Sugi Predict

Sugi Predict / Compounds / SCHEMBL162559

SCHEMBL162559

SCHEMBL162559

Nc1c(C(=O)O)cccc1[N+](=O)[O-]

nearest known ligand 0.64

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ TSHR P16473 1/20 0.64
▸ CASP6 P55212 2/20 0.53
▸ G6PD P11413 1/20 0.53
▸ CASP7 P55210 1/20 0.53
▸ DNA2 P51530 1/20 0.51
▸ CTDSP1 Q9GZU7 1/20 0.51
▸ TDP1 Q9NUW8 3/20 0.50
▸ CTSD P07339 1/20 0.50
▸ L3MBTL1 Q9Y468 1/20 0.50
▸ ALDH1A1 P00352 4/20 0.49
▸ KDM4E B2RXH2 1/20 0.49
▸ MEN1 O00255 1/20 0.49
▸ GAA P10253 1/20 0.49
▸ MAPT P10636 1/20 0.49
▸ KMT2A Q03164 1/20 0.49
▸ GPR35 Q9HC97 1/20 0.48
▸ LMNA P02545 2/20 0.46
▸ CYP3A4 P08684 2/20 0.46
▸ ALOX15 P16050 1/20 0.46
▸ DTYMK P23919 1/20 0.45

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
SCHEMBL1509448 0.98 TSHR (0.62) TSHRCASP6G6PDCASP7DNA2
Hydrochloric Acid SCHEMBL27908306 0.98 TSHR (0.62) TSHRCASP6G6PDCASP7DNA2
SCHEMBL28935981 0.98 TSHR (0.62) TSHRCASP6G6PDCASP7DNA2
SCHEMBL1509450 0.98 TSHR (0.62) TSHRCASP6G6PDCASP7DNA2
SCHEMBL6206355 0.89 TSHR (0.55) TSHRCASP6DNA2CTDSP1TDP1
SCHEMBL8411975 0.87 TSHR (0.51) TSHRCASP6DNA2CTDSP1TDP1
SCHEMBL631453 0.85 ALDH1A1 (0.57) TSHRCASP6DNA2CTDSP1TDP1
SCHEMBL4245567 0.85 TSHR (0.55) TSHRCASP6G6PDCASP7DNA2
SCHEMBL1509449 0.84 TSHR (0.49) TSHRCASP6DNA2CTDSP1TDP1
SCHEMBL7907999 0.84 CTSD (0.53) TSHRTDP1CTSDL3MBTL1ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-122010739-A Synthesis method of 2-fluoro-3-nitrobenzoic acid 山东佰隆医药有限公司 2026-05-12 — — CN claimed
CN-115594592-B Preparation method and application of 2-chloro-3-nitrobenzoic acid 江西天宇化工有限公司 2024-03-19 — — CN claimed
CN-116730871-A Synthesis method of candesartan intermediate 湖北郡泰医药化工有限公司 2023-09-12 — — CN claimed
CN-115594592-A Preparation method and application of 2-chloro-3-nitrobenzoic acid 江西天宇化工有限公司（CN） 2023-01-13 — — CN claimed
CN-112028811-A 4-iodo-indole compound and preparation method thereof 平顶山学院 2020-12-04 — — CN claimed
CN-109403101-B Low-temperature stripping method for dyed fabric 河南工程学院 2020-09-29 — — CN claimed
CN-109281208-B Low-temperature white discharge printing method for cotton fabric 河南工程学院 2020-09-29 — — CN claimed
CN-109403100-B Preparation of disperse dye thiourea dioxide low-temperature reduction cleaning catalyst and reduction cleaning method 河南工程学院 2020-09-29 — — CN claimed
CN-109338747-B Dyeing method for reducing dye thiourea dioxide at low temperature 河南工程学院 2020-09-04 — — CN claimed
CN-109183387-B Low-temperature neutral reduction bleaching method for protein fiber 河南工程学院 2020-08-21 — — CN claimed
US-7539006-B2 Electrolytic solution for driving electrolytic capacitor and electrolytic capacitor RUBYCON CORPORATION (JP) 2009-05-26 — — US claimed
CN-100456398-C Electrolyte for driving electrolytic capacitor and electrolytic capacitor RUBYCON CORP (JP) 2009-01-28 — — CN claimed
US-20070121276-A1 Electrolytic solution for use in electrolytic capacitor, and electrolytic capacitor RUBYCON CORPORATION (JP) 2007-05-31 — — US claimed
EP-1760737-A1 ELECTROLYTE FOR DRIVING ELECTROLYTIC CAPACITOR AND ELECTROLYTIC CAPACITOR Rubycon Corporation (JP) 2007-03-07 — — EP claimed
US-20070029529-A1 Electrolytic solution for driving electrolytic capacitor and electrolytic capacitor KOMATSU AKIHIKO 2007-02-08 — — US claimed
US-20040245105-A1 Electrolyte solution for driving electrolytic capacitor and electrolytic capacitor RUBYCON CORPORATION (JP) 2004-12-09 — — US claimed
CN-1529892-A Electrolyte for driving electrolytic capacitor and electrolytic capacitor 如碧空株式会社 2004-09-15 — — CN claimed
EP-1437749-A1 ELECTROLYTE SOLUTION FOR DRIVING ELECTROLYTIC CAPACITOR AND ELECTROLYTIC CAPACITOR Rubycon Corporation (JP) 2004-07-14 — — EP claimed
US-6608193-B2 Forming an intermediate by reacting the support-bound amino-substituted-tetrahydroisoquinoline compound with a reagent; and cyclizatively cleaving support-bound amino-substituted-tetrahydroisoquinoline compound THE PROCTER & GAMBLE COMPANY 2003-08-19 — — US claimed
US-20020077480-A1 Methods for synthesis of amino-tetrahydroisoquinoline ring compounds PROCTER & GAMBLE COMPANY, THE 2002-06-20 — — US claimed

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-20020077480-A1 Methods for synthesis of amino-tetrahydroisoquinoline ring compounds ASNS, QPCT, DAO TSHR 4338/4885CASP6 1437/4885G6PD 2271/4885

“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.