SCHEMBL8932203

SCHEMBL8932203

CCOC(=O)[C@H](Cc1cc(OC(=O)OC(C)(C)C)c(OC(=O)OC(C)(C)C)cc1[Sn](C)(C)C)NC=O

nearest known ligand 0.35

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
SCN9A Q15858 1/20 0.35
CYP1A2 P05177 1/20 0.35
CYP2C9 P11712 1/20 0.35
CYP2C19 P33261 1/20 0.35
HTT P42858 1/20 0.35
SMN1; SMN2 Q16637 1/20 0.33
ALDH1A1 P00352 3/20 0.32
MAPT P10636 3/20 0.32
KDM4E B2RXH2 1/20 0.32
GAA P10253 1/20 0.32
PKM P14618 1/20 0.32
HPGD P15428 1/20 0.32
ALOX12 P18054 1/20 0.32
TACR1 P25103 1/20 0.31

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
SCHEMBL8932195 0.85 MTNR1A (0.38) SCN9ACYP1A2CYP2C9CYP2C19HTT
SCHEMBL5664158 0.85 MTNR1A (0.38) SCN9ACYP1A2CYP2C9CYP2C19HTT
SCHEMBL28858611 0.83 CYP1A2 (0.34) SCN9ACYP1A2CYP2C9CYP2C19HTT
SCHEMBL4651817 0.78 KLK5 (0.41) SCN9ACYP1A2CYP2C9CYP2C19HTT
SCHEMBL29361110 0.73 SCN9A (0.50) SCN9ACYP1A2CYP2C9CYP2C19HTT
SCHEMBL584547 0.72 SCN9A (0.49) SCN9ACYP1A2CYP2C9CYP2C19HTT
SCHEMBL1571749 0.70 SCN9A (0.47) SCN9ACYP1A2CYP2C9CYP2C19HTT
SCHEMBL4651819 0.69 MMP13 (0.34)
SCHEMBL4651824 0.69 MMP13 (0.34)
SCHEMBL8932192 0.68 CA1 (0.39) CYP1A2CYP2C19ALDH1A1KDM4EHPGD

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5393908-A Storage stable intermediate NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 1995-02-28 US claimed
WO-1994000460-A9 SYNTHESIS OF N-FORMYL-3,4-DI-t-BUTOXYCARBONYLOXY-6-(TRIMETHYLSTANNYL)-L-PHENYLALANINE ETHYL ESTER AND ITS REGIOSELECTIVE RADIOFLUORODESTANNYLATION TO 6-[18F]FLUORO-L-DOPA 1994-02-17 WO claimed
WO-1994000460-A1 SYNTHESIS OF N-FORMYL-3,4-DI-t-BUTOXYCARBONYLOXY-6-(TRIMETHYLSTANNYL)-L-PHENYLALANINE ETHYL ESTER AND ITS REGIOSELECTIVE RADIOFLUORODESTANNYLATION TO 6-[18F]FLUORO-L-DOPA THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 1994-01-06 WO claimed
US-5510522-A AMIDATION, IODINATION, METALLIZATION, RADIOFLUORINATION OF DOPA AND DERIVATIVES THEREOF; SHELF STABLE PRECURSOR, HIGH YIELDS REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 1996-04-23 US disclosed
US-5510522-A AMIDATION, IODINATION, METALLIZATION, RADIOFLUORINATION OF DOPA AND DERIVATIVES THEREOF; SHELF STABLE PRECURSOR, HIGH YIELDS REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 1996-04-23 US disclosed
US-5393908-A Storage stable intermediate NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 1995-02-28 US disclosed
US-5393908-A Storage stable intermediate NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 1995-02-28 US disclosed
WO-1994000460-A9 SYNTHESIS OF N-FORMYL-3,4-DI-t-BUTOXYCARBONYLOXY-6-(TRIMETHYLSTANNYL)-L-PHENYLALANINE ETHYL ESTER AND ITS REGIOSELECTIVE RADIOFLUORODESTANNYLATION TO 6-[18F]FLUORO-L-DOPA 1994-02-17 WO disclosed
WO-1994000460-A1 SYNTHESIS OF N-FORMYL-3,4-DI-t-BUTOXYCARBONYLOXY-6-(TRIMETHYLSTANNYL)-L-PHENYLALANINE ETHYL ESTER AND ITS REGIOSELECTIVE RADIOFLUORODESTANNYLATION TO 6-[18F]FLUORO-L-DOPA THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 1994-01-06 WO disclosed