0.54) LMNAHIF1AEPAS1RARB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-116573981-B Resolution method of beta receptor blocker raceme medicine 中南大学 2025-05-06 CN claimed
CN-114409510-B Method for promoting hydrolysis of isooctyl isooctanoate and isooctyl formate 大连普莱瑞迪化学有限公司 2024-01-30 CN claimed
CN-116573981-A Resolution method of beta receptor blocker raceme medicine 中南大学 2023-08-11 CN claimed
CN-116375550-A Method for resolving racemate compound by enantioselective reverse micelle extraction 中南大学 2023-07-04 CN claimed
CN-114409510-A Method for promoting hydrolysis of isooctyl isooctanoate and isooctyl formate 大连普莱瑞迪化学有限公司 2022-04-29 CN claimed
CN-116573981-B Resolution method of beta receptor blocker raceme medicine 中南大学 2025-05-06 CN disclosed
CN-114409510-B Method for promoting hydrolysis of isooctyl isooctanoate and isooctyl formate 大连普莱瑞迪化学有限公司 2024-01-30 CN disclosed
CN-114409510-B Method for promoting hydrolysis of isooctyl isooctanoate and isooctyl formate 大连普莱瑞迪化学有限公司 2024-01-30 CN disclosed
CN-114409510-B Method for promoting hydrolysis of isooctyl isooctanoate and isooctyl formate 大连普莱瑞迪化学有限公司 2024-01-30 CN disclosed
CN-111090826-B Optimizing device, method implemented by optimizing device, and computer-readable storage medium 富士通株式会社 2023-09-29 CN disclosed
CN-116573981-A Resolution method of beta receptor blocker raceme medicine 中南大学 2023-08-11 CN disclosed
CN-111310930-B Optimizing apparatus, optimizing method, and non-transitory computer-readable storage medium 富士通株式会社 2023-07-21 CN disclosed
CN-114409510-A Method for promoting hydrolysis of isooctyl isooctanoate and isooctyl formate 大连普莱瑞迪化学有限公司 2022-04-29 CN disclosed
US-20100216736-A2 2'-CYANOPYRIMIDINE NUCLEOSIDE COMPOUND TAIHO PHARMACEUTICAL CO., LTD. (JP) 2010-08-26 US disclosed
US-20100056466-A1 2'-Cyanopyrimidine Nucleoside Compound MATSUDA, AKIRA (JP) 2010-03-04 US disclosed
EP-2045256-A1 2'-CYANOPYRIMIDINE NUCLEOSIDE COMPOUND TAIHO PHARMACEUTICAL COMPANY, LIMITED (JP) 2009-04-08 EP disclosed
US-5691319-A ANTICARCINOGENIC AGENTS SANKYO COMPANY, LIMITED (JP) 1997-11-25 US disclosed
EP-0536936-B1 Pyrimidine nucleoside derivatives having anti-tumor activity, their preparation and use SANKYO CO (JP) 1996-08-14 EP disclosed
EP-0536936-A1 Pyrimidine nucleoside derivatives having anti-tumor activity, their preparation and use Sankyo Company Limited (JP) 1993-04-14 EP disclosed
US-4795807-A Preparation of azo dyestuffs by diazotization and coupling in the presence of an ester CASSELLA AKTIENGESELLSCHAFT (DE) 1989-01-03 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-20100216736-A2 2'-CYANOPYRIMIDINE NUCLEOSIDE COMPOUND NUDT1, DPYD, SLC29A1 LMNA 1804/4885HIF1A 1355/4885EPAS1 4545/4885
US-20100056466-A1 2'-Cyanopyrimidine Nucleoside Compound NUDT1, DPYD, SLC29A1 LMNA 1804/4885HIF1A 1355/4885EPAS1 4545/4885

“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.