SCHEMBL2293546

SCHEMBL2293546

CC(C)(C)c1cc(CBr)c(Br)c(C(C)(C)C)c1

nearest known ligand 0.39

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HTT P42858 2/20 0.39
NPSR1 Q6W5P4 2/20 0.39
KDM4E B2RXH2 1/20 0.39
MEN1 O00255 1/20 0.39
MAPT P10636 1/20 0.39
KMT2A Q03164 1/20 0.39
CYP2C19 P33261 5/20 0.39
CYP2C9 P11712 4/20 0.39
CYP1A2 P05177 3/20 0.39
CYP2D6 P10635 3/20 0.39
HIF1A Q16665 2/20 0.39
ALDH1A1 P00352 1/20 0.33
GAA P10253 1/20 0.33
XBP1 P17861 1/20 0.33
MAPK1 P28482 1/20 0.33
NR5A2 O00482 1/20 0.33
NR5A1 Q13285 1/20 0.33
HSPA5 P11021 2/20 0.32
GABRA1 P14867 1/20 0.32
GABRB2 P47870 1/20 0.32

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
SCHEMBL29707205 1.00 HTT (0.39) HTTNPSR1KDM4EMEN1MAPT
SCHEMBL198146 0.80 GABRA1 (0.42) HTTNPSR1KDM4EMEN1MAPT
SCHEMBL15003248 0.80 CYP2C19 (0.36) HTTNPSR1CYP2C19CYP2C9CYP1A2
SCHEMBL17594504 0.80 CYP2C19 (0.36) HTTNPSR1CYP2C19CYP2C9CYP1A2
SCHEMBL28928342 0.78 CYP2C19 (0.35) HTTNPSR1CYP2C19CYP2C9CYP1A2
SCHEMBL9994766 0.78 ALDH1A1 (0.48) HTTNPSR1KDM4EMEN1MAPT
SCHEMBL17594925 0.74 POLB (0.44) HTTNPSR1KDM4EMEN1MAPT
SCHEMBL13529284 0.73 CYP19A1 (0.33)
SCHEMBL2292932 0.73 HSPA5 (0.37) HSPA5
SCHEMBL29516681 0.72 CYP2C19 (0.59) HTTNPSR1CYP2C19CYP2C9CYP1A2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114805068-B Preparation method of chiral alpha-hydroxy-beta-keto ester compound 南京工业大学 2023-07-21 CN disclosed
CN-113549062-B Chiral quaternary ammonium salt phase transfer catalyst with high steric hindrance derived from cinchona alkaloid and synthesis method thereof 南京工业大学 2022-08-09 CN disclosed
CN-114805068-A Preparation method of chiral alpha-hydroxy-beta-keto ester compound 南京工业大学 2022-07-29 CN disclosed
CN-113549062-A Chiral quaternary ammonium salt phase transfer catalyst with high steric hindrance derived from cinchona alkaloid and synthesis method thereof 南京工业大学 2021-10-26 CN disclosed
EP-2149545-B1 METHOD FOR PRODUCING BENZALDEHYDE COMPOUND SUMITOMO CHEMICAL CO (JP) 2016-10-05 EP disclosed
WO-2016039691-A1 CATALYSTS FOR MAKING CHIRAL HETEROCYCLIC SULFOXIDES NANYANG TECHNOLOGICAL UNIVERSITY (SG) 2016-03-17 WO disclosed
US-7994367-B2 Method for producing benzaldehyde compound SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2011-08-09 US disclosed
US-20100210879-A1 METHOD FOR PRODUCING BENZALDEHYDE COMPOUND SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2010-08-19 US disclosed
EP-2149545-A1 METHOD FOR PRODUCING BENZALDEHYDE COMPOUND Sumitomo Chemical Company, Limited (JP) 2010-02-03 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-20100210879-A1 METHOD FOR PRODUCING BENZALDEHYDE COMPOUND NQO1, C9, TRPA1 HTT 1687/4885NPSR1 3260/4885KDM4E 1499/4885

“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.