(+)-Tranylcypromine

(+)-Tranylcypromine

SCHEMBL56351

Cl.N[C@@H]1C[C@H]1c1ccccc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

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 9/20 1.00
MAOA known ✓ P21397 7/20 1.00
KDM1A O60341 14/20 1.00
TAAR1 Q96RJ0 2/20 1.00
LMNA P02545 2/20 1.00
KDM1B Q8NB78 2/20 1.00
BLM P54132 1/20 1.00
PMP22 Q01453 1/20 1.00
CYP2C19 P33261 4/20 0.95
CYP2B6 P20813 3/20 0.95
CYP1A2 P05177 2/20 0.95
CYP2D6 P10635 2/20 0.95
CYP2C9 P11712 2/20 0.95
KCNH2 Q12809 2/20 0.95
CYP3A4 P08684 1/20 0.95
HTR1A P08908 1/20 0.95
ADRA2A P08913 1/20 0.95
CYP2A6 P11509 1/20 0.95
SLC6A2 P23975 1/20 0.95
HTR2C P28335 1/20 0.95

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 SCHEMBL4380284 1.00 KDM1A (1.00) KDM1AMAOBMAOATAAR1LMNA
(+)-Tranylcypromine SCHEMBL56350 1.00 KDM1A (1.00) KDM1AMAOBMAOATAAR1LMNA
(+)-Tranylcypromine SCHEMBL145687 1.00 KDM1A (1.00) KDM1AMAOBMAOATAAR1LMNA
(+)-Tranylcypromine SCHEMBL56352 1.00 KDM1A (1.00) KDM1AMAOBMAOATAAR1LMNA
(+)-Tranylcypromine SCHEMBL6388781 1.00 KDM1A (1.00) KDM1AMAOBMAOATAAR1LMNA
(+)-Tranylcypromine SCHEMBL7759844 1.00 KDM1A (1.00) KDM1AMAOBMAOATAAR1LMNA
(+)-Tranylcypromine SCHEMBL13785162 0.97 KDM1A (1.00) KDM1AMAOBMAOATAAR1LMNA
(+)-Tranylcypromine SCHEMBL3406205 0.97 KDM1A (1.00) KDM1AMAOBMAOATAAR1LMNA
(+)-Tranylcypromine SCHEMBL40651 0.97 KDM1A (1.00) KDM1AMAOBMAOATAAR1LMNA
(+)-Tranylcypromine SCHEMBL1649712 0.97 KDM1A (1.00) KDM1AMAOBMAOATAAR1LMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118147053-A Culture system, kit and method for inducing mesenchymal stem cells 成都赛济元生物医药有限公司 2024-06-07 CN claimed
US-11788145-B2 Epigeneiic silencing of NMT2 PACYLEX PHARMACEUTICALS INC. (CA) 2023-10-17 US claimed
EP-3325662-B1 EPIGENETIC SILENCING OF NMT2 PACYLEX PHARMACEUTICALS INC (CA) 2023-08-30 EP claimed
US-20200131431-A1 CHEMICAL ADDITIVES AND SURFACTANT COMBINATIONS FOR FAVORABLE WETTABILITY ALTERATION AND IMPROVED HYDROCARBON RECOVERY FACTORS ALCHEMY SCIENCES INC (US) 2020-04-30 US claimed
EP-2841566-B1 DERIVATION OF NEURAL STEM CELLS AND DOPAMINERGIC NEURONS FROM HUMAN PLURIPOTENT STEM CELLS INT STEM CELL CORPORATION (US) 2019-03-13 EP claimed
US-20190010461-A1 HUMAN PLURIPOTENT STEM CELL-BASED SCREENING FOR SMOOTH MUSCLE CELL DIFFERENTIATION AND DISEASE NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2019-01-10 US claimed
US-20180371423-A1 NON-VIRAL IPSCS INDUCING METHOD, COMPOSITIONS, KITS AND IPSCS Guangzhou Biocare Biotechnology Co., Ltd (CN) 2018-12-27 US claimed
US-20180208990-A1 EPIGENETIC SILENCING OF NMT2 PACYLEX PHARMACEUTICALS INC. (CA) 2018-07-26 US claimed
US-20180185478-A1 TREATMENT FOR MYOPATHY CHILDREN'S MEDICAL CENTER CORPORATION (US) 2018-07-05 US claimed
EP-3325662-A1 EPIGENETIC SILENCING OF NMT2 Pacylex Pharmaceuticals Inc. (CA) 2018-05-30 EP claimed
