Predicted protein targets (top 12)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | ALOX15 | P16050 | 2/20 | 0.59 |
| ▸ | TSHR | P16473 | 6/20 | 0.57 |
| ▸ | ALDH1A1 | P00352 | 4/20 | 0.57 |
| ▸ | CYP2C9 | P11712 | 3/20 | 0.57 |
| ▸ | CYP2D6 | P10635 | 8/20 | 0.53 |
| ▸ | MAPK1 | P28482 | 2/20 | 0.51 |
| ▸ | CYP3A4 | P08684 | 8/20 | 0.51 |
| ▸ | CYP2C19 | P33261 | 5/20 | 0.51 |
| ▸ | LTA4H | P09960 | 1/20 | 0.50 |
| ▸ | USP2 | O75604 | 2/20 | 0.49 |
| ▸ | CYP1A2 | P05177 | 2/20 | 0.49 |
| ▸ | SMN1; SMN2 | Q16637 | 1/20 | 0.45 |
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 | |
|---|---|---|---|---|
| SCHEMBL807362 | 0.98 | ALOX15 (0.58) | ALOX15TSHRALDH1A1CYP2C9CYP2D6 | |
| SCHEMBL30341042 | 0.91 | ALOX15 (0.55) | ALOX15TSHRALDH1A1CYP2C9CYP2D6 | |
| SCHEMBL16221501 | 0.86 | ALOX15 (0.51) | ALOX15TSHRALDH1A1CYP2C9CYP2D6 | |
| SCHEMBL13940681 | 0.86 | ALOX15 (0.51) | ALOX15TSHRALDH1A1CYP2C9CYP2D6 | |
| SCHEMBL14338850 | 0.85 | ALOX15 (0.56) | ALOX15TSHRALDH1A1CYP2C9CYP2D6 | |
| SCHEMBL6482630 | 0.85 | ALOX15 (0.56) | ALOX15TSHRALDH1A1CYP2C9CYP2D6 | |
| SCHEMBL211751 | 0.83 | ALOX15 (0.72) | ALOX15TSHRALDH1A1CYP2C9CYP2D6 | |
| SCHEMBL4914558 | 0.83 | ALOX15 (0.72) | ALOX15TSHRALDH1A1CYP2C9CYP2D6 | |
| SCHEMBL952226 | 0.83 | ALOX15 (0.55) | ALOX15TSHRALDH1A1CYP2C9CYP2D6 | |
| SCHEMBL6218968 | 0.82 | ALOX15 (0.54) | ALOX15TSHRALDH1A1CYP2C9CYP2D6 |
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 |
|---|---|---|---|---|---|---|---|
| US-12344600-B2 | c-Myc mRNA translation modulators and uses thereof in the treatment of cancer | ANIMA BIOTECH INC. (US) | 2025-07-01 | — | — | US | disclosed |
| US-20250109128-A1 | C-MYC MRNA TRANSLATION MODULATORS AND USES THEREOF IN THE TREATMENT OF CANCER | ANIMA BIOTECH INC. (US) | 2025-04-03 | — | — | US | disclosed |
| EP-3381918-B1 | 7-(THIAZOL-5-YL) PYRROLOPYRIMIDINE COMPOUND AS TLR7 AGONIST | CHIA TAI TIANQING PHARMACEUTICAL GROUP CO LTD (CN) | 2020-09-16 | — | — | EP | disclosed |
| US-10676478-B2 | 7-(thiazol-5-yl) pyrrolopyrimidine compound as TLR7 agonist | CHIA TAI TIANQING PHARMACEUTICAL GROUP CO., LTD. (CN) | 2020-06-09 | — | — | US | disclosed |
| US-10676478-B2 | 7-(thiazol-5-yl) pyrrolopyrimidine compound as TLR7 agonist | CHIA TAI TIANQING PHARMACEUTICAL GROUP CO., LTD. (CN) | 2020-06-09 | — | — | US | disclosed |
| CN-108349982-B | 7- (thiazol-5-yl) pyrrolopyrimidine compounds as TLR7 agonists | 正大天晴药业集团股份有限公司 | 2020-05-05 | — | — | CN | disclosed |
| US-20180370976-A1 | 7-(THIAZOL-5-YL) PYRROLOPYRIMIDINE COMPOUND AS TLR7 AGONIST | CHIA TAI TIANQING PHARMACEUTICAL GROUP CO., LTD. (CN) | 2018-12-27 | — | — | US | disclosed |
| EP-3381918-A1 | 7-(THIAZOL-5-YL) PYRROLOPYRIMIDINE COMPOUND AS TLR7 AGONIST | Chai Tai Tianqing Pharmaceutical Group Co., Ltd. (CN) | 2018-10-03 | — | — | EP | disclosed |
| CN-108349982-A | 7- (thiazole -5- bases) Pyrrolopyrimidine compounds as TLR7 agonists | 正大天晴药业集团股份有限公司 | 2018-07-31 | — | — | CN | disclosed |
| CN-107567445-A | It can be used as 2 phenyl 3H imidazos [4,5 B] pyridine derivates of mammal EGFR-TK ROR1 activities inhibitor | 坎塞拉有限公司 | 2018-01-09 | — | — | CN | disclosed |
| EP-2049542-B1 | PYRROLOTRIAZINE KINASE INHIBITORS | BRISTOL MYERS SQUIBB CO (US) | 2012-09-19 | — | — | EP | disclosed |
| US-7550486-B2 | N-ureidoalkyl-piperidines as modulators of chemokine receptor activity | BRISTOL-MYERS SQUIBB COMPANY (US) | 2009-06-23 | — | — | US | disclosed |
| US-20080132523-A1 | N-UREIDOALKYL-PIPERIDINES AS MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY | BRISTOL-MYERS SQUIBB COMPANY | 2008-06-05 | — | — | US | disclosed |
| EP-0711290-A1 | METHYLGUANIDINE DERIVATIVES, METHODS FOR PREPARING SAME AND COMPOSITIONS CONTAINING SAID DERIVATIVES | SANOFI (FR) | 1996-05-15 | — | — | EP | disclosed |
| WO-1995004052-A1 | METHYLGUANIDINE DERIVATIVES, METHODS FOR PREPARING SAME AND COMPOSITIONS CONTAINING SAID DERIVATIVES | SANOFI (FR) | 1995-02-09 | — | — | 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 (5 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-20180370976-A1 | 7-(THIAZOL-5-YL) PYRROLOPYRIMIDINE COMPOUND AS TLR7 AGONIST | TLR7, TLR9, TLR5 | ALOX15 3533/4885TSHR 705/4885ALDH1A1 1624/4885 |
| US-10676478-B2 | 7-(thiazol-5-yl) pyrrolopyrimidine compound as TLR7 agonist | TLR7, TLR9, TLR5 | ALOX15 3533/4885TSHR 705/4885ALDH1A1 1624/4885 |
| US-12344600-B2 | c-Myc mRNA translation modulators and uses thereof in the treatment of cancer | MYC, MYCBP, MYCBP2 | ALOX15 3870/4885TSHR 4347/4885ALDH1A1 4471/4885 |
| US-20080132523-A1 | N-UREIDOALKYL-PIPERIDINES AS MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY | ACKR3, CCR7, CCR2 | ALOX15 886/4885TSHR 1168/4885ALDH1A1 914/4885 |
| US-20250109128-A1 | C-MYC MRNA TRANSLATION MODULATORS AND USES THEREOF IN THE TREATMENT OF CANCER | MYC, MYCBP, MYCBP2 | ALOX15 3870/4885TSHR 4347/4885ALDH1A1 4471/4885 |
“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.