(+)-Tranylcypromine

(+)-Tranylcypromine

SCHEMBL5070768

Cl.N[C@H]1C[C@@H]1c1ccccc1.O=S(=O)(O)O

nearest known ligand 0.96

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

MAOAMAOB

The experimentally established mechanism targets of (+)-Tranylcypromine. 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
MAOB known ✓ P27338 14/20 0.76
MAOA known ✓ P21397 12/20 0.76
KDM4E B2RXH2 1/20 0.96
MAPT P10636 1/20 0.96
HPGD P15428 1/20 0.96
KDM1A O60341 14/20 0.76
TAAR1 Q96RJ0 2/20 0.76
LMNA P02545 2/20 0.76
KDM1B Q8NB78 1/20 0.76
BLM P54132 1/20 0.76
PMP22 Q01453 1/20 0.76
CYP2C19 P33261 4/20 0.72
CYP2B6 P20813 3/20 0.72
CYP1A2 P05177 2/20 0.72
CYP2D6 P10635 2/20 0.72
CYP2C9 P11712 2/20 0.72
RCOR1 Q9UKL0 2/20 0.72
CYP3A4 P08684 1/20 0.72
HTR1A P08908 1/20 0.72
ADRA2A P08913 1/20 0.72

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
(+)-Tranylcypromine SCHEMBL40650 0.98 KDM4E (1.00) KDM4EMAPTHPGDMAOBKDM1A
(+)-Tranylcypromine SCHEMBL5075069 0.98 KDM4E (1.00) KDM4EMAPTHPGDMAOBKDM1A
(+)-Tranylcypromine SCHEMBL5070770 0.98 KDM4E (1.00) KDM4EMAPTHPGDMAOBKDM1A
(+)-Tranylcypromine SCHEMBL4332273 0.98 KDM4E (1.00) KDM4EMAPTHPGDMAOBKDM1A
(+)-Tranylcypromine SCHEMBL31133533 0.98 KDM4E (1.00) KDM4EMAPTHPGDMAOBKDM1A
(+)-Tranylcypromine SCHEMBL56352 0.87 KDM1A (1.00) KDM4EMAPTHPGDMAOBKDM1A
(+)-Tranylcypromine SCHEMBL7759844 0.87 KDM1A (1.00) KDM4EMAPTHPGDMAOBKDM1A
(+)-Tranylcypromine SCHEMBL56351 0.87 KDM1A (1.00) KDM4EMAPTHPGDMAOBKDM1A
(+)-Tranylcypromine SCHEMBL6388781 0.87 KDM1A (1.00) KDM4EMAPTHPGDMAOBKDM1A
(+)-Tranylcypromine SCHEMBL4380284 0.87 KDM1A (1.00) KDM4EMAPTHPGDMAOBKDM1A

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 10 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-3961073-A 2-PHENYL-CYCLOPROPYLAMINE NELSON RESEARCH & DEVELOPMENT COMPANY (US) 1976-06-01 US claimed
EP-3617181-A1 SYNTHESIS OF TRANS-2-PHENYLCYCLOPROPYLAMINE OR A SALT OR SOLVATE THEREOF Arevipharma GmbH (DE) 2020-03-04 EP disclosed
EP-3617181-A1 SYNTHESIS OF TRANS-2-PHENYLCYCLOPROPYLAMINE OR A SALT OR SOLVATE THEREOF Arevipharma GmbH (DE) 2020-03-04 EP disclosed
EP-1758600-A4 METHODS AND COMPOSITIONS FOR TREATING MOOD DISORDER MOOD MAN SCIENCES LLC (US) 2008-03-05 EP disclosed
US-20070264358-A1 Methods and Compositions for Treating Mood Disorder MOOD MANAGEMENT SCIENCES, INC. 2007-11-15 US disclosed
US-20070212428-A1 METHODS AND COMPOSITIONS FOR TREATING MOOD DISORDER MOOD MANAGEMENT SCIENCES, INC. (US) 2007-09-13 US disclosed
EP-1758600-A1 METHODS AND COMPOSITIONS FOR TREATING MOOD DISORDER Mood Management Sciences, LLC (US) 2007-03-07 EP disclosed
WO-2005120523-A1 METHODS AND COMPOSITIONS FOR TREATING MOOD DISORDER MOOD MANAGEMENT SCIENCES, LLC (US) 2005-12-22 WO disclosed
US-4156017-A TO PROTECT CROPS FROM CABBAGE MOTH AND BUTTERFLY AND COTTON MOTH; OVICIDES SCHERING AKTIENGESELLSCHAFT (DE) 1979-05-22 US disclosed
US-4016204-A ISOMERIZING ETHYL-2-PHENYL-CYCLOPROPANE CARBOXYLATE NELSON RESEARCH & DEVELOPMENT COMPANY (US) 1977-04-05 US disclosed