SCHEMBL8919552

SCHEMBL8919552

CC(C)(C)OC(=O)NC1C2CN(Cc3ccccc3)CC21

nearest known ligand 0.57

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KMT2A Q03164 2/20 0.57
L3MBTL1 Q9Y468 1/20 0.57
HTR4 Q13639 1/20 0.48
HRH3 Q9Y5N1 1/20 0.48
NPFFR1 Q9GZQ6 1/20 0.47
NPFFR2 Q9Y5X5 1/20 0.47
S1PR1 P21453 1/20 0.45
S1PR5 Q9H228 1/20 0.45
TEAD1 P28347 1/20 0.45
BCHE P06276 2/20 0.44
UBE2M P61081 1/20 0.44
DCUN1D1 Q96GG9 1/20 0.44
KCNA3 P22001 1/20 0.44
CA12 O43570 1/20 0.44
CA1 P00915 1/20 0.44
CA7 P43166 1/20 0.44
CA14 Q9ULX7 1/20 0.44
MEN1 O00255 1/20 0.44
MAOB P27338 1/20 0.44
JAK1 P23458 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
SCHEMBL2082398 0.89 KMT2A (0.57) KMT2AL3MBTL1NPFFR1NPFFR2BCHE
SCHEMBL4869666 0.88 TEAD1 (0.46) KMT2AL3MBTL1HRH3S1PR5TEAD1
SCHEMBL1815532 0.88 KMT2A (0.65) KMT2AL3MBTL1NPFFR1NPFFR2S1PR1
SCHEMBL17304781 0.86 KMT2A (0.65) KMT2AL3MBTL1NPFFR1NPFFR2S1PR1
SCHEMBL9052529 0.86 KMT2A (0.54) KMT2AL3MBTL1NPFFR1NPFFR2BCHE
SCHEMBL8863819 0.86 KMT2A (0.54) KMT2AL3MBTL1NPFFR1NPFFR2BCHE
SCHEMBL25473941 0.85 TEAD1 (0.49) KMT2AL3MBTL1TEAD1SIGMAR1
SCHEMBL22719762 0.85 TEAD1 (0.49) KMT2AL3MBTL1TEAD1SIGMAR1
SCHEMBL25473933 0.85 TEAD1 (0.49) KMT2AL3MBTL1TEAD1SIGMAR1
SCHEMBL3187533 0.85 KMT2A (0.55) KMT2AL3MBTL1NPFFR1NPFFR2S1PR1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5691366-A UNSATURATED NITRO OXIME FORMED BY REACTION OF DINITROGEN TRIOXIDE WITH DIOLEFIN ETHER, SULFIDE OR AMINE TO BE USED AS VASODILATORS FUJISAWA PHARMACEUTICAL CO., LTD. (JP) 1997-11-25 US claimed
US-20240317705-A1 POTASSIUM CHANNEL MODULATORS NOVARTIS AG (CH) 2024-09-26 US disclosed
US-10774064-B2 Potassium channel modulators CADENT THERAPEUTICS, INC. (US) 2020-09-15 US disclosed
US-20190218200-A1 POTASSIUM CHANNEL MODULATORS NOVARTIS AG (CH) 2019-07-18 US disclosed
WO-2017139697-A9 BACTERIA ENGINEERED TO TREAT DISEASES ASSOCIATED WITH HYPERAMMONEMIA SYNLOGIC, INC. (US) 2017-12-07 WO disclosed
US-5623078-A Process for producing an intermediate of a new quinolone compound CHISSO CORPORATION (JP) 1997-04-22 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 (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-20240317705-A1 POTASSIUM CHANNEL MODULATORS KCNJ11, KCNJ2, KCNJ1 KMT2A 1471/4885L3MBTL1 4021/4885HTR4 1976/4885
US-10774064-B2 Potassium channel modulators KCNJ11, KCNJ2, KCNJ1 KMT2A 1471/4885L3MBTL1 4021/4885HTR4 1976/4885
US-20190218200-A1 POTASSIUM CHANNEL MODULATORS KCNJ11, KCNJ2, KCNJ1 KMT2A 1471/4885L3MBTL1 4021/4885HTR4 1976/4885

“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.