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Peptide·modified or textual

ATLPC0008489

ATLPC0008489

HSDGIFTDSYSRYRKQMAVKKYLAAVL-NH2

Routes
Compare in workbenchDownload releaseAPI JSON
  • Length
    28 aa
On this page
  • 01 Sequence & molecular identity
  • 02 Physicochemical profile
  • 03 Distribution / Barrier
  • 04 Evidence landscape
  • 05 Product context
  • 06 Identity & reference map
  • 07 Data access & reproducibility
Coveragecounts only · not riskATLPC0008489
  • Measurements
    11
  • Endpoints
    1
  • Domains
    1/5
  • Products
    —
  • No matrix stability evidence
  • No clearance evidence
  • No immunogenicity context
  • No sequence liability cues
Jump to domain

Open the matching evidence section below

All evidence index · 11
Exposure / Absorption
No evidence
Distribution / Barrier
11 measurements
Metabolic & Proteolytic Stability
No evidence
Excretion / Persistence
No evidence
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.

HSDGIFTDSYSRYRKQMAVKKYLAAVL-NH2
Identity summarySpecific molecular form represented
Identity status
Specific molecular form represented
Residues
28
Peptidoform features
1
Documented molecular forms
1
Representations
2
Documented molecular forms1 form linked to this peptide identity
FormTopologyModificationsConnectionsRepresentationsMeasurements
ATLPF0009298———Notation only—
Residue view
Residue display
28 residues
H1S2D3G4I5F6T7D8S9Y10S11R12Y13R14K15Q16M17A18V19K20K21Y22L23A24A25V26L27X28X
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 28
X

Reported token NH2 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.

modified or textual
Parent-residue sequence

Residue string used for positional interpretation when available.

HSDGIFTDSYSRYRKQMAVKKYLAAVLX
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

Distribution / Barrier

11 records

What is known about distribution, binding, permeability, or barrier crossing?

Evidence records
11
Complete canonical measurements and observations attached to this domain.
Endpoint scope
1
Formal ADMET endpoints represented for this peptide.
Matched-context analysis
5
Quantitative results that may be analysed only with scientifically compatible records.
Reported-result review
6
Qualitative, narrative, or review-first results interpreted in their source context.
Endpoints in scopeBBB penetration
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.
5
Interpret as reported
Qualitative, narrative, or review-first findings preserved in source context.
6
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.

·
BBB penetration11 records · 5 matched-context · 6 as reported · 0 context only · 0 review required
#ValueAnalysis useAssay / modelResult contextReference
1

0.059 min^-1

Eligible when experimental context matches

Efflux study (ICV) · blood-brain barrier

Result: Reported point value · Molecular form: not reported · kout · saturable · Source: Primary reference linked

Reference
2

11.8 min

Eligible when experimental context matches

Efflux study (ICV) · blood-brain barrier

Result: Reported point value · Molecular form: not reported · t1/2, brain · saturable · Source: Primary reference linked

Reference
3

76.9 %/g

Eligible when experimental context matches

HPLC · blood-brain barrier

Result: Reported point value · Molecular form: not reported · % injected dose · NA · Source: Primary reference linked

Reference
4

0.00213 mL/g/min

Eligible when experimental context matches

Intravenous injection (multiple time regression) · blood-brain barrier

Result: Reported point value · Molecular form: not reported · Kin · non saturable · Source: Primary reference linked

Reference
5

0.0141 mL/g

Eligible when experimental context matches

Intravenous injection (multiple time regression) · blood-brain barrier

Result: Reported point value · Molecular form: not reported · Vi · NA · Source: Primary reference linked

Reference
6

-1.42

Interpret as reported

Not specified

Result: Reported point value · Molecular form: not reported · Source: Primary reference linked

Reference
7

76.9 %/g

Interpret as reported

Not specified

Result: Reported point value · Molecular form: not reported · Source: Primary reference linked

Reference
8

0.00213 mL/g/min

Interpret as reported

NA · NA · blood-brain barrier

Result: Reported point value · Molecular form: not reported · Route: Intravenous · non saturable · Source: Primary reference linked

Reference
9

0.0141 mL/g

Interpret as reported

NA · NA · blood-brain barrier

Result: Reported point value · Molecular form: not reported · Route: Intravenous · Permeability · Source: Primary reference linked

Reference
10

0.059 min^-1

Interpret as reported

NA · NA · blood-brain barrier

Result: Reported point value · Molecular form: not reported · Route: NA · saturable · Source: Primary reference linked

Reference
1–10 / 11
Barrier and permeability assay context

PAMPA, Caco-2, MDCK/RRCK, and BBB findings are assay/model contexts under Distribution / Barrier. They should not be read as interchangeable measurements.

