Phentermine

Phentermine

SCHEMBL677133

CC(C)(N)Cc1ccccc1.[Cl-].[H+]

nearest known ligand 0.91

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

SLC6A2

The experimentally established mechanism targets of Phentermine. 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 2/20 0.91
TAAR1 Q96RJ0 1/20 0.91
HTR2A P28223 1/20 0.56
SLC6A4 P31645 1/20 0.56
HRH1 P35367 1/20 0.56
HTR2B P41595 1/20 0.56
CHRNA4 P43681 1/20 0.56
SLC6A3 Q01959 1/20 0.56
CYP2D6 P10635 2/20 0.50
LMNA P02545 1/20 0.50
SMN1; SMN2 Q16637 1/20 0.48
HIF1A Q16665 1/20 0.48
TRPA1 O75762 1/20 0.44
CYP1A2 P05177 3/20 0.41
CYP2C9 P11712 1/20 0.41
CYP2C19 P33261 1/20 0.41
GHSR Q92847 2/20 0.41
CYP3A4 P08684 2/20 0.41
PRMT1 Q99873 1/20 0.41
TP53 P04637 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
Phentermine SCHEMBL10392295 0.95 SLC6A2 (1.00) SLC6A2TAAR1HTR2ASLC6A4HRH1
Phentermine SCHEMBL26615 0.95 SLC6A2 (1.00) SLC6A2TAAR1HTR2ASLC6A4HRH1
Phentermine SCHEMBL41585 0.93 SLC6A2 (0.95) SLC6A2TAAR1HTR2ASLC6A4HRH1
Phentermine SCHEMBL28695767 0.93 SLC6A2 (0.95) SLC6A2TAAR1HTR2ASLC6A4HRH1
Phentermine SCHEMBL3676484 0.93 SLC6A2 (0.95) SLC6A2TAAR1HTR2ASLC6A4HRH1
Phentermine SCHEMBL28729624 0.93 SLC6A2 (0.95) SLC6A2TAAR1HTR2ASLC6A4HRH1
Phentermine SCHEMBL25214698 0.91 SLC6A2 (0.91) SLC6A2TAAR1HTR2ASLC6A4HRH1
Phentermine SCHEMBL29261099 0.91 SLC6A2 (0.91) SLC6A2TAAR1HTR2ASLC6A4HRH1
Phentermine SCHEMBL8825530 0.87 SLC6A2 (0.76) SLC6A2TAAR1HTR2ASLC6A4HRH1
SCHEMBL11709671 0.86 SLC6A2 (0.83) SLC6A2TAAR1HTR2ASLC6A4HRH1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250205222-A1 ANTIOBESITY COMPOSITIONS JACKSON MILTON S (US) 2025-06-26 US disclosed
US-20250195455-A1 COMBINATION NASAL AND ORAL THERAPY FOR WEIGHT LOSS JACKSON MILTON S (US) 2025-06-19 US disclosed
EP-4493172-A1 ANTIOBESITY COMPOSITIONS Jackson, Milton S. (US) 2025-01-22 EP disclosed
CN-118922180-A Anti-obesity composition 米尔顿·S·杰克逊 2024-11-08 CN disclosed
CN-118871099-A Combined nasal and oral therapy for weight loss 米尔顿·S·杰克逊 2024-10-29 CN disclosed
WO-2023183153-A1 COMBINATION NASAL AND ORAL THERAPY FOR WEIGHT LOSS JACKSON MILTON S (US) 2023-09-28 WO disclosed
WO-2023177561-A1 ANTIOBESITY COMPOSITIONS JACKSON MILTON S (US) 2023-09-21 WO disclosed
US-20230265043-A1 CRYSTALLINE FORM OF PHENTERMINE HYDROCHLORIDE AND PROCESS FOR OBTAINING SAME EUROFARMA LABORATÓRIOS S.A. (BR) 2023-08-24 US disclosed
EP-4190320-A1 CRYSTALLINE FORM OF PHENTERMINE HYDROCHLORIDE AND PROCESS FOR OBTAINING SAME Eurofarma Laboratórios S.A. (BR) 2023-06-07 EP disclosed
WO-2022020910-A1 CRYSTALLINE FORM OF PHENTERMINE HYDROCHLORIDE AND PROCESS FOR OBTAINING SAME EUROFARMA LABORATÓRIOS S.A. (BR) 2022-02-03 WO 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
US-20070049576-A1 NEUROGENESIS BY MUSCARINIC RECEPTOR MODULATION BRAINCELLS, INC. (US) 2007-03-01 US disclosed
WO-2007025177-A2 NEUROGENESIS BY MUSCARINIC RECEPTOR MODULATION BRAINCELLS, INC. (US) 2007-03-01 WO 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 (6 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 330/4885TAAR1 282/4885HTR2A 524/4885
US-20070078083-A1 MODULATION OF NEUORGENESIS BY HDac INHIBITION DCX, BDNF, NTRK2 SLC6A2 2832/4885TAAR1 2834/4885HTR2A 3184/4885
US-20070208029-A1 MODULATION OF NEUROGENESIS BY PDE INHIBITION PDE2A, PDE4A, DCX SLC6A2 1018/4885TAAR1 944/4885HTR2A 1221/4885
US-20070244143-A1 MODULATION OF NEUROGENESIS BY NOOTROPIC AGENTS GAP43, BDNF, DCX SLC6A2 295/4885TAAR1 326/4885HTR2A 273/4885
US-20070049576-A1 NEUROGENESIS BY MUSCARINIC RECEPTOR MODULATION CHRNB2, CHAT, CHRNB4 SLC6A2 1348/4885TAAR1 207/4885HTR2A 406/4885
US-20230265043-A1 CRYSTALLINE FORM OF PHENTERMINE HYDROCHLORIDE AND PROCESS FOR OBTAINING SAME PNMT, HTR5A, TAAR5 SLC6A2 6/4885TAAR1 14/4885HTR2A 5/4885

“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.