SCHEMBL384813

SCHEMBL384813

Cc1ccc2cc(F)ccc2n1

nearest known ligand 0.63

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
CYP1A2 P05177 4/20 0.63
POLB P06746 2/20 0.59
KDM4E B2RXH2 2/20 0.59
BACE1 P56817 1/20 0.59
LMNA P02545 1/20 0.59
CASP6 P55212 1/20 0.59
RAB9A P51151 4/20 0.50
NPC1 O15118 3/20 0.50
CYP2A6 P11509 1/20 0.43
KDM1A O60341 1/20 0.42
TSHR P16473 1/20 0.41
CCR1 P32246 1/20 0.41
CCR5 P51681 1/20 0.41
ALDH1A1 P00352 1/20 0.41
HPGD P15428 1/20 0.41
NFKB1 P19838 1/20 0.41
NFKB2 Q00653 1/20 0.41
RELA Q04206 1/20 0.41
SMN1; SMN2 Q16637 1/20 0.41

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
SCHEMBL1193454 0.84 CYP1A2 (0.61) CYP1A2POLBKDM4ELMNACASP6
SCHEMBL30081474 0.84 CYP1A2 (0.61) CYP1A2POLBKDM4ELMNACASP6
SCHEMBL15831610 0.81 BACE1 (0.45) CYP1A2POLBKDM4EBACE1LMNA
SCHEMBL985631 0.81 CYP1A2 (0.47) CYP1A2POLBKDM4EBACE1LMNA
SCHEMBL15831571 0.80 CCR1 (0.53) CYP1A2POLBKDM4EBACE1LMNA
SCHEMBL4889091 0.77 BACE1 (0.63) CYP1A2KDM4EBACE1LMNARAB9A
SCHEMBL161703 0.77 CYP1A2 (1.00) CYP1A2POLBKDM4EBACE1LMNA
SCHEMBL29444268 0.77 CYP1A2 (1.00) CYP1A2POLBKDM4EBACE1LMNA
SCHEMBL10259445 0.76 CYP1A2 (0.68) CYP1A2POLBKDM4ELMNACASP6
SCHEMBL4058013 0.76 CYP1A2 (0.56) CYP1A2POLBKDM4ELMNACASP6

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-109689627-B Pyrazolylquinoline compounds, process for their preparation and pharmaceutical compositions containing them 高雄医学大学 2022-10-11 CN claimed
CN-113754583-A 2- ([2, 2' -biquinolyl ] -3-ether) -1-ethanol and derivative and synthetic method thereof 湖南工程学院 2021-12-07 CN claimed
CN-113512064-A Preparation method of aromatic phosphine oxide compound 中南大学 2021-10-19 CN claimed
CN-110606839-B Green synthesis method of polysubstituted quinazoline derivative 南方医科大学 2021-10-08 CN claimed
CN-109776406-B Method for cross coupling of ether compound and quinoline derivative 湘潭大学 2021-05-04 CN claimed
CN-108912070-B Synthetic method of epoxy compound and agricultural biological activity thereof 青岛农业大学 2020-06-02 CN claimed
EP-2119717-B1 8-[3-amino-piperidin-1-yl]-xanthins, their production and utilisation as DPP IV inhibitors BOEHRINGER INGELHEIM INT (DE) 2018-01-17 EP claimed
US-8697868-B2 8-[3-amino-piperidin-1-yl]-xanthines, their preparation and their use as pharmaceutical compositions BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2014-04-15 US claimed
US-20090137801-A1 8-[3-AMINO-PIPERIDIN-1-YL]-XANTHINES, THEIR PREPARATION AND THEIR USE AS PHARMACEUTICAL COMPOSITIONS BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2009-05-28 US claimed
EP-1758905-B1 8-[3-AMINO-PIPERIDIN-1-YL]-XANTHINE, THE PRODUCTION THEREOF AND THE USE IN THE FORM OF A DDP-IV INHIBITOR BOEHRINGER INGELHEIM INT (DE) 2009-04-29 EP claimed
US-20050234108-A1 8-[3-amino-piperidin-1-yl]-xanthines, their preparation and their use as pharmaceutical compositions BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2005-10-20 US claimed
EP-0245913-B1 Process for preparing 6,7-dihydro-5,8-dimethyl-9-fluoro-1-oxo-1H,5H-benzo[i,j]quinolizine-2-carboxylic acid RIKER LABORATORIES, INC. (US) 1992-03-25 EP claimed
US-4898945-A Process for 6,7-dihydro-5,8-dimethyl-9-fluoro-1-oxo-1H,5H-benzo[i,j]quinolizine-2-carboxylic acid MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1990-02-06 US claimed
EP-0245913-A1 Process for preparing 6,7-dihydro-5,8-dimethyl-9-fluoro-1-oxo-1H,5H-benzo[i,j]quinolizine-2-carboxylic acid RIKER LABORATORIES, INC. (US) 1987-11-19 EP claimed
US-4301289-A Process for 6,7-dihydro-9-fluoro-5-methyl-1-oxo-1H,5H-benzo(ij)quinolizine-2-carboxylic acid MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1981-11-17 US claimed
US-4301288-A Process for 6,7-dihydro-9-fluoro-5-methyl-1-oxo-1H,5H-benzo(ij)quinolizine-2-carboxylic acid MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1981-11-17 US claimed
US-20250382285-A1 BICYCLIC-SUBSTITUTED GLUTARIMIDE CEREBLON BINDERS C4 THERAPEUTICS, INC. (US) 2025-12-18 US disclosed
US-20250368631-A1 BICYCLIC-SUBSTITUTED GLUTARIMIDE CEREBLON BINDERS C4 THERAPEUTICS, INC. (US) 2025-12-04 US disclosed
US-4301289-A Process for 6,7-dihydro-9-fluoro-5-methyl-1-oxo-1H,5H-benzo(ij)quinolizine-2-carboxylic acid MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1981-11-17 US disclosed
US-4207320-A FUNGICIDES WARNER-LAMBERT COMPANY (US) 1980-06-10 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 (4 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-20250368631-A1 BICYCLIC-SUBSTITUTED GLUTARIMIDE CEREBLON BINDERS CRBN, STUB1, CUL1 CYP1A2 3894/4885POLB 4265/4885KDM4E 465/4885
US-20090137801-A1 8-[3-AMINO-PIPERIDIN-1-YL]-XANTHINES, THEIR PREPARATION AND THEIR USE AS PHARMACEUTICAL COMPOSITIONS DPP8, DPP4, DPP7 CYP1A2 592/4885POLB 2194/4885KDM4E 1036/4885
US-20250382285-A1 BICYCLIC-SUBSTITUTED GLUTARIMIDE CEREBLON BINDERS CRBN, STUB1, CUL1 CYP1A2 3894/4885POLB 4265/4885KDM4E 465/4885
US-20050234108-A1 8-[3-amino-piperidin-1-yl]-xanthines, their preparation and their use as pharmaceutical compositions DPP8, DPP4, DPP7 CYP1A2 616/4885POLB 2648/4885KDM4E 1140/4885

“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.