SCHEMBL5830700

SCHEMBL5830700

CCCCCCCCOC(=O)NCCCCCC

nearest known ligand 0.89

Predicted protein targets (top 3)

geneUniProtsupporting neighboursconfidence
▸ ACHE P22303 14/20 0.89
▸ EPHX1 P07099 2/20 0.68
▸ EPHX2 P34913 2/20 0.68

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
SCHEMBL13700185 1.00 ACHE (0.89) ACHEEPHX1EPHX2
SCHEMBL17602934 1.00 ACHE (0.89) ACHEEPHX1EPHX2
SCHEMBL7155278 1.00 ACHE (0.89) ACHEEPHX1EPHX2
SCHEMBL1952876 1.00 ACHE (0.89) ACHEEPHX1EPHX2
SCHEMBL13700201 1.00 ACHE (0.89) ACHEEPHX1EPHX2
SCHEMBL7155271 1.00 ACHE (0.89) ACHEEPHX1EPHX2
SCHEMBL13700183 1.00 ACHE (0.89) ACHEEPHX1EPHX2
SCHEMBL1026398 1.00 ACHE (0.89) ACHEEPHX1EPHX2
SCHEMBL13700182 1.00 ACHE (0.89) ACHEEPHX1EPHX2
SCHEMBL13700164 1.00 ACHE (0.89) ACHEEPHX1EPHX2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4446310-A1 METHOD FOR PRODUCING BLOCKED ISOCYANATE COMPOUND AND METHOD FOR PRODUCING ISOCYANATE COMPOUND Asahi Kasei Kabushiki Kaisha (JP) 2024-10-16 — — EP disclosed
CN-118382612-A Method for producing blocked isocyanate compound and method for producing isocyanate compound 旭化成株式会社 2024-07-23 — — CN disclosed
WO-2023106377-A1 METHOD FOR PRODUCING BLOCKED ISOCYANATE COMPOUND AND METHOD FOR PRODUCING ISOCYANATE COMPOUND 旭化成株式会社 2023-06-15 — — WO disclosed
CN-100387339-C Use of tin derivatives as catalysts for the transesterification of carbamates, carbamate compositions containing said catalysts and process for the transesterification of carbamates RHODIA CHIMIE SA (FR) 2008-05-14 — — CN disclosed
US-6998364-B2 Process for the formation of urethane via transcarbamation RHODIA CHIMIE (FR) 2006-02-14 — — US disclosed
US-20040044242-A1 Use as catalyst for forming urethanes,of fluorinated and of trivalent metal acid salts, composition containing same and methods using same VENCOREX FRANCE (FR) 2004-03-04 — — US disclosed
CN-1469777-A Use of tin derivatives as catalysts for transforming carbamates, carbamate compositions comprising said catalyst and method for transforming carbamates �Ϻ���ͨ��ѧ 2004-01-21 — — CN disclosed
CN-1469888-A Use as catalyst for forming urethanes, of fluorinated and trivalent metal acid salts, composition containing same and methods using same �޵��ǻ�ѧ��˾ 2004-01-21 — — CN disclosed
US-4713476-A REACTING DI- OR POLYAMINE, UREA AND ALCOHOL BASF AKTIENGESELLSCHAFT (DE) 1987-12-15 — — 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 (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-20040044242-A1 Use as catalyst for forming urethanes,of fluorinated and of trivalent metal acid salts, composition containing same and methods using same PHF2, UBE2T, UHRF1 ACHE 877/4885EPHX1 3358/4885EPHX2 2676/4885

“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.

Send feedback