SCHEMBL10071932

SCHEMBL10071932

CCc1nc2ccc3c(c2[nH]1)C(=O)c1ccccc1C3=O

nearest known ligand 0.47

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TNKS2 Q9H2K2 1/20 0.47
MAPT P10636 9/20 0.44
SMN1; SMN2 Q16637 7/20 0.44
KMT2A Q03164 5/20 0.44
ALDH1A1 P00352 4/20 0.44
MEN1 O00255 4/20 0.44
HTT P42858 3/20 0.44
HPGD P15428 2/20 0.44
POLB P06746 2/20 0.44
DDAH1 O94760 1/20 0.44
MAOA P21397 3/20 0.43
ACVR1 Q04771 1/20 0.41
MAPK1 P28482 4/20 0.41
L3MBTL1 Q9Y468 3/20 0.41
NPC1 O15118 3/20 0.41
RAB9A P51151 3/20 0.41
LMNA P02545 2/20 0.41
TP53 P04637 1/20 0.40
MITF O75030 1/20 0.40
ADORA3 P0DMS8 2/20 0.39

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
SCHEMBL12261351 0.87 PARP1 (0.51) MAPTSMN1; SMN2KMT2AALDH1A1MEN1
SCHEMBL711986 0.86 MAOA (0.43) MAPTSMN1; SMN2KMT2AALDH1A1MEN1
SCHEMBL711989 0.85 MAPT (0.40) MAPTSMN1; SMN2KMT2AALDH1A1MEN1
SCHEMBL719982 0.85 KMT2A (0.42) MAPTSMN1; SMN2KMT2AALDH1A1MEN1
SCHEMBL712224 0.85 MAPT (0.41) MAPTSMN1; SMN2KMT2AALDH1A1MEN1
SCHEMBL12261358 0.84 PARP1 (0.46) MAPTSMN1; SMN2KMT2AALDH1A1MEN1
SCHEMBL711990 0.83 MAPT (0.39) MAPTSMN1; SMN2KMT2AALDH1A1MEN1
SCHEMBL714445 0.83 MAPT (0.44) MAPTSMN1; SMN2KMT2AALDH1A1MEN1
SCHEMBL713014 0.83 MAOA (0.41) MAPTSMN1; SMN2KMT2AALDH1A1MEN1
SCHEMBL10044133 0.83 MAPT (0.43) MAPTSMN1; SMN2KMT2AALDH1A1MEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8470824-B2 Substituted naphto[2,3-f]quinoxaline-7,12-diones and pharmaceutical utility thereof NATIONAL DEFENSE MEDICAL CENTER (TW) 2013-06-25 US disclosed
US-8470824-B2 Substituted naphto[2,3-f]quinoxaline-7,12-diones and pharmaceutical utility thereof NATIONAL DEFENSE MEDICAL CENTER (TW) 2013-06-25 US disclosed
US-8445492-B2 Method for inhibiting growth of cancer cells and cell telomere and diseases of cell proliferation by using heteroannelated anthraquinone derivative compounds NATIONAL DEFENSE MEDICAL CENTER (TW) 2013-05-21 US disclosed
US-8445492-B2 Method for inhibiting growth of cancer cells and cell telomere and diseases of cell proliferation by using heteroannelated anthraquinone derivative compounds NATIONAL DEFENSE MEDICAL CENTER (TW) 2013-05-21 US disclosed
US-8222287-B2 Substituted anthra[1,2-D]imidazolediones and pharmaceutical utility thereof NATIONAL DEFENSE MEDICAL CENTER (TW) 2012-07-17 US disclosed
US-8222287-B2 Substituted anthra[1,2-D]imidazolediones and pharmaceutical utility thereof NATIONAL DEFENSE MEDICAL CENTER (TW) 2012-07-17 US disclosed
US-8124637-B2 Anthra [1, 2-d]imidazole-6,11-dione derivatives, preparation method and application thereof NATIONAL DEFENSE MEDICAL CENTER (TW) 2012-02-28 US disclosed
US-20110224218-A1 METHOD FOR INHIBITING GROWTH OF CANCER CELLS AND CELL TELOMERE AND DISEASES OF CELL PROLIFERATION BY USING HETEROANNELATED ANTHRAQUINONE DERIVATIVE COMPOUNDS NATIONAL DEFENSE MEDICAL CENTER (TW) 2011-09-15 US disclosed
