SCHEMBL2500684

SCHEMBL2500684

C[C@H](O[Si](C)(C)C(C)(C)C)c1ccc(O)cc1Cl

nearest known ligand 0.46

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
ESR1 P03372 6/20 0.46
HSD17B10 Q99714 1/20 0.37
ESR2 Q92731 3/20 0.34
PDE2A O00408 1/20 0.34
TTR P02766 2/20 0.33
APLNR P35414 2/20 0.33
PDK1 Q15118 1/20 0.32
PDK2 Q15119 1/20 0.32
PDK3 Q15120 1/20 0.32
PDK4 Q16654 1/20 0.32
TYR P14679 1/20 0.32
LMNA P02545 1/20 0.32
TP53 P04637 1/20 0.32
HTT P42858 1/20 0.32
MEN1 O00255 1/20 0.31
CYP1A2 P05177 1/20 0.31
CYP3A4 P08684 1/20 0.31
KMT2A Q03164 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
SCHEMBL2497862 0.81 APLNR (0.46) PDE2AAPLNRLMNATP53HTT
SCHEMBL737515 0.74 HSD17B10 (0.42) HSD17B10TTRLMNACYP1A2CYP3A4
SCHEMBL1100314 0.74 CYP3A4 (0.36) APLNRLMNATP53HTTCYP3A4
SCHEMBL2497084 0.74 AAK1 (0.41)
SCHEMBL1100412 0.72 APLNR (0.36) APLNR
SCHEMBL69021 0.72 ESR1 (0.63) ESR1HSD17B10ESR2PDE2ATTR
SCHEMBL6742674 0.72 ESR1 (0.63) ESR1HSD17B10ESR2PDE2ATTR
SCHEMBL30234474 0.72 ESR1 (0.63) ESR1HSD17B10ESR2PDE2ATTR
SCHEMBL3342503 0.70 APLNR (0.35) APLNR
SCHEMBL2499335 0.68 PDE2A (0.43) PDE2ALMNATP53MEN1KMT2A

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
EP-1813613-B1 NOVEL FUSED IMIDAZOLE DERIVATIVE MSD KK (JP) 2012-12-19 EP disclosed
US-8030327-B2 3-[1-(2-chlorophenyl)ethoxy]-5-imidazo[1,2-a]pyridin-3-ylthiophene-2-carboxyamide; polo like kinase inhibitor; antitumor and anticarcinogenic agent; mitotic phase (M phase) of the cell cycle MDS K.K. (JP) 2011-10-04 US disclosed
US-20080103136-A1 Novel Fused Imidazole Derivative MSD K.K. (JP) 2008-05-01 US disclosed
EP-1813613-A1 NOVEL FUSED IMIDAZOLE DERIVATIVE BANYU PHARMACEUTICAL CO., LTD. (JP) 2007-08-01 EP 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-20080103136-A1 Novel Fused Imidazole Derivative HRH4, H1-4, H1-3 ESR1 454/4885HSD17B10 1655/4885ESR2 1135/4885

“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.