SCHEMBL1320737

SCHEMBL1320737

CC(CCNC1(Cc2cccc(Cl)c2)C(=O)Nc2cc(Cl)ccc21)CC(=O)N1CCC(O)CC1

nearest known ligand 0.49

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
MDM2 Q00987 11/20 0.49
TP53 P04637 7/20 0.49
OPRK1 P41145 1/20 0.35
ADAMTS5 Q9UNA0 3/20 0.35
ADAM17 P78536 2/20 0.35
GHSR Q92847 1/20 0.35
MDM4 O15151 1/20 0.35
MMP13 P45452 1/20 0.34
ADORA2B P29275 1/20 0.34
THRB P10828 1/20 0.34
MMP2 P08253 1/20 0.34
PYGL P06737 1/20 0.34
CYP51A1 Q16850 1/20 0.34

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
SCHEMBL1321532 0.96 MDM2 (0.48) MDM2TP53OPRK1ADAMTS5ADAM17
SCHEMBL1320132 0.88 MDM2 (0.45) MDM2TP53GHSR
SCHEMBL1320122 0.79 MDM2 (0.47) MDM2TP53OPRK1ADAMTS5
SCHEMBL8204684 0.79 MDM2 (0.49) MDM2TP53ADAMTS5ADAM17PYGL
SCHEMBL8199660 0.78 MDM2 (0.49) MDM2TP53ADAMTS5ADAM17MMP13
SCHEMBL3239017 0.78 MDM2 (0.51) MDM2TP53PYGLCYP51A1
SCHEMBL1322509 0.77 CYP51A1 (0.51) MDM2TP53PYGLCYP51A1
SCHEMBL1321534 0.75 MDM2 (0.56) MDM2TP53
SCHEMBL3253003 0.75 MDM2 (0.50) MDM2TP53OPRK1ADORA2BPYGL
SCHEMBL1320804 0.74 MDM2 (0.59) MDM2TP53MDM4

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
US-8058269-B2 rac-6-chloro-3-(3-chloro-benzyl)-3-(3-isopropoxy-phenylamino)-1,3-dihydro-indol-2-one; murine double minute (MDM2 ) oncogene inhibitor; feedback control loop of p53 mutant cells; inhibit the interaction between p53 and MDM2 proteins HOFFMAN-LA ROCHE INC. (US) 2011-11-15 US claimed
EP-2066318-B1 OXINDOLE DERIVATIVES AS ANTICANCER AGENTS HOFFMANN LA ROCHE (CH) 2010-05-12 EP claimed
EP-2066318-A2 OXINDOLE DERIVATIVES AS ANTICANCER AGENTS F. Hoffmann-Roche AG (CH) 2009-06-10 EP claimed
US-20080081810-A1 OXINDOLE DERIVATIVES CHEN LI 2008-04-03 US claimed
WO-2008034736-A2 OXINDOLE DERIVATIVES AS ANTICANCER AGENTS F. HOFFMANN-LA ROCHE AG (CH) 2008-03-27 WO claimed
US-8058269-B2 rac-6-chloro-3-(3-chloro-benzyl)-3-(3-isopropoxy-phenylamino)-1,3-dihydro-indol-2-one; murine double minute (MDM2 ) oncogene inhibitor; feedback control loop of p53 mutant cells; inhibit the interaction between p53 and MDM2 proteins HOFFMAN-LA ROCHE INC. (US) 2011-11-15 US disclosed
EP-2066318-B1 OXINDOLE DERIVATIVES AS ANTICANCER AGENTS HOFFMANN LA ROCHE (CH) 2010-05-12 EP disclosed
EP-2066318-A2 OXINDOLE DERIVATIVES AS ANTICANCER AGENTS F. Hoffmann-Roche AG (CH) 2009-06-10 EP disclosed
US-20080081810-A1 OXINDOLE DERIVATIVES CHEN LI 2008-04-03 US disclosed
WO-2008034736-A2 OXINDOLE DERIVATIVES AS ANTICANCER AGENTS F. HOFFMANN-LA ROCHE AG (CH) 2008-03-27 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 (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-20080081810-A1 OXINDOLE DERIVATIVES CCNY, CCNI, RPS4Y1 MDM2 441/4885TP53 219/4885OPRK1 13/4885

“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.