SCHEMBL3476023

SCHEMBL3476023

Cn1c2nc(=O)[nH]c(=O)c-2nc2ccccc21

nearest known ligand 0.65

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
GSR P00390 4/20 0.65
MAPT P10636 4/20 0.56
MEN1 O00255 2/20 0.56
KMT2A Q03164 2/20 0.56
TDP2 O95551 1/20 0.56
NGF P01138 1/20 0.56
NTRK1 P04629 1/20 0.56
RECQL P46063 1/20 0.56
BLM P54132 1/20 0.56
KDM4E B2RXH2 6/20 0.51
ALDH1A1 P00352 4/20 0.51
GAA P10253 3/20 0.51
HPGD P15428 1/20 0.51
PDGFRB P09619 1/20 0.49
FGFR1 P11362 1/20 0.49
L3MBTL1 Q9Y468 2/20 0.49
THRB P10828 1/20 0.49
HSD17B10 Q99714 2/20 0.47
CASP1 P29466 1/20 0.47
CASP7 P55210 1/20 0.47

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
SCHEMBL9635901 0.82 MEN1 (0.61) GSRMAPTMEN1KMT2ATDP2
SCHEMBL8336453 0.80 MEN1 (0.52) GSRMAPTMEN1KMT2ATDP2
SCHEMBL4748217 0.80 TDP2 (0.62) GSRMAPTMEN1KMT2ATDP2
SCHEMBL9635970 0.80 HTT (0.54) GSRMAPTMEN1KMT2AKDM4E
SCHEMBL9635797 0.79 GSR (0.70) GSRMEN1KMT2ATDP2RECQL
Lumiflavin SCHEMBL29516802 0.79 MEN1 (0.76) GSRMAPTMEN1KMT2ATDP2
Lumiflavin SCHEMBL193713 0.79 MEN1 (0.76) GSRMAPTMEN1KMT2ATDP2
SCHEMBL28727266 0.78 TLR8 (0.54) GSRMAPTKDM4EALDH1A1GAA
Lumiflavin SCHEMBL6365933 0.78 MEN1 (0.74) GSRMAPTMEN1KMT2ATDP2
SCHEMBL24238131 0.77 MEN1 (0.55) GSRMAPTMEN1KMT2ATDP2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-113164483-B Pharmaceutical composition for preventing or treating cancer containing PLK1 inhibitor as active ingredient 国立癌症中心 2024-09-24 CN claimed
US-20230148252-A1 PROCESS FOR TREATING KERATIN MATERIALS USING A FLAVIN DERIVATIVE, A POLYMERIZABLE MOLECULE AND LIGHT RADIATION L'OREAL (FR) 2023-05-11 US claimed
US-20220033405-A1 PHARMACEUTICAL COMPOSITION FOR PREVENTING OR TREATING CANCER CONTAINING PLK1 INHIBITOR AS ACTIVE INGREDIENT NATIONAL CANCER CENTER (KR) 2022-02-03 US claimed
EP-3727318-B1 PROCESS FOR TREATING KERATIN MATERIALS USING A FLAVIN DERIVATIVE, A POLYMERIZABLE MOLECULE AND LIGHT RADIATION OREAL (FR) 2022-01-19 EP claimed
US-20200375866-A1 HAIR TREATMENT PROCESS USING A FLAVIN DERIVATIVE AND LIGHT RADIATION L'OREAL (FR) 2020-12-03 US claimed
WO-2020111325-A1 PHARMACEUTICAL COMPOSITION FOR PREVENTING OR TREATING CANCER, CONTAINING ACTIVATION INHIBITOR OF PLK1 AS ACTIVE INGREDIENT 국립암센터 2020-06-04 WO claimed
CN-113164483-B Pharmaceutical composition for preventing or treating cancer containing PLK1 inhibitor as active ingredient 国立癌症中心 2024-09-24 CN disclosed
US-20230148252-A1 PROCESS FOR TREATING KERATIN MATERIALS USING A FLAVIN DERIVATIVE, A POLYMERIZABLE MOLECULE AND LIGHT RADIATION L'OREAL (FR) 2023-05-11 US disclosed
US-20230148252-A1 PROCESS FOR TREATING KERATIN MATERIALS USING A FLAVIN DERIVATIVE, A POLYMERIZABLE MOLECULE AND LIGHT RADIATION L'OREAL (FR) 2023-05-11 US disclosed
US-20230148252-A1 PROCESS FOR TREATING KERATIN MATERIALS USING A FLAVIN DERIVATIVE, A POLYMERIZABLE MOLECULE AND LIGHT RADIATION L'OREAL (FR) 2023-05-11 US disclosed
EP-3492104-B1 USE OF 10H-BENZO [G] PTERIDIN-2,4-DION DERIVATIVES TRIOPTOTEC GMBH (DE) 2023-02-15 EP disclosed
EP-3586632-B1 10H-BENZO[G]PTERIDINE-2,4-DIONE DERIVATIVES, METHOD FOR PRODUCING SAME AND USE OF SAME TRIOPTOTEC GMBH (DE) 2022-09-28 EP disclosed
US-20220033405-A1 PHARMACEUTICAL COMPOSITION FOR PREVENTING OR TREATING CANCER CONTAINING PLK1 INHIBITOR AS ACTIVE INGREDIENT NATIONAL CANCER CENTER (KR) 2022-02-03 US disclosed
US-8193430-B2 Methods for separating carbon nanotubes THE UNIVERSITY OF CONNECTICUT (US) 2012-06-05 US disclosed
US-20100044230-A1 METHODS FOR SEPARATING CARBON NANOTUBES UNIVERSITY OF CONNECTICUT (US) 2010-02-25 US disclosed
EP-1297843-B1 METHOD OF PHOTOREDUCTION OF HEMOGLOBIN VESICLES UNIV WASEDA (JP) 2008-02-13 EP disclosed
US-6967020-B2 Oxygen carrier system, artificial oxygen carrier, and reducing agent OXYGENIX CO., LTD (JP) 2005-11-22 US disclosed
US-6916303-B2 Photoreduction method for hemoglobin-vesicle JAPAN SCIENCE AND TECHNOLOGY CORPORATION (JP) 2005-07-12 US disclosed
EP-1297843-A1 METHOD OF PHOTOREDUCTION OF HEMOGLOBIN VESICLES Japan Science and Technology Corporation (JP) 2003-04-02 EP disclosed
US-20020095108-A1 Photoreduction method for hemoglobin-visicle JAPAN SCIENCE AND TECHNOLOGY CORPORATION (JP) 2002-07-18 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-20100044230-A1 METHODS FOR SEPARATING CARBON NANOTUBES FSCN1, TTPA, FLNB GSR 366/4885MAPT 1575/4885MEN1 3231/4885
US-20230148252-A1 PROCESS FOR TREATING KERATIN MATERIALS USING A FLAVIN DERIVATIVE, A POLYMERIZABLE MOLECULE AND LIGHT RADIATION KRT18, FLNA, VIM GSR 1584/4885MAPT 240/4885MEN1 3617/4885
US-20220033405-A1 PHARMACEUTICAL COMPOSITION FOR PREVENTING OR TREATING CANCER CONTAINING PLK1 INHIBITOR AS ACTIVE INGREDIENT PLK1, PLK2, PLK4 GSR 4488/4885MAPT 919/4885MEN1 2253/4885
US-20200375866-A1 HAIR TREATMENT PROCESS USING A FLAVIN DERIVATIVE AND LIGHT RADIATION FH, BLVRB, NQO1 GSR 162/4885MAPT 757/4885MEN1 2096/4885

“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.