SCHEMBL10357692

SCHEMBL10357692

CC(=O)OC(C)OC(=O)N(CC(O)COc1cccc2[nH]ccc12)C(C)C

nearest known ligand 0.60

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HTR1A P08908 14/20 0.60
ADRB2 P07550 4/20 0.53
ADRB1 P08588 4/20 0.53
ADRB3 P13945 3/20 0.53
CYP1A2 P05177 2/20 0.53
CYP3A4 P08684 2/20 0.53
LMNA P02545 2/20 0.53
KDM4E B2RXH2 1/20 0.53
USP2 O75604 1/20 0.53
CYP2D6 P10635 1/20 0.53
THRB P10828 1/20 0.53
CYP2C9 P11712 1/20 0.53
TSHR P16473 1/20 0.53
TP53 P04637 1/20 0.53
GLA P06280 1/20 0.53
ALOX15 P16050 1/20 0.53
NFKB1 P19838 1/20 0.53
DRD4 P21917 1/20 0.53
HTR1B P28222 1/20 0.53
HTR2C P28335 1/20 0.53

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
SCHEMBL10865518 0.84 HTR1A (0.62) HTR1AADRB2ADRB1ADRB3CYP1A2
SCHEMBL10358158 0.84 NR2E1 (0.51) HTR1AADRB2ADRB1ADRB3CYP1A2
SCHEMBL13077527 0.76 HTR1A (0.57) HTR1AADRB2ADRB1ADRB3CYP1A2
SCHEMBL11308494 0.76 HTR1A (0.69) HTR1AADRB2ADRB1ADRB3CYP1A2
SCHEMBL13077528 0.76 HTR1A (0.56) HTR1AADRB2ADRB1ADRB3CYP1A2
SCHEMBL13077515 0.75 HTR1A (0.55) HTR1AADRB2ADRB1ADRB3CYP1A2
SCHEMBL14571136 0.73 HTR1A (0.53) HTR1AADRB2ADRB1ADRB3CYP1A2
SCHEMBL13040095 0.73 HTR1A (0.53) HTR1AADRB2ADRB1ADRB3CYP1A2
SCHEMBL10472395 0.72 HTR1A (0.69) HTR1AADRB2ADRB1ADRB3CYP1A2
SCHEMBL5759097 0.71 HTR1A (0.71) HTR1AADRB2ADRB1ADRB3CYP1A2

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
EP-0167451-B1 A NEW PROCESS FOR PREPARING NOVEL N-(ACYLOXY-ALKOXY) CARBONYL DERIVATIVES USEFUL AS BIOREVERSIBLE PRODRUG MOIETIES FOR PRIMARY AND SECONDARY AMINE FUNCTIONS IN DRUGS MERCK & CO. INC. (US) 1990-10-03 EP claimed
EP-0167451-A2 A new process for preparing novel N-(acyloxy-alkoxy) carbonyl derivatives useful as bioreversible prodrug moieties for primary and secondary amine functions in drugs MERCK & CO. INC. (US) 1986-01-08 EP claimed
EP-0167451-B1 A NEW PROCESS FOR PREPARING NOVEL N-(ACYLOXY-ALKOXY) CARBONYL DERIVATIVES USEFUL AS BIOREVERSIBLE PRODRUG MOIETIES FOR PRIMARY AND SECONDARY AMINE FUNCTIONS IN DRUGS MERCK & CO. INC. (US) 1990-10-03 EP disclosed
US-4916230-A Process for preparing novel N-(acyloxy-alkoxy)carbonyl derivatives useful as bioreversible prodrug moieties for primary and secondary amine functions in drugs MERCK & CO., INC. (US) 1990-04-10 US disclosed