SCHEMBL5346750

SCHEMBL5346750

Cn1nnc2c(C(=O)NC(C)(C)C)ncn2c1=O

nearest known ligand 0.64

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 1/20 0.64
PABPC1 P11940 1/20 0.64
KMT2A Q03164 1/20 0.64
CA12 O43570 3/20 0.55
CA1 P00915 3/20 0.55
CA2 P00918 3/20 0.55
CA9 Q16790 3/20 0.55
POLB P06746 1/20 0.44
MAPT P10636 1/20 0.44
RIPK1 Q13546 1/20 0.34
DPP4 P27487 1/20 0.34
PKM P14618 1/20 0.33
TP53 P04637 1/20 0.33
ALDH1A1 P00352 1/20 0.33
LMNA P02545 1/20 0.31

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
SCHEMBL25529330 0.86 MEN1 (0.61) MEN1PABPC1KMT2ACA12CA1
SCHEMBL891881 0.85 MEN1 (0.69) MEN1PABPC1KMT2ACA12CA1
SCHEMBL7876576 0.85 MEN1 (0.69) MEN1PABPC1KMT2ACA12CA1
SCHEMBL15788844 0.83 KMT2A (0.72) MEN1PABPC1KMT2ACA12CA1
SCHEMBL26911797 0.82 MEN1 (0.66) MEN1PABPC1KMT2ACA12CA1
SCHEMBL18737910 0.81 MEN1 (0.64) MEN1PABPC1KMT2ACA12CA1
SCHEMBL5355079 0.81 MEN1 (0.64) MEN1PABPC1KMT2ACA12CA1
SCHEMBL892401 0.81 MEN1 (0.77) MEN1PABPC1KMT2ACA12CA1
Hydrochloric Acid SCHEMBL1335355 0.80 MEN1 (0.75) MEN1PABPC1KMT2ACA12CA1
SCHEMBL5353245 0.80 MEN1 (0.75) MEN1PABPC1KMT2ACA12CA1

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 17 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20230303577-A1 TEMOZOLOMIDE ANALOGS AND METHODS OF USE ST. JOHN'S CANCER INSTITUTE (US) 2023-09-28 US disclosed
US-20230303577-A1 TEMOZOLOMIDE ANALOGS AND METHODS OF USE ST. JOHN'S CANCER INSTITUTE (US) 2023-09-28 US disclosed
WO-2022026756-A1 TEMOZOLOMIDE ANALOGS AND METHODS OF USE ST. JOHN'S CANCER INSTITUTE (US) 2022-02-03 WO disclosed
US-11014953-B2 Trigger-activatable metabolic sugar precursors for cancer-selective labeling and targeting THE BOARD OF TRUSTEES OF THE UNIVERSITY OF ILLINOIS (US) 2021-05-25 US disclosed
US-8258294-B2 Process for the preparation of temozolomide and analogs CIPLA LIMITED (IN) 2012-09-04 US disclosed
US-8232392-B2 Process for preparing temozolomide CHEMI S.P.A. (IT) 2012-07-31 US disclosed
US-8232392-B2 Process for preparing temozolomide CHEMI S.P.A. (IT) 2012-07-31 US disclosed
US-7737284-B2 Synthesis of temozolomide and analogs SCHERING PLOUGH CORP. (US) 2010-06-15 US disclosed
US-20100036121-A1 Process for preparing temozolomide CHEMI S.P.A. (IT) 2010-02-11 US disclosed
US-20100036121-A1 Process for preparing temozolomide CHEMI S.P.A. (IT) 2010-02-11 US disclosed
EP-2151442-A2 Process for preparing temozolomide Chemi SPA (IT) 2010-02-10 EP disclosed
US-20090326028-A1 Process for the preparation of temozolomide and analogs CIPLA LIMITED (IN) 2009-12-31 US disclosed
US-7612202-B2 Process for preparing temozolomide CHEMAGIS, LTD. (IL) 2009-11-03 US disclosed
US-20090023919-A1 SYNTHESIS OF TEMOZOLOMIDE AND ANALOGS SCHERING CORPORATION 2009-01-22 US disclosed
US-7446209-B2 Diazotizing a blocked 5-amino-1H-imidazole-4-carboxamide; hydrolysis; antitumor agents SCHERING CORPORATION (US) 2008-11-04 US disclosed
US-7173021-B2 Synthesis of temozolomide esters as potent anticancer pro-drugs for topical and transdermal applications in treatments of cancers TIANJIN NORTH PHARM SCI-TECH CO., LTD. (CN) 2007-02-06 US disclosed
US-20060047117-A1 Synthesis of temozolomide esters as potent anticancer pro-drugs for topical and transdermal applications in treatments of cancers TIANJIN NORTH PHARM SCI-TECH CO., LTD. (CN) 2006-03-02 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 (6 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-11014953-B2 Trigger-activatable metabolic sugar precursors for cancer-selective labeling and targeting GPI, SLC2A1, SLC2A4 MEN1 2008/4885PABPC1 2384/4885KMT2A 1397/4885
US-20060047117-A1 Synthesis of temozolomide esters as potent anticancer pro-drugs for topical and transdermal applications in treatments of cancers TET1, SLC16A1, ADH1A MEN1 222/4885PABPC1 4434/4885KMT2A 1472/4885
US-20090326028-A1 Process for the preparation of temozolomide and analogs IDH3A, IDH3B, IDH2 MEN1 81/4885PABPC1 4306/4885KMT2A 683/4885
US-20090023919-A1 SYNTHESIS OF TEMOZOLOMIDE AND ANALOGS MGMT, TYMS, MCL1 MEN1 42/4885PABPC1 2492/4885KMT2A 334/4885
US-20100036121-A1 Process for preparing temozolomide MGMT, NNMT, NOS2 MEN1 910/4885PABPC1 3423/4885KMT2A 248/4885
US-20230303577-A1 TEMOZOLOMIDE ANALOGS AND METHODS OF USE MGMT, TOP2B, IDH3B MEN1 882/4885PABPC1 2801/4885KMT2A 524/4885

“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.