Cadaverine Tartrate

Cadaverine Tartrate

SCHEMBL5628833

CCC(C)n1cnc2c(NCc3ccccc3)nc(N[C@H]3CC[C@H](N)CC3)nc21.O=C(O)C(O)C(O)C(=O)O

nearest known ligand 0.69

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3CHRM1CHRM2CHRM3CHRM4ESR1ESR2GABRA1GABRB1GABRG2GBA1HRH1HTR1DHTR2AOPRD1OPRK1OPRM1SLC6A2SLC6A3TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8rplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of Cadaverine Tartrate. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
CCNE2 O96020 20/20 0.69
CCNE1 P24864 20/20 0.69
CDK2 P24941 20/20 0.69
CCNA2 P20248 19/20 0.69
CCNA1 P78396 19/20 0.69
CCNB2 O95067 1/20 0.61
CDK1 P06493 1/20 0.61
CDK4 P11802 1/20 0.61
CCNB1 P14635 1/20 0.61
CCND1 P24385 1/20 0.61
FLT3 P36888 1/20 0.61
CCNB3 Q8WWL7 1/20 0.61

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
Cadaverine Tartrate SCHEMBL5629659 0.94 CCNE2 (0.66) CCNE2CCNE1CDK2CCNA2CCNA1
SCHEMBL5195310 0.93 CCNE2 (0.77) CCNE2CCNE1CDK2CCNA2CCNA1
SCHEMBL5196149 0.93 CCNE2 (0.77) CCNE2CCNE1CDK2CCNA2CCNA1
SCHEMBL5195563 0.86 CCNE2 (0.75) CCNE2CCNE1CDK2CCNA2CCNA1
SCHEMBL5195558 0.86 CCNE2 (0.75) CCNE2CCNE1CDK2CCNA2CCNA1
SCHEMBL6821203 0.86 CCNE2 (0.90) CCNE2CCNE1CDK2CCNA2CCNA1
SCHEMBL6821200 0.86 CCNE2 (0.90) CCNE2CCNE1CDK2CCNA2CCNA1
Hydrochloric Acid SCHEMBL6820812 0.85 CCNE2 (0.88) CCNE2CCNE1CDK2CCNA2CCNA1
Hydrochloric Acid SCHEMBL6824017 0.85 CCNE2 (0.88) CCNE2CCNE1CDK2CCNA2CCNA1
Hydrochloric Acid SCHEMBL6820813 0.85 CCNE2 (0.88) CCNE2CCNE1CDK2CCNA2CCNA1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7208598-B2 Derivatives of purine, their preparation process and pharmaceutical compositions containing them AVENTIS PHARMA (FR) 2007-04-24 US disclosed
US-7122669-B1 Purine derivatives, preparation method and pharmaceutical compositions containing same HOECHST MARION ROUSSEL (FR) 2006-10-17 US disclosed
US-20050187228-A1 Derivatives of purine, their preparation process and pharmaceutical compositions containing them AVENTIS PHARMA S.A. 2005-08-25 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.

PatentTitleText reads most aboutPredicted target · text-rank
US-20050187228-A1 Derivatives of purine, their preparation process and pharmaceutical compositions containing them CDK6, CDK1, CDK2 CCNE2 34/4885CCNE1 4/4885CDK2 3/4885

“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.