SCHEMBL6283678

SCHEMBL6283678

COc1ccc(C2=CC(=O)NC2=O)c(OC)c1OC

nearest known ligand 0.49

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
HDAC4 P56524 1/20 0.44
HDAC2 Q92769 1/20 0.44
HDAC8 Q9BY41 1/20 0.44
KDM4E B2RXH2 4/20 0.41
ALDH1A1 P00352 3/20 0.41
HPGD P15428 2/20 0.41
SMN1; SMN2 Q16637 2/20 0.41
NPC1 O15118 1/20 0.41
RAB9A P51151 1/20 0.41
PTGS2 P35354 2/20 0.39
CRBN Q96SW2 1/20 0.39
ACHE P22303 1/20 0.39
ERN1 O75460 1/20 0.38
HSD17B10 Q99714 2/20 0.37
TDP1 Q9NUW8 1/20 0.37
LMNA P02545 1/20 0.37
MAPT P10636 1/20 0.37
MAPK1 P28482 1/20 0.37
HTT P42858 1/20 0.37

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
SCHEMBL10433668 0.79 KDR (0.40) KDM4EALDH1A1HPGDHSD17B10MAPK1
SCHEMBL30824770 0.77 CHEK1 (0.44)
SCHEMBL211026 0.77 L3MBTL1 (0.51) KDM4EALDH1A1HPGDSMN1; SMN2NPC1
Ammonia Solution, Strong SCHEMBL27959164 0.75 L3MBTL1 (0.54) KDM4EALDH1A1HPGDSMN1; SMN2NPC1
SCHEMBL10480215 0.75 ALDH1A1 (0.43) KDM4EALDH1A1HPGDERN1HSD17B10
SCHEMBL10480168 0.75 STK10 (0.42) ALDH1A1SMN1; SMN2NPC1RAB9ALMNA
SCHEMBL2262245 0.74 ALDH1A1 (0.38) KDM4EALDH1A1HPGDSMN1; SMN2HSD17B10
SCHEMBL11323197 0.73 PRMT1 (0.44) KDM4EALDH1A1HPGDSMN1; SMN2RAB9A
SCHEMBL11327793 0.72 L3MBTL1 (0.49) KDM4EMAPT
SCHEMBL642228 0.72 HDAC4 (0.58) HDAC4HDAC2HDAC8KDM4EALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6958395-B2 Method for producing water-soluble saccharide conjugates and saccharide mimetics by Diels-Alder reaction DEUTSCHES KREBSFORSCHUNGSZENTRUM STIFTUNG DES OFFENTLICHEN RECHTS (DE) 2005-10-25 US disclosed
US-20040059101-A1 Method for producing water-soluble saccharide conjugates and saccharide mimetics by diels-alder reaction DEUTSCHES KREBSFORSCHUNGSZENTRUM STIFTUNG DES OFFENTLICHEN RECHTS (DE) 2004-03-25 US disclosed
EP-1313750-A1 METHOD FOR PRODUCING WATER-SOLUBLE SACCHARIDE CONJUGATES AND SACCHARIDE MIMETICS BY DIELS-ALDER REACTION Deutsches Krebsforschungszentrum Stiftung des öffentlichen Rechts (DE) 2003-05-28 EP disclosed
WO-2002016378-A1 METHOD FOR PRODUCING WATER-SOLUBLE SACCHARIDE CONJUGATES AND SACCHARIDE MIMETICS BY DIELS-ALDER REACTION Deutsches Krebsforschungszentrum Stiftung des öffentlichen Rechts (DE) 2002-02-28 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 (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-20040059101-A1 Method for producing water-soluble saccharide conjugates and saccharide mimetics by diels-alder reaction SI, MAN1B1, SORD HDAC4 2276/4885HDAC2 2604/4885HDAC8 1313/4885

“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.