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  3. ATLPC0031376
Peptide·plain sequence-like

ATLPC0031376

ATLPC0031376

VDKPPYLPRPRPPROIYNO

Routes
Compare in workbenchDownload releaseAPI JSON
  • Length
    19 aa
On this page
  • 01 Sequence & molecular identity
  • 02 Physicochemical profile
  • 03 Metabolic & Proteolytic Stability
  • 04 Excretion / Persistence
  • 05 Evidence landscape
  • 06 Product context
  • 07 Identity & reference map
  • 08 Data access & reproducibility
Coveragecounts only · not riskATLPC0031376
  • Measurements
    6
  • Endpoints
    2
  • Domains
    2/5
  • Products
    —
  • 1 stability measurement
  • 5 clearance measurements
  • No immunogenicity context
  • No sequence liability cues
Jump to domain

Open the matching evidence section below

All evidence index · 6
Exposure / Absorption
No evidence
Distribution / Barrier
No evidence
Metabolic & Proteolytic Stability
1 measurement
Excretion / Persistence
5 measurements
Toxicity / Safety
No evidence
01

Sequence & molecular identity

1 forms

Reviewed sequence, peptidoform forms, chemical representation, 3D references, and covalent topology used to interpret this peptide identity.

Sequence & peptidoform

·
Identity view

A peptidoform is one specific molecular form of the peptide — its sequence plus the modifications at given positions (HUPO-PSI term). This view preserves the reported terminal groups, residue modifications, and stereo markers from the source notation.

VDKPPYLPRPRPPROIYNO
Identity summarySpecific molecular form represented
Identity status
Specific molecular form represented
Residues
19
Peptidoform features
2
Documented molecular forms
1
Representations
2
Documented molecular forms1 form linked to this peptide identity
FormTopologyModificationsConnectionsRepresentationsMeasurements
ATLPF0034080———Notation only6
Residue view
Residue display
19 residues
V1D2K3P4P5Y6L7P8R9P10R11P12P13R14X15XI16Y17N18X19X
Side-chain classNonpolarPolarBasic (+)Acidic (−)Modified

Soft tints mark standard side-chain classes for scanning. Primary emphasis is reserved for reported modifications, termini, secondary-structure tracks, and topology links.

Peptidoform features

Features are shown only when a reported notation or topology record supports them.

Non-standard residue tokenpos 15
X

Reported token O is not one of the 20 standard residue symbols in this display.

Non-standard residue tokenpos 19
X

Reported token O is not one of the 20 standard residue symbols in this display.

Reported sequence notation was converted to parent-residue display for visualization; the original notation remains shown below.

Structure & chemistry

·
Chemical representationsequence / HELM only
Representation class

How the current release can interpret this identity chemically.

plain sequence-like
Parent-residue sequence

Residue string used for positional interpretation when available.

VDKPPYLPRPRPPRXIYNX
HELM

Polymer notation for modified peptide representation when available.

Not available
SMILES

Chemical graph string used for atom-level 2D depiction when available.

Not available
No atom-level graph

A reviewed SMILES is required before a 2D molecular depiction can be shown. Sequence and HELM remain useful for identity interpretation, but they do not replace a chemical graph.

3D structure referencesnone attached
3D structure not available

A 3D structure isn't available for this peptide in the current release. Chemistry and topology fields remain available when represented by sequence, HELM, or SMILES.

Covalent topology & modificationsnone
Exact topology not established

No reviewed form-level topology or residue-level connection annotation is attached to this peptide in the current release. This is not evidence that every molecular form is linear or unmodified.

02

Physicochemical profile

Computed sequence-derived descriptors and any measured physicochemical evidence such as lipophilicity. Computed values are interpretation aids, not experimental ADMET measurements.

Physicochemical descriptors unavailable

These descriptors require a standard parent-residue sequence. The module remains visible so modified or unresolved identities are not forced into unreliable computed values.

03

Metabolic & Proteolytic Stability

1 records

How stable is the peptide in biological matrices or protease systems?

