SCHEMBL2484352

SCHEMBL2484352

CN(C)Cc1ccc(-c2cc3onc(-c4ccccc4)c3c(=O)n2C)cc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
NR4A2 P43354 7/20 1.00
DCTPP1 Q9H773 5/20 1.00
TSHR P16473 1/20 1.00
NPC1 O15118 4/20 0.76
RAB9A P51151 4/20 0.76
CASP3 P42574 1/20 0.76
SENP8 Q96LD8 1/20 0.76
SENP7 Q9BQF6 1/20 0.76
SENP6 Q9GZR1 1/20 0.76
MITF O75030 1/20 0.72

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
SCHEMBL2486400 0.90 NR4A2 (0.82) NR4A2DCTPP1TSHRNPC1RAB9A
SCHEMBL11614993 0.90 NR4A2 (0.82) NR4A2DCTPP1TSHRNPC1RAB9A
SCHEMBL11617213 0.90 NR4A2 (0.82) NR4A2DCTPP1TSHRNPC1RAB9A
SCHEMBL11617795 0.89 NR4A2 (0.79) NR4A2DCTPP1TSHRNPC1RAB9A
SCHEMBL5532304 0.87 NPC1 (0.95) NR4A2DCTPP1TSHRNPC1RAB9A
SCHEMBL3663640 0.87 NPC1 (1.00) NR4A2DCTPP1TSHRNPC1RAB9A
SCHEMBL5533836 0.87 NPC1 (0.80) NR4A2DCTPP1TSHRNPC1RAB9A
SCHEMBL6068778 0.86 NPC1 (0.78) NR4A2DCTPP1TSHRNPC1RAB9A
SCHEMBL6069212 0.85 NPC1 (0.81) NR4A2DCTPP1TSHRNPC1RAB9A
SCHEMBL5535403 0.85 NR4A2 (0.83) NR4A2DCTPP1TSHRNPC1RAB9A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2376079-B1 METHODS OF USING SUBSTITUTED ISOXAZOLO PYRIDINONES AS DISSOCIATED GLUCOCORTICOIDS VAN ANDEL RES INST (US) 2016-08-10 EP claimed
US-8173670-B2 Methods of using substituted isoxazolo pyridinones as dissociated glucocorticoids VAN ANDEL RESEARCH INSTITUTE (US) 2012-05-08 US claimed
EP-2376079-A1 METHODS OF USING SUBSTITUTED ISOXAZOLO PYRIDINONES AS DISSOCIATED GLUCOCORTICOIDS Van Andel Research Institute (US) 2011-10-19 EP claimed
US-20110251211-A9 METHODS OF USING SUBSTITUTED ISOXAZOLO PYRIDINONES AS DISSOCIATED GLUCOCORTICOIDS NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2011-10-13 US claimed
WO-2010083218-A1 METHODS OF USING SUBSTITUTED ISOXAZOLO PYRIDINONES AS DISSOCIATED GLUCOCORTICOIDS VAN ANDEL RESEARCH INSTITUTE (US) 2010-07-22 WO claimed
US-20100179167-A1 METHODS OF USING SUBSTITUTED ISOXAZOLO PYRIDINONES AS DISSOCIATED GLUCOCORTICOIDS VAN ANDEL RESEARCH INSTITUTE 2010-07-15 US claimed
US-4049813-A HYPOLIPIDEMIC AGENTS SANDOZ, INC. (US) 1977-09-20 US claimed
CN-102361640-B Isoxazole pyridone is in the purposes prepared in the medicine of the symptom alleviating or alleviating warm-blooded mammals arthritis and asthma 范安德尔研究所 2016-10-19 CN disclosed
EP-2376079-B1 METHODS OF USING SUBSTITUTED ISOXAZOLO PYRIDINONES AS DISSOCIATED GLUCOCORTICOIDS VAN ANDEL RES INST (US) 2016-08-10 EP disclosed
US-8173670-B2 Methods of using substituted isoxazolo pyridinones as dissociated glucocorticoids VAN ANDEL RESEARCH INSTITUTE (US) 2012-05-08 US disclosed
US-8173670-B2 Methods of using substituted isoxazolo pyridinones as dissociated glucocorticoids VAN ANDEL RESEARCH INSTITUTE (US) 2012-05-08 US disclosed
US-8173670-B2 Methods of using substituted isoxazolo pyridinones as dissociated glucocorticoids VAN ANDEL RESEARCH INSTITUTE (US) 2012-05-08 US disclosed
CN-102361640-A Methods of using substituted isoxazolo pyridinones as dissociated glucocorticoids VAN ANDEL RES INST 2012-02-22 CN disclosed
US-20060003975-A1 Combination of an aldosterone receptor antagonist and an HMG CoA reductase inhibitor PHARMACIA CORPORATION 2006-01-05 US disclosed
CN-1537019-A Medical combination of aldosterone receptor antagonist and HMG CoA reductase inhibitor �ź㴫 2004-10-13 CN disclosed
CN-1527709-A Therapeutic combination for cardiovascular and inflammatory indications 2004-09-08 CN disclosed
US-6264938-B1 ADMINISTERING POLYDIALLYLAMINE AND HYDROXY-3-METHYLGLUTARYL/3-/, COENZYME A REDUCTASE GELTEX PHARMACEUTICALS, INC. 2001-07-24 US disclosed
US-4154928-A Substituted isoxazolo compounds SANDOZ, INC. (US) 1979-05-15 US disclosed
US-4086421-A HYPOLIPIDEMIC AGENTS SANDOZ, INC. (US) 1978-04-25 US disclosed
US-4049813-A HYPOLIPIDEMIC AGENTS SANDOZ, INC. (US) 1977-09-20 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 (3 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-20100179167-A1 METHODS OF USING SUBSTITUTED ISOXAZOLO PYRIDINONES AS DISSOCIATED GLUCOCORTICOIDS NR3C1, NR3C2, PDXK NR4A2 67/4885DCTPP1 2528/4885TSHR 442/4885
US-20060003975-A1 Combination of an aldosterone receptor antagonist and an HMG CoA reductase inhibitor HMGCR, NR3C2, LDLR NR4A2 449/4885DCTPP1 4608/4885TSHR 316/4885
US-20110251211-A9 METHODS OF USING SUBSTITUTED ISOXAZOLO PYRIDINONES AS DISSOCIATED GLUCOCORTICOIDS NR3C1, NR3C2, PDXK NR4A2 67/4885DCTPP1 2528/4885TSHR 442/4885

“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.