SCHEMBL519006

SCHEMBL519006

CC(C)CCCN(CCCC(C)C)CCCC(C)C

nearest known ligand 0.45

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 1/20 0.45
ALDH1A1 P00352 1/20 0.35
KDM4C Q9H3R0 2/20 0.33
KDM4A O75164 1/20 0.33
PHF8 Q9UPP1 1/20 0.33
KDM2A Q9Y2K7 1/20 0.33
BLM P54132 1/20 0.32
CYP1A2 P05177 1/20 0.32
MAPK1 P28482 1/20 0.32
OPRM1 P35372 2/20 0.31
OPRD1 P41143 2/20 0.31
OPRK1 P41145 2/20 0.31
HTR2A P28223 1/20 0.31
HRH1 P35367 1/20 0.31
PLA2G1B P04054 1/20 0.31
PLA2G2A P14555 1/20 0.31
CA12 O43570 1/20 0.31
CA1 P00915 1/20 0.31
CA2 P00918 1/20 0.31
CA9 Q16790 1/20 0.31

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
SCHEMBL20438511 0.94 LMNA (0.41) LMNAALDH1A1KDM4CKDM4APHF8
SCHEMBL517872 0.90 LMNA (0.50) LMNAALDH1A1KDM4CKDM4APHF8
SCHEMBL10225592 0.89 LMNA (0.38) LMNAALDH1A1CYP1A2MAPK1PLA2G1B
SCHEMBL22753506 0.89 LMNA (0.38) LMNAALDH1A1CYP1A2MAPK1PLA2G1B
SCHEMBL17277117 0.89 PLA2G1B (0.40) LMNAKDM4CPHF8MAPK1OPRM1
SCHEMBL8464998 0.88 LMNA (0.48) LMNAALDH1A1KDM4CKDM4APHF8
SCHEMBL1507508 0.88 LMNA (0.48) LMNAALDH1A1KDM4CKDM4APHF8
SCHEMBL20438365 0.88 LMNA (0.41) LMNAALDH1A1KDM4CKDM4APHF8
SCHEMBL1020474 0.88 LMNA (0.48) LMNAALDH1A1KDM4CKDM4APHF8
SCHEMBL1507494 0.88 LMNA (0.48) LMNAALDH1A1KDM4CKDM4APHF8

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115991633-B Method for preparing methanol and ethylene glycol and co-producing formic acid by photocatalysis of polyalcohol 中国科学院大连化学物理研究所 2024-06-25 CN claimed
CN-115991633-A Method for preparing methanol and ethylene glycol and co-producing formic acid by photocatalysis of polyalcohol 中国科学院大连化学物理研究所 2023-04-21 CN claimed
CN-110627832-A Preparation method for synthesizing tenofovir alafenamide by oxidation method 江西农业大学 2019-12-31 CN claimed
CN-110590844-A Preparation method for synthesizing tenofovir alafenamide by two-step method 江西农业大学 2019-12-20 CN claimed
CN-110551153-A Preparation method for synthesizing tenofovir alafenamide by three-step method UNIV JIANGXI AGRICULTURAL 2019-12-10 CN claimed
US-9226925-B1 Abuse deterrent and anti-dose dumping pharmaceutical salts useful for the treatment of attention deficit/hyperactivity disorder PISGAH LABORATORIES, INC. (US) 2016-01-05 US claimed
US-8940729-B1 Abuse deterrent and anti-dose dumping pharmaceutical salts useful for the treatment of attention deficit/hyperactivity disorder PISGAH LABORATORIES, INC. (US) 2015-01-27 US claimed
US-8912217-B1 Abuse deterrent and anti-dose dumping pharmaceutical salts useful for the treatment of attention deficit/hyperactivity disorder PISGAH LABORATORIES, INC. (US) 2014-12-16 US claimed
US-12620777-B2 Optical member, laser module including said optical member, and laser device DAICEL CORPORATION (JP) 2026-05-05 US disclosed
EP-4012726-B1 ADHESIVE CONDUCTIVE PASTE DAICEL CORP (JP) 2025-10-22 EP disclosed
US-20250269473-A1 CONDUCTIVE PASTE FOR BONDING DAICEL CORPORATION (JP) 2025-08-28 US disclosed
EP-4589607-A1 BONDING CONDUCTOR PASTE Daicel Corporation (JP) 2025-07-23 EP disclosed
CN-115777128-B Conductive ink 株式会社大赛璐 2025-06-03 CN disclosed
EP-4549055-A1 INK COMPOSITION Daicel Corporation (JP) 2025-05-07 EP disclosed
US-5739388-A Process for the preparation of aromatic compounds by decarboxylation of aromatic carboxylic acids HOECHST AKTIENGESELLSCHAFT (DE) 1998-04-14 US disclosed
EP-0811601-A1 Process for the preparation of aromatic carbonic acid esters Clariant GmbH (DE) 1997-12-10 EP disclosed
EP-0757028-A1 Process for the preparation of aromatic carbonic acid esters HOECHST AKTIENGESELLSCHAFT (DE) 1997-02-05 EP disclosed
EP-0741122-A1 Process for preparing aromatic compounds through decarboxylation of aromatic carboxylic acids HOECHST AKTIENGESELLSCHAFT (DE) 1996-11-06 EP disclosed
US-4615977-A AMINE DERIVATIVES PROMOTE GROWTH WITH LOW SERUM CONCENTRATIONS ASAHI KASEI KOGYO KABUSHIKI KAISHA (JP) 1986-10-07 US disclosed
EP-0082974-B1 METHOD FOR THE CULTIVATION OF NORMAL DIPLOID CELLS AND CULTIVATION MEDIUM USED THEREFOR Asahi Kasei Kogyo Kabushiki Kaisha (JP) 1986-05-14 EP 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 (1 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-12620777-B2 Optical member, laser module including said optical member, and laser device MARK3, OR10J3, ILK LMNA 2730/4885ALDH1A1 3032/4885KDM4C 619/4885

“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.