Evidence records
1
Complete canonical measurements and observations attached to this domain.
Endpoint scope
1
Formal ADMET endpoints represented for this peptide.
Matched-context analysis
0
Quantitative results that may be analysed only with scientifically compatible records.
Reported-result review
1
Qualitative, narrative, or review-first results interpreted in their source context.
Endpoints in scopeSerum/plasma stability
Evidence interpretation

Result type, analysis use, and source-check status are kept separate so a numerical value is not mistaken for a universally comparable result.

Eligible for matched-context analysis
Quantitative results whose endpoint and context must still be matched before analysis.
0
Interpret as reported
Qualitative, narrative, or review-first findings preserved in source context.
1
Supporting context only
Reference, label, clinical, or supporting context for interpretation.
0
Review before analysis
Records whose present structure does not establish a safe analysis role.
0
Evidence by endpoint

Rows are grouped by endpoint so value, assay context, interpretation layer, and reference can be checked in place.

·
Serum/plasma stability1 record · 0 matched-context · 1 as reported · 0 context only · 0 review required
#ValueAnalysis useAssay / modelResult contextReference
1
Observation

Medium Stable

Interpret as reported

RP-HPLC · mouse · Mouse blood/plasma/serum

Result: Qualitative or narrative result · Molecular form: ATLPF0034080 · Dose/window: 31.5 μmol/L · Time: Aliquots (20 or 40 μL) taken after 0 and 60 min (0, 10 and 30 min for Api88) · Mouse blood/plasma/serum protease · In Vitro · Source: Primary reference linked

Reference
04

Excretion / Persistence

5 records

What evidence describes clearance or persistence?

Evidence records
5
Complete canonical measurements and observations attached to this domain.
Endpoint scope
1
Formal ADMET endpoints represented for this peptide.
Matched-context analysis
4
Quantitative results that may be analysed only with scientifically compatible records.
Reported-result review
1
Qualitative, narrative, or review-first results interpreted in their source context.
Endpoints in scopeHalf Life
Evidence interpretation

Result type, analysis use, and source-check status are kept separate so a numerical value is not mistaken for a universally comparable result.

Eligible for matched-context analysis
Quantitative results whose endpoint and context must still be matched before analysis.
4
Interpret as reported
Qualitative, narrative, or review-first findings preserved in source context.
1
Supporting context only
Reference, label, clinical, or supporting context for interpretation.
0
Review before analysis
Records whose present structure does not establish a safe analysis role.
0
Evidence by endpoint

Rows are grouped by endpoint so value, assay context, interpretation layer, and reference can be checked in place.

·
Half Life5 records · 4 matched-context · 1 as reported · 0 context only · 0 review required
#ValueAnalysis useAssay / modelResult contextReference
1

systemic pk half life unspecified phase: 43 Minutes

2580 seconds
Eligible when experimental context matches

LC-MS · mouse · CD-1 mice plasma

Result: Reported point value · Molecular form: ATLPF0034080 · Route: SC · Dose/window: 4.34 mmol/kg · Time: Prodrug and Onc72 concentrations were determined 5 min, 15 min, 30 min, 1 h, 2 h, 4 h, 8 h, and 24 h postadmi... · CD-1 mice plasma protease · In Vivo · Source: Primary reference linked

Reference
2

systemic pk half life unspecified phase: 43 Minutes

2580 seconds
Eligible when experimental context matches

LC-MS · mouse · CD-1 mice plasma

Result: Reported point value · Molecular form: ATLPF0034080 · Route: SC · Dose/window: 4.34 mmol/kg · Time: Prodrug and Onc72 concentrations were determined 5 min, 15 min, 30 min, 1 h, 2 h, 4 h, 8 h, and 24 h postadmi... · CD-1 mice plasma protease · In Vivo · Source: Primary reference linked

Reference
3

systemic pk half life unspecified phase: 43 Minutes

2580 seconds
Eligible when experimental context matches

LC-MS · mouse · CD-1 mice plasma

Result: Reported point value · Molecular form: ATLPF0034080 · Route: SC · Dose/window: 4.34 mmol/kg · Time: Prodrug and Onc72 concentrations were determined 5 min, 15 min, 30 min, 1 h, 2 h, 4 h, 8 h, and 24 h postadmi... · CD-1 mice plasma protease · In Vivo · Source: Primary reference linked

