Predicted protein targets (top 5)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | POLB | P06746 | 1/20 | 0.51 |
| ▸ | LTA4H | P09960 | 7/20 | 0.50 |
| ▸ | CHRNB4 | P30926 | 1/20 | 0.44 |
| ▸ | CHRNA3 | P32297 | 1/20 | 0.44 |
| ▸ | HTR6 | P50406 | 4/20 | 0.43 |
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.
| Compound | similarity | top predicted | shared targets | |
|---|---|---|---|---|
| Biphenyl SCHEMBL5439264 | 1.00 | POLB (0.51) | POLBLTA4HCHRNB4CHRNA3HTR6 | |
| Biphenyl SCHEMBL16732521 | 0.88 | LTA4H (0.45) | POLBLTA4HCHRNB4CHRNA3 | |
| SCHEMBL9015256 | 0.86 | POLB (0.57) | POLBLTA4H | |
| SCHEMBL8135451 | 0.84 | POLB (0.47) | POLBLTA4HCHRNB4CHRNA3HTR6 | |
| SCHEMBL115932 | 0.82 | — | — | |
| SCHEMBL7787365 | 0.82 | FDPS (0.41) | POLBCHRNB4CHRNA3 | |
| SCHEMBL10141198 | 0.82 | — | — | |
| SCHEMBL10141207 | 0.82 | — | — | |
| SCHEMBL19071 | 0.82 | — | — | |
| SCHEMBL145266 | 0.82 | — | — |
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 45 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-113943317-B | Preparation method of MeCBS solid | 大连双硼医药化工有限公司 | 2024-02-27 | — | — | CN | claimed |
| CN-114853662-B | Process for preparing chiral hydrazinopiperidine derivatives | 四川青木制药有限公司 | 2024-01-12 | — | — | CN | claimed |
| CN-114853662-A | Preparation method of chiral hydrazinylpiperidine derivative | 四川青木制药有限公司 | 2022-08-05 | — | — | CN | claimed |
| CN-107188771-B | Chiral synthesis method of gamma-nitrophenol compound | 浙江工业大学 | 2021-08-24 | — | — | CN | claimed |
| CN-109265385-B | Synthesis process of chiral catalyst | 上海福乐医药科技有限公司 | 2020-10-27 | — | — | CN | claimed |
| CN-103772224-B | Preparation method of D-threonine | CHENGDU BAISHIXING SCIENCE AND TECHNOLOGY INDUSTRY CO LTD | 2015-04-15 | — | — | CN | claimed |
| CN-103772224-A | Preparation method of D-threonine | CHENGDU BAISHIXING SCIENCE AND TECHNOLOGY INDUSTRY CO LTD | 2014-05-07 | — | — | CN | claimed |
| CN-120623134-A | Dihydromyricetin-diphenyl prolinol chiral eutectic as well as preparation method and application thereof | 天津大学 | 2025-09-12 | — | — | CN | disclosed |
| CN-120623134-A | Dihydromyricetin-diphenyl prolinol chiral eutectic as well as preparation method and application thereof | 天津大学 | 2025-09-12 | — | — | CN | disclosed |
| CN-120623095-A | Crystalline as a racemic compound Deracemization method for chiral compound | 天津大学 | 2025-09-12 | — | — | CN | disclosed |
| EP-4140992-B1 | METHOD FOR PREPARING S-NICOTINE | SHENZHEN ZINWI BIO TECH CO LTD (CN) | 2024-10-16 | — | — | EP | disclosed |
| EP-4144727-B1 | METHOD FOR PREPARING CHIRAL SYNTHETIC NICOTINE | SHENZHEN ZINWI BIO TECH CO LTD (CN) | 2024-10-09 | — | — | EP | disclosed |
| EP-4144726-B1 | PREPARATION METHOD FOR SYNTHESIZING S-NICOTINE FROM GLUTARIC ACID ESTER | SHENZHEN ZINWI BIO TECH CO LTD (CN) | 2024-10-02 | — | — | EP | disclosed |
| EP-2132179-A1 | PROCESS FOR PREPARING ISOMERS OF CARMOTEROL | Cipla Limited (IN) | 2009-12-16 | — | — | EP | disclosed |
| WO-2008104781-A1 | PROCESS FOR PREPARING ISOMERS OF CARMOTEROL | CIPLA LIMITED (IN) | 2008-09-04 | — | — | WO | disclosed |
| US-20080200672-A1 | Highly enantioselective carbonyl reduction with borane catalyzed by chiral spiroborate esters derived from chiral beta-aminoalcohols | NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT | 2008-08-21 | — | — | US | disclosed |
| US-20070232813-A1 | Substituted Cyclohexadienals - Syntheses and Applications | THE TEXAS A&M UNIVERSITY SYSTEM | 2007-10-04 | — | — | US | disclosed |
| CN-1156448-C | Optical isomer of 3-methyl fentanyl, derivant, synthesizing and its analgesic activity | 中国科学院上海药物研究所 | 2004-07-07 | — | — | CN | disclosed |
| CN-1371903-A | Optical isomer of 3-methyl fentanyl, derivant, synthesizing and its analgesic activity | SHANGHAI INST OF DRUG CHINESE (CN) | 2002-10-02 | — | — | CN | disclosed |
| US-5527923-A | Process for preparing enantiomerically pure diarylprolinols | BOEHRINGER INGELHEIM KG (DE) | 1996-06-18 | — | — | US | 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 (2 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.
| Patent | Title | Text reads most about | Predicted target · text-rank |
|---|---|---|---|
| US-20070232813-A1 | Substituted Cyclohexadienals - Syntheses and Applications | DHPS, COASY, PPIE | POLB 702/4885LTA4H 659/4885CHRNB4 4740/4885 |
| US-20080200672-A1 | Highly enantioselective carbonyl reduction with borane catalyzed by chiral spiroborate esters derived from chiral beta-aminoalcohols | ADH1A, ALDH7A1, HSD11B1 | POLB 1177/4885LTA4H 3345/4885CHRNB4 801/4885 |
“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.