SCHEMBL14733400

SCHEMBL14733400

N[C@@H](CO)Cc1ccc(-c2ccccc2)cc1

nearest known ligand 0.58

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
EPHX1 P07099 1/20 0.58
SRR Q9GZT4 2/20 0.51
PSAT1 Q9Y617 2/20 0.51
TAAR1 Q96RJ0 1/20 0.50
ANPEP P15144 1/20 0.50
ACP3 P15309 1/20 0.47
FFAR1 O14842 1/20 0.47
PPARG P37231 6/20 0.46
PPARA Q07869 5/20 0.46
ABCC4 O15439 1/20 0.45
LMNA P02545 1/20 0.45
GAA P10253 1/20 0.45
TSHR P16473 1/20 0.45
PTGS1 P23219 1/20 0.45
HTT P42858 1/20 0.45
IDO1 P14902 1/20 0.45
AGXT P21549 1/20 0.45
MME P08473 1/20 0.44
ACE P12821 1/20 0.44

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
SCHEMBL7357350 1.00 EPHX1 (0.58) EPHX1SRRPSAT1TAAR1ANPEP
SCHEMBL7357345 1.00 EPHX1 (0.58) EPHX1SRRPSAT1TAAR1ANPEP
Hydrochloric Acid SCHEMBL30885862 0.98 EPHX1 (0.56) EPHX1SRRPSAT1TAAR1ANPEP
Hydrochloric Acid SCHEMBL16932212 0.98 EPHX1 (0.56) EPHX1SRRPSAT1TAAR1ANPEP
Hydrochloric Acid SCHEMBL16932213 0.98 EPHX1 (0.56) EPHX1SRRPSAT1TAAR1ANPEP
Biphenyl SCHEMBL7890864 0.90 EPHX1 (0.52) EPHX1SRRPSAT1TAAR1ANPEP
L-Phenylalaninol SCHEMBL81769 0.87 EPHX1 (0.76) EPHX1TAAR1ANPEPPTGS1
L-Phenylalaninol SCHEMBL2521 0.87 EPHX1 (0.76) EPHX1TAAR1ANPEPPTGS1
L-Phenylalaninol SCHEMBL87692 0.87 EPHX1 (0.76) EPHX1TAAR1ANPEPPTGS1
L-Phenylalaninol SCHEMBL177073 0.87 EPHX1 (0.76) EPHX1TAAR1ANPEPPTGS1

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 28 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119528749-A Synthesis method of (r) -tert-butyl (1- ([ 1,1' -biphenyl ] -4-yl) -3-hydroxy propane-2-yl) carbamate 河北八亿时空药业有限公司 2025-02-28 CN claimed
CN-121825923-A (S) -transaminase mutant and application thereof in preparation of (R) -3- ([ 1,1' -biphenyl ] -4-yl) -2-aminopropan-1-ol 浙江大学 2026-04-10 CN disclosed
CN-121825923-A (S) -transaminase mutant and application thereof in preparation of (R) -3- ([ 1,1' -biphenyl ] -4-yl) -2-aminopropan-1-ol 浙江大学 2026-04-10 CN disclosed
CN-119528749-A Synthesis method of (r) -tert-butyl (1- ([ 1,1' -biphenyl ] -4-yl) -3-hydroxy propane-2-yl) carbamate 河北八亿时空药业有限公司 2025-02-28 CN disclosed
CN-119528749-A Synthesis method of (r) -tert-butyl (1- ([ 1,1' -biphenyl ] -4-yl) -3-hydroxy propane-2-yl) carbamate 河北八亿时空药业有限公司 2025-02-28 CN disclosed
CN-115745841-B Preparation method of sakubi-qu intermediate 凯特立斯(深圳)科技有限公司 2024-04-16 CN disclosed
WO-2023206874-A1 SACUBITRIL INTERMEDIATE, PREPARATION METHOD THEREFOR, AND USE THEREOF 凯特立斯(深圳)科技有限公司 2023-11-02 WO disclosed
CN-116083497-A Synthesis method of sakubi qu intermediate 南通常佑药业科技有限公司 2023-05-09 CN disclosed
CN-116083497-A Synthesis method of sakubi qu intermediate 南通常佑药业科技有限公司 2023-05-09 CN disclosed
CN-115745841-A Preparation method of shakubiqu intermediate 凯特立斯(深圳)科技有限公司 2023-03-07 CN disclosed
US-20160200665-A1 SYNTHESIS OF BIPHENYLALANINOL VIA NOVEL INTERMEDIATES DPX HOLDINGS B.V. (NL) 2016-07-14 US disclosed
US-9139515-B2 Synthesis of R-biphenylalaninol DPX HOLDINGS B.V. (US) 2015-09-22 US disclosed
US-9139515-B2 Synthesis of R-biphenylalaninol DPX HOLDINGS B.V. (US) 2015-09-22 US disclosed
US-20150210632-A1 NEW PROCESS NOVARTIS AG (CH) 2015-07-30 US disclosed
US-20150210632-A1 NEW PROCESS NOVARTIS AG (CH) 2015-07-30 US disclosed
WO-2015024991-A1 SYNTHESIS OF BIPHENYLALANINOL VIA NOVEL INTERMEDIATES DPX HOLDINGS B.V. (NL) 2015-02-26 WO disclosed
US-20140296559-A1 SYNTHESIS OF R-BIPHENYLALANINOL DSM FINE CHEMICALS AUSTRIA NFG. GMBH & CO KG (AT) 2014-10-02 US disclosed
US-20140296559-A1 SYNTHESIS OF R-BIPHENYLALANINOL DSM FINE CHEMICALS AUSTRIA NFG. GMBH & CO KG (AT) 2014-10-02 US disclosed
WO-2014032627-A1 NEW PROCESS ZHEJIANG JIUZHOU PHARMACEUTICAL CO., LTD (CN) 2014-03-06 WO disclosed
WO-2013026773-A1 SYNTHESIS OF R-BIPHENYLALANINOL DSM IP ASSETS B.V. (NL) 2013-02-28 WO 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 (3 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-20150210632-A1 NEW PROCESS MME, DNPEP, ACE EPHX1 76/4885SRR 694/4885PSAT1 1374/4885
US-20140296559-A1 SYNTHESIS OF R-BIPHENYLALANINOL CYP2B6, CYP2A6, CYP2D6 EPHX1 725/4885SRR 517/4885PSAT1 2786/4885
US-20160200665-A1 SYNTHESIS OF BIPHENYLALANINOL VIA NOVEL INTERMEDIATES CYP1B1, UGT1A1, UGT2B7 EPHX1 499/4885SRR 680/4885PSAT1 969/4885

“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.