SCHEMBL5082241

SCHEMBL5082241

CS(=O)(=O)O.C[C@H](N[C@H](C)c1ccccc1)C(=O)c1ccc(OC(=O)c2ccccc2)cc1

nearest known ligand 0.48

Known targets — ChEMBL curated mechanism

ABL1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB2AGTR1BCL2BCL2A1BCL2L1BCL2L10BCL2L2BCRBRAFCHRM1CHRNA10CHRNA9DRD1DRD2DRD3DRD4DRD5EGFRF2FLT1FLT4GCKGHSRGNRHRGRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BHTR1AHTR1BHTR1DHTR2AHTR2CHTR3AIDH2KDRKITMAOBMCL1MTTPPP4HBPDGFRBPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PIKFYVEROCK1ROCK2SLC18A2SLC6A2SLC6A3SLC6A4TACR1TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8gyrAgyrBparCparEpol

The experimentally established mechanism targets of None. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
TMPRSS15 P98073 1/20 0.48
KMT2A Q03164 4/20 0.48
MEN1 O00255 3/20 0.48
MAPT P10636 4/20 0.47
POLB P06746 1/20 0.47
NPC1 O15118 1/20 0.47
RAB9A P51151 1/20 0.47
PARP10 Q53GL7 1/20 0.46
ALDH1A1 P00352 2/20 0.44
TDP1 Q9NUW8 1/20 0.44
L3MBTL1 Q9Y468 1/20 0.44
PKM P14618 1/20 0.44
SMN1; SMN2 Q16637 1/20 0.43
ACR P10323 1/20 0.43
NPSR1 Q6W5P4 1/20 0.42
ELANE P08246 1/20 0.41
KLK1 P06870 1/20 0.41
PRSS1 P07477 1/20 0.41
ACP3 P15309 2/20 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
SCHEMBL5082686 0.95 KMT2A (0.52) KMT2AMEN1MAPTPOLBNPC1
Hydrochloric Acid SCHEMBL5082767 0.94 KMT2A (0.51) KMT2AMEN1MAPTPOLBNPC1
SCHEMBL5082805 0.87 ACP3 (0.47) KMT2AMAPTPOLBNPC1ALDH1A1
SCHEMBL5079094 0.85 ALDH1A1 (0.41) KMT2AMEN1MAPTPOLBNPC1
SCHEMBL5082798 0.84 ALDH1A1 (0.42) KMT2AMEN1MAPTPOLBNPC1
SCHEMBL5079906 0.84 ALDH1A1 (0.42) KMT2AMEN1MAPTPOLBNPC1
Hydrochloric Acid SCHEMBL5082428 0.82 ACP3 (0.44) KMT2AMEN1MAPTPOLBNPC1
SCHEMBL5082435 0.81 ACP3 (0.53) NPC1ALDH1A1TDP1L3MBTL1SMN1; SMN2
SCHEMBL22828969 0.81 ACP3 (0.53) NPC1ALDH1A1TDP1L3MBTL1SMN1; SMN2
SCHEMBL5082443 0.81 MAOB (0.51) MAPTNPC1RAB9APARP10ALDH1A1

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-7408084-B2 Process for producing optically active β-amino alcohol KANEKA CORPORATION (JP) 2008-08-05 US disclosed
US-20050277791-A1 Process for producing optically active beta-amino alcohol KANEKA CORPORATION (JP) 2005-12-15 US disclosed
EP-1512677-A1 PROCESS FOR PRODUCING OPTICALLY ACTIVE s-AMINO ALCOHOL KANEKA CORPORATION (JP) 2005-03-09 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-20050277791-A1 Process for producing optically active beta-amino alcohol ADH1A, ALDH7A1, ADH1C TMPRSS15 1871/4885KMT2A 1460/4885MEN1 3339/4885

“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.