SCHEMBL9137646

SCHEMBL9137646

O=C(c1ccc(S)cc1)c1ccc([N+](=O)[O-])cc1

nearest known ligand 0.69

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
▸ SRD5A2 P31213 2/20 0.69
▸ LMNA P02545 1/20 0.67
▸ GAA P10253 1/20 0.67
▸ L3MBTL1 Q9Y468 1/20 0.65
▸ MAPK1 P28482 2/20 0.62
▸ POLB P06746 1/20 0.62
▸ CES1 P23141 2/20 0.61
▸ TDP1 Q9NUW8 2/20 0.59
▸ ALDH1A1 P00352 2/20 0.59
▸ MAPT P10636 1/20 0.59
▸ CA1 P00915 3/20 0.59
▸ CA2 P00918 3/20 0.59
▸ TSHR P16473 1/20 0.57
▸ CA12 O43570 1/20 0.56
▸ CA9 Q16790 1/20 0.56
▸ CA14 Q9ULX7 1/20 0.56
▸ CES2 O00748 1/20 0.53
▸ GSK3B P49841 1/20 0.52

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
SCHEMBL975118 0.89 SRD5A2 (0.83) SRD5A2LMNAGAAL3MBTL1MAPK1
SCHEMBL10723714 0.89 SRD5A2 (0.83) SRD5A2LMNAGAAL3MBTL1MAPK1
SCHEMBL1362 0.85 ALDH1A1 (0.56) LMNAL3MBTL1MAPK1CES1TDP1
SCHEMBL8764904 0.85 ALDH1A1 (0.56) LMNAL3MBTL1MAPK1CES1TDP1
SCHEMBL28914440 0.83 MAPK1 (0.85) SRD5A2LMNAGAAL3MBTL1MAPK1
SCHEMBL9798096 0.83 CES2 (0.62) LMNACES1TDP1ALDH1A1MAPT
SCHEMBL8934653 0.83 ALDH1A1 (0.54) LMNAL3MBTL1MAPK1CES1TDP1
SCHEMBL9804074 0.83 ALDH1A1 (0.54) LMNAL3MBTL1MAPK1CES1TDP1
SCHEMBL7143035 0.83 ALDH1A1 (0.54) LMNAL3MBTL1MAPK1CES1TDP1
Potassium Ion SCHEMBL7143040 0.83 ALDH1A1 (0.54) LMNAL3MBTL1MAPK1CES1TDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5464912-A Adduct with rodlike mesogenic moiety, adduct made by reacting polyepoxide with nitro/so/ compound having epoxy-reactive hydrogen; conversion of hydroxyl product to ether, ester, halide, urethane, ketone, alkane; reducing nitro/so/ to amine THE DOW CHEMICAL COMPANY (US) 1995-11-07 — — US disclosed
US-5412044-A Nitro group terminated mesogenic epoxy resin adducts THE DOW CHEMICAL COMPANY (US) 1995-05-02 — — US disclosed
US-5344898-A Curable composition with stilbene groups and molecular orientation THE DOW CHEMICAL COMPANY (US) 1994-09-06 — — US disclosed
US-5298575-A Consists of at least one compound having more than one vicinal epoxide group and at least one amine terminated adduct containing one or more mesogenic moities THE DOW CHEMICAL COMPANY (US) 1994-03-29 — — US disclosed
US-4996347-A Anticoagulant FOURNIER INNOVATION ET SYNERGIE (FR) 1991-02-26 — — US disclosed
US-4877808-A ANTITHROMBOTICS FOURNIER INNOVATION ET SYNERGIE (FR) 1989-10-31 — — US disclosed
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