Phendimetrazine

Phendimetrazine

SCHEMBL678276

CC1C(c2ccccc2)OCCN1C.Cl

nearest known ligand 0.96

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

SLC6A2SLC6A3

The experimentally established mechanism targets of Phendimetrazine. 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
SLC6A2 known ✓ P23975 5/20 0.50
SLC6A3 known ✓ Q01959 5/20 0.50
HTR1A P08908 1/20 0.96
HTR2B P41595 2/20 0.50
ADRA1A P35348 1/20 0.50
SMN1; SMN2 Q16637 2/20 0.46
CYP2C19 P33261 1/20 0.45
CYP2D6 P10635 4/20 0.44
SLC6A4 P31645 4/20 0.44
KCNH2 Q12809 2/20 0.44
TSHR P16473 2/20 0.42
CHRM2 P08172 1/20 0.42
CHRM1 P11229 1/20 0.42
ADRA2B P18089 1/20 0.42
ADRA2C P18825 1/20 0.42
CHRM3 P20309 1/20 0.42
HTR2A P28223 1/20 0.42
HTR2C P28335 1/20 0.42
HRH1 P35367 1/20 0.42
OPRM1 P35372 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
Phendimetrazine SCHEMBL598950 0.98 HTR1A (1.00) HTR1ASLC6A2SLC6A3HTR2BADRA1A
Phendimetrazine SCHEMBL49481 0.98 HTR1A (1.00) HTR1ASLC6A2SLC6A3HTR2BADRA1A
Phendimetrazine SCHEMBL344020 0.98 HTR1A (1.00) HTR1ASLC6A2SLC6A3HTR2BADRA1A
Phendimetrazine SCHEMBL15064942 0.98 HTR1A (1.00) HTR1ASLC6A2SLC6A3HTR2BADRA1A
Phendimetrazine SCHEMBL678073 0.95 HTR1A (0.93) HTR1ASLC6A2SLC6A3HTR2BADRA1A
Phendimetrazine SCHEMBL160376 0.85 HTR1A (0.75) HTR1ASLC6A2SLC6A3HTR2BADRA1A
Phendimetrazine SCHEMBL29353044 0.85 HTR1A (0.75) HTR1ASLC6A2SLC6A3HTR2BADRA1A
Phendimetrazine SCHEMBL160375 0.85 HTR1A (0.75) HTR1ASLC6A2SLC6A3HTR2BADRA1A
Phendimetrazine SCHEMBL29554688 0.85 HTR1A (0.75) HTR1ASLC6A2SLC6A3HTR2BADRA1A
Phendimetrazine SCHEMBL4381184 0.85 HTR1A (0.75) HTR1ASLC6A2SLC6A3HTR2BADRA1A

