P-Nitrophenol

P-Nitrophenol

SCHEMBL1324262

O=S(=O)(O)C(F)(F)F.O=[N+]([O-])c1ccc(O)cc1

nearest known ligand 0.67

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CA1 P00915 6/20 0.50
CA2 P00918 6/20 0.50
CA9 Q16790 5/20 0.50
CA5A P35218 4/20 0.50
HSD11B1 P28845 1/20 0.46
PTGS1 P23219 1/20 0.46
PTGS2 P35354 1/20 0.46
MMP1 P03956 1/20 0.46
MMP2 P08253 1/20 0.46
MMP9 P14780 1/20 0.46
MMP8 P22894 1/20 0.46
MMP13 P45452 1/20 0.46
CA12 O43570 4/20 0.46
CA14 Q9ULX7 4/20 0.46
CA3 P07451 3/20 0.46
CA4 P22748 3/20 0.46
CA6 P23280 3/20 0.46
CA7 P43166 3/20 0.46
CA13 Q8N1Q1 3/20 0.46
CA5B Q9Y2D0 3/20 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
P-Nitrophenol SCHEMBL2906482 0.86 CA1 (0.54) CA1CA2CA9CA5APTGS1
Trifluoromethanesulfonic Acid SCHEMBL28570941 0.85 CA1 (0.50) CA1CA2CA9CA5AHSD11B1
4-Nitroaniline SCHEMBL28189154 0.84 ALDH1A1 (0.64) CA1CA2CA9CA5AHSD11B1
Trifluoromethanesulfonic Acid SCHEMBL4574955 0.84 CA1 (0.49) CA1CA2CA9CA5AHSD11B1
Trifluoromethanesulfonic Acid SCHEMBL22389552 0.84 CA1 (0.49) CA1CA2CA9CA5AHSD11B1
Nitrobenzene SCHEMBL2888054 0.83 ALDH1A1 (0.61) CA1CA2CA9CA5AHSD11B1
Trifluoromethanesulfonic Acid SCHEMBL576036 0.82 LMNA (0.52) CA1CA2CA9CA5APTGS1
P-Nitrophenol SCHEMBL29806213 0.82 CES1 (0.58) CA1CA2PTGS1PTGS2CES1
P-Nitrophenol SCHEMBL11048842 0.82 CES1 (0.58) CA1CA2PTGS1PTGS2CES1
P-Nitrophenol SCHEMBL1839 0.82 CES1 (0.58) CA1CA2PTGS1PTGS2CES1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111517902-B Aerobic oxidation system containing sulfinic acid, sulfonic acid or derivatives thereof and photo-oxidation promoting method thereof 清华大学 2022-06-14 CN disclosed
CN-111517902-A Aerobic oxidation system containing sulfinic acid, sulfonic acid or derivatives thereof and photo-oxidation promoting method thereof 清华大学 2020-08-11 CN disclosed
WO-2020155595-A1 AEROBIC OXIDATION SYSTEM CONTAINING SULFINIC ACID, SULFONIC ACID OR DERIVATIVES THEREOF AND PHOTOCATALYTIC OXIDATION METHOD THEREFOR 清华大学 2020-08-06 WO disclosed
CN-102093150-B Method for synthesizing aromatic amine BEIJING INST TECHNOLOGY 2013-10-09 CN disclosed
EP-1937689-B1 INTERMEDIATE AND PROCESS OF PREPARATION OF ECTEINASCIDINS SUCH AS ECTEINASCIDINS 583 AND 597 USING SUCH INTERMEDIATE CENTRE NAT RECH SCIENT (FR) 2012-04-18 EP disclosed
US-8058435-B2 Intermediate and process of preparation of ecteinascidin such as ecteinascidines-583,597 using such intermediate CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (CNRS) (FR) 2011-11-15 US disclosed
US-7999090-B2 reporter system reflecting the transport process that transports GPI-anchored proteins to the cell wall was constructed and compounds inhibiting this process were discovered; antifungal agents; inhibiting expression of cell wall glycoproteins and preventing pathogens from showing pathogenicity; DNA EISAI CO., LTD (JP) 2011-08-16 US disclosed
CN-102093150-A Method for synthesizing aromatic amine BEIJING INST TECHNOLOGY 2011-06-15 CN disclosed
US-7928209-B2 reporter system reflecting the transport process that transports GPI-anchored proteins to the cell wall was constructed and compounds inhibiting this process were discovered; antifungal agents; inhibiting expression of cell wall glycoproteins and preventing pathogens from showing pathogenicity; DNA EISAI R & D MANAGEMENT CO. LTD. (JP) 2011-04-19 US disclosed
US-7910712-B2 Fungal cell wall synthesis gene EISAI R&D MANAGEMENT CO., LTD (JP) 2011-03-22 US disclosed
US-7375204-B2 Fungal cell wall synthesis gene EISAI R&D MANAGEMENT CO., LTD. (JP) 2008-05-20 US disclosed
EP-1792904-A1 Intermediate and process of preparation of ecteinascidin using such intermediate Centre National de la Recherche Scientifique (CNRS) (FR) 2007-06-06 EP disclosed
CN-1873002-A Fungal cell wall synthesis gene EISAI CO LTD (JP) 2006-12-06 CN disclosed
CN-1873003-A Fungal cell wall synthesis gene EISAI CO LTD (JP) 2006-12-06 CN disclosed
US-20060234283-A1 Fungal cell wall synthesis gene EISAI CO., LTD. (JP) 2006-10-19 US disclosed
US-20060234349-A1 Fungal cell wall synthesis gene EISAI CO., LTD. (JP) 2006-10-19 US disclosed
CN-1249227-C Fungal cell wall synthetic genes EISAI CO LTD (JP) 2006-04-05 CN disclosed
US-20040038239-A1 Fungal cell wall synthesis gene EISAI CO., LTD. (JP) 2004-02-26 US disclosed
CN-1449443-A Fungal cell wall synthetic genes EISAI CO LTD (JP) 2003-10-15 CN disclosed
EP-1300464-A1 FUNGAL CELL WALL SYNTHESIS GENE Eisai Co., Ltd. (JP) 2003-04-09 EP 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 (2 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-20040038239-A1 Fungal cell wall synthesis gene ERG28, GPI, DPM1 CA1 4497/4885CA2 3944/4885CA9 3394/4885
US-20060234349-A1 Fungal cell wall synthesis gene ERG28, GPI, DPM1 CA1 4497/4885CA2 3944/4885CA9 3394/4885

“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.