SCHEMBL6171379

SCHEMBL6171379

CCOC(=O)C(C)n1ccnc1

nearest known ligand 0.43

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
TBXA2R P21731 1/20 0.41
KMT2A Q03164 3/20 0.41
KDM4E B2RXH2 2/20 0.40
ALDH1A1 P00352 3/20 0.40
MAPT P10636 2/20 0.40
PKM P14618 1/20 0.40
HPGD P15428 1/20 0.40
ALOX12 P18054 1/20 0.40
HTT P42858 1/20 0.40
HSD17B10 Q99714 1/20 0.40
TDP1 Q9NUW8 1/20 0.40
CYP26A1 O43174 4/20 0.39
MEN1 O00255 1/20 0.39
MITF O75030 1/20 0.39
SMN1; SMN2 Q16637 1/20 0.39
CYP19A1 P11511 1/20 0.39
FPR2 P25090 1/20 0.38
TBXAS1 P24557 1/20 0.38

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
SCHEMBL9460010 1.00 TBXA2R (0.41) TBXA2RKMT2AKDM4EALDH1A1MAPT
SCHEMBL27455193 0.84 ALDH1A1 (0.41) KMT2AKDM4EALDH1A1MAPTPKM
SCHEMBL28789383 0.84 TBXA2R (0.44) TBXA2RKMT2AKDM4EALDH1A1MAPT
SCHEMBL27553812 0.82 CYP26A1 (0.50) TBXA2RKMT2AKDM4EALDH1A1MAPT
SCHEMBL27819912 0.82 PIK3R1 (0.45) TBXA2RHTTCYP26A1SMN1; SMN2CYP19A1
SCHEMBL27565163 0.82 PIK3R1 (0.45) TBXA2RHTTCYP26A1SMN1; SMN2CYP19A1
SCHEMBL26660824 0.81 CYP26A1 (0.41) KMT2AKDM4EALDH1A1MAPTPKM
SCHEMBL25196732 0.80 CYP26A1 (0.40) TBXA2RKMT2AKDM4EALDH1A1MAPT
SCHEMBL4552326 0.79 KMT2A (0.39) TBXA2RKMT2AKDM4EALDH1A1MAPT
SCHEMBL29852421 0.79 KMT2A (0.50) KMT2AKDM4EALDH1A1MAPTPKM

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 19 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-101531636-B Method for synthesizing 2-(1-imidazol)ethylamine UNIV HEFEI TECHNOLOGY 2010-12-08 CN claimed
CN-101531636-A Method for synthesizing 2-(1-imidazol)ethylamine UNIV HEFEI TECHNOLOGY 2009-09-16 CN claimed
CN-101531636-B Method for synthesizing 2-(1-imidazol)ethylamine UNIV HEFEI TECHNOLOGY 2010-12-08 CN disclosed
CN-101531636-B Method for synthesizing 2-(1-imidazol)ethylamine UNIV HEFEI TECHNOLOGY 2010-12-08 CN disclosed
CN-101531636-A Method for synthesizing 2-(1-imidazol)ethylamine UNIV HEFEI TECHNOLOGY 2009-09-16 CN disclosed
CN-101531636-A Method for synthesizing 2-(1-imidazol)ethylamine UNIV HEFEI TECHNOLOGY 2009-09-16 CN disclosed
EP-0966446-B1 BICYCLIC INHIBITORS OF PROTEIN FARNESYL TRANSFERASE WARNER LAMBERT CO (US) 2005-10-19 EP disclosed
US-6528535-B2 Anticancer agents; restenosis WARNER-LAMBERT COMPANY 2003-03-04 US disclosed
CN-1086701-C Chloropyridylcarbonylazoles and fungicides for agriculture and horticulture BAYER AGROCHEM KK (JP) 2002-06-26 CN disclosed
US-20020006936-A1 Bicyclic inhibitors of protein farnesyl transferase BIKKER JACK (US) 2002-01-17 US disclosed
EP-0763530-B1 Chloropyridylcarbonyl derivatives and their use as microbiocides BAYER AGROCHEM KK (JP) 2001-12-05 EP disclosed
US-6265422-B1 ANTICANCER AGENTS; CARDIOVASCULAR DISORDERS WARNER-LAMBERT COMPANY 2001-07-24 US disclosed
US-6133303-A VARIOUS INDENE DERIVATIVES, WITH THE EXCEPTION OF 5-(2-IMIDAZOLE-1-YL-ETHOXY)INDAN-1-ONE; TREATING CANCER AND TREATING OR PREVENTING RESTENOSIS OR ATHEROSCLEROSIS WARNER-LAMBERT COMPANY (US) 2000-10-17 US disclosed
EP-0966446-A1 BICYCLIC INHIBITORS OF PROTEIN FARNESYL TRANSFERASE WARNER-LAMBERT COMPANY (US) 1999-12-29 EP disclosed
US-5973156-A Piperidine and tetrahydropyridine derivatives MERCK SHARP & DOME LTD. (GB) 1999-10-26 US disclosed
US-5849767-A Chloropyridylcarbonyl derivatives NIHON BAYER AGROCHEM K.K. (JP) 1998-12-15 US disclosed
WO-1998034921-A1 BICYCLIC INHIBITORS OF PROTEIN FARNESYL TRANSFERASE WARNER-LAMBERT COMPANY (US) 1998-08-13 WO disclosed
CN-1147505-A Chloropyridylcarbonylazoles and fungicides for agriculture and horticulture BAYER AGROCHEM KK (JP) 1997-04-16 CN disclosed
EP-0763530-A1 Chloropyridylcarbonyl derivatives and their use as microbiocides NIHON BAYER AGROCHEM K.K. (JP) 1997-03-19 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 (1 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-20020006936-A1 Bicyclic inhibitors of protein farnesyl transferase FNTA, FNTB, SREBF1 TBXA2R 1720/4885KMT2A 3893/4885KDM4E 3607/4885

“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.