SCHEMBL708675

SCHEMBL708675

Clc1ccc(-c2ccc3ccccc3n2)cc1

nearest known ligand 0.67

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
NPC1 O15118 13/20 0.67
RAB9A P51151 13/20 0.67
MEN1 O00255 3/20 0.67
KMT2A Q03164 3/20 0.67
AR P10275 2/20 0.67
KDM4E B2RXH2 9/20 0.65
SMN1; SMN2 Q16637 8/20 0.65
ALDH1A1 P00352 7/20 0.65
MAPT P10636 5/20 0.65
HPGD P15428 3/20 0.65
HSD17B10 Q99714 3/20 0.65
CYP3A4 P08684 2/20 0.65
TP53 P04637 2/20 0.65
PKM P14618 2/20 0.65
GMNN O75496 1/20 0.65
THPO P40225 1/20 0.65
BLM P54132 1/20 0.65
PMP22 Q01453 1/20 0.65
CYP1A2 P05177 1/20 0.63
CYP2D6 P10635 1/20 0.63

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
SCHEMBL30644241 1.00 NPC1 (0.67) NPC1RAB9AMEN1KMT2AAR
SCHEMBL26826802 0.98 NPC1 (0.65) NPC1RAB9AMEN1KMT2AAR
SCHEMBL12112870 0.89 RAB9A (0.80) NPC1RAB9AMEN1KMT2AAR
SCHEMBL31571831 0.83 RAB9A (0.71) NPC1RAB9AMEN1KMT2AAR
SCHEMBL706884 0.83 RAB9A (0.71) NPC1RAB9AMEN1KMT2AAR
2-Phenylquinoline SCHEMBL29399739 0.83 RAB9A (0.73) NPC1RAB9AMEN1KMT2AAR
2-Phenylquinoline SCHEMBL44999 0.83 RAB9A (0.73) NPC1RAB9AMEN1KMT2AAR
SCHEMBL26824826 0.83 NPC1 (0.56) NPC1RAB9AMEN1KMT2AAR
SCHEMBL1924662 0.82 NPC1 (0.56) NPC1RAB9AMEN1KMT2AAR
2-Phenylquinoline SCHEMBL6130707 0.82 RAB9A (0.66) NPC1RAB9AMEN1KMT2AAR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111116466-B Catalytic synthesis method of polysubstituted quinoline derivative 浙江万里学院 2023-02-10 CN claimed
US-20230337527-A1 ORGANIC COMPOUND AND ORGANIC ELECTROLUMINESCENT DEVICE COMPRISING SAME LAPTO CO., LTD. (KR) 2023-10-19 US disclosed
US-20230337527-A1 ORGANIC COMPOUND AND ORGANIC ELECTROLUMINESCENT DEVICE COMPRISING SAME LAPTO CO., LTD. (KR) 2023-10-19 US disclosed
CN-111116466-B Catalytic synthesis method of polysubstituted quinoline derivative 浙江万里学院 2023-02-10 CN disclosed
CN-113979956-A Method for synthesizing 2-arylquinoxaline and 3-arylquinoxaline-2 (1H) -one based on mechanical grinding of aryldiazonium salts 广西师范大学 2022-01-28 CN disclosed
CN-111116466-A Catalytic synthesis method of polysubstituted quinoline derivative 浙江万里学院 2020-05-08 CN disclosed
CN-107400084-B Method for synthesizing quinoline derivative 南京理工大学 2020-04-10 CN disclosed
EP-3197900-B1 INHIBITORS OF HIF PROLYL HYDROXYLASE MERCK SHARP & DOHME (US) 2020-02-12 EP disclosed
CN-110467568-A A kind of synthetic method of aryl quinoline derivatives UNIV WENZHOU 2019-11-19 CN disclosed
CN-106831565-B The restoring method of benzo aromatic aza cyclics 三峡大学 2019-11-08 CN disclosed
US-8053445-B2 Utilities of olefin derivatives SHIONOGI & CO., LTD. (JP) 2011-11-08 US disclosed
EP-2217070-A1 NUCLEIC ACID FLUORESCENT STAINS Sigma-Aldrich Co. (US) 2010-08-18 EP disclosed
CN-101691354-A Method for chemically synthesizing 2-heteroaryl substituted quinoline derivatives UNIV ZHEJIANG TECHNOLOGY 2010-04-07 CN disclosed
US-20100041045-A1 NUCLEIC ACID FLUORESCENT STAINS SIGMA-ALDRICH CO. (US) 2010-02-18 US disclosed
WO-2009064943-A1 NUCLEIC ACID FLUORESCENT STAINS SIGMA-ALDRICH CO. (US) 2009-05-22 WO disclosed
US-20090131279-A1 NUCLEIC ACID FLUORESCENT STAINS SIGMA ALDRICH COMPANY (US) 2009-05-21 US disclosed
US-20090036457-A1 Utilities of olefin derivatives YAMAMORI TERUO 2009-02-05 US disclosed
US-20040242615-A1 Utilities of olefin derivatives SHIONOGI & CO., LTD. (JP) 2004-12-02 US disclosed
US-6815447-B2 6-N-(2-AMINO-PYRIMIDIN-4-YL)QUINOLINE-6-AMINE DERIVATIVES; ANALGESICS ASTRAZENECA AB (SE) 2004-11-09 US disclosed
US-5532374-A Method of preparation of bis-quinolines HITACHI CHEMICAL COMPANY, LTD. (JP) 1996-07-02 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-20040242615-A1 Utilities of olefin derivatives APOL1, NR1H2, APOB NPC1 19/4885RAB9A 4723/4885MEN1 3997/4885
US-20230337527-A1 ORGANIC COMPOUND AND ORGANIC ELECTROLUMINESCENT DEVICE COMPRISING SAME AOC1, ODC1, PIEZO1 NPC1 1199/4885RAB9A 3157/4885MEN1 1661/4885
US-20090131279-A1 NUCLEIC ACID FLUORESCENT STAINS POLRMT, HNRNPH3, EWSR1 NPC1 1437/4885RAB9A 4009/4885MEN1 3100/4885
US-20090036457-A1 Utilities of olefin derivatives APOL1, APOB, NR1H2 NPC1 48/4885RAB9A 4606/4885MEN1 3163/4885

“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.