SCHEMBL1820644

SCHEMBL1820644

[c]1c2ccccc2c(-c2ccccc2)c2ccccc12

nearest known ligand 0.45

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
ACHE P22303 4/20 0.45
ESR1 P03372 6/20 0.40
ESR2 Q92731 6/20 0.40
MAPT P10636 3/20 0.40
LMNA P02545 2/20 0.40
HTT P42858 1/20 0.40
ALDH1A1 P00352 2/20 0.38
EGFR P00533 1/20 0.36
KDM4E B2RXH2 2/20 0.35
MAPK1 P28482 1/20 0.35
TDP1 Q9NUW8 1/20 0.35
L3MBTL1 Q9Y468 1/20 0.35
HPGD P15428 1/20 0.34
CA1 P00915 1/20 0.33
CA2 P00918 1/20 0.33

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
SCHEMBL15453046 0.95 ACHE (0.42) ACHEESR1ESR2MAPTLMNA
SCHEMBL3875883 0.87 ALDH1A1 (0.38) ACHEESR1ESR2ALDH1A1EGFR
SCHEMBL28762429 0.86 ESR1 (0.39) ACHEESR1ESR2MAPTLMNA
SCHEMBL22635772 0.85 MAOA (0.39) ACHEESR1ESR2ALDH1A1
SCHEMBL15453009 0.84 ACHE (0.35) ACHEESR1ESR2MAPTLMNA
SCHEMBL28762446 0.84 ACHE (0.35) ACHEESR1ESR2MAPTLMNA
SCHEMBL6759020 0.84 CYP2A6 (0.33) ALDH1A1TDP1
SCHEMBL27800484 0.83 DCLK1 (0.39) ACHEESR1ESR2MAPTALDH1A1
SCHEMBL27849808 0.83 ALDH1A1 (0.38) ACHEESR1ESR2MAPTALDH1A1
SCHEMBL21295977 0.82 IMPDH2 (0.49) MAPTLMNAALDH1A1KDM4EMAPK1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117964502-A Method for asymmetric catalytic synthesis of alpha-aminoketone 南开大学 2024-05-03 CN claimed
CN-117800900-A Polysubstituted chiral bicyclo [2.1.1] hexane compound and synthesis method thereof 河南师范大学 2024-04-02 CN claimed
CN-115057762-B Aggregation-resistant induced quenching type rigid Gemini fluorescent amphiphilic molecule and synthesis method thereof 武汉大学 2023-09-08 CN claimed
CN-103534331-B Naphthalene derivatives, comprise its organic material and comprise its organic electroluminescent device 大州电子材料株式会社 2016-06-08 CN claimed
CN-103805167-B Organic blue luminescent material and its preparation method and application Jilin Optical and Electronic Materials Co., Ltd. (CN) 2015-12-02 CN claimed
US-9024304-B2 Naphthalene derivative, organic material including the same, and organic electroluminescent device including the same DAE JOO ELECTRONIC MATERIALS CO., LTD. (KR) 2015-05-05 US claimed
US-9006503-B2 Organic electroluminescence devices containing substituted benzo[C]phenanthrenes MERCK PATENT GMBH (DE) 2015-04-14 US claimed
US-20140299849-A1 NAPHTHALENE DERIVATIVE, ORGANIC MATERIAL INCLUDING THE SAME, AND ORGANIC ELECTROLUMINESCENT DEVICE INCLUDING THE SAME DAE JOO ELECTRONIC MATERIALS CO., LTD. (KR) 2014-10-09 US claimed
CN-103805167-A Organic blue luminescent material, and preparation method and application thereof JILIN OPTICAL & ELECTRONIC MATERIALS CO LTD 2014-05-21 CN claimed
EP-2692823-A2 NAPHTHALENE DERIVATIVES, ORGANIC MATERIAL USING SAME, AND ORGANIC ELECTROLUMINESCENT DEVICE USING SAME Dae Joo Electronic Materials Co., Ltd. (KR) 2014-02-05 EP claimed
CN-103534331-A Naphthalene derivatives, organic material using same, and organic electroluminescent device using same DAE JOO ELECTRONIC MAT CO LTD 2014-01-22 CN claimed
US-7482490-B2 Amine compound having fluorene group as framework, process for producing the amine compound, and use of the amine compound TOSOH CORPORATION (JP) 2009-01-27 US claimed
US-20080194878-A1 Amine Compound Having Fluorene Group as Framework, Process for Producing the Amine Compound, and Use of the Amine Compound TOSOH CORPORATION (JP) 2008-08-14 US claimed
EP-1752440-A1 AMINE COMPOUND HAVING FLUORENE GROUP AS FRAMEWORK, PROCESS FOR PRODUCING THE AMINE COMPOUND, AND USE OF THE AMINE COMPOUND Tosoh Corporation (JP) 2007-02-14 EP claimed
CN-1263825-C Liquid crystal orientation agent, formation method of liquid crystal orientation membrane and liquid crystal display unit JSR CORP (JP) 2006-07-12 CN claimed
CN-114315742-B Fluorene-containing compound and application thereof 湖北尚赛光电材料有限公司 2024-06-28 CN disclosed
CN-118221708-A Organic electroluminescent material and device 环球展览公司 2024-06-21 CN disclosed
US-20040110958-A1 Novel arylamine derivatives having fluorene skeleton, synthetic intermediates thereof, processes of producing those, and organic electrolumivescene devices TOSOH CORPORATION 2004-06-10 US disclosed
EP-1400578-A1 Electrolumisescent 9,9-bis(4-amino)-1,1'-biphenyl)fluorene derivatives Tosoh Corporation (JP) 2004-03-24 EP disclosed
CN-1442466-A Liquid crystal orientation agent, formation method of liquid crystal orientation membrane and liquid crystal display unit JSR CORP (JP) 2003-09-17 CN 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 (2 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-20040110958-A1 Novel arylamine derivatives having fluorene skeleton, synthetic intermediates thereof, processes of producing those, and organic electrolumivescene devices AHR, NAT1, AR ACHE 3669/4885ESR1 139/4885ESR2 38/4885
US-20080194878-A1 Amine Compound Having Fluorene Group as Framework, Process for Producing the Amine Compound, and Use of the Amine Compound TAAR1, SLC18A1, ADRB2 ACHE 2539/4885ESR1 521/4885ESR2 603/4885

“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.