SCHEMBL1962245

SCHEMBL1962245

NC(=O)c1n[nH]c2ccccc2c1=O

nearest known ligand 0.54

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ CYP1A2 P05177 1/20 0.54
▸ KDM4E B2RXH2 5/20 0.53
▸ YTHDC1 Q96MU7 1/20 0.53
▸ STAT3 P40763 1/20 0.53
▸ HIF1A Q16665 1/20 0.53
▸ NPC1 O15118 4/20 0.51
▸ RAB9A P51151 4/20 0.51
▸ ALDH1A1 P00352 2/20 0.51
▸ TP53 P04637 1/20 0.51
▸ FLT3 P36888 2/20 0.50
▸ CDK2 P24941 2/20 0.50
▸ CCNA2 P20248 1/20 0.50
▸ CCNA1 P78396 1/20 0.50
▸ CTNNB1 P35222 3/20 0.49
▸ WNT3A P56704 3/20 0.49
▸ PDPK1 O15530 1/20 0.48
▸ CYP3A4 P08684 1/20 0.48
▸ GAA P10253 1/20 0.48
▸ IDO1 P14902 1/20 0.48
▸ EPHB3 P54753 1/20 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
SCHEMBL27750743 0.87 KDM4E (0.62) KDM4EYTHDC1STAT3HIF1ANPC1
SCHEMBL82761 0.87 KDM4E (0.62) KDM4EYTHDC1STAT3HIF1ANPC1
Hydrochloric Acid SCHEMBL5071439 0.86 KDM4E (0.60) KDM4EYTHDC1STAT3HIF1ANPC1
SCHEMBL28139037 0.86 KDM4E (0.60) KDM4EYTHDC1STAT3HIF1ANPC1
Hydrochloric Acid SCHEMBL30404733 0.86 KDM4E (0.60) KDM4EYTHDC1STAT3HIF1ANPC1
Hydrochloric Acid SCHEMBL29962256 0.86 KDM4E (0.60) KDM4EYTHDC1STAT3HIF1ANPC1
Hydrochloric Acid SCHEMBL2175299 0.86 KDM4E (0.60) KDM4EYTHDC1STAT3HIF1ANPC1
SCHEMBL5908296 0.84 KDM4E (0.57) CYP1A2KDM4EYTHDC1STAT3HIF1A
Oxalic Acid SCHEMBL6033591 0.83 FLT3 (0.58) KDM4EYTHDC1STAT3HIF1ANPC1
SCHEMBL8067938 0.83 CYP1A2 (0.54) CYP1A2KDM4EYTHDC1STAT3HIF1A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11911364-B2 Positive allosteric modulators of GABAA receptor PEPTICOM LTD. (IL) 2024-02-27 — — US disclosed
US-20210353592-A1 POSITIVE ALLOSTERIC MODULATORS OF GABAA RECEPTOR PEPTICOM LTD. (IL) 2021-11-18 — — US disclosed
US-20200283502-A1 POSITIVE ALLOSTERIC MODULATORS OF GABA A RECEPTOR PEPTICOM LTD. (IL) 2020-09-10 — — US disclosed
WO-2020065642-A1 POSITIVE ALLOSTERIC MODULATORS OF GABAA RECEPTOR PEPTICOM LTD. (IL) 2020-04-02 — — WO disclosed
WO-2019058349-A1 POSITIVE ALLOSTERIC MODULATORS OF GABA A RECEPTOR PEPTICOM LTD (IL) 2019-03-28 — — WO disclosed
EP-1966158-B1 SUBSTITUTED CINNOLINE DERIVATIVES AS GABAA-RECEPTOR MODULATORS AND METHOD FOR THEIR SYNTHESIS ASTRAZENECA AB (SE) 2012-08-08 — — EP disclosed
US-20110144331-A1 Cinnoline Compounds for the Treatment of Anxiety, Cognitive and Mood Disorders ASTRAZENECA AB (SE) 2011-06-16 — — US disclosed
US-20100184738-A1 Uses of cinnoline compounds to treat schizophrenia ASTRAZENECA AB (SE) 2010-07-22 — — US disclosed