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 123 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260000653-A1 TREATMENT OF CNS DISEASES WITH sGC STIMULATORS TISENTO THERAPEUTICS INC (US) 2026-01-01 US disclosed
US-20250326761-A1 sGC STIMULATORS TISENTO THERAPEUTICS INC (US) 2025-10-23 US disclosed
US-12435080-B2 sGC stimulators TISENTO THERAPEUTICS INC. (US) 2025-10-07 US disclosed
US-20250243205-A1 sGC STIMULATORS TISENTO THERAPEUTICS INC (US) 2025-07-31 US disclosed
US-20250115611-A1 CRYSTALLINE FORMS OF 8-(2-FLUOROBENZYL)-6-(3-(TRIFLUOROMETHYL)-1H-1,2,4-TRIAZOL-5-YL)IMIDAZO[1,2-a]PYRAZINE AS sGC STIMULATORS TISENTO THERAPEUTICS INC. 2025-04-10 US disclosed
US-20250108040-A1 TREATMENT OF CNS DISEASES WITH sGC STIMULATORS TISENTO THERAPEUTICS INC (US) 2025-04-03 US disclosed
US-20250059197-A1 sGC STIMULATORS TISENTO THERAPEUTICS INC (US) 2025-02-20 US disclosed
US-12220414-B2 Use of sGC stimulators for the treatment of mitochondrial disorders TISENTO THERAPEUTICS INC. (US) 2025-02-11 US disclosed
US-12122782-B2 Crystalline forms of 8-(2-fluorobenzyl)-6-(3-(trifluoromethyl)-1H-1,2,4-triazol-5-yl)imidazo[1,2-a]pyrazine as sGC stimulators TISENTO THERAPEUTICS INC. (US) 2024-10-22 US disclosed
US-20240342188-A1 Use of NEP Inhibitors for the Treatment of Laminitis CURTAILS LLC (US) 2024-10-17 US disclosed
US-20070244143-A1 MODULATION OF NEUROGENESIS BY NOOTROPIC AGENTS BRAINCELLS, INC (US) 2007-10-18 US disclosed
WO-2007104035-A1 MODULATION OF NEUROGENESIS BY NOOTROPIC AGENTS BRAINCELLS, INC. (US) 2007-09-13 WO disclosed
US-20070208029-A1 MODULATION OF NEUROGENESIS BY PDE INHIBITION BRAINCELLS, INC. (US) 2007-09-06 US disclosed
US-20070112017-A1 GABA RECEPTOR MEDIATED MODULATION OF NEUROGENESIS BRAINCELLS, INC. (US) 2007-05-17 US disclosed
WO-2007053596-A1 GABA RECEPTOR MEDIATED MODULATION OF NEUROGENESIS BRAINCELLS, INC. (US) 2007-05-10 WO disclosed
WO-2007047978-A2 MODULATION OF NEUROGENESIS BY PDE INHIBITION BRAINCELLS, INC. (US) 2007-04-26 WO disclosed
US-20070078083-A1 MODULATION OF NEUORGENESIS BY HDac INHIBITION BRAINCELLS, INC. (US) 2007-04-05 US disclosed
WO-2007030697-A2 MODULATION OF NEUROGENESIS BY HDAC INHIBITION BRAINCELLS, INC. (US) 2007-03-15 WO disclosed
WO-2007025177-A2 NEUROGENESIS BY MUSCARINIC RECEPTOR MODULATION BRAINCELLS, INC. (US) 2007-03-01 WO disclosed
US-20070049576-A1 NEUROGENESIS BY MUSCARINIC RECEPTOR MODULATION BRAINCELLS, INC. (US) 2007-03-01 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 (15 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-20070112017-A1 GABA RECEPTOR MEDIATED MODULATION OF NEUROGENESIS GABRB2, GAP43, GABRB1 SLC6A2 330/4885SLC6A3 266/4885HTR1A 777/4885
US-20070078083-A1 MODULATION OF NEUORGENESIS BY HDac INHIBITION DCX, BDNF, NTRK2 SLC6A2 2832/4885SLC6A3 2839/4885HTR1A 3606/4885
US-12220414-B2 Use of sGC stimulators for the treatment of mitochondrial disorders CS, COQ8A, GLS SLC6A2 2145/4885SLC6A3 2569/4885HTR1A 3404/4885
US-20250059197-A1 sGC STIMULATORS GMPS, GUCY1A2, PDE2A SLC6A2 1983/4885SLC6A3 2536/4885HTR1A 1929/4885
US-20250326761-A1 sGC STIMULATORS GUCY1A2, PRKG1, GMPS SLC6A2 2812/4885SLC6A3 3555/4885HTR1A 1614/4885
US-12435080-B2 sGC stimulators GUCY1A2, PRKG1, PDE2A SLC6A2 3025/4885SLC6A3 3515/4885HTR1A 1751/4885
US-20070208029-A1 MODULATION OF NEUROGENESIS BY PDE INHIBITION PDE2A, PDE4A, DCX SLC6A2 1018/4885SLC6A3 777/4885HTR1A 1691/4885
US-20070244143-A1 MODULATION OF NEUROGENESIS BY NOOTROPIC AGENTS GAP43, BDNF, DCX SLC6A2 295/4885SLC6A3 333/4885HTR1A 385/4885
US-12122782-B2 Crystalline forms of 8-(2-fluorobenzyl)-6-(3-(trifluoromethyl)-1H-1,2,4-triazol-5-yl)imidazo[1,2-a]pyrazine as sGC stimulators GUCY1A2, GUCY1B2, GUCY1A1 SLC6A2 3694/4885SLC6A3 4068/4885HTR1A 756/4885
US-20070049576-A1 NEUROGENESIS BY MUSCARINIC RECEPTOR MODULATION CHRNB2, CHAT, CHRNB4 SLC6A2 1348/4885SLC6A3 1109/4885HTR1A 486/4885
US-20260000653-A1 TREATMENT OF CNS DISEASES WITH sGC STIMULATORS PDE9A, PDE2A, GUCY1A2 SLC6A2 99/4885SLC6A3 140/4885HTR1A 1249/4885
US-20250115611-A1 CRYSTALLINE FORMS OF 8-(2-FLUOROBENZYL)-6-(3-(TRIFLUOROMETHYL)-1H-1,2,4-TRIAZOL-5-YL)IMIDAZO[1,2-a]PYRAZINE AS sGC STIMULATORS GUCY1A2, GUCY1B2, GUCY1A1 SLC6A2 3694/4885SLC6A3 4068/4885HTR1A 756/4885
US-20240342188-A1 Use of NEP Inhibitors for the Treatment of Laminitis MME, REN, ACE SLC6A2 79/4885SLC6A3 824/4885HTR1A 1475/4885
US-20250243205-A1 sGC STIMULATORS GMPS, GUCY1A2, PDE2A SLC6A2 1983/4885SLC6A3 2536/4885HTR1A 1929/4885
US-20250108040-A1 TREATMENT OF CNS DISEASES WITH sGC STIMULATORS GUCY1A2, GUCY1B2, PDE2A SLC6A2 710/4885SLC6A3 668/4885HTR1A 1900/4885

“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.