Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | L3MBTL1 | Q9Y468 | 4/20 | 0.52 |
| ▸ | KMT2A | Q03164 | 3/20 | 0.52 |
| ▸ | POLB | P06746 | 3/20 | 0.52 |
| ▸ | PKM | P14618 | 1/20 | 0.52 |
| ▸ | PTPN1 | P18031 | 1/20 | 0.52 |
| ▸ | PTPN7 | P35236 | 1/20 | 0.52 |
| ▸ | BLM | P54132 | 1/20 | 0.52 |
| ▸ | ESR2 | Q92731 | 1/20 | 0.52 |
| ▸ | CYP2C19 | P33261 | 1/20 | 0.50 |
| ▸ | HSD17B10 | Q99714 | 1/20 | 0.48 |
| ▸ | HPGD | P15428 | 2/20 | 0.44 |
| ▸ | RECQL | P46063 | 2/20 | 0.44 |
| ▸ | GLA | P06280 | 1/20 | 0.44 |
| ▸ | LMNA | P02545 | 1/20 | 0.43 |
| ▸ | MEN1 | O00255 | 2/20 | 0.42 |
| ▸ | AGTR1 | P30556 | 1/20 | 0.42 |
| ▸ | ALDH1A1 | P00352 | 6/20 | 0.42 |
| ▸ | SMN1; SMN2 | Q16637 | 1/20 | 0.41 |
| ▸ | MIF | P14174 | 1/20 | 0.41 |
| ▸ | MAPT | P10636 | 3/20 | 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.
| Compound | similarity | top predicted | shared targets | |
|---|---|---|---|---|
| SCHEMBL477460 | 1.00 | L3MBTL1 (0.52) | L3MBTL1KMT2APOLBPKMPTPN1 | |
| SCHEMBL9707878 | 0.88 | POLB (0.46) | L3MBTL1KMT2APOLBPKMPTPN1 | |
| SCHEMBL7684954 | 0.83 | KMT2A (0.56) | L3MBTL1KMT2APOLBPKMPTPN1 | |
| SCHEMBL24516966 | 0.81 | KMT2A (0.42) | L3MBTL1KMT2APOLBPKMPTPN1 | |
| SCHEMBL23089955 | 0.78 | KMT2A (0.48) | L3MBTL1KMT2APOLBPKMPTPN1 | |
| SCHEMBL24515979 | 0.77 | UGT2B7 (0.52) | L3MBTL1KMT2APOLBPKMPTPN1 | |
| SCHEMBL24516523 | 0.77 | GAA (0.47) | L3MBTL1KMT2APOLBPKMCYP2C19 | |
| SCHEMBL1934617 | 0.76 | CYP2C19 (0.48) | L3MBTL1KMT2APOLBPKMPTPN1 | |
| SCHEMBL8627683 | 0.76 | CYP2C19 (0.48) | L3MBTL1KMT2APOLBPKMPTPN1 | |
| SCHEMBL23089951 | 0.75 | KMT2A (0.46) | L3MBTL1KMT2APOLBPKMPTPN1 |
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 15 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-101210017-A | Synthesis of middle position-tetraaryldiphenanthrene dioxyporphyrin derivative and application thereof | NANJING UNIVERSITY OF TECHNOLOGY (CN) | 2008-07-02 | — | — | CN | claimed |
| CN-115066428-B | Boric acid derivatives | 首药控股(北京)股份有限公司 | 2025-06-13 | — | — | CN | disclosed |
| CN-115413657-A | Application of cinnamic acid derivative in mosquito control | 五邑大学 | 2022-12-02 | — | — | CN | disclosed |
| WO-2022122975-A1 | CYCLOPENTENONES DERIVATIVES AND THEIR USE AS ANTIBIOTICS | CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (CNRS) (FR) | 2022-06-16 | — | — | WO | disclosed |
| CN-112264089-B | SAPO-11 Ni-loaded composite catalyst and preparation method and application thereof | 江南大学 | 2021-11-23 | — | — | CN | disclosed |
| CN-112264089-A | SAPO-11 Ni-loaded composite catalyst and preparation method and application thereof | 江南大学 | 2021-01-26 | — | — | CN | disclosed |
| CN-109180624-A | A kind of preparation method of novel 6- hydroxyl -2H- pyrans -3- ketone | 大连理工大学 | 2019-01-11 | — | — | CN | disclosed |
| US-8563786-B2 | Method for producing optically active alcohol | MITSUI CHEMICALS, INC. (JP) | 2013-10-22 | — | — | US | disclosed |
| US-20120088938-A1 | METHOD FOR PRODUCING OPTICALLY ACTIVE ALCOHOL | AGENCY FOR SCIENCE, TECHNOLOGY AND RESEARCH (SG) | 2012-04-12 | — | — | US | disclosed |
| EP-2412694-A1 | PROCESS FOR PRODUCING OPTICALLY ACTIVE ALCOHOL | Mitsui Chemicals, Inc. (JP) | 2012-02-01 | — | — | EP | disclosed |
| CN-101210017-A | Synthesis of middle position-tetraaryldiphenanthrene dioxyporphyrin derivative and application thereof | NANJING UNIVERSITY OF TECHNOLOGY (CN) | 2008-07-02 | — | — | CN | disclosed |
| US-6211374-B1 | REVERSE COLOR CHANGE; DISPLAYING | IPPOLITI JOSEPH THOMAS (US) | 2001-04-03 | — | — | US | disclosed |
| US-4536349-A | Furan derivatives useful as aroma compounds | NATIONAL DISTILLERS AND CHEMICAL CORPORATION (US) | 1985-08-20 | — | — | US | disclosed |
| US-4496767-A | REARRANGEMENT, ESTERIFICATION AND REDUCTION OF A FURAN-CARBINOL | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1985-01-29 | — | — | US | disclosed |
| US-4246178-A | CHEMICAL INTERMEDIATE FOR THE FLAVOR MALTOL | SHIN-ETSU CHEMICAL CO., LTD. (JP) | 1981-01-20 | — | — | 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 (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.
| Patent | Title | Text reads most about | Predicted target · text-rank |
|---|---|---|---|
| US-20120088938-A1 | METHOD FOR PRODUCING OPTICALLY ACTIVE ALCOHOL | ADH1A, ADH1C, FHIT | L3MBTL1 4093/4885KMT2A 1166/4885POLB 1884/4885 |
“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.