SCHEMBL5374608

SCHEMBL5374608

CCOC(=O)C(N)CC(N)=O

nearest known ligand 0.48

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALOX15 P16050 2/20 0.48
ALDH1A1 P00352 6/20 0.40
CAD P27708 1/20 0.39
LMNA P02545 1/20 0.39
HSD17B10 Q99714 1/20 0.39
CPB2 Q96IY4 1/20 0.38
MGAM O43451 1/20 0.37
GAA P10253 1/20 0.37
SI P14410 1/20 0.37
MGAM2 Q2M2H8 1/20 0.37
SOAT1 P35610 1/20 0.37
CYP2D6 P10635 1/20 0.37
CYP2C9 P11712 1/20 0.37
CYP2C19 P33261 1/20 0.37
HPGD P15428 1/20 0.36
MEN1 O00255 1/20 0.35
NPC1 O15118 1/20 0.35
KMT2A Q03164 1/20 0.35
KDM4E B2RXH2 1/20 0.35
HTT P42858 1/20 0.35

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
SCHEMBL1178957 1.00 ALOX15 (0.48) ALOX15ALDH1A1CADLMNAHSD17B10
Hydrochloric Acid SCHEMBL21247032 0.98 ALOX15 (0.46) ALOX15ALDH1A1CADLMNAHSD17B10
Hydrochloric Acid SCHEMBL21247031 0.98 ALOX15 (0.46) ALOX15ALDH1A1CADLMNAHSD17B10
SCHEMBL14016339 0.83 ALOX15 (0.48) ALOX15ALDH1A1CADLMNAHSD17B10
SCHEMBL31589297 0.83 HCAR2 (0.35) ALOX15ALDH1A1LMNAHSD17B10KMT2A
SCHEMBL1172849 0.82 MGAM (0.48) ALOX15ALDH1A1LMNAHSD17B10MGAM
SCHEMBL2617390 0.82 MGAM (0.48) ALOX15ALDH1A1LMNAHSD17B10MGAM
SCHEMBL20028702 0.82 ALDH1A1 (0.44) ALOX15ALDH1A1CADLMNAHSD17B10
SCHEMBL1074665 0.82 ALOX15 (0.42) ALOX15ALDH1A1LMNAHSD17B10MGAM
SCHEMBL1172846 0.82 MGAM (0.48) ALOX15ALDH1A1LMNAHSD17B10MGAM

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4673426-A1 FUNCTIONALIZED BIODEGRADABLE SURFACTANTS AND METHODS USE Locus Solutions IPCO, LLC (US) 2026-01-07 EP claimed
US-20240301322-A1 FUNCTIONALIZED BIODEGRADABLE SURFACTANTS AND METHODS USE LOCUS SOLUTIONS IPCO LLC (US) 2024-09-12 US claimed
WO-2024182125-A1 FUNCTIONALIZED BIODEGRADABLE SURFACTANTS AND METHODS USE LOCUS SOLUTIONS IPCO, LLC (US) 2024-09-06 WO claimed
EP-4673426-A1 FUNCTIONALIZED BIODEGRADABLE SURFACTANTS AND METHODS USE Locus Solutions IPCO, LLC (US) 2026-01-07 EP disclosed
CN-120040435-A Mangiferin and derivatives thereof, preparation method and medical application thereof 安徽中医药大学 2025-05-27 CN disclosed
US-20240301322-A1 FUNCTIONALIZED BIODEGRADABLE SURFACTANTS AND METHODS USE LOCUS SOLUTIONS IPCO LLC (US) 2024-09-12 US disclosed
WO-2024182125-A1 FUNCTIONALIZED BIODEGRADABLE SURFACTANTS AND METHODS USE LOCUS SOLUTIONS IPCO, LLC (US) 2024-09-06 WO disclosed
WO-2019104851-A4 BETA-HYDROXYBUTYRYL-AMINO ACID COMPOUND, PREPARATION METHOD THEREFOR AND USE THEREOF 刘成 2019-08-15 WO disclosed
CN-109153670-A Nicotinyl alcohol ether derivative, preparation method thereof, pharmaceutical composition and application 中国医学科学院药物研究所 2019-01-04 CN disclosed
US-20110263539-A1 SHIP 1 MODULATOR COMPOUNDS THE UNIVERSITY OF BRITISH COLUMBIA (CA) 2011-10-27 US disclosed
US-20100323990-A1 SHIP 1 MODULATOR PRODRUGS THE UNIVERSITY OF BRITISH COLUMBIA (CA) 2010-12-23 US disclosed
EP-1135398-A1 CYANOPHOSPHONAMIDES AND METHOD FOR PREPARATION Monsanto Technology LLC (US) 2001-09-26 EP disclosed
US-6218563-B1 Cyanophosphonamides and method for preparation MONSANTO COMPANY 2001-04-17 US disclosed
WO-2000032611-A1 CYANOPHOSPHONAMIDES AND METHOD FOR PREPARATION MONSANTO TECHNOLOGY LLC (US) 2000-06-08 WO disclosed
EP-0948506-A1 CYANOPHOSPHONATE DERIVATIVES MONSANTO COMPANY (US) 1999-10-13 EP disclosed
EP-0948502-A1 CYANOPHOSPHORUS COMPOUNDS AND THEIR PREPARATION MONSANTO COMPANY (US) 1999-10-13 EP disclosed
US-5945082-A HERBICIDES, INSECTICIDES, FLAME RETARDANTS, PLASTICIZERS; CYANATION, SALT FORMATION, PHOSPHONATION, PHOSPHATING MONSANTO COMPANY (US) 1999-08-31 US disclosed
US-5935542-A Cyanphosphonate derivatives and method for their preparation MONSANTO COMPANY (US) 1999-08-10 US disclosed
WO-1998029422-A1 CYANOPHOSPHONATE DERIVATIVES MONSANTO COMPANY (US) 1998-07-09 WO disclosed
WO-1998029419-A1 CYANOPHOSPHORUS COMPOUNDS AND THEIR PREPARATION MONSANTO COMPANY (US) 1998-07-09 WO 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-20100323990-A1 SHIP 1 MODULATOR PRODRUGS PPM1D, PPM1G, PPM1F ALOX15 1115/4885ALDH1A1 598/4885CAD 3593/4885
US-20110263539-A1 SHIP 1 MODULATOR COMPOUNDS PPM1F, PPM1D, PPP1R1B ALOX15 1048/4885ALDH1A1 980/4885CAD 4138/4885

“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.