SCHEMBL1509271

SCHEMBL1509271

O=C(O)C(O)C(O)C(=O)Nc1ccccc1[N+](=O)[O-]

nearest known ligand 0.58

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ KMT2A Q03164 2/20 0.58
▸ MEN1 O00255 1/20 0.58
▸ PHGDH O43175 1/20 0.54
▸ RAB9A P51151 3/20 0.52
▸ GAA P10253 2/20 0.52
▸ CYP3A4 P08684 1/20 0.52
▸ CYP2C9 P11712 1/20 0.52
▸ CYP2C19 P33261 1/20 0.52
▸ NPSR1 Q6W5P4 1/20 0.52
▸ TP53 P04637 1/20 0.52
▸ KCNMA1 Q12791 1/20 0.51
▸ NPC1 O15118 3/20 0.51
▸ MAPT P10636 2/20 0.51
▸ L3MBTL1 Q9Y468 2/20 0.51
▸ ALDH1A1 P00352 2/20 0.50
▸ POLB P06746 1/20 0.50
▸ CXCR1 P25024 1/20 0.49
▸ CXCR2 P25025 1/20 0.49
▸ MAPK1 P28482 1/20 0.49
▸ CASP7 P55210 1/20 0.49

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
SCHEMBL11758703 1.00 KMT2A (0.58) KMT2AMEN1PHGDHRAB9AGAA
SCHEMBL11758088 1.00 KMT2A (0.58) KMT2AMEN1PHGDHRAB9AGAA
Quinoline SCHEMBL11096417 0.86 NPC1 (0.51) KMT2AMEN1PHGDHRAB9AGAA
Isoquinoline SCHEMBL10997368 0.86 NPC1 (0.46) KMT2AMEN1PHGDHRAB9AGAA
Cadaverine Tartrate SCHEMBL28015425 0.82 CYP1A2 (0.56) KMT2AMEN1MAPTL3MBTL1ALDH1A1
SCHEMBL11332310 0.80 KMT2A (0.73) KMT2AMEN1PHGDHRAB9AGAA
SCHEMBL4729142 0.80 KMT2A (0.63) KMT2AMEN1PHGDHRAB9AGAA
SCHEMBL13390947 0.80 KMT2A (0.63) KMT2AMEN1PHGDHRAB9AGAA
SCHEMBL175272 0.79 MEN1 (0.71) KMT2AMEN1PHGDHRAB9AGAA
SCHEMBL113558 0.79 MEN1 (0.71) KMT2AMEN1PHGDHRAB9AGAA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-4556712-A OPTICAL RESOLUTION THROUGH SALT FORMATION AND SOLUBILITY THE UNITED STATES OF AMERICA AS REPRESENTED BY THE SECRETARY OF THE DEPARTMENT OF HEALTH AND HUMAN SERVICES (US) 1985-12-03 — — US claimed
EP-0079383-A4 PREPARATION OF CHIRAL 1-BENZYL-1,2,3,4-TETRAHYDROISOQUINOLINES BY OPTICAL RESOLUTION. US SECRETARY UNITED STATES DEP (US) 1984-01-12 — — EP claimed
EP-0079383-A1 PREPARATION OF CHIRAL 1-BENZYL-1,2,3,4-TETRAHYDROISOQUINOLINES BY OPTICAL RESOLUTION THE UNITED STATES OF AMERICA as represented by the Secretary UNITED STATES DEPARTMENT OF COMMERCE (US) 1983-05-25 — — EP claimed
WO-1982004049-A1 PREPARATION OF CHIRAL 1-BENZYL-1,2,3,4-TETRAHYDROISOQUINOLINES BY OPTICAL RESOLUTION US HEALTH (US) 1982-11-25 — — WO claimed
US-8158796-B2 Process for the preparation of Rho-kinase inhibitor compounds INSPIRE PHARMACEUTICALS, INC. (US) 2012-04-17 — — US disclosed
EP-2291077-A1 PROCESS FOR THE PREPARATION OF RHO-KINASE INHIBITOR COMPOUNDS Inspire Pharmaceuticals, Inc. (US) 2011-03-09 — — EP disclosed
EP-1638970-B1 PYRID (2, 1-A) - ISOQUINOLINE DERIVATIVES AS DPP-IV INHIBITORS HOFFMANN LA ROCHE (CH) 2010-11-24 — — EP disclosed
US-20100022775-A1 PROCESS FOR THE PREPARATION OF RHO-KINASE INHIBITOR COMPOUNDS INSPIRE PHARMACEUTICALS, INC. 2010-01-28 — — US disclosed
WO-2009154940-A1 PROCESS FOR THE PREPARATION OF RHO-KINASE INHIBITOR COMPOUNDS INSPIRE PHARMACEUTICALS, INC. (US) 2009-12-23 — — WO disclosed
US-7122555-B2 Pyrido [2,1-a] isoquinoline derivatives HOFFMANN-LA ROCHE INC. (US) 2006-10-17 — — US disclosed
EP-1638970-A1 PYRID (2, 1-A) - ISOQUINOLINE DERIVATIVES AS DPP-IV INHIBITORS F. HOFFMANN-LA ROCHE AG (CH) 2006-03-29 — — EP disclosed
WO-2005000848-A1 PYRIDO` 2, 1-A - ISOQUINOLINE DERIVATIVES AS DPP-IV INHIBITORS F. HOFFMANN-LA ROCHE AG (CH) 2005-01-06 — — WO disclosed
US-4410700-A Preparation of chiral 1-benzyl-1,2,3,4-tetrahydroisoquinolines by optical resolution THE UNITED STATES OF AMERICA AS REPRESENTED BY THE DEPARTMENT OF HEALTH AND HUMAN SERVICES (US) 1983-10-18 — — US disclosed
EP-0079383-A1 PREPARATION OF CHIRAL 1-BENZYL-1,2,3,4-TETRAHYDROISOQUINOLINES BY OPTICAL RESOLUTION THE UNITED STATES OF AMERICA as represented by the Secretary UNITED STATES DEPARTMENT OF COMMERCE (US) 1983-05-25 — — EP disclosed
WO-1982004049-A1 PREPARATION OF CHIRAL 1-BENZYL-1,2,3,4-TETRAHYDROISOQUINOLINES BY OPTICAL RESOLUTION US HEALTH (US) 1982-11-25 — — WO disclosed
US-4162316-A ANALGESICS DAINIPPON PHARMACEUTICAL CO., LTD. (JP) 1979-07-24 — — US disclosed
US-4105695-A LEARNING ENHANCEMENT, IMPROVES MENTAL ALERTNESS OF GERIATRICS BRISTOL-MYERS COMPANY (US) 1978-08-08 — — US disclosed
US-4080453-A ANALGESICS, ANTITUSSIVE DAINIPPON PHARMACEUTICAL CO., LTD. (JA) 1978-03-21 — — US disclosed
US-4034113-A Treatment of senile geriatric patients to restore performance SHULGIN ALEXANDER T 1977-07-05 — — US disclosed
US-3988456-A ANALGESICS, ANTITUSSIVE DAINIPPON PHARMACEUTICAL CO., LTD. (JA) 1976-10-26 — — 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-20100022775-A1 PROCESS FOR THE PREPARATION OF RHO-KINASE INHIBITOR COMPOUNDS ROCK1, ROCK2, RHOA KMT2A 2945/4885MEN1 2053/4885PHGDH 2558/4885

“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.

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