Imipramine

Imipramine

SCHEMBL518586

CCCCCCCCCCCCCCCCCCOC(=O)c1cc2ccccc2c(Cc2c(O)c(C(=O)O)cc3ccccc23)c1O.CN(C)CCCN1c2ccccc2CCc2ccccc21.N

nearest known ligand 0.44

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

SLC6A2SLC6A4

The experimentally established mechanism targets of Imipramine. 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
SLC6A4 known ✓ P31645 14/20 0.43
SLC6A2 known ✓ P23975 2/20 0.43
KMT2A Q03164 3/20 0.44
LMNA P02545 3/20 0.43
MAPT P10636 3/20 0.43
HRH1 P35367 3/20 0.43
SLC22A1 O15245 2/20 0.43
CHRM2 P08172 2/20 0.43
CHRM4 P08173 2/20 0.43
HTR1A P08908 2/20 0.43
CHRM5 P08912 2/20 0.43
ADORA3 P0DMS8 2/20 0.43
CYP2D6 P10635 2/20 0.43
CHRM1 P11229 2/20 0.43
DRD2 P14416 2/20 0.43
ADRA2B P18089 2/20 0.43
ADRA2C P18825 2/20 0.43
CHRM3 P20309 2/20 0.43
DRD1 P21728 2/20 0.43
HRH2 P25021 2/20 0.43

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 SCHEMBL517584 0.88 SLC6A4 (0.47) KMT2ASLC6A4LMNAMAPTHRH1
Pamoic Acid SCHEMBL21834068 0.88 SLC6A4 (0.56) KMT2ASLC6A4LMNAMAPTHRH1
Pamoic Acid SCHEMBL41090 0.88 SLC6A4 (0.56) KMT2ASLC6A4LMNAMAPTHRH1
Pamoic Acid SCHEMBL517502 0.86 SLC6A4 (0.51) KMT2ASLC6A4LMNAMAPTHRH1
Pamoic Acid SCHEMBL16222836 0.82 SLC6A4 (0.63) KMT2ASLC6A4LMNAMAPTHRH1
Imipramine SCHEMBL2098515 0.74 LMNA (0.62) KMT2ASLC6A4LMNAMAPTHRH1
Pamoic Acid SCHEMBL15533092 0.73 SLC6A4 (0.48) KMT2ASLC6A4LMNAMAPTHRH1
SCHEMBL5608291 0.72 SLC6A4 (0.47) KMT2ASLC6A4LMNAMAPTHRH1
SCHEMBL220778 0.71 SLC6A4 (0.62) KMT2ASLC6A4LMNAMAPTHRH1
Imipramine SCHEMBL4283852 0.71 SLC6A4 (0.71) KMT2ASLC6A4LMNAMAPTHRH1

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-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-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-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 SLC6A4 4/4885SLC6A2 3/4885KMT2A 1087/4885

“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.