EP-2841566-A1 DERIVATION OF NEURAL STEM CELLS AND DOPAMINERGIC NEURONS FROM HUMAN PLURIPOTENT STEM CELLS International Stem Cell Corporation (US) 2015-03-04 EP claimed
CN-104379732-A Derivation of neural stem cells and dopaminergic neurons from human pluripotent stem cells INT STEM CELL CORP 2015-02-25 CN claimed
WO-2013163228-A1 DERIVATION OF NEURAL STEM CELLS AND DOPAMINERGIC NEURONS FROM HUMAN PLURIPOTENT STEM CELLS INTERNATIONAL STEM CELL CORPORATION (US) 2013-10-31 WO claimed
EP-2572192-A2 A GENERAL MASS SPECTROMETRY ASSAY USING CONTINUOUSLY ELUTING CO-FRACTIONATING REPORTERS OF MASS SPECTROMETRY DETECTION EFFICIENCY The UAB Research Foundation (US) 2013-03-27 EP claimed
WO-2011146521-A2 A GENERAL MASS SPECTROMETRY ASSAY USING CONTINUOUSLY ELUTING CO-FRACTIONATING REPORTERS OF MASS SPECTROMETRY DETECTION EFFICIENCY THE UAB RESEARCH FOUNDATION (US) 2011-11-24 WO claimed
US-8003080-B2 Heating a coating, which includes an amine drug salt on a substrate to a temperature sufficient to volatilize the amine drug from the coating by heating, forming an amine drug vapor, drawing air, condensing vapor to form aerosol particles ALEXZA PHARMACEUTICALS, INC. (US) 2011-08-23 US claimed
US-7109377-B2 Synthesis of combinatorial libraries of compounds reminiscent of natural products PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) 2006-09-19 US claimed
US-20060171945-A1 Ip receptor antagonists for the treatment of pathological uterine conditions UNIVERSITY COURT OF THE UNIVERSITY OF EDINBURGH, THE (GB) 2006-08-03 US claimed
US-20030082830-A1 Synthesis of combinatorial libraries of compounds reminiscent of natural products NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2003-05-01 US claimed
US-6448443-B1 GENERATED FROM DIVERSIFIABLE SCAFFOLDS SYNTHESIZED FROM THE PYRIDINE-BASED TEMPLATE ISONICOTINAMIDE; ALSO PROVIDES A NOVEL ORTHO-NITROBENZYL PHOTOLINKER; SYNTHESIZED FROM A SHIKIMIC ACID BASED EPOXYOL TEMPLATE PRESIDENT AND FELLOWS OF HARVARD COLLEGE 2002-09-10 US claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (4 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-20180208990-A1 EPIGENETIC SILENCING OF NMT2 NMT2, NNMT, NMT1 MAOB 1825/4885MAOA 2403/4885KDM1A 66/4885
US-20190010461-A1 HUMAN PLURIPOTENT STEM CELL-BASED SCREENING FOR SMOOTH MUSCLE CELL DIFFERENTIATION AND DISEASE MYH10, MYH14, MYH2 MAOB 3258/4885MAOA 3220/4885KDM1A 495/4885
US-11788145-B2 Epigeneiic silencing of NMT2 NNMT, NMT2, NMT1 MAOB 1662/4885MAOA 2633/4885KDM1A 103/4885
US-20030082830-A1 Synthesis of combinatorial libraries of compounds reminiscent of natural products TKFC, NISCH, PTGIS MAOB 183/4885MAOA 290/4885KDM1A 1299/4885

“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.