SCHEMBL9435674

SCHEMBL9435674

CC(C)c1cccc(C(C)C)c1NC(=O)Nc1ccccc1

nearest known ligand 0.63

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
KMT2A Q03164 4/20 0.63
LMNA P02545 1/20 0.63
LPAR1 Q92633 1/20 0.60
SMN1; SMN2 Q16637 2/20 0.59
TP53 P04637 1/20 0.59
EPHX1 P07099 1/20 0.59
TSHR P16473 1/20 0.59
EPHX2 P34913 1/20 0.59
CDK9 P50750 1/20 0.59
CLK4 Q9HAZ1 1/20 0.59
NPC1 O15118 1/20 0.53
RAB9A P51151 1/20 0.53
TAAR1 Q96RJ0 1/20 0.53
CASP3 P42574 1/20 0.52
SENP7 Q9BQF6 1/20 0.52
MEN1 O00255 1/20 0.51

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
SCHEMBL462304 0.89 LPAR1 (0.66) KMT2ALMNALPAR1SMN1; SMN2MEN1
SCHEMBL28757102 0.88 SMN1; SMN2 (0.57) KMT2ALMNALPAR1SMN1; SMN2TP53
SCHEMBL12048116 0.87 KMT2A (0.58) KMT2ALMNALPAR1SMN1; SMN2EPHX1
SCHEMBL5642336 0.85 MDM2 (0.59) KMT2ALMNALPAR1SMN1; SMN2RAB9A
SCHEMBL8536693 0.83 SMN1; SMN2 (0.51) KMT2ALMNALPAR1SMN1; SMN2MEN1
SCHEMBL9723517 0.82 KMT2A (0.61) KMT2ALMNALPAR1SMN1; SMN2MEN1
SCHEMBL9723538 0.81 KMT2A (0.60) KMT2ALMNALPAR1SMN1; SMN2MEN1
SCHEMBL8845511 0.80 KMT2A (0.68) KMT2ALMNALPAR1SMN1; SMN2MEN1
SCHEMBL9504118 0.79 LMNA (0.58) KMT2ALMNALPAR1
SCHEMBL9723484 0.78 KMT2A (0.57) KMT2ALMNALPAR1SMN1; SMN2MEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-113444024-A Method for synthesizing polysubstituted ureas, thioureas, chiral ureas and thioureas compounds without catalyst and solvent 安徽师范大学 2021-09-28 CN claimed
CN-113444024-A Method for synthesizing polysubstituted ureas, thioureas, chiral ureas and thioureas compounds without catalyst and solvent 安徽师范大学 2021-09-28 CN disclosed
US-9663452-B2 Method for preparing formamidines COMMISSARIAT A L'ENERGIE ATOMIQUE ET AUX ENERGIES ALTERNATIVES (FR) 2017-05-30 US disclosed
US-9663452-B2 Method for preparing formamidines COMMISSARIAT A L'ENERGIE ATOMIQUE ET AUX ENERGIES ALTERNATIVES (FR) 2017-05-30 US disclosed
US-20150266813-A1 Method For Preparing Formamidines COMMISSARIAT A L'ENERGIE ATOMIQUE ET AUX ENERGIES ALTERNATIVES (FR) 2015-09-24 US disclosed
US-20150266813-A1 Method For Preparing Formamidines COMMISSARIAT A L'ENERGIE ATOMIQUE ET AUX ENERGIES ALTERNATIVES (FR) 2015-09-24 US disclosed
WO-2014057466-A1 METHOD FOR PREPARING FORMAMIDINES COMMISSARIAT A L'ENERGIE ATOMIQUE ET AUX ENERGIES ALTERNATIVES (FR) 2014-04-17 WO disclosed
US-5283362-A Reacting with an amine, terminating the reaction before the formation of by-product CHEMIE LINZ GESELLSCHAFT M.B.H. (AT) 1994-02-01 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 (1 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-20150266813-A1 Method For Preparing Formamidines PFAS, CYP4F3, CYP2F1 KMT2A 1822/4885LMNA 1592/4885LPAR1 4271/4885

“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.