SCHEMBL1459360

SCHEMBL1459360

O=C(c1ccc(Cl)cc1)c1c(Cl)cc(CO)cc1Cl

nearest known ligand 0.49

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 2/20 0.49
GALR3 O60755 1/20 0.49
CYP3A4 P08684 1/20 0.49
CYP2C9 P11712 1/20 0.49
NR2F2 P24468 1/20 0.49
HIF1A Q16665 1/20 0.49
SRD5A2 P31213 3/20 0.47
MAPK1 P28482 1/20 0.47
CES2 O00748 1/20 0.43
CES1 P23141 1/20 0.43
GSK3B P49841 2/20 0.42
HPGD P15428 2/20 0.42
ALOX15 P16050 1/20 0.42
TSHR P16473 1/20 0.42
NPC1 O15118 1/20 0.42
RAB9A P51151 1/20 0.42
MAPT P10636 2/20 0.41
L3MBTL1 Q9Y468 2/20 0.41
KDM4E B2RXH2 1/20 0.41
ALDH1A1 P00352 1/20 0.41

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
SCHEMBL1459380 0.89 GALR3 (0.49) SMN1; SMN2GALR3CYP3A4CYP2C9NR2F2
SCHEMBL7265825 0.84 GSK3B (0.48) SMN1; SMN2GALR3CYP3A4CYP2C9NR2F2
SCHEMBL7015674 0.80 SRD5A2 (0.59) SRD5A2MAPK1CES2CES1GSK3B
SCHEMBL4746218 0.79 MAPK1 (0.63) CYP3A4SRD5A2MAPK1CES2CES1
SCHEMBL7264321 0.77 CES2 (0.53) SRD5A2MAPK1CES2CES1HPGD
SCHEMBL1460161 0.77 SRD5A2 (0.50) SMN1; SMN2GALR3CYP3A4CYP2C9NR2F2
SCHEMBL14706277 0.76 GALR3 (0.43) SMN1; SMN2GALR3CYP3A4CYP2C9NR2F2
SCHEMBL543118 0.74 SMN1; SMN2 (0.44) SMN1; SMN2MAPK1HPGDTSHRNPC1
SCHEMBL11850279 0.74 SRD5A2 (0.56) SRD5A2MAPK1CES2CES1GSK3B
SCHEMBL4288308 0.74 HPGD (0.50) CYP3A4MAPK1HPGDNPC1RAB9A

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
EP-2963023-B1 PROCESS FOR PREPARING 5-AMINO-1, 2, 3-TRIAZOLE OROTATE DERIVATIVES TACTICAL THERAPEUTICS INC (US) 2018-04-18 EP claimed
EP-2963023-A1 PROCESS FOR PREPARING 5-AMINO-1, 2, 3-TRIAZOLE OROTATE DERIVATIVES Tactical Therapeutics Inc. (US) 2016-01-06 EP claimed
US-8912223-B2 Compositions and processes for preparing 5-amino or substituted amino 1,2,3-triazoles and triazoles orotate formulations TACTICAL THERAPEUTICS INC (US) 2014-12-16 US claimed
US-20140200247-A1 Novel compositions and processes for preparing 5-amino or substituted amino 1,2,3-triazoles and triazoles orotate formulations KARMALI RASHIDA A (US) 2014-07-17 US claimed
CN-119977778-A Preparation method of carboxyamidotriazole intermediate 广东银珠医药科技有限公司 2025-05-13 CN disclosed
CN-112358451-B Synthetic method of carboxyamidotriazole 广东银珠医药科技有限公司 2021-04-13 CN disclosed
CN-112358451-A Synthetic method of carboxyamidotriazole 广东银珠医药科技有限公司 2021-02-12 CN disclosed
EP-2963023-B1 PROCESS FOR PREPARING 5-AMINO-1, 2, 3-TRIAZOLE OROTATE DERIVATIVES TACTICAL THERAPEUTICS INC (US) 2018-04-18 EP disclosed
EP-2473051-B1 NOVEL COMPOSITIONS AND PROCESSES FOR PREPARING 5-AMINO OR SUBSTITUTED AMINO 1,2,3-TRIAZOLES AND TRIAZOLE OROTATE FORMULATIONS TACTICAL THERAPEUTICS INC (US) 2016-02-10 EP disclosed
EP-2963023-A1 PROCESS FOR PREPARING 5-AMINO-1, 2, 3-TRIAZOLE OROTATE DERIVATIVES Tactical Therapeutics Inc. (US) 2016-01-06 EP disclosed
US-8912223-B2 Compositions and processes for preparing 5-amino or substituted amino 1,2,3-triazoles and triazoles orotate formulations TACTICAL THERAPEUTICS INC (US) 2014-12-16 US disclosed
US-8912223-B2 Compositions and processes for preparing 5-amino or substituted amino 1,2,3-triazoles and triazoles orotate formulations TACTICAL THERAPEUTICS INC (US) 2014-12-16 US disclosed
WO-2011028288-A1 NOVEL COMPOSITIONS AND PROCESSES FOR PREPARING 5-AMINO OR SUBSTITUTED AMINO 1,2,3-TRIAZOLES AND TRIAZOLE OROTATE FORMULATIONS Tactical Therapeutics, Inc (US) 2011-03-10 WO disclosed
US-20110060142-A1 Novel compositions and processes for preparing 5-amino or substituted amino 1,2,3-triazoles and triazole orotate formulations Tactical Therapeutics, Inc 2011-03-10 US disclosed
US-20110060142-A1 Novel compositions and processes for preparing 5-amino or substituted amino 1,2,3-triazoles and triazole orotate formulations Tactical Therapeutics, Inc 2011-03-10 US disclosed
US-20110060142-A1 Novel compositions and processes for preparing 5-amino or substituted amino 1,2,3-triazoles and triazole orotate formulations Tactical Therapeutics, Inc 2011-03-10 US disclosed
EP-0304221-B1 5-amino or substituted amino 1,2,3-triazoles useful as antiproliferative agents MERCK & CO INC (US) 1994-02-16 EP disclosed
US-5045543-A Treatment of cancer with high probability of metastasis MERCK & CO., INC. (US) 1991-09-03 US disclosed
US-4847257-A PSORIASIS MERCK & CO., INC. (US) 1989-07-11 US disclosed
EP-0304221-A2 5-amino or substituted amino 1,2,3-triazoles useful as antiproliferative agents MERCK & CO. INC. (US) 1989-02-22 EP 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.

PatentTitleText reads most aboutPredicted target · text-rank
US-20110060142-A1 Novel compositions and processes for preparing 5-amino or substituted amino 1,2,3-triazoles and triazole orotate formulations MCL1, MALT1, MYD88 SMN1; SMN2 1028/4885GALR3 489/4885CYP3A4 232/4885
US-20140200247-A1 Novel compositions and processes for preparing 5-amino or substituted amino 1,2,3-triazoles and triazoles orotate formulations MCL1, MALT1, ABAT SMN1; SMN2 773/4885GALR3 467/4885CYP3A4 106/4885

“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.