SCHEMBL7148579

SCHEMBL7148579

C[C@H](Cc1ccccc1)NC[C@H](O)c1ccccc1Cl

nearest known ligand 0.68

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
▸ ADRB2 P07550 6/20 0.68
▸ ADRB1 P08588 4/20 0.68
▸ LMNA P02545 1/20 0.56
▸ CYP2D6 P10635 2/20 0.54
▸ NFKB1 P19838 1/20 0.54
▸ HIF1A Q16665 1/20 0.54
▸ BLM P54132 1/20 0.52
▸ SIGMAR1 Q99720 5/20 0.50
▸ ADRB3 P13945 2/20 0.50
▸ CYP1A2 P05177 1/20 0.50
▸ CYP3A4 P08684 1/20 0.50
▸ TSHR P16473 1/20 0.50
▸ SLC2A1 P11166 1/20 0.49

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
SCHEMBL7148585 1.00 ADRB2 (0.68) ADRB2ADRB1LMNACYP2D6NFKB1
SCHEMBL7153661 0.88 ADRB2 (0.52) ADRB2ADRB1LMNACYP2D6SIGMAR1
SCHEMBL7153665 0.88 ADRB2 (0.52) ADRB2ADRB1LMNACYP2D6SIGMAR1
SCHEMBL11089904 0.87 ADRB2 (0.59) ADRB2ADRB1CYP2D6SIGMAR1ADRB3
Hydrochloric Acid SCHEMBL11093309 0.86 ADRB2 (0.58) ADRB2ADRB1CYP2D6BLMSIGMAR1
SCHEMBL7148365 0.85 ADRB2 (0.68) ADRB2ADRB1LMNACYP2D6NFKB1
SCHEMBL7148362 0.85 ADRB2 (0.68) ADRB2ADRB1LMNACYP2D6NFKB1
SCHEMBL7153283 0.85 ADRB2 (0.62) ADRB2ADRB1CYP2D6HIF1AADRB3
SCHEMBL7153280 0.85 ADRB2 (0.62) ADRB2ADRB1CYP2D6HIF1AADRB3
SCHEMBL10659768 0.85 ADRB1 (0.56) ADRB2ADRB1CYP2D6NFKB1HIF1A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20030143701-A1 Processes for producing optically active 2-amino-1-phenylethanol derivatives DAICEL CHEMICAL INDUSTRIES, LTD. 2003-07-31 — — US disclosed
EP-0924194-B1 Processes for producing optically active 2-amino-1-phenylethanol derivatives DAICEL CHEM (JP) 2003-05-14 — — EP disclosed
US-6528686-B1 Reacting primary amine and ketone functionalized derivatives; catalytically reducing DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 2003-03-04 — — US disclosed
EP-0924193-B1 Processes for producing optically active 2-amino-1-phenylethanol derivatives DAICEL CHEM (JP) 2003-02-19 — — EP disclosed
EP-0939134-B1 Processes for producing optically active 2-amino-1-phenylethanol derivatives DAICEL CHEM (JP) 2002-09-11 — — EP disclosed
US-6114582-A DECYCLIZATION TO FORM A CHEMICAL INTERMEDIATE FOR PRODUCING AN ANTI-OBESITY AGENT AND ANTIDIABETIC AGENT DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 2000-09-05 — — US disclosed
EP-0654534-B1 Processes for producing optically active 2-amino-1-phenylethanol derivatives DAICEL CHEM (JP) 2000-03-01 — — EP disclosed
EP-0939134-A1 Processes for producing optically active 2-amino-1-phenylethanol derivatives DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 1999-09-01 — — EP disclosed
EP-0924194-A2 Processes for producing optically active 2-amino-1-phenylethanol derivatives DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 1999-06-23 — — EP disclosed
EP-0924193-A1 Processes for producing optically active 2-amino-1-phenylethanol derivatives DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 1999-06-23 — — EP disclosed
US-5811293-A CULTURE PRODUCT AS CHEMICAL INTERMEDIATE FOR ANTI-OBESITY AGENT DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 1998-09-22 — — US disclosed
US-5629200-A MICROORGANISM DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 1997-05-13 — — US disclosed
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