SCHEMBL524803

SCHEMBL524803

CC(=O)N(C)c1cccc(C(=O)/C=C/N(C)C)c1

nearest known ligand 0.61

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
MAPT P10636 11/20 0.61
ALDH1A1 P00352 10/20 0.61
HTT P42858 4/20 0.61
GAA P10253 3/20 0.61
HPGD P15428 3/20 0.61
RECQL P46063 2/20 0.58
RAB9A P51151 5/20 0.56
LMNA P02545 3/20 0.49
CYP1A2 P05177 2/20 0.47
CYP2C19 P33261 2/20 0.47
ALOX12 P18054 1/20 0.47
TDP1 Q9NUW8 1/20 0.46
SMN1; SMN2 Q16637 3/20 0.46
NPC1 O15118 3/20 0.46
POLB P06746 2/20 0.46
HSP90AA1 P07900 1/20 0.46
KMT2A Q03164 1/20 0.43

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
SCHEMBL524804 1.00 MAPT (0.61) MAPTALDH1A1HTTGAAHPGD
SCHEMBL13916105 0.92 MAPT (0.56) MAPTALDH1A1HTTGAAHPGD
SCHEMBL9533849 0.88 RECQL (0.63) MAPTALDH1A1HTTGAAHPGD
SCHEMBL7367457 0.84 MAPT (0.57) MAPTALDH1A1HTTGAAHPGD
SCHEMBL7367460 0.84 MAPT (0.57) MAPTALDH1A1HTTGAAHPGD
SCHEMBL5946453 0.84 MAPT (0.77) MAPTALDH1A1HTTGAAHPGD
SCHEMBL31531972 0.83 MAPT (0.56) MAPTALDH1A1HTTGAAHPGD
SCHEMBL899889 0.83 MAPT (0.56) MAPTALDH1A1HTTGAAHPGD
SCHEMBL3162509 0.83 MAPT (0.56) MAPTALDH1A1HTTGAAHPGD
SCHEMBL6071233 0.82 MAPT (0.55) MAPTALDH1A1HTTGAAHPGD

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111747422-B Preparation method of ultrapure sodium silicate for silicon dioxide 安徽龙泉硅材料有限公司 2023-07-28 CN claimed
US-20120028045-A1 Processes for the Preparation of Indiplon and Intermediates Thereof GLENMARK GENERICS LTD (IN) 2012-02-02 US claimed
EP-1713808-B1 TWO-PHASE METHOD FOR THE SYNTHESIS OF SELECTED PYRAZOLOPYRIMIDINES MALLINCKRODT INC (US) 2010-02-24 EP claimed
US-7498434-B2 Two-phase method for the synthesis of selected pyrazolopyrimidines MALLINCKRODT INC (US) 2009-03-03 US claimed
US-20070155995-A1 Two-phase method for the synthesis of selected pyrazolopyrimidines MALLINCKRODT INC, (US) 2007-07-05 US claimed
CN-111747422-B Preparation method of ultrapure sodium silicate for silicon dioxide 安徽龙泉硅材料有限公司 2023-07-28 CN disclosed
CN-111747422-A Preparation method of ultrapure sodium silicate for silicon dioxide 安徽龙泉硅材料有限公司 2020-10-09 CN disclosed
US-20120028045-A1 Processes for the Preparation of Indiplon and Intermediates Thereof GLENMARK GENERICS LTD (IN) 2012-02-02 US disclosed
US-20120028045-A1 Processes for the Preparation of Indiplon and Intermediates Thereof GLENMARK GENERICS LTD (IN) 2012-02-02 US disclosed
US-20120028045-A1 Processes for the Preparation of Indiplon and Intermediates Thereof GLENMARK GENERICS LTD (IN) 2012-02-02 US disclosed
WO-2010109480-A2 PROCESSES FOR THE PREPARATION OF INDIPLON AND INTERMEDIATES THEREOF GLENMARK GENERICS LIMITED (IN) 2010-09-30 WO disclosed
WO-2010109480-A2 PROCESSES FOR THE PREPARATION OF INDIPLON AND INTERMEDIATES THEREOF GLENMARK GENERICS LIMITED (IN) 2010-09-30 WO disclosed
US-6399621-B1 SEDATIVE, HYPNOTIC, ANXIOLYTIC, ANTICONVULSANT, AND SKELETAL MUSCLE RELAXANT AGENT AMERICAN CYANAMID COMPANY 2002-06-04 US disclosed
US-5219857-A Method of treating cognitive and related neural behavioral problems AMERICAN CYANAMID COMPANY (US) 1993-06-15 US disclosed
US-5126340-A Antidepressants AMERICAN CYANAMID COMPANY (US) 1992-06-30 US disclosed
US-4963553-A TREATING COGNITIVE AND NEURAL BEHAVIORAL PROBLEMS IN MAMMALS AMERICAN CYANAMID CO. (US) 1990-10-16 US disclosed
US-4847256-A HYPOTENSIVE AGENTS AMERICAN CYANAMID COMPANY (US) 1989-07-11 US disclosed
EP-0264773-A1 4,5-dihydro and 4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidines AMERICAN CYANAMID COMPANY (US) 1988-04-27 EP disclosed
US-4521422-A ANTICONVULSANT, ANTIEPILEPTIC AGENTS, SEDATIVES, MUSCLE RELAXANTS AMERICAN CYANAMID COMPANY (US) 1985-06-04 US disclosed
EP-0129847-A2 Aryl and heteroaryl[7-(aryl and heteroaryl)-pyrazolo-[1,5-a]-pyrimidin-3-yl]methanones AMERICAN CYANAMID COMPANY (US) 1985-01-02 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-20120028045-A1 Processes for the Preparation of Indiplon and Intermediates Thereof CYP2D6, HLA-B, HLA-DRB1 MAPT 4124/4885ALDH1A1 406/4885HTT 748/4885
US-20070155995-A1 Two-phase method for the synthesis of selected pyrazolopyrimidines AZI2, CDK2, TPMT MAPT 1611/4885ALDH1A1 1128/4885HTT 2398/4885

“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.