SCHEMBL5563158

SCHEMBL5563158

CC1=C(C(=O)O)C(c2cccc([N+](=O)[O-])c2)N(CCCN(C)C(=O)c2ccc(C(C)(C)C)cc2)C(=O)N1

nearest known ligand 0.44

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
CACNA1H O95180 2/20 0.44
CACNA1F O60840 6/20 0.44
CACNA1D Q01668 6/20 0.44
CACNA1S Q13698 6/20 0.44
CACNA1C Q13936 6/20 0.44
ALDH1A1 P00352 2/20 0.39
LMNA P02545 2/20 0.39
POLB P06746 1/20 0.39
GUSB P08236 1/20 0.39
MEN1 O00255 1/20 0.38
NPC1 O15118 1/20 0.38
MAPT P10636 1/20 0.38
NFKB1 P19838 1/20 0.38
RAB9A P51151 1/20 0.38
NFKB2 Q00653 1/20 0.38
KMT2A Q03164 1/20 0.38
RELA Q04206 1/20 0.38
SMN1; SMN2 Q16637 1/20 0.38

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
SCHEMBL5567923 0.92 CACNA1H (0.49) CACNA1HCACNA1FCACNA1DCACNA1SCACNA1C
SCHEMBL5567327 0.91 CACNA1H (0.46) CACNA1HCACNA1FCACNA1DCACNA1SCACNA1C
SCHEMBL5567034 0.91 CACNA1H (0.46) CACNA1HCACNA1FCACNA1DCACNA1SCACNA1C
SCHEMBL5568432 0.91 CACNA1H (0.47) CACNA1HCACNA1FCACNA1DCACNA1SCACNA1C
SCHEMBL5568260 0.90 CACNA1H (0.48) CACNA1HCACNA1FCACNA1DCACNA1SCACNA1C
SCHEMBL5567957 0.89 CACNA1H (0.46) CACNA1HCACNA1FCACNA1DCACNA1SCACNA1C
SCHEMBL5568170 0.89 CACNA1H (0.46) CACNA1HCACNA1FCACNA1DCACNA1SCACNA1C
SCHEMBL5567165 0.88 CACNA1H (0.44) CACNA1HCACNA1FCACNA1DCACNA1SCACNA1C
SCHEMBL5567236 0.88 CACNA1H (0.47) CACNA1HCACNA1FCACNA1DCACNA1SCACNA1C
SCHEMBL5568152 0.88 CACNA1F (0.46) CACNA1HCACNA1FCACNA1DCACNA1SCACNA1C

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
US-7166603-B2 Dihydropyrimidone inhibitors of calcium channel function BRISTOL-MYERS SQUIBB CO. (US) 2007-01-23 US claimed
US-20050043339-A1 Dihydropyrimidone inhibitors of calcium channel function BRISTOL-MYERS SQUIBB COMPANY 2005-02-24 US claimed
WO-2005009392-A2 DIHYDROPYRIMIDONE INHIBITORS OF CALCIUM CHANNEL FUNCTION BRISTOL-MYERS SQUIBB COMPANY (US) 2005-02-03 WO claimed
US-7166603-B2 Dihydropyrimidone inhibitors of calcium channel function BRISTOL-MYERS SQUIBB CO. (US) 2007-01-23 US disclosed
EP-1525205-A2 NOVEL SUBSTITUTED PYRAZOLO( 1,5-A /I ]-1,3,5-TRIAZINE DERIVATIVES AND THEIR ANALOGUES, PHARMACEUTICAL COMPOSITIONS CONTAINING SAME, USE THEREOF AS MEDICINE AND METHODS FOR PREPARING SAME Greenpharma (FR) 2005-04-27 EP disclosed
US-20050043339-A1 Dihydropyrimidone inhibitors of calcium channel function BRISTOL-MYERS SQUIBB COMPANY 2005-02-24 US disclosed
WO-2005009392-A2 DIHYDROPYRIMIDONE INHIBITORS OF CALCIUM CHANNEL FUNCTION BRISTOL-MYERS SQUIBB COMPANY (US) 2005-02-03 WO disclosed
WO-2004011464-A2 NOVEL SUBSTITUTED PYRAZOLO[1,5 A]-1,3,5-TRIAZINE DERIVATIVES AND THEIR ANALOGUES, PHARMACEUTICAL COMPOSITIONS CONTAINING SAME, USE THEREOF AS MEDICINE AND METHODS FOR PREPARING SAME GREENPHARMA (FR) 2004-02-05 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-20050043339-A1 Dihydropyrimidone inhibitors of calcium channel function CACNA1E, CACNA1C, CACNA1S CACNA1H 10/4885CACNA1F 6/4885CACNA1D 4/4885

“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.