SCHEMBL486290

SCHEMBL486290

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

nearest known ligand 0.41

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CALM1 P0DP23 1/20 0.41
CES2 O00748 1/20 0.39
CES1 P23141 1/20 0.39
TSHR P16473 3/20 0.38
ALDH1A1 P00352 2/20 0.38
LOXL2 Q9Y4K0 2/20 0.38
IDO1 P14902 1/20 0.38
TP53 P04637 1/20 0.38
TRPA1 O75762 1/20 0.38
MAOB P27338 1/20 0.36
HPGD P15428 1/20 0.36
ALOX15 P16050 1/20 0.36
ALOX12 P18054 1/20 0.36
CASP1 P29466 1/20 0.36
HSD17B10 Q99714 1/20 0.36
TAAR1 Q96RJ0 3/20 0.36
SLC6A2 P23975 2/20 0.36
CYP2A6 P11509 2/20 0.36
MAOA P21397 1/20 0.36
SLC6A4 P31645 1/20 0.36

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
SCHEMBL9512532 0.78 TSHR (0.48) CALM1CES2CES1TSHRALDH1A1
Iodide SCHEMBL7700643 0.76 TSHR (0.46) CALM1CES2CES1TSHRALDH1A1
SCHEMBL8726910 0.75 TAAR1 (0.39) IDO1TAAR1CYP2A6HTR2ASMN1; SMN2
SCHEMBL6045125 0.75 CYP3A4 (0.38) IDO1CYP1A2
SCHEMBL7903067 0.74 TP53 (0.43) CALM1TSHRALDH1A1LOXL2IDO1
SCHEMBL14306650 0.74 TSHR (0.43) CALM1CES2CES1TSHRALDH1A1
SCHEMBL73253 0.74 CPA1 (0.47) CALM1CES2CES1ALDH1A1CYP1A2
SCHEMBL27673225 0.74 CPA1 (0.47) CALM1CES2CES1ALDH1A1CYP1A2
SCHEMBL6045093 0.73 IDO1 (0.46) TSHRIDO1MAOBSIGMAR1CYP1A2
SCHEMBL31211948 0.72 CPA1 (0.46) CALM1CES2CES1ALDH1A1CYP1A2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-113292446-B Method for preparing N-benzylhydroxylamine hydrochloride with high yield 广州康瑞泰药业有限公司 2022-04-26 CN claimed
CN-113292446-A Method for preparing N-benzylhydroxylamine hydrochloride with high yield 广州康瑞泰药业有限公司 2021-08-24 CN claimed
EP-0366560-A1 Tylosin derivatives, process for their preparation and pharmaceutical compositions containing them ADIR ET COMPAGNIE (FR) 1990-05-02 EP claimed
CN-120647596-A Trifluoromethyl isoxazolidine-containing compound and synthetic method and pharmaceutical application thereof 河南师范大学 2025-09-16 CN disclosed
US-20240239771-A1 BACTERIAL EFFLUX PUMP INHIBITORS TAXIS PHARMACEUTICALS, INC. 2024-07-18 US disclosed
US-20240239771-A1 BACTERIAL EFFLUX PUMP INHIBITORS TAXIS PHARMACEUTICALS, INC. 2024-07-18 US disclosed
CN-116239492-B Continuous synthesis process of N-benzyl hydroxylamine hydrochloride 中南大学 2024-06-14 CN disclosed
CN-116239492-A Continuous synthesis process of N-benzyl hydroxylamine hydrochloride 湖南华纳大药厂科技开发有限公司 2023-06-09 CN disclosed
EP-3863632-B1 QUINOLYLNITRONE FOR USE IN THE TREATMENT AND PREVENTION OF A CEREBRAL STROKE OR ISCHAEMIA ISQUAEMIA BIOTECH S L (ES) 2023-06-07 EP disclosed
CN-113292446-B Method for preparing N-benzylhydroxylamine hydrochloride with high yield 广州康瑞泰药业有限公司 2022-04-26 CN disclosed
CN-114292207-A Production process of N-benzylhydroxylamine hydrochloride 苏州诚和医药化学有限公司 2022-04-08 CN disclosed
WO-2000006525-A9 SYNTHESIS OF COMBINATORIAL LIBRARIES OF COMPOUNDS REMINISCENT OF NATURAL PRODUCTS HARVARD COLLEGE (US) 2000-04-20 WO disclosed
WO-2000006525-A2 SYNTHESIS OF COMBINATORIAL LIBRARIES OF COMPOUNDS REMINISCENT OF NATURAL PRODUCTS PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) 2000-02-10 WO disclosed
US-5998627-A Preparation and uses of hydrocarbylnitrones ALBEMARLE CORPORATION (US) 1999-12-07 US disclosed
WO-1999006362-A1 PREPARATION AND USES OF HYDROCARBYLNITRONES ALBEMARLE CORPORATION (US) 1999-02-11 WO disclosed
US-5122610-A Renin inhibitor intermediates BAYER AKTIENGESELLSCHAFT (DE) 1992-06-16 US disclosed
EP-0366560-A1 Tylosin derivatives, process for their preparation and pharmaceutical compositions containing them ADIR ET COMPAGNIE (FR) 1990-05-02 EP disclosed
US-4080340-A Nitroimidazoles MERCK & CO., INC. (US) 1978-03-21 US disclosed
US-4010176-A Isoxazole substituted nitroimidazoles MERCK & CO., INC. (US) 1977-03-01 US disclosed
US-4006225-A Method of using reduction products of everninomicins as antibacterial agents and pharmaceutical compositions useful therefor SCHERING CORPORATION (US) 1977-02-01 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-20240239771-A1 BACTERIAL EFFLUX PUMP INHIBITORS ABCB11, ABCB1, SLC47A1 CALM1 3712/4885CES2 543/4885CES1 504/4885

“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.