SCHEMBL997615

SCHEMBL997615

CC(=O)CCC(C)[N+](=O)[O-]

nearest known ligand 0.39

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 3/20 0.39
CA1 P00915 2/20 0.34
LMNA P02545 2/20 0.33
TDP1 Q9NUW8 1/20 0.33
SLC15A2 Q16348 1/20 0.33
CPA1 P15085 1/20 0.31
BBOX1 O75936 1/20 0.30
MEN1 O00255 1/20 0.30
BLM P54132 1/20 0.30
HBB P68871 1/20 0.30
KMT2A Q03164 1/20 0.30
HIF1A Q16665 1/20 0.30

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
Nitroethane SCHEMBL6381909 0.83 TSHR (0.34) ALDH1A1
SCHEMBL3331716 0.82 GABRP (0.48) LMNACPA1MEN1BLMHBB
SCHEMBL28060367 0.80 TSHR (0.37) ALDH1A1CA1CPA1
SCHEMBL20261755 0.79 ALDH1A1 (0.41) ALDH1A1CA1LMNASLC15A2MEN1
SCHEMBL4434496 0.78 ALDH1A1 (0.32) ALDH1A1
SCHEMBL17673923 0.77 TSHR (0.46) ALDH1A1LMNAMEN1KMT2A
SCHEMBL23829566 0.76
SCHEMBL21549962 0.76 GABRR1 (0.32) CPA1
SCHEMBL19283717 0.75 MEN1 (0.34) CA1LMNACPA1MEN1BLM
SCHEMBL3239628 0.74 LMNA (0.41) ALDH1A1LMNAMEN1BLMHBB

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 35 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-3941846-A Preparation of nitrocarbonyl compounds TEXACO INC. (US) 1976-03-02 US claimed
US-9421513-B2 Catalyst-coated support, method for the production thereof, a reactor equipped therewith, and use thereof THYSSENKRUPP UHDE GMBH (DE) 2016-08-23 US disclosed
US-8729277-B2 Processes for the synthesis of gamma nitrocarbonyl and gamma dicarbonyl compounds and their pyrrole derivatives CHEVRON PHILIPS CHEMICAL COMPANY LP (US) 2014-05-20 US disclosed
US-8729277-B2 Processes for the synthesis of gamma nitrocarbonyl and gamma dicarbonyl compounds and their pyrrole derivatives CHEVRON PHILIPS CHEMICAL COMPANY LP (US) 2014-05-20 US disclosed
US-8729277-B2 Processes for the synthesis of gamma nitrocarbonyl and gamma dicarbonyl compounds and their pyrrole derivatives CHEVRON PHILIPS CHEMICAL COMPANY LP (US) 2014-05-20 US disclosed
US-8338325-B2 Tethered catalyst processes in microchannel reactors and systems containing a tethered catalyst or tethered chiral auxiliary VELOCYS, INC. (US) 2012-12-25 US disclosed
US-8338325-B2 Tethered catalyst processes in microchannel reactors and systems containing a tethered catalyst or tethered chiral auxiliary VELOCYS, INC. (US) 2012-12-25 US disclosed
US-8338325-B2 Tethered catalyst processes in microchannel reactors and systems containing a tethered catalyst or tethered chiral auxiliary VELOCYS, INC. (US) 2012-12-25 US disclosed
US-20120198769-A1 CATALYST-COATED SUPPORT, METHOD FOR THE PRODUCTION THEREOF, A REACTOR EQUIPPED THEREWITH, AND USE THEREOF THYSSENKRUPP INDUSTRIAL SOLUTIONS AG (DE) 2012-08-09 US disclosed
US-20120157692-A1 Processes for the Synthesis of Gamma Nitrocarbonyl and Gamma Dicarbonyl Compounds and Their Pyrrole Derivatives CHEVRON PHILLIPS CHEMICAL COMPANY LP (US) 2012-06-21 US disclosed
US-4066780-A Pyranoindole derivatives as antiulcer agents AYERST MCKENNA AND HARRISON LTD. (CA) 1978-01-03 US disclosed
US-4066779-A ANTIDEPRESSANT, ANTIULCER AYERST, MCKENNA AND HARRISON LTD. (CA) 1978-01-03 US disclosed
US-4056538-A ANTIDEPRESSANTS, ANTIULCER AGENTS AYERST, MCKENNA & HARRISON LIMITED (CA) 1977-11-01 US disclosed
US-4056537-A CYCLIZATION, ACID CATALYST AYERST MCKENNA AND HARRISON LTD. (CA) 1977-11-01 US disclosed
US-4041169-A TREATING AND PREVENTING ULCERS AYERST MCKENNA AND HARRISON LTD. (CA) 1977-08-09 US disclosed
US-4012511-A ANTIULCER AGENTS AYERST MCKENNA & HARRISON LTD. (CA) 1977-03-15 US disclosed
US-4003913-A ANTIDEPRESSANTS, ANTIULCER AGENTS AYERST MCKENNA AND HARRISON LTD. (CA) 1977-01-18 US disclosed
US-3995052-A Indenopyran- and indenothiopyranalkylamines III in the treatment of depression AYERST MCKENNA AND HARRISON LTD. (CA) 1976-11-30 US disclosed
US-3962236-A ANTIDEPRESSANTS, ANTI-ULCER AYERST MCKENNA AND HARRISON LTD. (CA) 1976-06-08 US disclosed
US-3941846-A Preparation of nitrocarbonyl compounds TEXACO INC. (US) 1976-03-02 US 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-20120157692-A1 Processes for the Synthesis of Gamma Nitrocarbonyl and Gamma Dicarbonyl Compounds and Their Pyrrole Derivatives DHPS, DNPH1, DDT ALDH1A1 2354/4885CA1 3082/4885LMNA 2633/4885

“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.