SCHEMBL10620689

SCHEMBL10620689

CCC(C(=O)c1ccc(C(=O)O)cc1)C(=O)c1ccc(C(=O)O)cc1

nearest known ligand 0.54

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 2/20 0.54
TSHR P16473 2/20 0.52
TP53 P04637 1/20 0.52
HTT P42858 1/20 0.50
MAPT P10636 1/20 0.49
SMN1; SMN2 Q16637 1/20 0.48
SRD5A2 P31213 2/20 0.46
CA1 P00915 3/20 0.44
CA2 P00918 3/20 0.44
LMNA P02545 1/20 0.44
HSD17B10 Q99714 1/20 0.44
CA12 O43570 1/20 0.44
CA3 P07451 1/20 0.44
TYR P14679 1/20 0.44
DRD1 P21728 1/20 0.44
CA4 P22748 1/20 0.44
CA6 P23280 1/20 0.44
CA5A P35218 1/20 0.44
CA7 P43166 1/20 0.44
CA9 Q16790 1/20 0.44

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
SCHEMBL1704486 0.84 MDM2 (0.61) ALDH1A1HTTMAPTSMN1; SMN2LMNA
SCHEMBL5434510 0.81 ALDH1A1 (0.52) ALDH1A1TSHRTP53HTTMAPT
Terephthalic Acid SCHEMBL11564620 0.79 TSHR (0.60) ALDH1A1TSHRTP53HTTMAPT
Terephthalic Acid SCHEMBL2160594 0.79 TSHR (0.60) ALDH1A1TSHRTP53HTTMAPT
SCHEMBL2289091 0.79 ALDH1A1 (0.50) ALDH1A1HTTMAPTSMN1; SMN2SRD5A2
SCHEMBL16553310 0.79 LMNA (0.59) ALDH1A1TSHRTP53HTTMAPT
SCHEMBL442090 0.78 MDM2 (0.59) ALDH1A1TSHRHTTMAPTLMNA
Terephthalic Acid SCHEMBL27306913 0.78 TSHR (0.75) ALDH1A1TSHRTP53SMN1; SMN2SRD5A2
SCHEMBL5217775 0.78 GSK3B (0.56) ALDH1A1HTTSMN1; SMN2CA1CA2
SCHEMBL342966 0.78 GSK3B (0.48) ALDH1A1HTTMAPTCA1CA2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-4789724-A POLYMERIZING ISOLATED AND PURIFIED MIXED DIANHYDRIDES PREPARED BY REACTING ACETIC ANHYDRIDE AND DIACIDS MASSACHUSETTS INSTITUTE OF TECHNOLOGY (US) 1988-12-06 US disclosed