Reference
4

systemic pk half life unspecified phase: 43 Minutes

2580 seconds
Eligible when experimental context matches

LC-MS · mouse · CD-1 mice plasma

Result: Reported point value · Molecular form: ATLPF0034080 · Route: SC · Dose/window: 4.34 mmol/kg · Time: Prodrug and Onc72 concentrations were determined 5 min, 15 min, 30 min, 1 h, 2 h, 4 h, 8 h, and 24 h postadmi... · CD-1 mice plasma protease · In Vivo · Source: Primary reference linked

Reference
5

~ 4800 seconds

Interpret as reported

RP-HPLC · E. coli BW25113 cell lysate

Result: Approximate quantitative measurement · Molecular form: ATLPF0034080 · Dose/window: 31.5 μmol/L · Time: Aliquots weretaken in triplicates after 0, 1, 2, 4, and 8 h for Onc72 and 0, 4, 8, and 24 hfor both prodrugs · Cell lysate protease (Obtained From An E. Coli Bw25113 Culture) · In Vitro · Source: Primary reference linked

Reference
05

Evidence landscape

6 records

Cross-domain evidence distribution and measurement-level detail; the domain modules above show evidence in context, and every row remains available for audit here.

Evidence landscape

A cross-domain view of evidence volume, scientifically permitted analysis use, and source traceability.

ADMET domain
Eligible when context matches
Interpret as reported
Supporting context only
Review before analysis
Exposure / Absorption
0 evidence records
0
0
0
0
Distribution / Barrier
0 evidence records
0
0
0
0
Metabolic & Proteolytic Stability
1 evidence record
0
1
0
0
Excretion / Persistence
5 evidence records
4
1
0
0
Toxicity / Safety
0 evidence records
0
0
0
0
Endpoint distribution

Top evidence-bearing endpoint questions.

Half Life
5
Serum Plasma Stability
1
Assay context

Broad context buckets, useful before comparing values.

In vivo / route
5
Matrix / stability
1
Traceability

Reference-link availability for measurement-level audit.

Linked reference
6
Not linked
0
All evidence index

Every evidence record remains available for audit and drilldown. Counts describe evidence volume, not confidence.

#ADMET domainEndpointReported valueResult typeAnalysis useAssay / modelConditionReference
1
Metabolic & Proteolytic Stability
Stability
Serum Plasma Stability
Observation

Medium Stable

Qualitative or narrative resultInterpret as reportedRP-HPLC · mouse · Mouse blood/plasma/serumTime: Aliquots (20 or 40 μL) taken after 0 and 60 min (0, 10 and 30 min for Api88) · Dose/window: 31.5 μmol/L · Protease: Mouse blood/plasma/serum protease · In Vitro
Reference
Primary reference linked
2
Excretion / Persistence
Persistence
Half Life
43 Minutes
2,580 seconds
Result metric: SYSTEMIC_PK_HALF_LIFE_UNSPECIFIED_PHASE
Reported point valueEligible when experimental context matchesLC-MS · mouse · CD-1 mice plasmaRoute: SC · Time: Prodrug and Onc72 concentrations were determined 5 min, 15 min, 30 min, 1 h, 2 h, 4 h, 8 h, and 24 h postadministration · Dose/window: 4.34 mmol/kg · Protease: CD-1 mice p...
Reference
Primary reference linked
3
Excretion / Persistence
Persistence
Half Life
43 Minutes
2,580 seconds
Result metric: SYSTEMIC_PK_HALF_LIFE_UNSPECIFIED_PHASE
Reported point valueEligible when experimental context matchesLC-MS · mouse · CD-1 mice plasmaRoute: SC · Time: Prodrug and Onc72 concentrations were determined 5 min, 15 min, 30 min, 1 h, 2 h, 4 h, 8 h, and 24 h postadministration · Dose/window: 4.34 mmol/kg · Protease: CD-1 mice p...
Reference
Primary reference linked
4
Excretion / Persistence
Persistence
Half Life
43 Minutes
2,580 seconds
Result metric: SYSTEMIC_PK_HALF_LIFE_UNSPECIFIED_PHASE
Reported point valueEligible when experimental context matchesLC-MS · mouse · CD-1 mice plasmaRoute: SC · Time: Prodrug and Onc72 concentrations were determined 5 min, 15 min, 30 min, 1 h, 2 h, 4 h, 8 h, and 24 h postadministration · Dose/window: 4.34 mmol/kg · Protease: CD-1 mice p...
Reference
Primary reference linked
5
Excretion / Persistence
Persistence
Half Life
43 Minutes
2,580 seconds
Result metric: SYSTEMIC_PK_HALF_LIFE_UNSPECIFIED_PHASE
Reported point valueEligible when experimental context matchesLC-MS · mouse · CD-1 mice plasmaRoute: SC · Time: Prodrug and Onc72 concentrations were determined 5 min, 15 min, 30 min, 1 h, 2 h, 4 h, 8 h, and 24 h postadministration · Dose/window: 4.34 mmol/kg · Protease: CD-1 mice p...
Reference
Primary reference linked
6
Excretion / Persistence
Persistence
Half Life
~ 4,800 seconds
Approximate quantitative measurementInterpret as reportedRP-HPLC · E. coli BW25113 cell lysateTime: Aliquots weretaken in triplicates after 0, 1, 2, 4, and 8 h for Onc72 and 0, 4, 8, and 24 hfor both prodrugs · Dose/window: 31.5 μmol/L · Protease: Cell lysate protease (Obtained From...
Reference
Primary reference linked
1–6 / 6
06

