SCHEMBL4837398

SCHEMBL4837398

COC(=O)C(CC(=O)NOC(c1ccccc1)(c1ccccc1)c1ccccc1)CC(=O)OC(C)(C)C

nearest known ligand 0.44

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
KMT2A Q03164 2/20 0.44
CYP3A4 P08684 2/20 0.43
CYP2C9 P11712 1/20 0.43
KCNH2 Q12809 1/20 0.43
CA2 P00918 1/20 0.40
CA9 Q16790 1/20 0.40
L3MBTL1 Q9Y468 1/20 0.39
KLK5 Q9Y337 2/20 0.38
KIF11 P52732 1/20 0.35
CYP1A2 P05177 1/20 0.34
RECQL P46063 1/20 0.34
MAPK1 P28482 1/20 0.34
MDM4 O15151 1/20 0.34
MDM2 Q00987 1/20 0.34
USP2 O75604 3/20 0.34
KCNN4 O15554 1/20 0.33
BIRC2 Q13490 1/20 0.33

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
SCHEMBL4837207 0.90 CYP3A4 (0.44) CYP3A4CYP2C9KCNH2CA2CA9
SCHEMBL4839501 0.82 L3MBTL1 (0.49) CYP3A4CYP2C9KCNH2CA2CA9
SCHEMBL4835594 0.82 CYP3A4 (0.47) KMT2ACYP3A4CYP2C9KCNH2CA2
SCHEMBL4831283 0.80 CA2 (0.49) KMT2ACYP3A4CYP2C9KCNH2CA2
SCHEMBL4838181 0.80 CYP3A4 (0.36) CYP3A4CYP2C9KCNH2CA2CA9
SCHEMBL4840448 0.80 L3MBTL1 (0.43) CYP3A4CYP2C9KCNH2CA2CA9
SCHEMBL4838164 0.80 NPC1 (0.48) KMT2ACYP2C9CA2CA9L3MBTL1
SCHEMBL4886128 0.79 KMT2A (0.45) KMT2ACYP2C9CA2CA9USP2
SCHEMBL4839942 0.78 CA2 (0.45) KMT2ACA2CA9L3MBTL1
SCHEMBL4840798 0.76 MMP2 (0.45) CA2CA9L3MBTL1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7365091-B2 Derivatives of succinic and glutaric acids and analogs thereof useful as inhibitors of PHEX ENOBIA PHARMA (CA) 2008-04-29 US disclosed
US-20060287280-A1 Derivatives of succinic and glutaric acids and analogs thereof useful as inhibitors of PHEX ENOBIA PHARMA (CA) 2006-12-21 US disclosed
US-7105539-B2 Derivatives of succinic and glutaric acids and analogs thereof useful as inhibitors of phex ENOBIA PHARMA (CA) 2006-09-12 US disclosed
US-20060135480-A1 Derivatives of succinic and glutaric acids and analogs thereof useful as inhibitors of phex ENOBIA PHARMA (CA) 2006-06-22 US disclosed
EP-1572645-A2 DERIVATIVES OF SUCCINIC AND GLUTARIC ACIDS AND ANALOGS THEREOF USEFUL AS INHIBITORS OF PHEX Enobia Pharma Inc. (CA) 2005-09-14 EP disclosed
US-20040186301-A1 Derivatives of succinic and glutaric acids and analogs thereof useful as inhibitors of phex BIOMEP INC. 2004-09-23 US disclosed
WO-2004050620-A2 DERIVATIVES OF SUCCINIC AND GLUTARIC ACIDS AND ANALOGS THEREOF USEFUL AS INHIBITORS OF PHEX ENOBIA PHARMA (CA) 2004-06-17 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-20060287280-A1 Derivatives of succinic and glutaric acids and analogs thereof useful as inhibitors of PHEX GLS, SUCNR1, PGD KMT2A 2453/4885CYP3A4 1480/4885CYP2C9 1090/4885
US-20040186301-A1 Derivatives of succinic and glutaric acids and analogs thereof useful as inhibitors of phex GLS, SUCNR1, PGD KMT2A 2577/4885CYP3A4 1294/4885CYP2C9 940/4885
US-20060135480-A1 Derivatives of succinic and glutaric acids and analogs thereof useful as inhibitors of phex GLS, SUCNR1, GCDH KMT2A 2487/4885CYP3A4 1300/4885CYP2C9 941/4885

“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.