SCHEMBL2479265

SCHEMBL2479265

N#Cc1ccc(-c2nc(-c3ccc(C#N)cc3)nc(-c3ccc(C#N)cc3)n2)cc1

nearest known ligand 0.52

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
MMP3 P08254 1/20 0.52
ABCG2 Q9UNQ0 7/20 0.50
ABCB1 P08183 4/20 0.50
GAA P10253 1/20 0.47
CYP11B2 P19099 1/20 0.47
NOTUM Q6P988 1/20 0.47
KIF11 P52732 2/20 0.46
HRH4 Q9H3N8 1/20 0.46
CA12 O43570 2/20 0.46
CA2 P00918 2/20 0.46
CA9 Q16790 2/20 0.46
ALDH1A1 P00352 1/20 0.46
CYP2A6 P11509 1/20 0.46
CA3 P07451 1/20 0.46
CA6 P23280 1/20 0.46
CA14 Q9ULX7 1/20 0.46
CA1 P00915 1/20 0.45
ABCC1 P33527 1/20 0.44
TSHR P16473 1/20 0.43

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
SCHEMBL31663591 0.91 ABCG2 (0.62) ABCG2ABCB1CYP11B2ABCC1TSHR
SCHEMBL20385208 0.89 AHR (0.57) MMP3ABCG2ABCB1GAACYP11B2
SCHEMBL22360641 0.89 ABCG2 (0.60) MMP3ABCG2ABCB1CYP11B2ABCC1
SCHEMBL18483365 0.89 L3MBTL1 (0.54) MMP3ABCG2ABCB1GAACYP11B2
SCHEMBL23383904 0.89 ABCG2 (0.60) MMP3ABCG2ABCB1CYP11B2ABCC1
SCHEMBL23384091 0.89 ABCG2 (0.60) MMP3ABCG2ABCB1CYP11B2ABCC1
SCHEMBL20222785 0.89 ABCG2 (0.44) MMP3ABCG2ABCB1GAACYP11B2
SCHEMBL23383850 0.89 ABCG2 (0.60) MMP3ABCG2ABCB1CYP11B2ABCC1
SCHEMBL22883053 0.89 ABCG2 (0.60) MMP3ABCG2ABCB1CYP11B2ABCC1
SCHEMBL22106575 0.89 ABCG2 (0.60) MMP3ABCG2ABCB1CYP11B2ABCC1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-122032521-A Triazinyl COF biochar composite material and preparation method and application thereof 武汉轻工大学 2026-05-15 CN claimed
CN-119978413-A Conjugated organic framework compound, preparation method thereof and application thereof in lithium ion battery anode material 宁波维科电池有限公司 2025-05-13 CN claimed
CN-114790286-A Preparation method of covalent triazine framework polymer microspheres 绍兴文理学院 2022-07-26 CN claimed
CN-122032521-A Triazinyl COF biochar composite material and preparation method and application thereof 武汉轻工大学 2026-05-15 CN disclosed
CN-119978413-A Conjugated organic framework compound, preparation method thereof and application thereof in lithium ion battery anode material 宁波维科电池有限公司 2025-05-13 CN disclosed
CN-119486482-A Thin film, preparation method thereof, photoelectric device and display device TCL科技集团股份有限公司 2025-02-18 CN disclosed
CN-114790286-A Preparation method of covalent triazine framework polymer microspheres 绍兴文理学院 2022-07-26 CN disclosed
US-20180066180-A1 ORGANIC LIGHT-EMITTING DEVICE LG CHEM, LTD. (KR) 2018-03-08 US disclosed
US-20130299807-A1 ELECTROACTIVE COMPOSITION E I DU PONT DE NEMOURS AND COMPANY (US) 2013-11-14 US disclosed
US-8420230-B2 Organic light emitting diode employing luminescent efficiency improvement layer SAMSUNG DISPLAY CO., LTD. (KR) 2013-04-16 US disclosed
US-8212080-B2 Production method of xylylenediamine MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) 2012-07-03 US disclosed
EP-2202218-B1 Production method of xylylenediamine MITSUBISHI GAS CHEMICAL CO (JP) 2011-10-12 EP disclosed
US-20100280216-A1 METHOD OF PREPARING ORGANIC POROUS SOLIDS AND SOLIDS OBTAINABLE BY THIS METHOD MAX-PLANCK-GESELLSCHAFT ZUR FOERDERUNG DER WISSENSCHAFTEN E.V. (DE) 2010-11-04 US disclosed
US-20100168474-A1 PRODUCTION METHOD OF XYLYLENEDIAMINE MITSUBISHI GAS CHEMICAL COMPANY, INC (JP) 2010-07-01 US disclosed
US-20100168474-A1 PRODUCTION METHOD OF XYLYLENEDIAMINE MITSUBISHI GAS CHEMICAL COMPANY, INC (JP) 2010-07-01 US disclosed
EP-2202218-A1 Production method of xylylenediamine Mitsubishi Gas Chemical Company, Inc. (JP) 2010-06-30 EP disclosed
EP-2202218-A1 Production method of xylylenediamine Mitsubishi Gas Chemical Company, Inc. (JP) 2010-06-30 EP disclosed
US-20100039026-A1 Organic light emitting diode employing luminescent efficiency improvement layer SAMSUNG DISPLAY CO., LTD. (KR) 2010-02-18 US disclosed
EP-2014699-B1 Method of preparing organic porous solids and solids obtainable by this method MAX PLANCK GESELLSCHAFT (DE) 2009-09-02 EP disclosed
EP-2014699-A1 Method of preparing organic porous solids and solids obtainable by this method Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. (DE) 2009-01-14 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 (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-20180066180-A1 ORGANIC LIGHT-EMITTING DEVICE CRY1, CRY2, PPOX MMP3 4265/4885ABCG2 3620/4885ABCB1 3211/4885
US-20100168474-A1 PRODUCTION METHOD OF XYLYLENEDIAMINE XDH, HNMT, DDC MMP3 3792/4885ABCG2 2358/4885ABCB1 3228/4885

“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.