SCHEMBL13738271

SCHEMBL13738271

OB(O)c1ccccc1CNc1ccccc1

nearest known ligand 0.47

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPT P10636 6/20 0.47
HIF1A Q16665 5/20 0.46
LIPG Q9Y5X9 1/20 0.46
HPGD P15428 2/20 0.44
L3MBTL1 Q9Y468 3/20 0.41
MEN1 O00255 3/20 0.41
KMT2A Q03164 3/20 0.41
ALDH1A1 P00352 2/20 0.41
GAA P10253 2/20 0.41
THRB P10828 2/20 0.41
BLM P54132 2/20 0.41
TDP1 Q9NUW8 2/20 0.41
RECQL P46063 1/20 0.41
ATM Q13315 1/20 0.41
PLEC Q15149 1/20 0.41
PKM P14618 1/20 0.41
CYP1A2 P05177 1/20 0.41
CYP3A4 P08684 1/20 0.41
CYP2C9 P11712 1/20 0.41
CYP2C19 P33261 1/20 0.41

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
SCHEMBL24274961 0.83 MAPT (0.68) MAPTHPGDL3MBTL1MEN1KMT2A
SCHEMBL26085708 0.80 CFD (0.53) MAPTLIPGHPGDL3MBTL1LMNA
SCHEMBL13830817 0.80 CA1 (0.62) MAPTHIF1AHPGDMEN1KMT2A
SCHEMBL10055008 0.79 MAPT (0.53) MAPTHIF1AHPGDL3MBTL1MEN1
SCHEMBL902105 0.78 LIPG (0.50) MAPTLIPGMEN1KMT2AALDH1A1
SCHEMBL30949224 0.78 LIPG (0.50) MAPTLIPGMEN1KMT2AALDH1A1
SCHEMBL30949223 0.78 LIPG (0.50) MAPTLIPGMEN1KMT2AALDH1A1
SCHEMBL28433585 0.77 MAPT (0.63) MAPTLIPGL3MBTL1MEN1KMT2A
SCHEMBL13830752 0.76 EGFR (0.62) HIF1AHPGDALDH1A1CYP1A2CYP3A4
SCHEMBL13287109 0.76 LIPG (0.48) HIF1ALIPGPKMKDM4E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118453643-A Antioxidant high polymer hydrogel and preparation method and application thereof 哈尔滨医科大学 2024-08-09 CN disclosed
US-20240083857-A1 2-Methyl-Quinazolines Bayer Pharma AG (DE) 2024-03-14 US disclosed
CN-111848668-B Pyridinylamino IVB group binuclear metal complex and preparation and application thereof 万华化学集团股份有限公司 2023-03-03 CN disclosed
US-20220340893-A1 BI-FUNCTIONAL COMPLEXES AND METHODS FOR MAKING AND USING SUCH COMPLEXES NUEVOLUTION A/S (DK) 2022-10-27 US disclosed
US-20220235013-A1 2-METHYL-QUINAZOLINES BAYER PHARMA AKTIENGESELLSCHAFT (DE) 2022-07-28 US disclosed
CN-111848668-A Pyridinylamino IVB group binuclear metal complex and preparation and application thereof 万华化学集团股份有限公司 2020-10-30 CN disclosed
EP-3601267-A1 2-METHYL-QUINAZOLINES Bayer Pharma Aktiengesellschaft (DE) 2020-02-05 EP disclosed
WO-2018172250-A1 2-METHYL-QUINAZOLINES BAYER PHARMA AKTIENGESELLSCHAFT (DE) 2018-09-27 WO disclosed
US-20140161729-A1 COFLUORONS AND METHODS OF MAKING AND USING THEM CORNELL UNIVERSITY (US) 2014-06-12 US disclosed
WO-2012154213-A1 COFLUORONS AND METHODS OF MAKING AND USING THEM CORNELL UNIVERSITY (US) 2012-11-15 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 (3 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-20240083857-A1 2-Methyl-Quinazolines NRAS, KRAS, KSR2 MAPT 4627/4885HIF1A 2197/4885LIPG 3777/4885
US-20140161729-A1 COFLUORONS AND METHODS OF MAKING AND USING THEM TNFSF11, CD14, TNFRSF1A MAPT 418/4885HIF1A 2817/4885LIPG 2627/4885
US-20220235013-A1 2-METHYL-QUINAZOLINES NRAS, KRAS, KSR2 MAPT 4627/4885HIF1A 2197/4885LIPG 3777/4885

“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.