Aminorex

Aminorex

SCHEMBL6803173

NC1=NCC(c2ccccc2)O1.O=C(O)/C=C/C(=O)O

nearest known ligand 0.41

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADRB1ADRB2ATP4AATP4BAXLCHRM2CHRM3DRD2FLT3HRH1HTR2AHTR2BHTR2CKCNH2KMT2AMAP2K1MAP2K2MEN1MLNRPLK4RENS1PR1SLC6A2SLC6A4atpAatpBatpCatpDatpEatpFatpFHatpGpol

The experimentally established mechanism targets of Aminorex. 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
MEN1 known ✓ O00255 1/20 0.37
KMT2A known ✓ Q03164 1/20 0.37
HDAC3 O15379 3/20 0.41
HDAC1 Q13547 3/20 0.41
HDAC2 Q92769 3/20 0.41
NCOR2 Q9Y618 2/20 0.41
HDAC8 Q9BY41 2/20 0.41
RAB9A P51151 1/20 0.37
SLC6A3 Q01959 1/20 0.37
POLB P06746 3/20 0.37
LMNA P02545 1/20 0.37
GLA P06280 1/20 0.37
MAPK1 P28482 1/20 0.37
PMP22 Q01453 1/20 0.37
SMN1; SMN2 Q16637 1/20 0.37
KDM4E B2RXH2 3/20 0.36
HTT P42858 1/20 0.36
TSHR P16473 2/20 0.35
HSD17B10 Q99714 2/20 0.35
TP53 P04637 1/20 0.35

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
Aminorex SCHEMBL123039 0.87 TSHR (0.45) HDAC3HDAC1HDAC2NCOR2HDAC8
SCHEMBL31158568 0.70 TSHR (0.50) HDAC3HDAC1HDAC2NCOR2HDAC8
SCHEMBL34460861 0.70 TSHR (0.50) HDAC3HDAC1HDAC2NCOR2HDAC8
Clominorex SCHEMBL121090 0.70 TAAR1 (0.46) RAB9ASLC6A3SMN1; SMN2TAAR1
SCHEMBL27806570 0.68 HDAC3 (0.41) HDAC3HDAC1HDAC2NCOR2HDAC8
SCHEMBL27848552 0.68 HDAC3 (0.41) HDAC3HDAC1HDAC2NCOR2HDAC8
SCHEMBL14301430 0.66 TSHR (0.45) SMN1; SMN2KDM4ETSHRHSD17B10ALDH1A1
SCHEMBL1548278 0.66 ALDH1A1 (0.54) KMT2ASMN1; SMN2KDM4ETSHRHSD17B10
SCHEMBL2399688 0.66 TSHR (0.45) SMN1; SMN2KDM4ETSHRHSD17B10ALDH1A1
SCHEMBL11748610 0.66 TSHR (0.41) HDAC3HDAC1HDAC2NCOR2HDAC8

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20040038890-A1 Human voltage-gated potassium channel subunit AIYAR JAYASHREE (US) 2004-02-26 US disclosed
WO-1999058666-A1 POTASSIUM CHANNEL SUBUNIT ASTRAZENECA AB (SE) 1999-11-18 WO disclosed
WO-1999055331-A1 USE OF ALPHA LIPOIC ACID TO REDUCE APPETITE AND/OR BODY WEIGHT SKW TROSTBERG AKTIENGESELLSCHAFT (DE) 1999-11-04 WO disclosed