SCHEMBL38206

SCHEMBL38206

COC(=O)c1cccc(Br)n1

nearest known ligand 0.59

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPT P10636 4/20 0.59
CYP1A2 P05177 3/20 0.59
GAA P10253 1/20 0.59
RECQL P46063 1/20 0.59
SMN1; SMN2 Q16637 2/20 0.51
GRM5 P41594 2/20 0.51
NPC1 O15118 2/20 0.51
RAB9A P51151 2/20 0.51
TP53 P04637 1/20 0.51
CYP3A4 P08684 1/20 0.51
CYP2C9 P11712 1/20 0.51
CYP2C19 P33261 1/20 0.51
ALDH1A1 P00352 3/20 0.49
HPGD P15428 2/20 0.49
IRAK4 Q9NWZ3 1/20 0.48
MEN1 O00255 1/20 0.44
KMT2A Q03164 1/20 0.44
CA12 O43570 1/20 0.44
CA1 P00915 1/20 0.44
CA2 P00918 1/20 0.44

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
SCHEMBL29457944 1.00 MAPT (0.59) MAPTCYP1A2GAARECQLSMN1; SMN2
SCHEMBL17258327 0.90 MAPT (0.54) MAPTCYP1A2GAARECQLSMN1; SMN2
SCHEMBL25434694 0.86 MAPT (0.48) MAPTCYP1A2GAARECQLSMN1; SMN2
SCHEMBL69653 0.86 MAPT (0.64) MAPTCYP1A2GAARECQLSMN1; SMN2
SCHEMBL31264286 0.81 MAPT (0.55) MAPTCYP1A2GAARECQLSMN1; SMN2
SCHEMBL875715 0.81 MAPT (0.55) MAPTCYP1A2GAARECQLSMN1; SMN2
SCHEMBL27633761 0.81 GRM5 (0.47) MAPTCYP1A2GAARECQLSMN1; SMN2
SCHEMBL594691 0.80 GRM5 (0.44) MAPTCYP1A2GAARECQLSMN1; SMN2
SCHEMBL22940095 0.80 MAPT (0.64) MAPTCYP1A2GAARECQLGRM5
SCHEMBL31746517 0.80 GRM5 (0.44) MAPTCYP1A2GAARECQLSMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-106749189-A A kind of pyridine radicals bridging NNN bimetallics part and its synthetic method 中国科学院大连化学物理研究所 2017-05-31 CN claimed
EP-4225762-B1 MODULATORS OF CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR VERTEX PHARMA (US) 2026-05-27 EP disclosed
EP-4212523-B1 PYRAZOLE AMIDE COMPOUNDS AS IRAK INHIBITORS RIGEL PHARMACEUTICALS INC (US) 2026-05-06 EP disclosed
US-12612416-B2 Modulators of cystic fibrosis transmembrane conductance regulator VERTEX PHARMACEUTICALS INCORPORATED (US) 2026-04-28 US disclosed
US-20260076962-A1 LANTHIONINE SYNTHETASE C-LIKE 2-BASED THERAPEUTICS NIMMUNE BIOPHARMA, INC. (US) 2026-03-19 US disclosed
EP-3867249-B1 (ISOPROPYL-TRIAZOLYL)PYRIDINYL-SUBSTITUTED BENZOTHIAZINONE DERIVATIVES AS ASK1 INHIBTORS FOR THE TREATMENT OF METABOLIC DISORDERS HK INNO N CORP (KR) 2026-03-04 EP disclosed
US-12565491-B2 (Isopropyl-triazolyl)pyridinyl-substituted benzooxazinone or benzothiazinone derivatives and use thereof HK INNO.N CORPORATION (KR) 2026-03-03 US disclosed
US-20260042749-A1 IRAK DEGRADERS AND USES THEREOF KYMERA THERAPEUTICS, INC. 2026-02-12 US disclosed
US-12545689-B2 Macrocyclic LRRK2 kinase inhibitors ONCODESIGN PRECISION MEDICINE (FR) 2026-02-10 US disclosed
US-12545659-B2 IRAK degraders and uses thereof KYMERA THERAPEUTICS, INC. (US) 2026-02-10 US disclosed
US-20020151715-A1 Imidazole derivatives EVOTEC INTERNATIONAL GMBH (DE) 2002-10-17 US disclosed
US-20020143034-A1 Aminoalcohol derivatives and their use as beta 3 adrenergic agonists FUJISAWA PHARMACEUTICAL CO. LTD. (JP) 2002-10-03 US disclosed
WO-2002060877-A1 IMIDAZOLE DERIVATIVES F. HOFFMANN-LA ROCHE AG (CH) 2002-08-08 WO disclosed
EP-1140849-A1 AMINOALCOHOL DERIVATIVES AND THEIR USE AS BETA 3 ADRENERGIC AGONISTS FUJISAWA PHARMACEUTICAL CO., LTD. (JP) 2001-10-10 EP disclosed
WO-2001042217-A1 BETA-3 ADRENOCEPTOR AGONISTS GLAXO GROUP LIMITED (GB) 2001-06-14 WO disclosed
WO-2000040560-A1 AMINOALCOHOL DERIVATIVES AND THEIR USE AS BETA 3 ADRENERGIC AGONISTS FUJISAWA PHARMACEUTICAL CO., LTD. (JP) 2000-07-13 WO disclosed
US-5502065-A TREATING HEADACHES PFIZER INC. (US) 1996-03-26 US disclosed
EP-0636129-A1 INDOLE DERIVATIVES AS 5-HT1-LIKE AGONISTS Pfizer Limited (GB) 1995-02-01 EP disclosed
CN-1082040-A Indoles PFIZER RES & DEV (IE) 1994-02-16 CN disclosed
WO-1993021178-A1 INDOLE DERIVATIVES AS 5-HT1-LIKE AGONISTS PFIZER LIMITED (GB) 1993-10-28 WO 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 (8 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-12565491-B2 (Isopropyl-triazolyl)pyridinyl-substituted benzooxazinone or benzothiazinone derivatives and use thereof IRAK1, PEAK1, IRAK4 MAPT 1221/4885CYP1A2 3315/4885GAA 2463/4885
US-12545659-B2 IRAK degraders and uses thereof IRAK2, IRAK3, IRAK4 MAPT 3470/4885CYP1A2 4592/4885GAA 4657/4885
US-12545689-B2 Macrocyclic LRRK2 kinase inhibitors LRRK2, SNCA, ROS1 MAPT 717/4885CYP1A2 3281/4885GAA 1504/4885
US-12612416-B2 Modulators of cystic fibrosis transmembrane conductance regulator CFTR, CLCN2, CLIC1 MAPT 4622/4885CYP1A2 2748/4885GAA 3751/4885
US-20020151715-A1 Imidazole derivatives GRIN2B, GRIN1, GRIN2A MAPT 448/4885CYP1A2 4578/4885GAA 2716/4885
US-20020143034-A1 Aminoalcohol derivatives and their use as beta 3 adrenergic agonists ADRB1, ADRB2, ADRB3 MAPT 3245/4885CYP1A2 167/4885GAA 4354/4885
US-20260042749-A1 IRAK DEGRADERS AND USES THEREOF IRAK2, IRAK3, IRAK4 MAPT 4151/4885CYP1A2 2456/4885GAA 4452/4885
US-20260076962-A1 LANTHIONINE SYNTHETASE C-LIKE 2-BASED THERAPEUTICS SCLY, CLCN2, CBS MAPT 4651/4885CYP1A2 4799/4885GAA 2016/4885

“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.