Pamoic Acid

Pamoic Acid

SCHEMBL517883

CCN(CC)CC.CCN(CC)CC.O=C(O)c1cc2ccccc2c(Cc2c(O)c(C(=O)O)cc3ccccc23)c1O

nearest known ligand 0.81

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

DRD2DRD3DRD4GNRHRHRH1HTR2AHTR2CSLC6A2SLC6A4SSTR1SSTR2SSTR3SSTR5

The experimentally established mechanism targets of Pamoic Acid. 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
POLB P06746 3/20 0.81
GPR35 Q9HC97 2/20 0.81
ME2 P23368 1/20 0.64
ME1 P48163 1/20 0.64
ME3 Q16798 1/20 0.64
MEN1 O00255 8/20 0.51
KMT2A Q03164 8/20 0.51
MAPT P10636 5/20 0.51
CYP3A4 P08684 3/20 0.51
ALOX15 P16050 3/20 0.51
HPGD P15428 3/20 0.51
MAPK1 P28482 2/20 0.51
TP53 P04637 1/20 0.51
SMN1; SMN2 Q16637 1/20 0.51
TDP1 Q9NUW8 1/20 0.51
HSD17B10 Q99714 6/20 0.51
GALK1 P51570 1/20 0.51
CYP2D6 P10635 1/20 0.49
HMGB1 P09429 1/20 0.47
CXCL12 P48061 1/20 0.47

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
Pamoic Acid SCHEMBL5721 0.90 GPR35 (1.00) POLBGPR35ME2ME1ME3
Pamoic Acid SCHEMBL30293211 0.90 GPR35 (1.00) POLBGPR35ME2ME1ME3
Pamoic Acid SCHEMBL446833 0.90 GPR35 (1.00) POLBGPR35ME2ME1ME3
Pamoic Acid SCHEMBL30293206 0.90 GPR35 (1.00) POLBGPR35ME2ME1ME3
Pamoic Acid SCHEMBL29362189 0.90 GPR35 (1.00) POLBGPR35ME2ME1ME3
Pamoic Acid SCHEMBL5379175 0.88 GPR35 (0.91) POLBGPR35ME2ME1ME3
Pamoic Acid SCHEMBL15955719 0.88 GPR35 (0.91) POLBGPR35ME2ME1ME3
Pamoic Acid SCHEMBL5014428 0.88 GPR35 (0.97) POLBGPR35ME2ME1ME3
Pamoic Acid SCHEMBL5014030 0.88 GPR35 (0.97) POLBGPR35ME2ME1ME3
Pamoic Acid SCHEMBL5012888 0.88 GPR35 (0.97) POLBGPR35ME2ME1ME3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9226925-B1 Abuse deterrent and anti-dose dumping pharmaceutical salts useful for the treatment of attention deficit/hyperactivity disorder PISGAH LABORATORIES, INC. (US) 2016-01-05 US disclosed
US-8980880-B1 Abuse deterrent and anti-dose dumping pharmaceutical salts useful for the treatment of attention deficit/hyperactivity disorder PISGAH LABORATORIES, INC. (US) 2015-03-17 US disclosed
US-8957067-B1 Abuse deterrent and anti-dose dumping pharmaceutical salts useful for the treatment of attention deficit/hyperactivity disorder PISGAH LABORATORIES, INC. (US) 2015-02-17 US disclosed
US-8940729-B1 Abuse deterrent and anti-dose dumping pharmaceutical salts useful for the treatment of attention deficit/hyperactivity disorder PISGAH LABORATORIES, INC. (US) 2015-01-27 US disclosed
US-8916587-B1 Abuse deterrent and anti-dose dumping pharmaceutical salts useful for the treatment of attention deficit/hyperactivity disorder PISGAH LABORATORIES, INC. (US) 2014-12-23 US disclosed
US-8912217-B1 Abuse deterrent and anti-dose dumping pharmaceutical salts useful for the treatment of attention deficit/hyperactivity disorder PISGAH LABORATORIES, INC. (US) 2014-12-16 US disclosed
US-8716278-B1 Abuse deterrent and anti-dose dumping pharmaceutical salts useful for the treatment of attention deficit/hyperactivity disorder PISGAH LABORATORIES, INC. (US) 2014-05-06 US disclosed
US-8716337-B1 Abuse deterrent and anti-dose dumping pharmaceutical salts useful for the treatment of attention deficit/hyperactivity disorder PISGAH LABORATORIES, INC. (US) 2014-05-06 US disclosed
US-8653065-B1 Abuse deterrent and anti-dose dumping pharmaceutical salts useful for the treatment of attention deficit/hyperactivity disorder PISGAH LABORATORIES, INC. (US) 2014-02-18 US disclosed
US-8653106-B2 Abuse deterrent and anti-dose dumping pharmaceutical salts useful for the treatment of attention deficit/hyperactivity disorder PISGAH LABORATORIES, INC. (US) 2014-02-18 US disclosed
US-8586575-B1 Abuse deterrent and anti-dose dumping pharmaceutical salts useful for the treatment of attention deficit/hyperactivity disorder PISGAH LABORATORIES, INC. (US) 2013-11-19 US disclosed
US-20120028960-A1 ABUSE DETERRENT AND ANTI-DOSE DUMPING PHARMACEUTICAL SALTS USEFUL FOR THE TREATMENT OF ATTENTION DEFICIT/HYPERACTIVITY DISORDER PISGAH LABORATORIES, INC. 2012-02-02 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 (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-20120028960-A1 ABUSE DETERRENT AND ANTI-DOSE DUMPING PHARMACEUTICAL SALTS USEFUL FOR THE TREATMENT OF ATTENTION DEFICIT/HYPERACTIVITY DISORDER COMT, SLC6A3, SLC6A2 POLB 2001/4885GPR35 427/4885ME2 2101/4885

“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.