SCHEMBL2648020

SCHEMBL2648020

Nc1ccc(OCc2ccccc2)cn1

nearest known ligand 0.61

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAOB P27338 4/20 0.61
GAA P10253 2/20 0.61
MAPT P10636 1/20 0.61
MAOA P21397 1/20 0.61
RAB9A P51151 1/20 0.61
SMN1; SMN2 Q16637 1/20 0.61
L3MBTL1 Q9Y468 1/20 0.61
P4HTM Q9NXG6 1/20 0.58
LMNA P02545 1/20 0.53
CYP1A2 P05177 1/20 0.53
PTGS1 P23219 1/20 0.53
SLC6A2 P23975 1/20 0.53
CYP2C19 P33261 1/20 0.53
PTGS2 P35354 1/20 0.53
SLC6A3 Q01959 1/20 0.53
HIF1A Q16665 1/20 0.53
HDAC6 Q9UBN7 1/20 0.53
MGAM O43451 1/20 0.50
SI P14410 1/20 0.50
MGAM2 Q2M2H8 1/20 0.50

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
SCHEMBL30362841 1.00 MAOB (0.61) MAOBGAAMAPTMAOARAB9A
Hydrochloric Acid SCHEMBL1330115 0.98 MAOB (0.59) MAOBGAAMAPTMAOARAB9A
SCHEMBL1258945 0.82 APP (0.59) MAOBMAPTRAB9ASMN1; SMN2
SCHEMBL11177596 0.82 MAOB (0.59) MAOBMAOARAB9ALMNACYP1A2
SCHEMBL11186146 0.82 APP (0.54) MAOBMAOARAB9ASMN1; SMN2CA12
SCHEMBL504815 0.81 MAOB (0.60) MAOBGAAMAPTMAOARAB9A
SCHEMBL15435397 0.81 NPC1 (0.53) MAOBMAOARAB9ALMNA
SCHEMBL13535008 0.79 P4HTM (0.60) MAOBGAAMAPTMAOARAB9A
SCHEMBL1680607 0.79 MAOB (0.59) MAOBGAAMAPTMAOARAB9A
SCHEMBL11183436 0.78 MAOB (0.67) MAOBMAOA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118206548-A Synthesis method of [1,2,4] triazolo [1,5-a ] pyridin-6-ol 江苏工程职业技术学院 2024-06-18 CN claimed
US-12551580-B2 Heterocyclic compounds and imaging agents for imaging Huntington protein CHDI FOUNDATION, INC. (US) 2026-02-17 US disclosed
EP-4615839-A1 INHIBITORS OF PROTEIN TYROSINE PHOSPHATASE, COMPOSITIONS, AND METHODS OF USE Bristol-Myers Squibb Company (US) 2025-09-17 EP disclosed
EP-4612151-A1 PREPARATION OF IMIDAZOPYRIDINE AND IMIDAZOPYRIDAZINE DERIVATIVES AS NOVEL DIACYLGLYCERIDE O-ACYLTRANSFERASE 2 INHIBITORS Merck Sharp & Dohme LLC (US) 2025-09-10 EP disclosed
CN-120152973-A Protein tyrosine phosphatase inhibitors, compositions, and methods of use 百时美施贵宝公司 2025-06-13 CN disclosed
CN-120092003-A CDK protein degrading agents, pharmaceutical compositions and therapeutic uses 拜欧斯瑞克斯公司 2025-06-03 CN disclosed
EP-4539840-A1 KINASE MODULATORS AND METHODS OF USE THEREOF Neuron23, Inc. (US) 2025-04-23 EP disclosed
CN-119730846-A Kinase modulators and methods of use thereof 神经元23公司 2025-03-28 CN disclosed
US-12234220-B2 Immunomodulatory compounds DANA-FARBER CANCER INSTITUTE, INC. (US) 2025-02-25 US disclosed
US-20250034171-A1 IMIDAZOPYRIDINE AMIDES AND RELATED COMPOUNDS FOR USE IN THE TREATMENT OF BACTERIAL INFECTIONS Janssen Sciences Ireland Unlimited Company (IE) 2025-01-30 US disclosed
US-6951945-B2 Heteroaromatic glucokinase activators HOFFMAN-LA ROCHE INC. (US) 2005-10-04 US disclosed
EP-1169312-B1 GLUCOKINASE ACTIVATORS HOFFMANN LA ROCHE (CH) 2004-10-06 EP disclosed
US-20040014968-A1 Heteroaromatic glucokinase activators BIZZARRO FRED THOMAS (US) 2004-01-22 US disclosed
US-6610846-B1 Increase insulin secretion; type II diabetes; 2,3-Di-substituted N-heteroaromatic propionamides with 3- a phenyl group and 2- a methyl cycloalkyl ring; 3-cyclopentyl-2-(3,4-dichlorophenyl)-N-pyridazin-3-yl-propionamide HOFFMAN-LA ROCHE INC. 2003-08-26 US disclosed
US-6320050-B1 2-SUBSTITUTED PHENYL-3-CYCLOALKYL SUBSTITUTED N-HETEROAROMATIC PROPIONAMIDES; USED TO INCREASE INSULIN SECRETION IN THE TREATMENT OF TYPE II DIABETES. HOFFMANN-LA ROCHE INC. 2001-11-20 US disclosed
US-20010039344-A1 Heteroaromatic glucokinase activators HOFFMANN-LA ROCHE INC. 2001-11-08 US disclosed
EP-0120589-B1 IMIDAZO-HETEROCYCLIC COMPOUNDS, PROCESSES FOR PREPARATION THEREOF AND PHARMACEUTICAL COMPOSITION COMPRISING THE SAME FUJISAWA PHARMACEUTICAL CO., LTD. (JP) 1988-06-08 EP disclosed
US-4450164-A ANTIULCER AND ANTISECRETORY AGENTS SCHERING CORPORATION (US) 1984-05-22 US disclosed
US-4406690-A Certain aralkyloxy or aralkylthio-pyridyl-phthalimides and their use as herbicides ZOECON CORPORATION (US) 1983-09-27 US disclosed
US-4406689-A Certain aralkyloxy or thio-pyridyl-imidazo-pyridines and their herbicidal use ZOECON CORPORATION (US) 1983-09-27 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 (5 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-20040014968-A1 Heteroaromatic glucokinase activators GCKR, GCK, PDXK MAOB 3813/4885GAA 589/4885MAPT 4407/4885
US-12234220-B2 Immunomodulatory compounds CRBN, CD47, CD58 MAOB 3653/4885GAA 1182/4885MAPT 1799/4885
US-20250034171-A1 IMIDAZOPYRIDINE AMIDES AND RELATED COMPOUNDS FOR USE IN THE TREATMENT OF BACTERIAL INFECTIONS TPMT, QDPR, BRD4 MAOB 740/4885GAA 709/4885MAPT 1783/4885
US-20010039344-A1 Heteroaromatic glucokinase activators GCKR, GCK, PDXK MAOB 3663/4885GAA 384/4885MAPT 4402/4885
US-12551580-B2 Heterocyclic compounds and imaging agents for imaging Huntington protein HTT, HYPK, HIRA MAOB 3676/4885GAA 2749/4885MAPT 17/4885

“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.