1,2,3,4-Tetrahydroisoquinoline

1,2,3,4-Tetrahydroisoquinoline

SCHEMBL2084613

NCCO.c1ccc2c(c1)CCNC2

nearest known ligand 0.70

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

MPL

The experimentally established mechanism targets of 1,2,3,4-Tetrahydroisoquinoline. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 8)

geneUniProtsupporting neighboursconfidence
PNMT P11086 3/20 0.70
CD44 P16070 2/20 0.70
MAOB P27338 1/20 0.70
HTR2C P28335 1/20 0.54
PRCP P42785 1/20 0.45
ADRA2A P08913 1/20 0.42
ADRA2B P18089 1/20 0.42
ADRA2C P18825 1/20 0.42

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
1,2,3,4-Tetrahydroisoquinoline SCHEMBL29360217 0.84 PNMT (1.00) PNMTCD44MAOBHTR2CPRCP
1,2,3,4-Tetrahydroisoquinoline SCHEMBL19085 0.84 PNMT (1.00) PNMTCD44MAOBHTR2CPRCP
1,2,3,4-Tetrahydroisoquinoline SCHEMBL28236302 0.84 PNMT (1.00) PNMTCD44MAOBHTR2CPRCP
1,2,3,4-Tetrahydroisoquinoline SCHEMBL16291557 0.82 PNMT (0.86) PNMTCD44MAOBHTR2CADRA2A
1,2,3,4-Tetrahydroisoquinoline SCHEMBL2082936 0.82 PNMT (0.95) PNMTCD44MAOBHTR2CPRCP
1,2,3,4-Tetrahydroisoquinoline SCHEMBL4243903 0.82 PNMT (0.95) PNMTCD44MAOBHTR2CPRCP
1,2,3,4-Tetrahydroisoquinoline SCHEMBL6635293 0.82 PNMT (0.95) PNMTCD44MAOBHTR2CPRCP
1,2,3,4-Tetrahydroisoquinoline SCHEMBL20524019 0.82 PNMT (0.95) PNMTCD44MAOBHTR2CPRCP
1,2,3,4-Tetrahydroisoquinoline SCHEMBL5411332 0.82 PNMT (0.95) PNMTCD44MAOBHTR2CPRCP
SCHEMBL11838922 0.82 PNMT (0.95) PNMTCD44MAOBHTR2CPRCP

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-7902218-B2 Inhibit production of A beta -peptide; neurological disorders, Alzheimer's disease; (S)-2-((S)-3-Acetamido-3-((R)-sec-butyl)-2-oxopyrrolidin-1-yl)-N-((1R,2S)-3-(3,5-difluorophenyl)-1-hydroxy-1-((R)-1,2,3,4-tetrahydroisoquinolin-3-yl)propan-2-yl)-4-phenylbutanamide BRISTOL-MYERS SQUIBB COMPANY (US) 2011-03-08 US disclosed
US-20080153868-A1 Substituted Tetrahydroisoquinolines as Beta-secretase Inhibitors BRISTOL-MYERS SQUIBB COMPANY 2008-06-26 US disclosed
US-7388007-B2 Gamma-lactams as beta-secretase inhibitors BRISTOL-MYERS SQUIBB COMPANY (US) 2008-06-17 US disclosed
WO-2006026204-A2 NOVEL GAMMA-LACTAMS AS BETA-SECRETASE INHIBITORS BRISTOL-MYERS SQUIBB COMPANY (US) 2006-03-09 WO disclosed
US-20060046984-A1 Novel gamma-lactams as beta-secretase inhibitors THOMPSON LORIN A III 2006-03-02 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 (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-20080153868-A1 Substituted Tetrahydroisoquinolines as Beta-secretase Inhibitors BACE1, APP, BACE2 PNMT 1489/4885CD44 4883/4885MAOB 1464/4885
US-20060046984-A1 Novel gamma-lactams as beta-secretase inhibitors BACE1, BACE2, APP PNMT 3578/4885CD44 4645/4885MAOB 1880/4885

“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.