Phenylalanine

Phenylalanine

SCHEMBL5154392

CC(=O)N1CCC(OC(c2ccc(Cl)cc2)c2ccccn2)CC1.N[C@@H](Cc1ccccc1)C(=O)O

nearest known ligand 0.49

Full drug profile on Sugi Atlas →

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
FAAH O00519 12/20 0.49
CNR1 P21554 2/20 0.44
CNR2 P34972 2/20 0.44
POLB P06746 1/20 0.44
LMNA P02545 1/20 0.41
CHRM2 P08172 1/20 0.41
ADRA2B P18089 1/20 0.41
SLC6A2 P23975 1/20 0.41
SLC6A4 P31645 1/20 0.41
HRH1 P35367 1/20 0.41
SLC6A3 Q01959 1/20 0.41
KCNH2 Q12809 1/20 0.41
HRH3 Q9Y5N1 1/20 0.41
CYP2D6 P10635 1/20 0.41
CYP2C19 P33261 1/20 0.41
FNTA P49354 1/20 0.40
FNTB P49356 1/20 0.40

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
SCHEMBL28850336 0.89 FAAH (0.51) FAAHCNR1CNR2POLBLMNA
SCHEMBL28850271 0.82 FAAH (0.50) FAAHCNR1CNR2POLBLMNA
SCHEMBL20898384 0.80 NOS2 (0.51) FAAHCNR1CNR2POLBLMNA
SCHEMBL20900383 0.80 NOS2 (0.51) FAAHCNR1CNR2POLBLMNA
SCHEMBL29631806 0.80 NOS2 (0.51) FAAHCNR1CNR2POLBLMNA
SCHEMBL5154387 0.78 FAAH (0.41) FAAHCNR1CNR2POLB
SCHEMBL28097062 0.78 POLB (0.46) FAAHCNR1CNR2POLBLMNA
SCHEMBL8583410 0.78 FAAH (0.53) FAAHLMNACHRM2ADRA2BSLC6A2
SCHEMBL7683665 0.78 DRD2 (0.46) FAAH
SCHEMBL28093862 0.77 GPR119 (0.51) FAAHCNR1POLBLMNACHRM2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7282589-B2 Acid addition salt of optically active piperidine compound and process for preparing the same UBE INDUSTRIES, LTD. (JP) 2007-10-16 US disclosed
US-20040220226-A1 Acid addition salt of optically active piperidine compound and process for preparing the same UBE INDUSTRIES, LTD. 2004-11-04 US disclosed
US-6780877-B2 ANTIHISTAMINIC ACTIVITY, ANTI-ALLERGIC ACTIVITY UBE INDUSTRIES, LTD. (JP) 2004-08-24 US disclosed
EP-0949260-A1 ACID-ADDITION SALTS OF OPTICALLY ACTIVE PIPERIDINE COMPOUND AND PROCESS FOR PRODUCING THE SAME UBE INDUSTRIES, LTD. (JP) 1999-10-13 EP 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 (1 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-20040220226-A1 Acid addition salt of optically active piperidine compound and process for preparing the same DCTPP1, SSRP1, ITPA FAAH 1684/4885CNR1 1689/4885CNR2 1904/4885

“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.