Methamphetamine

Methamphetamine

SCHEMBL8534227

CNC(C)Cc1ccccc1.O=C(O)C(O)C(O)C(=O)O

nearest known ligand 0.72

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

SLC6A2SLC6A3SLC6A4

The experimentally established mechanism targets of Methamphetamine. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
TAAR1 Q96RJ0 4/20 0.72
SIGMAR1 Q99720 4/20 0.72
SLC18A2 Q05940 1/20 0.72
NPC1 O15118 2/20 0.59
RAB9A P51151 2/20 0.59
CYP1A2 P05177 2/20 0.52
TP53 P04637 1/20 0.52
CYP2D6 P10635 1/20 0.52
ALOX15 P16050 1/20 0.52
TSHR P16473 1/20 0.52
CYP2C19 P33261 1/20 0.52
LMNA P02545 1/20 0.51
MEN1 O00255 1/20 0.50
KMT2A Q03164 1/20 0.50
TRPA1 O75762 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
Levmetamfetamine SCHEMBL29878484 1.00 TAAR1 (0.72) TAAR1SIGMAR1SLC18A2NPC1RAB9A
Mucic Acid SCHEMBL6466756 0.93 TAAR1 (0.68) TAAR1SIGMAR1SLC18A2NPC1RAB9A
Methamphetamine SCHEMBL7036430 0.87 SIGMAR1 (0.81) TAAR1SIGMAR1SLC18A2NPC1RAB9A
Methamphetamine SCHEMBL7036433 0.87 SIGMAR1 (0.81) TAAR1SIGMAR1SLC18A2NPC1RAB9A
Methamphetamine SCHEMBL29112697 0.87 SIGMAR1 (0.81) TAAR1SIGMAR1SLC18A2NPC1RAB9A
Methamphetamine SCHEMBL27438559 0.87 SIGMAR1 (0.95) TAAR1SIGMAR1SLC18A2NPC1RAB9A
Methamphetamine SCHEMBL28233460 0.86 SIGMAR1 (0.78) TAAR1SIGMAR1SLC18A2NPC1RAB9A
Methamphetamine SCHEMBL20490091 0.85 SIGMAR1 (0.84) TAAR1SIGMAR1SLC18A2NPC1RAB9A
Methamphetamine SCHEMBL18227057 0.85 SIGMAR1 (0.91) TAAR1SIGMAR1SLC18A2NPC1RAB9A
Methamphetamine SCHEMBL20211416 0.85 SIGMAR1 (1.00) TAAR1SIGMAR1SLC18A2NPC1RAB9A

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
CN-110642721-B Preparation method of selegiline hydrochloride 安徽贝克生物制药有限公司 2022-09-30 CN disclosed
CN-110642721-A Preparation method of selegiline hydrochloride 安徽贝克生物制药有限公司 2020-01-03 CN disclosed
EP-0713858-B1 Improved process for the preparation of propargyl ammonium-chloride derivatives CHINOIN GYOGYSZER ES VEGYESZET (HU) 1998-07-29 EP disclosed
EP-0713858-A1 Improved process for the preparation of propargyl ammonium-chloride derivatives CHINOIN Gyogyszer és Vegyészeti Termékek Gyára RT. (HU) 1996-05-29 EP disclosed
US-5449828-A Process for the preparation of propargyl ammonium-chloride CHINOIN GYOGYSZER- ES VEGYESZETI TERMEKEK GYARA RT. (HU) 1995-09-12 US disclosed