SCHEMBL9332856

SCHEMBL9332856

CC(=O)OC[C@H]1O[C@H](OCc2ccccc2)[C@@H](N2C(=O)c3ccccc3C2=O)[C@@H](OC(C)=O)[C@@H]1OC(C)=O

nearest known ligand 0.52

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ LMNA P02545 3/20 0.52
▸ POLB P06746 1/20 0.51
▸ KMT2A Q03164 1/20 0.50
▸ TSHR P16473 1/20 0.50
▸ CYP2D6 P10635 3/20 0.49
▸ ALDH1A1 P00352 1/20 0.49
▸ MAPK1 P28482 1/20 0.49
▸ P4HB P07237 1/20 0.44
▸ PDIA4 P13667 1/20 0.44
▸ PDIA3 P30101 1/20 0.44
▸ PAX8 Q06710 1/20 0.43
▸ PRKCA P17252 1/20 0.43
▸ AKT1 P31749 1/20 0.43
▸ PTK2 Q05397 1/20 0.43
▸ CYP2C19 P33261 1/20 0.42
▸ THRB P10828 1/20 0.42
▸ SMN1; SMN2 Q16637 1/20 0.42
▸ HIF1A Q16665 1/20 0.42
▸ CA9 Q16790 2/20 0.42
▸ CA1 P00915 1/20 0.42

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
SCHEMBL29865166 1.00 LMNA (0.52) LMNAPOLBKMT2ATSHRCYP2D6
SCHEMBL9332848 1.00 LMNA (0.52) LMNAPOLBKMT2ATSHRCYP2D6
SCHEMBL24804649 1.00 LMNA (0.52) LMNAPOLBKMT2ATSHRCYP2D6
SCHEMBL25736465 0.92 LMNA (0.48) LMNAPOLBKMT2ATSHRCYP2D6
SCHEMBL8002809 0.92 CYP3A4 (0.46) LMNAPOLBKMT2ATSHRCYP2D6
SCHEMBL827827 0.89 NT5E (0.47) LMNAPOLBKMT2ATSHRCYP2D6
SCHEMBL827826 0.89 NT5E (0.47) LMNAPOLBKMT2ATSHRCYP2D6
SCHEMBL17456128 0.89 NT5E (0.48) LMNAPOLBKMT2ACYP2D6ALDH1A1
SCHEMBL17456127 0.89 NT5E (0.48) LMNAPOLBKMT2ACYP2D6ALDH1A1
SCHEMBL8699189 0.89 TSHR (0.50) LMNAPOLBKMT2ATSHRCYP2D6

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5352811-A To produce homoallylic alcohol, acylation, oxidation of double bond E. I. DU PONT DE NEMOURS AND COMPANY (US) 1994-10-04 — — US disclosed
US-5158941-A Lipid A analog as stimulant for production of interleukin-1 in human monocytes and tumor cell growth inhibitor E. I. DU PONT DE NEMOURS AND COMPANY (US) 1992-10-27 — — US disclosed
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