Silver

Silver

SCHEMBL4232127

O=C([O-])c1ccc(P(=O)(OCc2ccccc2)OCc2ccccc2)cc1.[Ag+]

nearest known ligand 0.50

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

folP

The experimentally established mechanism targets of Silver. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TSHR P16473 1/20 0.50
CA2 P00918 2/20 0.44
CA4 P22748 1/20 0.44
CETP P11597 3/20 0.43
ALDH1A1 P00352 1/20 0.42
NPC1 O15118 3/20 0.41
RAB9A P51151 3/20 0.41
NR4A1 P22736 1/20 0.41
NR4A2 P43354 1/20 0.41
NR4A3 Q92570 1/20 0.41
LMNA P02545 1/20 0.41
SLC6A2 P23975 1/20 0.41
SLC6A3 Q01959 1/20 0.41
KMT2A Q03164 1/20 0.41
TDP1 Q9NUW8 1/20 0.41
LTA4H P09960 1/20 0.40
EPHX2 P34913 1/20 0.40
MAOB P27338 1/20 0.40
PARP10 Q53GL7 1/20 0.40
ALPG P10696 1/20 0.40

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
SCHEMBL4232124 0.84 NR4A2 (0.56) TSHRCETPALDH1A1NR4A1NR4A2
SCHEMBL5400948 0.81 TSHR (0.61) TSHRCA2CETPALDH1A1KMT2A
Silver SCHEMBL4220651 0.80 TSHR (0.49) TSHRCA2CA4CETPNPC1
SCHEMBL21805836 0.76 MEN1 (0.53) TSHRCETPALDH1A1NPC1RAB9A
SCHEMBL20710698 0.73 LTA4H (0.52) TSHRCA2CA4CETPALDH1A1
Potassium Ion SCHEMBL10916773 0.72 KMT2A (0.73) CA2CA4ALDH1A1NPC1RAB9A
SCHEMBL11098403 0.72 NR4A1 (0.72) ALDH1A1NPC1RAB9ANR4A1NR4A2
SCHEMBL5969733 0.72 NR4A1 (0.72) ALDH1A1NPC1RAB9ANR4A1NR4A2
SCHEMBL21805851 0.72 LMNA (0.56) TSHRCA2CETPALDH1A1NPC1
SCHEMBL21891867 0.71 TSHR (0.53) TSHRCETPALDH1A1ALPGPTK2B

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7572795-B2 Pyrrolotriazine aniline prodrug compounds useful as kinase inhibitors BRISTOL-MYERS SQUIBB COMPANY (US) 2009-08-11 US disclosed
US-20090156555-A1 PYRROLOTRIAZINE ANILINE PRODRUG COMPOUNDS USEFUL AS KINASE INHIBITORS BRISTOL-MYERS SQUIBB COMPANY 2009-06-18 US disclosed
EP-2001886-A2 PYRROLOTRIAZINE ANILINE PRODRUG COMPOUNDS USEFUL AS KINASE INHIBITORS Bristol-Myers Squibb Company (US) 2008-12-17 EP disclosed
WO-2007103839-A2 PYRROLOTRIAZINE ANILINE PRODRUG COMPOUNDS USEFUL AS KINASE INHIBITORS BRISTOL-MYERS SQUIBB COMPANY (US) 2007-09-13 WO disclosed
US-20070213300-A1 PYRROLOTRIAZINE ANILINE PRODRUG COMPOUNDS USEFUL AS KINASE INHIBITORS BRISTOL-MYERS SQUIBB COMPANY 2007-09-13 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-20090156555-A1 PYRROLOTRIAZINE ANILINE PRODRUG COMPOUNDS USEFUL AS KINASE INHIBITORS CDK2, CDK3, CDK1 TSHR 612/4885CA2 1586/4885CA4 3728/4885
US-20070213300-A1 PYRROLOTRIAZINE ANILINE PRODRUG COMPOUNDS USEFUL AS KINASE INHIBITORS CDK2, CDK3, CDK1 TSHR 697/4885CA2 1602/4885CA4 3685/4885

“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.