PAMPA
0

artificial membrane

Caco-2
0

cell monolayer

MDCK
0

cell monolayer

RRCK
0

cell monolayer

BBB
11

barrier evidence

04

Evidence landscape

11 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
11 evidence records
5
6
0
0
Metabolic & Proteolytic Stability
0 evidence records
0
0
0
0
Excretion / Persistence
0 evidence records
0
0
0
0
Toxicity / Safety
0 evidence records
0
0
0
0
Endpoint distribution

Top evidence-bearing endpoint questions.

Blood Brain Barrier Penetration
11
Assay context

Broad context buckets, useful before comparing values.

Matrix / stability
5
In vivo / route
4
Unspecified
2
Traceability

Reference-link availability for measurement-level audit.

Linked reference
11
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
Distribution / Barrier
Distribution
Blood Brain Barrier Penetration
0.059 min^-1
Reported point valueInterpret as reportedNA · blood-brain barrierRoute: NA
Reference
Primary reference linked
2
Distribution / Barrier
Distribution
Blood Brain Barrier Penetration
-1.42
Reported point valueInterpret as reportedNot specifiedNot specified
Reference
Primary reference linked
3
Distribution / Barrier
Distribution
Blood Brain Barrier Penetration
0.002 mL/g/min
Reported point valueInterpret as reportedNA · blood-brain barrierRoute: Intravenous
Reference
Primary reference linked
4
Distribution / Barrier
Distribution
Blood Brain Barrier Penetration
0.014 mL/g
Reported point valueInterpret as reportedNA · blood-brain barrierRoute: Intravenous
Reference
Primary reference linked
5
Distribution / Barrier
Distribution
Blood Brain Barrier Penetration
11.8 min
Reported point valueInterpret as reportedNA · blood-brain barrierRoute: NA
Reference
Primary reference linked
6
Distribution / Barrier
Distribution
Blood Brain Barrier Penetration
76.9 %/g
Reported point valueInterpret as reportedNot specifiedNot specified
Reference
Primary reference linked
7
Distribution / Barrier
Distribution
Blood Brain Barrier Penetration
0.014 mL/g
Reported point valueEligible when experimental context matchesIntravenous injection (multiple time regression) · blood-brain barrierNot specified
Reference
Primary reference linked
8
Distribution / Barrier
Distribution
Blood Brain Barrier Penetration
76.9 %/g
Reported point valueEligible when experimental context matchesHPLC · blood-brain barrierNot specified
Reference
Primary reference linked
9
Distribution / Barrier
Distribution
Blood Brain Barrier Penetration
0.059 min^-1
Reported point valueEligible when experimental context matchesEfflux study (ICV) · blood-brain barrierNot specified
Reference
Primary reference linked
10
Distribution / Barrier
Distribution
Blood Brain Barrier Penetration
11.8 min
Reported point valueEligible when experimental context matchesEfflux study (ICV) · blood-brain barrierNot specified
Reference
Primary reference linked
1–10 / 11
05

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
06

Identity & reference map

11 sources

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

·
Summary1 reference group
Identity type
reported modified sequence
Reported notation
0
Reference groups
1
Measurements
11
ATL peptide ID
ATLPC0008489
Identity concordance
Identity concordance
Exact reported notation

Reported sequence string matches the current peptide notation.

0 / 11
Parent-residue compatible

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

0 / 11
Different notation

Reported notation does not resolve to the current display sequence.

0 / 11
Source sequence not captured

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

11 / 11
Reported sequence notation

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

Current identity
HSDGIFTDSYSRYRKQMAVKKYLAAVL-NH2
Reported names
No distinct human-readable aliases are exposed.
Reference map1 reference group
Reference map

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

ReferenceSupportsReported identityRecords
Reference
Open
Distribution
Blood Brain Barrier Penetration
No reported alias
11 identity
11 evidence
07

Data access & reproducibility

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

·
Record scopePublic release
ATL peptide ID
ATLPC0008489
Identity type
reported modified sequence
ADMET endpoints
1
Evidence records
11
Reference groups
1
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/ATLPC0008489
open
curl -sS 'https://admetatlas.scbdd.com/api/v1/peptides/ATLPC0008489' \
  -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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