Predicted protein targets (top 18)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | ALDH1A1 | P00352 | 5/20 | 0.47 |
| ▸ | L3MBTL1 | Q9Y468 | 2/20 | 0.46 |
| ▸ | KMT2A | Q03164 | 2/20 | 0.46 |
| ▸ | MAPK1 | P28482 | 1/20 | 0.46 |
| ▸ | SLC6A2 | P23975 | 1/20 | 0.46 |
| ▸ | SLC6A3 | Q01959 | 1/20 | 0.46 |
| ▸ | TDP1 | Q9NUW8 | 1/20 | 0.46 |
| ▸ | CCNE1 | P24864 | 1/20 | 0.45 |
| ▸ | CDK2 | P24941 | 1/20 | 0.45 |
| ▸ | GSK3B | P49841 | 1/20 | 0.45 |
| ▸ | NPC1 | O15118 | 1/20 | 0.44 |
| ▸ | RAB9A | P51151 | 1/20 | 0.44 |
| ▸ | DDB1 | Q16531 | 1/20 | 0.43 |
| ▸ | CRBN | Q96SW2 | 1/20 | 0.43 |
| ▸ | MEN1 | O00255 | 1/20 | 0.43 |
| ▸ | NPSR1 | Q6W5P4 | 1/20 | 0.43 |
| ▸ | PKM | P14618 | 1/20 | 0.43 |
| ▸ | LMNA | P02545 | 1/20 | 0.42 |
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 | |
|---|---|---|---|---|
| SCHEMBL11323517 | 1.00 | ALDH1A1 (0.47) | ALDH1A1L3MBTL1KMT2AMAPK1SLC6A2 | |
| SCHEMBL1279658 | 0.98 | ALDH1A1 (0.46) | ALDH1A1L3MBTL1KMT2AMAPK1SLC6A2 | |
| Carbamic Acid SCHEMBL28871401 | 0.95 | CYP2C19 (0.44) | ALDH1A1L3MBTL1KMT2AMAPK1SLC6A2 | |
| SCHEMBL6363978 | 0.93 | CCNE1 (0.42) | ALDH1A1L3MBTL1KMT2AMAPK1SLC6A2 | |
| SCHEMBL9942943 | 0.90 | ALDH1A1 (0.41) | ALDH1A1L3MBTL1KMT2AMAPK1SLC6A2 | |
| SCHEMBL5469498 | 0.90 | ALDH1A1 (0.47) | ALDH1A1L3MBTL1KMT2AMAPK1SLC6A2 | |
| SCHEMBL15999210 | 0.87 | NOTUM (0.51) | ALDH1A1L3MBTL1KMT2AMAPK1SLC6A2 | |
| SCHEMBL406279 | 0.87 | KMT2A (0.41) | ALDH1A1L3MBTL1KMT2AMAPK1SLC6A2 | |
| SCHEMBL5963233 | 0.86 | CA2 (0.43) | ALDH1A1L3MBTL1KMT2AMAPK1CCNE1 | |
| SCHEMBL19763139 | 0.86 | ALDH1A1 (0.50) | ALDH1A1L3MBTL1KMT2AMAPK1SLC6A2 |
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
Appears in 4833 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-122036924-A | Synthetic method of bionic collagen hexapeptide | 成都欣肽生物科技有限公司 | 2026-05-15 | — | — | CN | claimed |
| CN-119350189-A | Method for preparing N-methyl-N-benzyloxycarbonyl-L-aspartic acid-4-tert-butyl ester | 上海农林职业技术学院 | 2025-01-24 | — | — | CN | claimed |
| CN-118791403-A | Refining method of compound intermediate containing gamma-glutamyl transpeptidase response motif | 安徽普利药业有限公司 | 2024-10-18 | — | — | CN | claimed |
| CN-118084735-A | Photo-delay synthesis method of O- [2- [ [ tert-butyloxycarbonyl ] amino ] ethyl ] -N- [ fluorenylmethoxycarbonyl ] -L-tyrosine | 吉尔多肽生物制药(大连市)有限公司 | 2024-05-28 | — | — | CN | claimed |
| CN-118005554-A | Synthesis method of 5, 6-dihydroxyindole and intermediate thereof | 北京颖诺凯胜科技有限公司 | 2024-05-10 | — | — | CN | claimed |
| CN-117924113-A | AEEA-AEEA synthesis method | 成都普康唯新生物科技有限公司 | 2024-04-26 | — | — | CN | claimed |
| CN-117820136-A | Synthesis method of 2- (2- (2-amino ethoxy) acetic acid | 康羽生命科学技术(苏州)有限公司 | 2024-04-05 | — | — | CN | claimed |
| CN-114105848-B | Preparation method of cis-D-hydroxyproline derivative | 四川同晟生物医药有限公司 | 2024-01-12 | — | — | CN | claimed |
| US-11799085-B2 | Method of manufacturing negative electrode for lithium secondary battery and lithium secondary battery | LG ENERGY SOLUTION, LTD. (KR) | 2023-10-24 | — | — | US | claimed |
| US-11788080-B2 | Modified cleavases, uses thereof and related kits | Encodia, Inc. (US) | 2023-10-17 | — | — | US | claimed |
| US-5621085-A | Process for the preparation of amikacin precursors | BIOCHIMICA OPOS S.P.A. (IT) | 1997-04-15 | — | — | US | claimed |
| US-5426190-A | Preparation of N-(organocarbonyloxy)-succinimide derivatives of N-hydroxysuccinimide | PPG INDUSTRIES, INC. (US) | 1995-06-20 | — | — | US | claimed |
| EP-0446798-B1 | 1-alkyl-, 1-alkenyl- and 1-alkynylaryl-2-amino-1, 3-propanediols and related compounds, a process and intermediates for their preparation and their use as medicaments | HOECHST ROUSSEL PHARMA (US) | 1994-11-23 | — | — | EP | claimed |
| EP-0446670-B1 | Method of preparation of amikacin precursors | OPOS BIOCHIMICA SRL (IT) | 1994-09-21 | — | — | EP | claimed |
| EP-0446798-A1 | 1-alkyl-, 1-alkenyl- and 1-alkynylaryl-2-amino-1, 3-propanediols and related compounds, a process and intermediates for their preparation and their use as medicaments | HOECHST-ROUSSEL PHARMACEUTICALS INCORPORATED (US) | 1991-09-18 | — | — | EP | claimed |
| EP-0446670-A1 | Method of preparation of amikacin precursors | BIOCHIMICA OPOS SPA (IT) | 1991-09-18 | — | — | EP | claimed |
| US-4231924-A | ACYLATION, HYDROLYSIS | ABBOTT LABORATORIES (US) | 1980-11-04 | — | — | US | claimed |
| US-4169941-A | ANTIBIOTICS, URETHANE-TYPE AMINO PROTECTION REACTION | ABBOTT LABORATORIES (US) | 1979-10-02 | — | — | US | claimed |
| US-4155902-A | ACYLATION, HYDROGENOLYSIS | ABBOTT LABORATORIES (US) | 1979-05-22 | — | — | US | claimed |
| US-4124756-A | REACTION WITH PROTECTED AMINO ACIDS TO FORM 3-DE-O-METHYL-N-ACYLFORTIMICINS; ANTIBACTERIAL | ABBOTT LABORATORIES (US) | 1978-11-07 | — | — | US | claimed |