SCHEMBL30358050

SCHEMBL30358050

COC(=O)[C@H]1CCc2cc(Br)ccc2N1

nearest known ligand 0.46

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
▸ IGF1R P08069 1/20 0.46
▸ ALDH1A1 P00352 2/20 0.38
▸ SMN1; SMN2 Q16637 2/20 0.38
▸ KMT2A Q03164 2/20 0.38
▸ TP53 P04637 1/20 0.38
▸ CYP1A2 P05177 1/20 0.38
▸ HPGD P15428 1/20 0.38
▸ HSD17B10 Q99714 1/20 0.38
▸ SMYD3 Q9H7B4 1/20 0.37
▸ RIPK1 Q13546 1/20 0.37
▸ SLC6A4 P31645 1/20 0.36
▸ SLC6A3 Q01959 1/20 0.36
▸ BRD4 O60885 1/20 0.35
▸ MTNR1A P48039 1/20 0.35
▸ HTT P42858 1/20 0.35
▸ MEN1 O00255 1/20 0.35
▸ POLB P06746 1/20 0.35
▸ ESR1 P03372 1/20 0.35
▸ ESR2 Q92731 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
SCHEMBL3893061 1.00 IGF1R (0.46) IGF1RALDH1A1SMN1; SMN2KMT2ATP53
SCHEMBL8646992 0.86 GAA (0.40) KMT2ASLC6A4SLC6A3BRD4MEN1
SCHEMBL7335768 0.83 ALDH1A1 (0.51) IGF1RALDH1A1SMN1; SMN2TP53CYP1A2
SCHEMBL30357998 0.83 IGF1R (0.46) IGF1RALDH1A1SMN1; SMN2KMT2ATP53
SCHEMBL30358032 0.83 ALDH1A1 (0.51) IGF1RALDH1A1SMN1; SMN2TP53CYP1A2
SCHEMBL30358011 0.83 IGF1R (0.46) IGF1RALDH1A1SMN1; SMN2KMT2ATP53
SCHEMBL7433964 0.80 SMYD3 (0.56) IGF1RALDH1A1KMT2ACYP1A2HPGD
SCHEMBL926907 0.80 SMYD3 (0.56) IGF1RALDH1A1KMT2ACYP1A2HPGD
SCHEMBL30357995 0.80 SMYD3 (0.56) IGF1RALDH1A1KMT2ACYP1A2HPGD
SCHEMBL8567081 0.80 SMYD3 (0.56) IGF1RALDH1A1KMT2ACYP1A2HPGD

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115872820-B Method for synthesizing chiral 2-functionalized tetrahydroquinoline through biomimetic catalysis and asymmetric hydrogenation 中国科学院大连化学物理研究所 2024-08-06 — — CN disclosed
CN-115872820-A Method for synthesizing chiral 2-functional group tetrahydroquinoline by biomimetic catalytic asymmetric hydrogenation 中国科学院大连化学物理研究所 2023-03-31 — — CN disclosed
Send feedback