SCHEMBL12600156

SCHEMBL12600156

CCOC(=O)C[C@H](O[Si](C)(C)C(C)(C)C)c1ccc2nc(C)sc2c1

nearest known ligand 0.43

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 5/20 0.41
SMN1; SMN2 Q16637 5/20 0.41
MAPT P10636 4/20 0.41
KMT2A Q03164 3/20 0.41
MEN1 O00255 2/20 0.41
KDM4E B2RXH2 2/20 0.41
TSHR P16473 2/20 0.41
HPGD P15428 1/20 0.39
SHMT2 P34897 1/20 0.39
LDHA P00338 2/20 0.38
RAB9A P51151 5/20 0.37
NPC1 O15118 4/20 0.37
RXFP1 Q9HBX9 2/20 0.37
TDP1 Q9NUW8 1/20 0.37
ROCK2 O75116 1/20 0.36
POLB P06746 1/20 0.36
P2RX3 P56373 1/20 0.36
GAA P10253 1/20 0.36
PTPN1 P18031 1/20 0.36
TP53 P04637 1/20 0.36

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
SCHEMBL12600052 0.92 SMN1; SMN2 (0.41) ALDH1A1SMN1; SMN2MAPTKMT2AMEN1
SCHEMBL12600038 0.92 SMN1; SMN2 (0.41) ALDH1A1SMN1; SMN2MAPTKMT2AMEN1
SCHEMBL12600169 0.81 SMN1; SMN2 (0.38) ALDH1A1SMN1; SMN2MAPTKMT2AMEN1
SCHEMBL12600109 0.80 ALDH1A1 (0.47) ALDH1A1SMN1; SMN2MAPTKMT2AMEN1
SCHEMBL12600157 0.79 FFAR1 (0.39) ALDH1A1SMN1; SMN2KDM4EHPGDRAB9A
SCHEMBL12600131 0.79 KDM4E (0.43) ALDH1A1SMN1; SMN2MAPTKDM4EHPGD
SCHEMBL22397218 0.78 DRD2 (0.35) ALDH1A1MAPTKMT2AMEN1KDM4E
SCHEMBL2818376 0.78 TAS1R3 (0.39) SMN1; SMN2MAPTKMT2AMEN1KDM4E
SCHEMBL12600150 0.76 ALDH1A1 (0.36) ALDH1A1MAPTKMT2AKDM4EHPGD
SCHEMBL12600129 0.76 CYP2D6 (0.35) ALDH1A1KDM4EROCK2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7935827-B2 Optically active, heteroaromatic β-hydroxy esters and processes for their preparation from β-keto esters and processes for the preparation of these β-keto esters BAYER SCHERING PHARMA AG (DE) 2011-05-03 US disclosed
US-20100248313-A1 NOVEL OPTICALLY ACTIVE, HETEROAROMATIC BETA-HYDROXY ESTERS AND PROCESSES FOR THEIR PREPARATION FROM BETA-KETO ESTERS AND PROCESSES FOR THE PREPARATION OF THESE BETA-KETO ESTERS BAYER SCHERING PHARMA AG (DE) 2010-09-30 US disclosed
US-7626035-B2 Ethyl 2-(benzothiazol-2-yl),2-oxo-acetate; useful in the synthesis of epothilonederivatives; antitumor,-carcinogenic agents; high chemical purity, optical purity,in very good yields and allows an industrial-scale production BAYER SCHERING PHARMA AG (DE) 2009-12-01 US 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-20100248313-A1 NOVEL OPTICALLY ACTIVE, HETEROAROMATIC BETA-HYDROXY ESTERS AND PROCESSES FOR THEIR PREPARATION FROM BETA-KETO ESTERS AND PROCESSES FOR THE PREPARATION OF THESE BETA-KETO ESTERS CYP8B1, HSD17B7, CYP51A1 ALDH1A1 286/4885SMN1; SMN2 4806/4885MAPT 3068/4885

“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.