SCHEMBL10999840

SCHEMBL10999840

O=C(O)CC(=O)CCc1ccc([N+](=O)[O-])cc1

nearest known ligand 0.58

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
▸ MMP12 P39900 1/20 0.58
▸ TSHR P16473 1/20 0.56
▸ MEN1 O00255 1/20 0.51
▸ KMT2A Q03164 1/20 0.51
▸ CCR5 P51681 1/20 0.51
▸ SMN1; SMN2 Q16637 3/20 0.49
▸ NPC1 O15118 2/20 0.49
▸ RAB9A P51151 2/20 0.49
▸ TAAR1 Q96RJ0 1/20 0.49
▸ ALDH1A1 P00352 3/20 0.49
▸ CYP2C19 P33261 2/20 0.49
▸ MAPT P10636 3/20 0.48
▸ FFAR1 O14842 1/20 0.48
▸ KCNH2 Q12809 2/20 0.47
▸ L3MBTL1 Q9Y468 1/20 0.47
▸ CYP1A2 P05177 1/20 0.46
▸ KCNJ1 P48048 1/20 0.46
▸ LMNA P02545 1/20 0.46
▸ LOXL2 Q9Y4K0 1/20 0.46

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
SCHEMBL27590304 0.90 TSHR (0.53) MMP12TSHRMEN1KMT2ASMN1; SMN2
SCHEMBL7999122 0.88 TSHR (0.66) TSHRMEN1KMT2ACCR5SMN1; SMN2
SCHEMBL350869 0.86 TSHR (0.63) TSHRMEN1KMT2ASMN1; SMN2NPC1
SCHEMBL1536704 0.85 TSHR (0.54) TSHRMEN1KMT2ACCR5SMN1; SMN2
SCHEMBL14896389 0.83 TSHR (0.51) TSHRMEN1KMT2ACCR5SMN1; SMN2
SCHEMBL17986241 0.81 TSHR (0.58) TSHRMEN1KMT2ACCR5SMN1; SMN2
SCHEMBL8041387 0.81 TSHR (0.58) TSHRMEN1KMT2ACCR5SMN1; SMN2
SCHEMBL11239432 0.80 TSHR (0.56) TSHRMEN1KMT2ACCR5SMN1; SMN2
SCHEMBL135651 0.79 TSHR (0.59) TSHRMEN1KMT2ASMN1; SMN2NPC1
SCHEMBL6585903 0.79 LMNA (0.54) TSHRMEN1KMT2ACCR5SMN1; SMN2

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-4525582-A Silyl, benzyl, p-nitrobenyl, or methyl esters of diazoacetate, a synthon used in the conversion of penicillin to thienamycin MERCK & CO., INC. (US) 1985-06-25 — — US disclosed
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