Product context

Product-level route, label, and clinical context that frames peptide-level evidence. A peptide-level summary only; product pages keep the full drilldown.

No product association in this release

This peptide is currently interpreted from sequence, structure, physicochemical, and ADMET evidence only.

Browse products
07

Identity & reference map

6 sources

Reference-level support for checking reported names, sequence notation, and peptide identity agreement.

·
Summary2 reference groups
Identity type
identity record
Reported notation
0
Reference groups
2
Measurements
6
ATL peptide ID
ATLPC0031376
Identity concordance
Identity concordance
Exact reported notation

Reported sequence string matches the current peptide notation.

0 / 6
Parent-residue compatible

Reported notation differs, but resolves to the same parent-residue display.

0 / 6
Different notation

Reported notation does not resolve to the current display sequence.

0 / 6
Source sequence not captured

No source-specific sequence was captured for comparison; this is not interpreted as agreement or disagreement.

6 / 6
Reported sequence notation

No source-specific sequence notation has been captured in the current identity references.

Current identity
VDKPPYLPRPRPPROIYNO
Reported names
No distinct human-readable aliases are exposed.
Reference map2 reference groups
Reference map

Grouped by reference link, with endpoint scope and reported identity kept visible.

ReferenceSupportsReported identityRecords
Reference
Open
Persistence
Half Life
No reported alias
5 identity
5 evidence
Reference
Open
Stability
Serum Plasma Stability
No reported alias
1 identity
1 evidence
08

Data access & reproducibility

Stable record access, analysis-ready files, and scripted retrieval for reproducing this profile view.

·
Record scopePublic release
ATL peptide ID
ATLPC0031376
Identity type
identity record
ADMET endpoints
2
Evidence records
6
Reference groups
2
Release view
Public release
Data access

Structured peptide profile

JSON

Peptide-specific profile used by this page, including identity and evidence context.

Open JSON

Peptide catalogue

TSV

Complete frozen peptide table. Filter the ATL peptide ID column locally to isolate this record.

Download catalogue

Measurement catalogue

TSV

Complete frozen measurement table. Join or filter by ATL peptide ID for peptide-level analysis.

Download measurements
Programmatic access

The request returns the same structured peptide record used by this profile. The tabular downloads are complete frozen release tables and should be filtered locally by ATL peptide ID.

Open endpoint
GET /api/v1/peptides/ATLPC0031376
open
curl -sS 'https://admetatlas.scbdd.com/api/v1/peptides/ATLPC0031376' \
  -H 'accept: application/json' \
  -H 'X-Visibility: public_release'
ADMETatlas
peptide evidence atlas

ADMETatlas is an open, curated atlas of ADMET evidence for therapeutic peptides — spanning developability, membrane permeability and blood–brain-barrier transport, immune-recognition context, and approved-product context. Every measurement stays linked to its original source, with stable identifiers and transparent curation, so results can be traced, cited, and reproduced.

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