US-20110224218-A1 METHOD FOR INHIBITING GROWTH OF CANCER CELLS AND CELL TELOMERE AND DISEASES OF CELL PROLIFERATION BY USING HETEROANNELATED ANTHRAQUINONE DERIVATIVE COMPOUNDS NATIONAL DEFENSE MEDICAL CENTER (TW) 2011-09-15 US disclosed
US-20110207719-A1 Novel Anthra [1, 2-d]imidazole-6,11-dione Derivatives, Preparation Method and application thereof NATIONAL DEFENSE MEDICAL CENTER (TW) 2011-08-25 US disclosed
US-20100256155-A1 METHOD FOR INHIBITING GROWTH OF CANCER CELLS AND CELL TELOMERE AND DISEASES OF CELL PROLIFERATION BY USING HETEROANNELATED ANTHRAQUINONE DERIVATIVE COMPOUNDS NATIONAL DEFENSE MEDICAL CENTER (TW) 2010-10-07 US disclosed
US-20100256155-A1 METHOD FOR INHIBITING GROWTH OF CANCER CELLS AND CELL TELOMERE AND DISEASES OF CELL PROLIFERATION BY USING HETEROANNELATED ANTHRAQUINONE DERIVATIVE COMPOUNDS NATIONAL DEFENSE MEDICAL CENTER (TW) 2010-10-07 US disclosed
US-20100249143-A1 METHOD FOR INHIBITING GROWTH OF CANCER CELLS AND CELL TELOMERE AND DISEASES OF CELL PROLIFERATION BY USING HETEROANNELATED ANTHRAQUINONE DERIVATIVE COMPOUNDS NATIONAL DEFENSE MEDICAL CENTER (TW) 2010-09-30 US disclosed
US-20100249143-A1 METHOD FOR INHIBITING GROWTH OF CANCER CELLS AND CELL TELOMERE AND DISEASES OF CELL PROLIFERATION BY USING HETEROANNELATED ANTHRAQUINONE DERIVATIVE COMPOUNDS NATIONAL DEFENSE MEDICAL CENTER (TW) 2010-09-30 US disclosed
US-20090253707-A1 HETEROANNELATED ANTHRAQUINONE DERIVATIVES AND THE SYNTHESIS METHOD THEREOF NATIONAL DEFENSE MEDICAL CENTER (TW) 2009-10-08 US disclosed
US-20090253707-A1 HETEROANNELATED ANTHRAQUINONE DERIVATIVES AND THE SYNTHESIS METHOD THEREOF NATIONAL DEFENSE MEDICAL CENTER (TW) 2009-10-08 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 (5 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-20110224218-A1 METHOD FOR INHIBITING GROWTH OF CANCER CELLS AND CELL TELOMERE AND DISEASES OF CELL PROLIFERATION BY USING HETEROANNELATED ANTHRAQUINONE DERIVATIVE COMPOUNDS TELO2, TERT, H4C1; H4C2; H4C3; H4C4; H4C5; H4C6; H4C8; H4C9; H4C11; H4C12; H4C13; H4C14; H4C15; H4C16 TNKS2 111/4885MAPT 4584/4885SMN1; SMN2 3777/4885
US-20090253707-A1 HETEROANNELATED ANTHRAQUINONE DERIVATIVES AND THE SYNTHESIS METHOD THEREOF ANTXR2, RCC2, H4C1; H4C2; H4C3; H4C4; H4C5; H4C6; H4C8; H4C9; H4C11; H4C12; H4C13; H4C14; H4C15; H4C16 TNKS2 1682/4885MAPT 4881/4885SMN1; SMN2 4752/4885
US-20100249143-A1 METHOD FOR INHIBITING GROWTH OF CANCER CELLS AND CELL TELOMERE AND DISEASES OF CELL PROLIFERATION BY USING HETEROANNELATED ANTHRAQUINONE DERIVATIVE COMPOUNDS TELO2, TERT, POT1 TNKS2 241/4885MAPT 4799/4885SMN1; SMN2 2839/4885
US-20100256155-A1 METHOD FOR INHIBITING GROWTH OF CANCER CELLS AND CELL TELOMERE AND DISEASES OF CELL PROLIFERATION BY USING HETEROANNELATED ANTHRAQUINONE DERIVATIVE COMPOUNDS TELO2, TERT, POT1 TNKS2 241/4885MAPT 4799/4885SMN1; SMN2 2839/4885
US-20110207719-A1 Novel Anthra [1, 2-d]imidazole-6,11-dione Derivatives, Preparation Method and application thereof TERT, ACIN1, AK2 TNKS2 55/4885MAPT 3490/4885SMN1; SMN2 3811/4885

“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.