SCHEMBL6934174

SCHEMBL6934174

CC(=O)OCC(Cl)=NOC(C)=O

nearest known ligand 0.37

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 5/20 0.37
LMNA P02545 2/20 0.37
HSD17B10 Q99714 1/20 0.37
FAAH O00519 1/20 0.32
CHRM5 P08912 2/20 0.31
CHRM1 P11229 2/20 0.31
CHRM3 P20309 2/20 0.31
SMN1; SMN2 Q16637 2/20 0.31
PGR P06401 1/20 0.31
CHRM2 P08172 1/20 0.31
CHRM4 P08173 1/20 0.31
HTR1A P08908 1/20 0.31
CHRNB2 P17787 1/20 0.31
TBXA2R P21731 1/20 0.31
CHRNB4 P30926 1/20 0.31
CHRNA3 P32297 1/20 0.31
CHRNA7 P36544 1/20 0.31
CHRNA4 P43681 1/20 0.31
CHRNA10 Q9GZZ6 1/20 0.31
CHRNA9 Q9UGM1 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
SCHEMBL27934957 0.79 ALDH1A1 (0.44) ALDH1A1LMNAHSD17B10FAAHTSHR
SCHEMBL6235031 0.77
SCHEMBL6235022 0.77
SCHEMBL6940725 0.72 LMNA (0.41) LMNATSHR
SCHEMBL6940728 0.72 LMNA (0.41) LMNATSHR
SCHEMBL5288 0.71
Acetic Acid SCHEMBL27488764 0.69 ALDH1A1 (0.38) ALDH1A1LMNAHSD17B10FAAHSMN1; SMN2
Hydrochloric Acid SCHEMBL4967118 0.69
SCHEMBL28458016 0.68
SCHEMBL9311644 0.67 ALDH1A1 (0.43) ALDH1A1LMNAHSD17B10FAAHCHRM5

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0979814-B1 Improved synthesis of haloformimine compounds ROHM & HAAS (US) 2003-10-22 EP claimed
US-6207863-B1 MAINTAINING A PH BETWEEN 2 AND 5 DURING THE HALOGENATION OF FORMIMINES GREATLY INCREASES THE YIELDS OF HALOFORMIMINES AND GREATLY DECREASES THE RATE OF BY-PRODUCT FORMATION. ROHM AND HAAS COMPANY 2001-03-27 US claimed
EP-0979814-A1 Improved synthesis of haloformimine compounds ROHM AND HAAS COMPANY (US) 2000-02-16 EP claimed
EP-0979814-B1 Improved synthesis of haloformimine compounds ROHM & HAAS (US) 2003-10-22 EP disclosed
US-6207863-B1 MAINTAINING A PH BETWEEN 2 AND 5 DURING THE HALOGENATION OF FORMIMINES GREATLY INCREASES THE YIELDS OF HALOFORMIMINES AND GREATLY DECREASES THE RATE OF BY-PRODUCT FORMATION. ROHM AND HAAS COMPANY 2001-03-27 US disclosed
EP-0979814-A1 Improved synthesis of haloformimine compounds ROHM AND HAAS COMPANY (US) 2000-02-16 EP disclosed