EP-2167091-A1 CINNOLINE COMPOUNDS FOR USE IN THE TREATMENT OF SCHIZOPHRENIA AstraZeneca AB (SE) 2010-03-31 — — EP disclosed
US-20090036454-A1 Compounds and Uses Thereof ASTRAZENECA AB (SE) 2009-02-05 — — US disclosed
EP-1265873-A2 4-OXO-1,4-DIHYDRO-3-CINNOLINECARBOXAMIDES AS ANTIVIRAL AGENTS PHARMACIA & UPJOHN COMPANY (US) 2002-12-18 — — EP disclosed
US-20020045619-A1 4-oxo-1,4-dihydro-3-cinnolinecarboxamides as antiviral agents PHARMACIA & UPJOHN COMPANY 2002-04-18 — — US disclosed
US-20020045619-A1 4-oxo-1,4-dihydro-3-cinnolinecarboxamides as antiviral agents PHARMACIA & UPJOHN COMPANY 2002-04-18 — — US disclosed
WO-2001070706-A2 4-OXO-1,4-DIHYDRO-3-CINNOLINECARBOXAMIDES AS ANTIVIRAL AGENTS PHARMACIA & UPJOHN COMPANY (US) 2001-09-27 — — WO disclosed
EP-0328282-B1 PHARMACEUTICAL ICI AMERICAS INC. (US) 1992-08-19 — — EP disclosed
EP-0205272-B1 CINNOLINE DERIVATIVES ICI AMERICAS INC. (US) 1991-08-14 — — EP disclosed
US-4925844-A ADMINISTERING 4-AMINO-8-PHENYL-N-PROPYL-3-CINNOLINECARBOXAMIDE ICI AMERICAS INC. (US) 1990-05-15 — — US disclosed
US-4886800-A Substituted cinnoline derivatives as CNS depressants ICI AMERICAS INC. (US) 1989-12-12 — — US disclosed
EP-0328282-A2 Pharmaceutical ICI AMERICAS INC. (US) 1989-08-16 — — EP disclosed
EP-0205272-A2 Cinnoline derivatives ICI AMERICAS INC. (US) 1986-12-17 — — 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 (7 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-20210353592-A1 POSITIVE ALLOSTERIC MODULATORS OF GABAA RECEPTOR GABRP, GABRB2, GABRB1 CYP1A2 1134/4885KDM4E 2877/4885YTHDC1 4832/4885
US-11911364-B2 Positive allosteric modulators of GABAA receptor GABRP, GABRB2, GABRB1 CYP1A2 1134/4885KDM4E 2877/4885YTHDC1 4832/4885
US-20110144331-A1 Cinnoline Compounds for the Treatment of Anxiety, Cognitive and Mood Disorders HTR7, HTR2C, CRH CYP1A2 455/4885KDM4E 3855/4885YTHDC1 4868/4885
US-20020045619-A1 4-oxo-1,4-dihydro-3-cinnolinecarboxamides as antiviral agents ZC3HAV1, ZC3HAV1L, EIF2AK2 CYP1A2 1659/4885KDM4E 1153/4885YTHDC1 679/4885
US-20200283502-A1 POSITIVE ALLOSTERIC MODULATORS OF GABA A RECEPTOR GABRB3, GABRB1, GABRB2 CYP1A2 1785/4885KDM4E 570/4885YTHDC1 2288/4885
US-20090036454-A1 Compounds and Uses Thereof MAPT, BDNF, PYGB CYP1A2 428/4885KDM4E 3031/4885YTHDC1 4774/4885
US-20100184738-A1 Uses of cinnoline compounds to treat schizophrenia COMT, BACE1, CHAT CYP1A2 367/4885KDM4E 4245/4885YTHDC1 4842/4885

“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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