(2-Nitrovinyl)Benzene

(2-Nitrovinyl)Benzene

SCHEMBL1226359

O=[N+]([O-])C=Cc1ccccc1.c1ccccc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
▸ FBP1 P09467 16/20 1.00
▸ TLR4 O00206 2/20 0.69
▸ TLR2 O60603 2/20 0.69
▸ MEN1 O00255 1/20 0.65
▸ S1PR4 O95977 1/20 0.65
▸ ALDH1A1 P00352 1/20 0.65
▸ LMNA P02545 1/20 0.65
▸ HSP90AA1 P07900 1/20 0.65
▸ HPGD P15428 1/20 0.65
▸ S1PR1 P21453 1/20 0.65
▸ MAPK1 P28482 1/20 0.65
▸ CCR6 P51684 1/20 0.65
▸ KMT2A Q03164 1/20 0.65
▸ SMN1; SMN2 Q16637 1/20 0.65
▸ NPSR1 Q6W5P4 1/20 0.65
▸ TLR9 Q9NR96 1/20 0.65
▸ EGFR P00533 1/20 0.63
▸ VCP P55072 2/20 0.60

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
(2-Nitrovinyl)Benzene SCHEMBL28065845 1.00 FBP1 (1.00) FBP1TLR4TLR2MEN1S1PR4
(2-Nitrovinyl)Benzene SCHEMBL30591 1.00 FBP1 (1.00) FBP1TLR4TLR2MEN1S1PR4
(2-Nitrovinyl)Benzene SCHEMBL1226357 1.00 FBP1 (1.00) FBP1TLR4TLR2MEN1S1PR4
(2-Nitrovinyl)Benzene SCHEMBL30590 1.00 FBP1 (1.00) FBP1TLR4TLR2MEN1S1PR4
SCHEMBL19088017 1.00 FBP1 (1.00) FBP1TLR4TLR2MEN1S1PR4
(2-Nitrovinyl)Benzene SCHEMBL18132133 1.00 FBP1 (1.00) FBP1TLR4TLR2MEN1S1PR4
SCHEMBL7829071 0.96 FBP1 (0.91) FBP1TLR4TLR2MEN1S1PR4
SCHEMBL7829067 0.96 FBP1 (0.91) FBP1TLR4TLR2MEN1S1PR4
(2-Nitrovinyl)Benzene SCHEMBL28758634 0.94 FBP1 (0.88) FBP1TLR4TLR2MEN1S1PR4
Hexamethylbenzene SCHEMBL29275075 0.92 FBP1 (0.84) FBP1TLR4TLR2MEN1S1PR4

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
CN-110372514-B Method for catalyzing asymmetric Michael addition reaction and catalyst thereof 常州大学 2022-09-27 — — CN claimed
CN-108727241-A A kind of cup [4] thiocarbamide cyclohexanediamine derivative and its method for being catalyzed asymmetric Michael addition reaction 常州大学 2018-11-02 — — CN claimed
CN-108727241-A A kind of cup [4] thiocarbamide cyclohexanediamine derivative and its method for being catalyzed asymmetric Michael addition reaction 常州大学 2018-11-02 — — CN disclosed
EP-2459727-A2 BIOCATALYST FOR CATALYTIC HYDROAMINATION BASF SE (DE) 2012-06-06 — — EP disclosed
US-20120123155-A1 BIOCATALYST FOR CATALYTIC HYDROAMINATION BASF SE (DE) 2012-05-17 — — US disclosed
WO-2011012632-A2 BIOCATALYST FOR CATALYTIC HYDROAMINATION BASF SE (DE) 2011-02-03 — — WO 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-20120123155-A1 BIOCATALYST FOR CATALYTIC HYDROAMINATION HDHD5, PAH, GRHPR FBP1 317/4885TLR4 4174/4885TLR2 3181/4885

“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.

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