SCHEMBL309636

SCHEMBL309636

CCOc1cc(Br)ccc1[N+](=O)[O-]

nearest known ligand 0.57

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
MAPT P10636 5/20 0.57
FBP1 P09467 1/20 0.51
LMNA P02545 5/20 0.50
ALDH1A1 P00352 3/20 0.50
RECQL P46063 2/20 0.47
MAPK1 P28482 2/20 0.47
MEN1 O00255 1/20 0.47
KMT2A Q03164 1/20 0.47
POLB P06746 1/20 0.44
NPC1 O15118 2/20 0.42
RAB9A P51151 2/20 0.42
HPGD P15428 1/20 0.42
TSHR P16473 1/20 0.42
GAA P10253 1/20 0.41
GBA1 P04062 1/20 0.41
SMN1; SMN2 Q16637 1/20 0.40
TDP1 Q9NUW8 1/20 0.40
S1PR4 O95977 1/20 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
SCHEMBL29508979 1.00 MAPT (0.57) MAPTFBP1LMNAALDH1A1RECQL
SCHEMBL3039038 0.87 LMNA (0.51) MAPTFBP1LMNAALDH1A1RECQL
SCHEMBL22897608 0.84 MAPT (0.42) MAPTFBP1LMNAALDH1A1RECQL
SCHEMBL29212458 0.83 NPC1 (0.42) MAPTFBP1LMNAALDH1A1RECQL
SCHEMBL23589335 0.83 ALDH1A1 (0.53) MAPTLMNAALDH1A1MAPK1MEN1
SCHEMBL15508187 0.83 NPC1 (0.50) MAPTLMNAALDH1A1RECQLMAPK1
SCHEMBL10197531 0.81 NPC1 (0.46) MAPTALDH1A1MAPK1MEN1KMT2A
SCHEMBL20577146 0.81 NPC1 (0.45) MAPTLMNAALDH1A1RECQLKMT2A
SCHEMBL10197528 0.81 NPC1 (0.49) MAPTALDH1A1MAPK1MEN1KMT2A
SCHEMBL11058768 0.81 MAPT (0.58) MAPTLMNAALDH1A1RECQLMAPK1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250179059-A1 ANTICANCER COMPOUNDS THE REGENTS OF THE UNIVERSITY OF CALIFORNIA 2025-06-05 US disclosed
US-12312339-B2 Polo like kinase 4 inhibitors ORIC PHARMACEUTICALS, INC. (US) 2025-05-27 US disclosed
US-12162870-B2 Anticancer compounds THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2024-12-10 US disclosed
US-20240270722-A1 POLO LIKE KINASE 4 INHIBITORS ORIC PHARMACEUTICALS, INC. 2024-08-15 US disclosed
US-20240124426-A1 POLO LIKE KINASE 4 INHIBITORS ORIC PHARMACEUTICALS, INC. 2024-04-18 US disclosed
EP-4351560-A1 ANTICANCER COMPOUNDS The Regents of the University of California (US) 2024-04-17 EP disclosed
CN-117794529-A POLO-like kinase 4 inhibitors 欧瑞克制药公司 2024-03-29 CN disclosed
CN-117794525-A Anticancer compounds 加利福尼亚大学董事会 2024-03-29 CN disclosed
EP-4337198-A1 POLO LIKE KINASE 4 INHIBITORS Oric Pharmaceuticals, Inc. (US) 2024-03-20 EP disclosed
US-20240067648-A1 N-OXIDE INHIBITORS OF NLRP3 INFLAMMASOME BioAge Labs, Inc. 2024-02-29 US disclosed
US-20070208054-A1 MACROCYCLIC FACTOR VIIA INHIBITORS USEFUL AS ANTICOAGULANTS BRISTOL-MYERS SQUIBB COMPANY 2007-09-06 US disclosed
US-20070208054-A1 MACROCYCLIC FACTOR VIIA INHIBITORS USEFUL AS ANTICOAGULANTS BRISTOL-MYERS SQUIBB COMPANY 2007-09-06 US disclosed
US-20070208054-A1 MACROCYCLIC FACTOR VIIA INHIBITORS USEFUL AS ANTICOAGULANTS BRISTOL-MYERS SQUIBB COMPANY 2007-09-06 US disclosed
WO-2007076431-A1 MACROCYCLIC FACTOR VIIA INHIBITORS USEFUL AS ANTICOAGULANTS BRISTOL-MYERS SQUIBB COMPANY (US) 2007-07-05 WO disclosed
US-20070088067-A1 Novel amidine compounds for treating microbial infections GEORGIA STATE UNIVERSITY RESEARCH FOUNDATION, INC. 2007-04-19 US disclosed
EP-1663959-A1 NOVEL AMIDINE COMPOUNDS FOR TREATING MICROBIAL INFECTIONS UNIVERSITY OF NORTH CAROLINA AT CHAPEL HILL (US) 2006-06-07 EP disclosed
WO-2005033065-A1 NOVEL AMIDINE COMPOUNDS FOR TREATING MICROBIAL INFECTIONS UNIVERSITY OF NORTH CAROLINA AT CHAPEL HILL (US) 2005-04-14 WO disclosed
US-6706754-B2 ANTIPROTOZOA AGENTS, PARASITICIDES THE UNITED STATES OF AMERICA AS REPRESENTED BY THE SECRETARY OF THE ARMY 2004-03-16 US disclosed
US-20020156098-A1 Reversed amidines and methods of using for treating, preventing, or inhibiting leishmaniasis ARMY, UNITED STATES 2002-10-24 US disclosed
WO-2002036588-A2 REVERSED AMIDINES AND METHODS OF USING FOR TREATING, PREVENTING, OR INHIBITING LEISHMANIASIS U.S. ARMY MEDICAL RESEARCH AND MATERIEL COMMAND (US) 2002-05-10 WO 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 (9 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-20250179059-A1 ANTICANCER COMPOUNDS BET1, BRD4, BICRA MAPT 2666/4885FBP1 2236/4885LMNA 4337/4885
US-20240124426-A1 POLO LIKE KINASE 4 INHIBITORS PLK4, PLK2, PLK3 MAPT 1102/4885FBP1 1932/4885LMNA 2193/4885
US-20070088067-A1 Novel amidine compounds for treating microbial infections ARG1, ARG2, GSDMD MAPT 2490/4885FBP1 1786/4885LMNA 4384/4885
US-12312339-B2 Polo like kinase 4 inhibitors PLK4, PLK2, PLK3 MAPT 1102/4885FBP1 1932/4885LMNA 2193/4885
US-20070208054-A1 MACROCYCLIC FACTOR VIIA INHIBITORS USEFUL AS ANTICOAGULANTS F12, F7, F2 MAPT 1936/4885FBP1 667/4885LMNA 217/4885
US-20240067648-A1 N-OXIDE INHIBITORS OF NLRP3 INFLAMMASOME NLRP3, NOD1, CASP1 MAPT 940/4885FBP1 3339/4885LMNA 407/4885
US-20020156098-A1 Reversed amidines and methods of using for treating, preventing, or inhibiting leishmaniasis ARG1, NAT1, CTSA MAPT 4882/4885FBP1 2158/4885LMNA 515/4885
US-20240270722-A1 POLO LIKE KINASE 4 INHIBITORS PLK4, PLK2, PLK3 MAPT 1151/4885FBP1 1817/4885LMNA 2199/4885
US-12162870-B2 Anticancer compounds BET1, BRD4, BICRA MAPT 2666/4885FBP1 2236/4885LMNA 4337/4885

“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.