(+)-Tranylcypromine

(+)-Tranylcypromine

SCHEMBL13764364

NC1C[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 11/20 1.00
▸ MAOA known ✓ P21397 7/20 1.00
▸ KDM1A O60341 14/20 1.00
▸ CYP2C19 P33261 4/20 1.00
▸ CYP2B6 P20813 3/20 1.00
▸ KCNH2 Q12809 3/20 1.00
▸ RCOR1 Q9UKL0 3/20 1.00
▸ CYP1A2 P05177 2/20 1.00
▸ CYP2D6 P10635 2/20 1.00
▸ CYP2C9 P11712 2/20 1.00
▸ LMNA P02545 2/20 1.00
▸ TAAR1 Q96RJ0 2/20 1.00
▸ CYP3A4 P08684 1/20 1.00
▸ HTR1A P08908 1/20 1.00
▸ ADRA2A P08913 1/20 1.00
▸ CYP2A6 P11509 1/20 1.00
▸ SLC6A2 P23975 1/20 1.00
▸ HTR2C P28335 1/20 1.00
▸ ADRA1A P35348 1/20 1.00
▸ DRD3 P35462 1/20 1.00

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 SCHEMBL145650 1.00 KDM1A (1.00) KDM1AMAOBMAOACYP2C19CYP2B6
(+)-Tranylcypromine SCHEMBL13785162 1.00 KDM1A (1.00) KDM1AMAOBMAOACYP2C19CYP2B6
(+)-Tranylcypromine SCHEMBL29360959 1.00 KDM1A (1.00) KDM1AMAOBMAOACYP2C19CYP2B6
(+)-Tranylcypromine SCHEMBL3406205 1.00 KDM1A (1.00) KDM1AMAOBMAOACYP2C19CYP2B6
(+)-Tranylcypromine SCHEMBL34339 1.00 KDM1A (1.00) KDM1AMAOBMAOACYP2C19CYP2B6
(+)-Tranylcypromine SCHEMBL1720497 1.00 KDM1A (1.00) KDM1AMAOBMAOACYP2C19CYP2B6
(+)-Tranylcypromine SCHEMBL40651 1.00 KDM1A (1.00) KDM1AMAOBMAOACYP2C19CYP2B6
(+)-Tranylcypromine SCHEMBL4740285 1.00 KDM1A (1.00) KDM1AMAOBMAOACYP2C19CYP2B6
(+)-Tranylcypromine SCHEMBL1649712 1.00 KDM1A (1.00) KDM1AMAOBMAOACYP2C19CYP2B6
(+)-Tranylcypromine SCHEMBL2755938 1.00 KDM1A (1.00) KDM1AMAOBMAOACYP2C19CYP2B6

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2024110649-A1 COMBINATIONS OF LSD1 INHIBITORS AND MENIN INHIBITORS FOR TREATING CANCER ORYZON GENOMICS, S.A. (ES) 2024-05-30 — — WO disclosed
CN-117337281-A Piperidine urea derivatives as soluble epoxide hydrolase inhibitors 纽若平治疗公司 2024-01-02 — — CN disclosed
WO-2023217758-A1 METHODS OF TREATING MALIGNANT PERIPHERAL NERVE SHEATH TUMOR (MPNST) USING LSD1 INHIBITORS ORYZON GENOMICS, S.A. (ES) 2023-11-16 — — WO disclosed
WO-2023217784-A1 METHODS OF TREATING NF1-MUTANT TUMORS USING LSD1 INHIBITORS ORYZON GENOMICS, S.A. (ES) 2023-11-16 — — WO disclosed
EP-3292100-B1 SOLID FORMS ORYZON GENOMICS SA (ES) 2023-11-15 — — EP disclosed
EP-3955929-A1 NEW PYRIMIDINE DERIVATIVES FOR PREVENTION AND TREATMENT OF GRAM-NEGATIVE BACTERIAL INFECTION, CONTAMINATION AND FOULING Université de Liège (BE) 2022-02-23 — — EP disclosed
US-9918959-B2 TLR-independent small molecule adjuvants THE BOARD OF REGENTS OF THE UNIVERSITY OF TEXAS SYSTEM (US) 2018-03-20 — — US disclosed
WO-2017157825-A1 COMBINATIONS OF LSD1 INHIBITORS FOR USE IN THE TREATMENT OF SOLID TUMORS F. HOFFMANN-LA ROCHE AG (CH) 2017-09-21 — — WO disclosed
WO-2017157813-A1 COMBINATIONS OF LSD1 INHIBITORS FOR THE TREATMENT OF HEMATOLOGICAL MALIGNANCIES F. HOFFMANN-LA ROCHE AG (CH) 2017-09-21 — — WO disclosed
US-20170224653-A1 TLR-INDEPENDENT SMALL MOLECULE ADJUVANTS THE SCRIPPS RESEARCH INSTITUTE 2017-08-10 — — US disclosed
US-20170224653-A1 TLR-INDEPENDENT SMALL MOLECULE ADJUVANTS THE SCRIPPS RESEARCH INSTITUTE 2017-08-10 — — US disclosed
WO-2017060319-A1 GENE EXPRESSION BIOMARKERS FOR PERSONALIZED CANCER CARE TO EPIGENETIC MODIFYING AGENTS F. HOFFMANN-LA ROCHE AG (CH) 2017-04-13 — — WO disclosed
CN-103857393-B Cyclopropylamine is as LSD1 inhibitor 葛兰素史密斯克莱知识产权(第2 号)有限公司 2016-08-17 — — CN disclosed
CN-103857393-A Cyclopropylamines as LSD1 inhibitors GLAXOSMITHKLINE LLC 2014-06-11 — — CN disclosed
US-20130165696-A1 NOVEL PROCESSES FOR THE PREPARATION OF PHENYLCYCLOPROPYLAMINE DERIVATIVES AND USE THEREOF FOR PREPARING TICAGRELOR ACTAVIS GROUP PTC EHF (IS) 2013-06-27 — — US disclosed
US-7566722-B2 Triazolopyrimidine derivatives as ADP P2Y12 receptor antagonists JANSSEN PHARMACEUTICA, N.V. (BE) 2009-07-28 — — US disclosed
US-20080108635-A1 Triazolopyrimidine derivatives as ADP P2Y12 receptor antagonists JANSSEN PHARMACEUTICA, N.V. (BE) 2008-05-08 — — US disclosed
US-20080108635-A1 Triazolopyrimidine derivatives as ADP P2Y12 receptor antagonists JANSSEN PHARMACEUTICA, N.V. (BE) 2008-05-08 — — 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 (3 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-20080108635-A1 Triazolopyrimidine derivatives as ADP P2Y12 receptor antagonists P2RY12, P2RY1, P2RY2 MAOB 1571/4885MAOA 1911/4885KDM1A 3744/4885
US-20130165696-A1 NOVEL PROCESSES FOR THE PREPARATION OF PHENYLCYCLOPROPYLAMINE DERIVATIVES AND USE THEREOF FOR PREPARING TICAGRELOR THPO, P2RY4, TBXA2R MAOB 610/4885MAOA 405/4885KDM1A 3290/4885
US-20170224653-A1 TLR-INDEPENDENT SMALL MOLECULE ADJUVANTS TLR1, TLR9, TLR3 MAOB 3524/4885MAOA 3935/4885KDM1A 2575/4885

“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.

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