SCHEMBL5892

SCHEMBL5892

O=P(O)(Cl)N(c1ccccc1)c1ccccc1

nearest known ligand 0.52

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HTT P42858 2/20 0.44
KMT2A Q03164 2/20 0.44
MEN1 O00255 1/20 0.44
CA2 P00918 1/20 0.42
CA4 P22748 1/20 0.42
CA5A P35218 1/20 0.42
NPSR1 Q6W5P4 2/20 0.41
ALDH1A1 P00352 2/20 0.39
NPC1 O15118 1/20 0.39
POLB P06746 1/20 0.39
RAB9A P51151 1/20 0.39
TDP1 Q9NUW8 1/20 0.38
L3MBTL1 Q9Y468 1/20 0.38
SRC P12931 2/20 0.38
CFTR P13569 1/20 0.38
PTPN1 P18031 1/20 0.37
PTPN5 P54829 1/20 0.36
KCNA5 P22460 1/20 0.36
ALOX15 P16050 2/20 0.36
TSHR P16473 1/20 0.35

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
SCHEMBL8530739 0.80 MEN1 (0.48) HTTKMT2AMEN1CA2CA4
SCHEMBL2309806 0.80 MEN1 (0.48) HTTKMT2AMEN1CA2CA4
SCHEMBL27651298 0.80 HTT (0.48) HTTKMT2AMEN1CA2CA4
SCHEMBL7526246 0.80 HTT (0.48) HTTKMT2AMEN1CA2CA4
Hydrochloric Acid SCHEMBL27627985 0.78 MEN1 (0.46) HTTKMT2AMEN1CA2CA4
SCHEMBL9386233 0.76 SRC (0.43) HTTKMT2AMEN1CA2CA4
SCHEMBL8370301 0.74 HTT (0.59) HTTKMT2AMEN1CA2CA4
Phosphoric Acid SCHEMBL1242659 0.72 ALDH1A1 (0.50) HTTKMT2AMEN1CA2CA4
Phosphoric Acid SCHEMBL29898200 0.72 ALDH1A1 (0.50) HTTKMT2AMEN1CA2CA4
SCHEMBL6748159 0.71 POLB (0.39) HTTKMT2AMEN1CA2CA4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2024075736-A1 NITROGEN-CONTAINING COMPOUND, COMPOSITION COMPRISING SAID NITROGEN-CONTAINING COMPOUND, AND MARKER FOR PREDICTING TUMOR GRADE 学校法人関西医科大学 2024-04-11 WO disclosed
US-20080293701-A1 1-Acylamino-2-Hydroxy-3-Amino- -Arylalkanes as Renin Inhibitors VITAE PHARMACEUTICALS, INC. 2008-11-27 US disclosed
US-7329660-B2 Phthalazine derivatives for treating inflammatory diseases NOVARTIS AG (CH) 2008-02-12 US disclosed
EP-1844002-A1 1-ACYLAMINO-2-HYDROXY-3-AMINO-W-ARYLALKANES AS RENIN INHIBITORS Vitae Pharmaceuticals, Inc. (US) 2007-10-17 EP disclosed
US-7115777-B2 Amide derivatives as inhibitors of the enzymatic activity of renin NOVARTIS AG (CH) 2006-10-03 US disclosed
US-20060217388-A1 Phthalazine derivatives for treating inflammatory diseases BOLD GUIDO 2006-09-28 US disclosed
WO-2006083924-A1 1-ACYLAMINO-2-HYDROXY-3-AMINO-W-ARYLALKANES AS RENIN INHIBITORS VITAE PHARMACEUTICALS, INC. (US) 2006-08-10 WO disclosed
US-20060154926-A1 Methods of treating alzheimer's disease using aryl alkanoic acid amides ELAN PHARMACEUTICALS, INC. 2006-07-13 US disclosed
EP-1165085-B1 PHTHALAZINE DERIVATIVES FOR TREATING INFLAMMATORY DISEASES NOVARTIS AG (CH) 2006-06-14 EP disclosed
US-20060089355-A1 Methods of treating alzheimer's disease using aromatically substituted w-amino-alkanoic acid amides and alkanoic acid diamides ELAN PHARMACEUTICALS, INC. 2006-04-27 US disclosed
US-4595677-A Substituted tetrapeptides CIBA-GEIGY CORPORATION (US) 1986-06-17 US disclosed
EP-0184550-A2 5-Amino-4-hydroxy valeryl amide derivatives CIBA-GEIGY AG (CH) 1986-06-11 EP disclosed
EP-0175570-A2 Process for the preparation of aromatic-1,4-oxazepinones and thiones A.H. ROBINS COMPANY, INCORPORATED (a Delaware corporation) (US) 1986-03-26 EP disclosed
EP-0144290-A2 Substituted ethylenediamine derivatives CIBA-GEIGY AG (CH) 1985-06-12 EP disclosed
EP-0143746-A2 5-Amino 4-hydroxy-valeryl-substituted derivatives CIBA-GEIGY AG (CH) 1985-06-05 EP disclosed
US-4483977-A TETRAMINOBIPHENYL AND ISOPHTHALIC ACID CELANESE CORPORATION (US) 1984-11-20 US disclosed
EP-0111266-A2 Substituted tetrapeptides CIBA-GEIGY AG (CH) 1984-06-20 EP disclosed
US-4452967-A MELT POLYMERIZATION OF AROMATIC CARBOXY DIAMINE CELANESE CORPORATION (US) 1984-06-05 US disclosed
EP-0095348-A2 High molecular weight polybenzimidazoles CELANESE CORPORATION (US) 1983-11-30 EP disclosed
US-4414383-A High molecular weight polybenzimidazole preparation with phosphorus containing polymerization catalyst CELANESE CORPORATION (US) 1983-11-08 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 (4 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-20060217388-A1 Phthalazine derivatives for treating inflammatory diseases KDR, NR2E3, FLT1 HTT 1544/4885KMT2A 2072/4885MEN1 3878/4885
US-20060089355-A1 Methods of treating alzheimer's disease using aromatically substituted w-amino-alkanoic acid amides and alkanoic acid diamides APP, BACE1, BACE2 HTT 161/4885KMT2A 2309/4885MEN1 1992/4885
US-20060154926-A1 Methods of treating alzheimer's disease using aryl alkanoic acid amides BACE1, APP, PSEN1 HTT 133/4885KMT2A 2294/4885MEN1 3795/4885
US-20080293701-A1 1-Acylamino-2-Hydroxy-3-Amino- -Arylalkanes as Renin Inhibitors REN, AGTR1, AGTR2 HTT 1710/4885KMT2A 2789/4885MEN1 4386/4885

“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.