SCHEMBL4601555

SCHEMBL4601555

COC(=O)CCC(=O)O[Si](C)(C)C(C)(C)C

nearest known ligand 0.54

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TSHR P16473 4/20 0.54
LMNA P02545 3/20 0.41
KDM4E B2RXH2 1/20 0.41
ALDH1A1 P00352 4/20 0.39
KMT2A Q03164 2/20 0.39
HSD17B10 Q99714 2/20 0.39
HTT P42858 2/20 0.39
MAPT P10636 1/20 0.39
MEN1 O00255 1/20 0.38
CA12 O43570 1/20 0.36
CA14 Q9ULX7 1/20 0.36
RECQL P46063 1/20 0.36
MGAM O43451 1/20 0.34
GAA P10253 1/20 0.34
SI P14410 1/20 0.34
MGAM2 Q2M2H8 1/20 0.34
TET2 Q6N021 1/20 0.33
VCAM1 P19320 1/20 0.33
POLB P06746 1/20 0.33
L3MBTL1 Q9Y468 1/20 0.33

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
SCHEMBL6545278 0.91 TSHR (0.38) TSHR
SCHEMBL4921832 0.83 EGLN1 (0.42) TSHRLMNAKDM4EALDH1A1VCAM1
SCHEMBL6545080 0.83 TSHR (0.42) TSHRLMNAALDH1A1RECQLGLA
SCHEMBL28163566 0.82 MGAM (0.35) TSHRMGAMGAASIMGAM2
SCHEMBL6309457 0.81 ALDH1A1 (0.46) TSHRLMNAALDH1A1
SCHEMBL20168030 0.78 TSHR (0.46) TSHRLMNAKDM4EALDH1A1KMT2A
SCHEMBL11905663 0.77 TSHR (0.32) TSHRCA12CA14RECQL
SCHEMBL12227359 0.77 LDHA (0.33) TSHR
SCHEMBL12540531 0.76 ALDH1A1 (0.33) ALDH1A1
SCHEMBL26108395 0.76

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
EP-1912953-B1 PROCESS FOR THE SYNTHESIS OF ROSUVASTATIN CALCIUM LEK PHARMACEUTICALS (SI) 2016-08-17 EP disclosed
US-8354530-B2 Preparation of HMG-CoA reductase inhibitors, in particular rosuvastatin calcium, introducing L-malic acid as source of chirality for side chain; statin core moiety is consecutively coupled with chiral segment containing 4 carbon atoms and segment containing 2 carbon atoms; treating hypercholesterolemia Lek Pharmaceuticals d. d (SI) 2013-01-15 US disclosed
US-20080255170-A1 Process for the Synthesis of Rosuvastatin Calcium LEK PHARMACEUTICALS D.D (SI) 2008-10-16 US disclosed
EP-1912953-A1 PROCESS FOR THE SYNTHESIS OF ROSUVASTATIN CALCIUM LEK Pharmaceuticals D.D. (SI) 2008-04-23 EP disclosed
WO-2007017117-A1 PROCESS FOR THE SYNTHESIS OF ROSUVASTATIN CALCIUM LEK PHARMACEUTICALS D.D. (SI) 2007-02-15 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-20080255170-A1 Process for the Synthesis of Rosuvastatin Calcium HMGCR, ME1, COASY TSHR 4795/4885LMNA 555/4885KDM4E 1762/4885

“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.