SCHEMBL5665404

SCHEMBL5665404

CCOC(COC(=O)c1cccc(OC)c1)OCC

nearest known ligand 0.55

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 3/20 0.55
MEN1 O00255 2/20 0.55
KMT2A Q03164 2/20 0.55
CES2 O00748 1/20 0.51
CES1 P23141 1/20 0.51
NPC1 O15118 3/20 0.49
RAB9A P51151 2/20 0.49
ALDH1A1 P00352 1/20 0.49
MAPT P10636 1/20 0.49
NPSR1 Q6W5P4 1/20 0.49
ESR1 P03372 1/20 0.49
ESR2 Q92731 1/20 0.49
PARP1 P09874 1/20 0.49
POLB P06746 1/20 0.48
CASP3 P42574 1/20 0.48
SENP8 Q96LD8 1/20 0.48
SENP7 Q9BQF6 1/20 0.48
SENP6 Q9GZR1 1/20 0.48
TAS1R3 Q7RTX0 1/20 0.48
TAS1R1 Q7RTX1 1/20 0.48

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
SCHEMBL5664068 0.87 SMN1; SMN2 (0.56) SMN1; SMN2MEN1KMT2ACES2CES1
SCHEMBL5662779 0.85 MEN1 (0.49) SMN1; SMN2MEN1KMT2ACES2CES1
SCHEMBL5663461 0.84 KMT2A (0.53) SMN1; SMN2MEN1KMT2ACES2CES1
SCHEMBL1248647 0.84 SMN1; SMN2 (0.65) SMN1; SMN2MEN1KMT2ACES2CES1
SCHEMBL3070514 0.83 TDP1 (0.51) SMN1; SMN2MEN1KMT2ANPC1RAB9A
SCHEMBL7095551 0.83 ADRB2 (0.56) NPC1RAB9AALDH1A1MAPTADRB2
SCHEMBL5663951 0.83 MAPK1 (0.55) SMN1; SMN2MEN1KMT2ANPC1RAB9A
SCHEMBL1930664 0.82 ADRB2 (0.56) SMN1; SMN2MEN1KMT2ACES2CES1
SCHEMBL5664129 0.82 CHRM2 (0.50) RAB9AALDH1A1PARP1TP53ELANE
SCHEMBL714676 0.81 ALDH1A1 (0.61) SMN1; SMN2MEN1KMT2ANPC1RAB9A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20030162992-A1 Reacting a 2,2-dialkoxyethyl halide with an appropriate carboxylate compound to obtain acetal compound; hydrolyzing the acetal to form the alpha -acyloxyacetaldehyde PHARMASSET, INC. 2003-08-28 US claimed
EP-1461041-A4 PREPARATION OF INTERMEDIATES USEFUL IN THE SYNTHESIS OF ANTIVIRAL NUCLEOSIDES PHARMASSET LTD (BB) 2006-03-29 EP disclosed
EP-1461041-A2 PREPARATION OF INTERMEDIATES USEFUL IN THE SYNTHESIS OF ANTIVIRAL NUCLEOSIDES Pharmasset Ltd. (BB) 2004-09-29 EP disclosed
US-20030162992-A1 Reacting a 2,2-dialkoxyethyl halide with an appropriate carboxylate compound to obtain acetal compound; hydrolyzing the acetal to form the alpha -acyloxyacetaldehyde PHARMASSET, INC. 2003-08-28 US disclosed
WO-2003051298-A2 PREPARATION OF INTERMEDIATES USEFUL IN THE SYNTHESIS OF ANTIVIRAL NUCLEOSIDES PHARMASSET LTD. (BB) 2003-06-26 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-20030162992-A1 Reacting a 2,2-dialkoxyethyl halide with an appropriate carboxylate compound to obtain acetal compound; hydrolyzing the acetal to form the alpha -acyloxyacetaldehyde DERA, DPYD, DHPS SMN1; SMN2 1839/4885MEN1 2878/4885KMT2A 624/4885

“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.