SCHEMBL3040420

SCHEMBL3040420

CC(C)C[C@H](C(=O)O)N1CC[C@]2(CCCN2C(=O)C(C)C)C1=O

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
NTSR1 P30989 3/20 0.40
GRIN2B Q13224 1/20 0.34
GRIN2C Q14957 1/20 0.34
SMN1; SMN2 Q16637 1/20 0.33
HSD11B1 P28845 1/20 0.33
ADAM10 O14672 3/20 0.32
MMP1 P03956 3/20 0.32
MMP2 P08253 3/20 0.32
MMP3 P08254 3/20 0.32
MMP7 P09237 3/20 0.32
MMP9 P14780 3/20 0.32
MMP8 P22894 3/20 0.32
MMP13 P45452 3/20 0.32
MMP14 P50281 3/20 0.32
ADAM17 P78536 3/20 0.32
SLC6A2 P23975 1/20 0.32
SLC6A4 P31645 1/20 0.32
SLC6A3 Q01959 1/20 0.32
ACE P12821 2/20 0.32
MME P08473 1/20 0.32

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
SCHEMBL7171906 1.00 NTSR1 (0.40) NTSR1GRIN2BGRIN2CSMN1; SMN2HSD11B1
SCHEMBL9734966 0.90 NTSR1 (0.37) NTSR1GRIN2BGRIN2CSMN1; SMN2HSD11B1
SCHEMBL14219500 0.89 NTSR1 (0.36) NTSR1GRIN2BGRIN2CSMN1; SMN2HSD11B1
SCHEMBL16317418 0.87 NTSR1 (0.35) NTSR1GRIN2BGRIN2CSMN1; SMN2HSD11B1
SCHEMBL3053658 0.87 NTSR1 (0.35) NTSR1GRIN2BGRIN2CSMN1; SMN2HSD11B1
SCHEMBL16317411 0.85 NTSR1 (0.35) NTSR1GRIN2BGRIN2CSMN1; SMN2HSD11B1
SCHEMBL3051772 0.85 NTSR1 (0.35) NTSR1GRIN2BGRIN2CSMN1; SMN2HSD11B1
SCHEMBL3164763 0.83 GRIN2B (0.54) NTSR1GRIN2BGRIN2CSMN1; SMN2HSD11B1
SCHEMBL16317480 0.83 GRIN2B (0.54) NTSR1GRIN2BGRIN2CSMN1; SMN2HSD11B1
SCHEMBL3054791 0.82 NTSR1 (0.40) NTSR1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7678765-B2 Synthetic methods for aplidine and new antitumoral derivatives, methods of making and using them PHARMA MAR, S.A. (ES) 2010-03-16 US disclosed
US-7678765-B2 Synthetic methods for aplidine and new antitumoral derivatives, methods of making and using them PHARMA MAR, S.A. (ES) 2010-03-16 US disclosed
US-7678765-B2 Synthetic methods for aplidine and new antitumoral derivatives, methods of making and using them PHARMA MAR, S.A. (ES) 2010-03-16 US disclosed
EP-1294747-B1 SYNTHETIC METHODS FOR APLIDINE AND NEW ANTITUMORAL DERIVATIVES, METHODS OF MAKING AND USING THEM PHARMA MAR SA (ES) 2008-04-30 EP disclosed
US-7348310-B2 Synthetic methods for aplidine and new antitumoral derivatives, methods of making and using them PHARMA MAR, S.A. (ES) 2008-03-25 US disclosed
US-7348310-B2 Synthetic methods for aplidine and new antitumoral derivatives, methods of making and using them PHARMA MAR, S.A. (ES) 2008-03-25 US disclosed
US-7348310-B2 Synthetic methods for aplidine and new antitumoral derivatives, methods of making and using them PHARMA MAR, S.A. (ES) 2008-03-25 US disclosed
US-20080009435-A1 Synthetic methods for aplidine and new antitumoral derivatives, methods of making and using them PHARMA MAR, S.A., A SPAIN CORPORATION 2008-01-10 US disclosed
US-20080009435-A1 Synthetic methods for aplidine and new antitumoral derivatives, methods of making and using them PHARMA MAR, S.A., A SPAIN CORPORATION 2008-01-10 US disclosed
US-20080009435-A1 Synthetic methods for aplidine and new antitumoral derivatives, methods of making and using them PHARMA MAR, S.A., A SPAIN CORPORATION 2008-01-10 US disclosed
US-20040097413-A1 Synthetic methods for aplidine and new antitumoral derivatives, methods of making and using them PHARMA MAR, S.A. (ES) 2004-05-20 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 (2 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-20040097413-A1 Synthetic methods for aplidine and new antitumoral derivatives, methods of making and using them MCL1, PML, APLNR NTSR1 3472/4885GRIN2B 2605/4885GRIN2C 3233/4885
US-20080009435-A1 Synthetic methods for aplidine and new antitumoral derivatives, methods of making and using them MCL1, APLNR, PAICS NTSR1 2662/4885GRIN2B 2925/4885GRIN2C 3786/4885

“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.